The DOI matches its Crossref record; 94 of the 96 references it cites were found in a registry or an index; 2 of the 223 sources its claims cite were checked for support.
Current and Future Treatments in Alzheimer Disease: An Update
Open accessAbstract
Disease-modifying treatment strategies for Alzheimer disease (AD) are still under extensive research. Nowadays, only symptomatic treatments exist for this disease, all trying to counterbalance the neurotransmitter disturbance: 3 cholinesterase inhibitors and memantine. To block the progression of the disease, therapeutic agents are supposed to interfere with the pathogenic steps responsible for the clinical symptoms, classically including the deposition of extracellular amyloid β plaques and intracellular neurofibrillary tangle formation. Other underlying mechanisms are targeted by neuroprotective, anti-inflammatory, growth factor promotive, metabolic efficacious agents and stem cell therapies. Recent therapies have integrated multiple new features such as novel biomarkers, new neuropsychological outcomes, enrollment of earlier populations in the course of the disease, and innovative trial designs. In the near future different specific agents for every patient might be used in a “precision medicine” context, where aberrant biomarkers accompanied with a particular pattern of neuropsychological and neuroimaging findings could determine a specific treatment regimen within a customized therapeutic framework. In this review, we discuss potential disease-modifying therapies that are currently being studied and potential individualized therapeutic frameworks that can be proved beneficial for patients with AD.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
This narrative review summarizes current FDA-approved symptomatic treatments for Alzheimer disease and the 2019 pipeline of disease-modifying and symptomatic agents. It emphasizes that no disease-modifying therapy is approved and that future treatment may move toward biomarker-guided precision medicine.
Key findings
Current approved pharmacotherapy remains symptomatic: the 3 AChEIs donepezil, galantamine, and rivastigmine plus the NMDA antagonist memantine; no new FDA drug for AD has been approved since 2003 and there are no approved DMTs.
- A clinicaltrials.gov search accessed August 19, 2019 found 165 recruiting or active-but-not-recruiting phase 1–3 AD trials; the February 2019 pipeline review cited found 132 agents in 156 trials (28 drugs in 42 phase 3 trials, 74 drugs in 83 phase 2 trials, and 30 drugs in 31 phase 1 trials), classified as 73% DMTs, 13% symptomatic cognitive enhancers, and 11% for BPSD.
- Anti-amyloid failures include semagacestat, bapineuzumab, solanezumab, and the BACE inhibitors lanabecestat, verubecestat, and atabecestat; BACE inhibitors reduced CSF Aβ42 dose-dependently but without cognitive or functional benefit.
- Tau-directed agents remain earlier-stage: only 1 tau-related agent was in phase 2/3, 10 in phase 2, and 5 in phase 1; other DMT mechanisms include neuroprotection, anti-inflammatory effects, growth factor promotion, metabolic effects, and stem cell therapies.
Methods
Design: narrative review of current nonpharmacological and pharmacological AD management, FDA-approved medications, BPSD treatments, and phase 1–3 investigational agents.
- Data/sample: literature review plus a clinicaltrials.gov search for recruiting or active-but-not-recruiting phase 1–3 AD trials accessed August 19, 2019 (165 outcomes), and citation of the February 2019 AD drug development pipeline review (132 agents in 156 trials).
- Analysis: narrative synthesis and classification of agents by proposed mechanism—amyloid-related, tau-related, other DMT mechanisms, and symptomatic—without a formal systematic review or meta-analysis described.
Limitations
Stated: no effective treatment options and no approved DMTs exist; many trial failures are attributed to starting therapy too late, inappropriate drug doses, wrong treatment targets, inadequate understanding of AD pathophysiology, and variability in diagnostic markers and endpoints.
- Evident from the text: this is a narrative review without a stated systematic search strategy, inclusion/exclusion criteria, or risk-of-bias assessment.
- Evident from the text: pipeline findings are a cross-sectional 2019 snapshot and efficacy claims for many agents are brief, based on cited trials or conference reports rather than independent quantitative synthesis.
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Claims the paper makes
172 Not checked yet · 4 Own interpretation · 3 Sources not found · 1 Supported so far · 1 Partly supported · 1 Own result · 1 No basis given · accuracy not yet measured
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“However, the clinical trials with the BACE inhibitors lanabecestat,32 verubecestat,33 and atabecestat34 have been recently discontinued due to unexpected difficulties.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [32] Burki T Alzheimer’s disease research: the future of BACE inhibitors. Lancet. 2018; 391: 2486. 29976459 source
- Supportedcites [33] Egan MF Kost J Voss T, et al Randomized trial of verubecestat for prodromal Alzheimer’s disease. N Engl J Med. 2019; 380: 1408- 1420. 30970186 PMC6776078 source
The Results (Patient Characteristics) state that the verubecestat trial was stopped in February 2018 on the data and safety monitoring committee’s recommendation because neither dose was expected to show superiority over placebo. This supports the verubecestat portion of the sentence, to which this citation is attached; it does not need to establish what happened in the separately cited lanabecestat and atabecestat trials. (LLM, conf=0.93)
- Not checked yetcites [34] Henley D Raghavan N Sperling R Aisen P Raman R Romano G Preliminary results of a trial of atabecestat in preclinical Alzheimer’s disease. N Engl J Med. 2019; 380: 1483- 1485. 30970197 source
plaindirect- Asserted: passes — The authors put it forward as true.
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“One of them, compound γ-AA26, seems almost 100-fold as efficient as the compound 18 of the KLVFF in the inhibition of the aggregation of Aβ42.52”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Partly supportedcites [52] Nimmagadda A Shi Y Cai J γ-AApeptides as a new strategy for therapeutic development. Curr Med Chem. 2019; 26: 2313- 2329. 29110596 PMC5936681 sourceExperimental — accuracy not yet measured
Section 6 reports that γ-AA26 was almost 100-fold as potent as KLVFF at inhibiting Aβ aggregation. It describes screening and binding tests with Aβ40, but does not specify Aβ42 for the inhibition comparison; it also calls the comparator P4 (KLVFF), not “compound 18.” (LLM, conf=0.88)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“A search for phases 1, 2, and 3 “recruiting” or “active but not recruiting” clinical trials for AD in clinicaltrials.gov (accessed August 19, 2019) showed 165 outcomes.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
None of the sources cited for this claim have been checked yet.
In the paper
“However, despite all arduous research efforts, at the moment, there are no effective treatment options for the disease.3,4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [3] Scheltens P Blennow K Breteler MMB, et al Alzheimer’s disease. Lancet. 2016; 388: 505- 517. 26921134 source
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“Initiation of AChEI treatment as soon as possible after the diagnosis is preferred as patients who started the AChEI 6 months later showed more rapid cognitive decline than those who started the drug immediately.17”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [17] Farlow M Anand R Messina J Hartman R Jr Veach J A 52-week study of the efficacy of rivastigmine in patients with mild to moderately severe Alzheimer’s disease. Eur Neurol. 2000; 44: 236- 241. 11096224 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“The elements of the cascade include local inflammation, oxidation, excitoxicity (excessive glutamate), and tau hyperphosphorylation.5”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“Progressive neuronal destruction leads to shortage and imbalance between various neurotransmitters (eg, acetylcholine, dopamine, serotonin) and to the cognitive deficiencies seen in AD.5”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“The basic pathophysiology and neuropathology of AD that drives the current research suggests that the primary histopathologic lesions of AD are the extracellular amyloid plaques and the intracellular Tau neurofibrillary tangles (NFTs).5”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
None of the sources cited for this claim have been checked yet.
In the paper
“All 3 AChEIs have proved their treatment benefits in delaying decline, stabilizing, or even improving cognition and activities of daily living in randomized placebo-controlled trials up to 52 weeks duration.10,18”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“In clinical trials, both Aβ and tau are prime targets for disease-modifying treatments (DMTs) in AD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [7] Hampel H Mesulam MM Cuello AC, et al The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease. Brain. 2018; 141: 1917- 1933. 29850777 PMC6022632 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 78
- Probably not a substantial claim. 16
- The quote only partly states this claim. 1
None of the sources cited for this claim have been checked yet.
In the paper
“Thus, AChEIs are contraindicated in conditions including severe cardiac arrhythmias, especially bradycardia or syncope. They are also contraindicated in active peptic ulcer or gastrointestinal bleeding history and uncontrolled seizures.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [17] Farlow M Anand R Messina J Hartman R Jr Veach J A 52-week study of the efficacy of rivastigmine in patients with mild to moderately severe Alzheimer’s disease. Eur Neurol. 2000; 44: 236- 241. 11096224
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“It is the forming of amyloid oligomers to which neurotoxicity is mainly attributed and initiates the amyloid cascade.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Memantine binds preferentially to open NMDA receptor–operated calcium channels blocking NMDA-mediated ion flux and ameliorating the dangerous effects of pathologically elevated glutamate levels that lead to neuronal dysfunction.8”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [8] Matsunaga S Kishi T Iwata N Memantine monotherapy for Alzheimer’s disease: a systematic review and meta-analysis. PLoS ONE. 2015; 10:e0123289. PMC4393306 25860130
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Further decline occurs, but even temporary discontinuation of these drugs results in rapid decline and is associated with greater risk of nursing home placement.16”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [16] Howard R McShane R Lindesay J, et al Nursing home placement in the donepezil and memantine in moderate to severe Alzheimer’s disease (DOMINO-AD) trial: secondary and post-hoc analyses. Lancet Neurol. 2015; 14: 1171- 1181. 26515660
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Memantine is a noncompetitive low-affinity NMDA-receptor open-channel blocker and affects glutamatergic transmission.5”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Donepezil and rivastigmine have been approved by FDA for mild, moderate, and severe AD, whereas galantamine for mild and moderate AD.18”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, AChEIs enhance central cholinergic neurotransmission and finally tend to mitigate decline in cognition at least during the first year of treatment.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Although in the amyloid hypothesis, tau hyperphosphorylation was thought to be a downstream event of Aβ deposition, it is equally probable that tau and Aβ act in parallel pathways causing AD and enhancing each other’s toxic effects.3”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [3] Scheltens P Blennow K Breteler MMB, et al Alzheimer’s disease. Lancet. 2016; 388: 505- 517. 26921134 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“According to the “amyloid hypothesis” Aβ production in the brain initiates a cascade of events leading to the clinical syndrome of AD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Pharmacokinetic characteristics differ among AChEIs: the primary route of elimination for donepezil and galantamine is hepatic metabolism, whereas for rivastigmine is liver and intestine metabolism.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
- Not checked yetcites [17] Farlow M Anand R Messina J Hartman R Jr Veach J A 52-week study of the efficacy of rivastigmine in patients with mild to moderately severe Alzheimer’s disease. Eur Neurol. 2000; 44: 236- 241. 11096224
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“From this point of view, AD could be prevented or effectively treated by decreasing the production of Aβ and tau; preventing aggregation or misfolding of these proteins; neutralizing or removing the toxic aggregate or misfolded forms of these proteins; or a combination of these modalities.7”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [7] Hampel H Mesulam MM Cuello AC, et al The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease. Brain. 2018; 141: 1917- 1933. 29850777 PMC6022632 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The AChEIs increase the availability of acetylcholine at synapses and have been proven clinically useful in delaying the cognitive decline in AD.7”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction
What the sources say
- Not checked yetcites [7] Hampel H Mesulam MM Cuello AC, et al The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease. Brain. 2018; 141: 1917- 1933. 29850777 PMC6022632 source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Donepezil and galantamine inhibit selectively and reversibly the acetylcholinesterase, whereas rivastigmine is a “pseudo-irreversible” inhibitor of acetylcholinesterase and butyrylcholinesterase.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
- Not checked yetcites [17] Farlow M Anand R Messina J Hartman R Jr Veach J A 52-week study of the efficacy of rivastigmine in patients with mild to moderately severe Alzheimer’s disease. Eur Neurol. 2000; 44: 236- 241. 11096224
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The AChEIs may also trigger bradycardia and increase the risk of syncope.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [17] Farlow M Anand R Messina J Hartman R Jr Veach J A 52-week study of the efficacy of rivastigmine in patients with mild to moderately severe Alzheimer’s disease. Eur Neurol. 2000; 44: 236- 241. 11096224
- Not checked yetcites [18] Rountree SD Atri A Lopez OL Doody RS Effectiveness of antidementia drugs in delaying Alzheimer disease progression. Alzheimers Dement. 2013; 9: 338- 345. 23102979 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The most popular and broadly accepted explanations for the multiple failures of clinical trials of DMT agents for AD include the too late starting of therapies in disease development, the inappropriate drug doses, the wrong main target of the treatment, and mainly an inadequate understanding of the pathophysiology of AD.35”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [35] Gauthier S Albert M Fox N, et al Why has therapy development for dementia failed in the last two decades. Alzheimers Dement. 2016; 12: 60- 64. 26710325
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The DMT agents were further separated into small molecules or biologics (monoclonal antibodies [mAbs] and other immunotherapies).”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The DMT agents were also classified according to their potential MOA as amyloid targeting, as tau-related targeting, and as having other MOA such as anti-inflammatory or metabolic protection, neuroprotection, and growth factor support.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Symptomatic agents are supposed to show symptomatic benefits over weeks to many months in cognition improvement or BPSD elimination.10”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“In addition, the use of clinical trial simulators, Bayesian statistics, and modifiable trial designs is strongly suggested.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
boosted- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Given the fact that longer trial durations increase the probability of detecting a significant effect but at the same time increase tremendously the costs, the proposed solution seems to be the use of clinical trial simulators.28”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [28] Anderson RM Hadjichrysanthou C Evans S Wong MM Why do so many clinical trials of therapies for Alzheimer’s disease fail? Lancet. 2017; 390: 2327- 2329. 29185425 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“A novel approach to the problem seems more technical and mathematical than biological and suggests that the selected trials’ clinical endpoint may be extremely premature, and additionally, the variability in diagnostic markers and end points may result in inaccurate diagnosis of patients’ disease state and is finally a definite source of errors.28”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [28] Anderson RM Hadjichrysanthou C Evans S Wong MM Why do so many clinical trials of therapies for Alzheimer’s disease fail? Lancet. 2017; 390: 2327- 2329. 29185425 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
In the paper
“They can also help in the perfecting of the design of the study; hence, they may augment the probability of success of estimated new drugs or save invaluable time and resources, by indicating earlier the forthcoming failure of any inappropriate therapy.37”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [37] Hadjichrysanthou C Ower AK de Wolf F Anderson RM The development of a stochastic mathematical model of Alzheimer’s disease to help improve the design of clinical trials of potential treatments. PLoS ONE. 2018; 13:e0190615. PMC5788351 29377891
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The crucial step in AD pathogenesis is the production of amyloid (Aβ), which forms SPs (insoluble and proteolysis-resistant fibrils).”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Selective serotonin reuptake inhibitors are preferred for treating depression and anxiety.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [21] Bessey LJ Walaszek A Management of behavioral and psychological symptoms of dementia. Curr Psychiatry Rep. 2019; 21: 66. 31264056
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The tested agents are classified as DMTs (73%), symptomatic cognitive enhancers (13%), and symptomatic for the treatment of BPSDs (11%).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The APP cleavage by α-secretase leads to nonamyloidogenic pathway, whereas APP cleavage by β-secretase (BACE1) leads to amyloidogenic pathway.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“These simulators are constructed with mathematical, computational, and statistical tools and can predict the likelihood that a strategy and clinical end point selection of a given trial are proper or not, before the initiation of the trial.36”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [36] Romero K Ito K Rogers JA, et al The future is now: model-based clinical trial design for Alzheimer’s disease. Clin Pharmacol Ther. 2015; 97: 210- 214. 25669145 PMC6463482
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“No new drug has been approved by FDA for AD since 2003 and there are no approved DMTs for AD, despite many long and expensive trials.22,28”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [22] Hukins D Macleod U Boland JW Identifying potentially inappropriate prescribing in older people with dementia: a systematic review. Eur J Clin Pharmacol. 2019; 75: 467- 481. 30610274
- Not checked yetcites [28] Anderson RM Hadjichrysanthou C Evans S Wong MM Why do so many clinical trials of therapies for Alzheimer’s disease fail? Lancet. 2017; 390: 2327- 2329. 29185425 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The National Institute on Aging and the Alzheimer’s Association (NIA-AA) proposed a new framework for research,39 which requires the application of amyloid, tau, and neurodegeneration biomarkers to clinical trials, succeeds in precise classification of patients in AD stages, and can be used to assist clinical trials design.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [39] Jack CR Jr Bennett DA Blennow K, et al NIA-AA research framework: toward a biological definition of Alzheimer’s disease. Alzheimers Dement. 2018; 14: 535- 562. 29653606 PMC5958625 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Consequently, current guidance provided by the FDA for AD clinical trials further includes use of fluid or neuroradiological biomarkers in disease staging for preclinical and prodromal AD trials and of a single primary outcome in prodromal AD trials.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The last annual review of the drug development pipeline for AD examined clinicaltrials.gov in February, 2019 (132 agents in 156 trials) and provides information and conclusions available at that time: 28 drugs in 42 clinical trials in phase 3 trials, 74 drugs in 83 phase 2 trials, and 30 drugs in 31 phase 1 trials.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Their combination benefits patients with usually additive effects, without any increase in adverse effects.14,15”
§ Current and Future Treatments in Alzheimer Disease: An Update > Introduction > Current management of AD
What the sources say
- Not checked yetcites [14] Na R Yang JH Yeom Y, et al A systematic review and meta-analysis of nonpharmacological interventions for moderate to severe dementia. Psychiatry Investig. 2019; 16: 325- 335. PMC6539264 31132836
- Not checked yetcites [15] Kishita N Backhouse T Mioshi E Nonpharmacological interventions to improve depression, anxiety, and quality of life (QoL) in people with dementia: an overview of systematic reviews. J Geriatr Psychiatry Neurol. 2019; 33: 28- 41. 31203712 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Two BACE inhibitors are still elaborated: elenbecestat (E2609) in phase 2 and umibecestat (CNP520) in phase 3.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The phase 3 lanabecestat trial was discontinued due to lack of efficacy, whereas verubecestat and atabecestat trials were ceased due to ineffectiveness, as well as safety reasons (rash, falls, liver toxicity, and neuropsychiatric symptoms).10,32-34”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
- Not checked yetcites [32] Burki T Alzheimer’s disease research: the future of BACE inhibitors. Lancet. 2018; 391: 2486. 29976459 source
- Not checked yetcites [33] Egan MF Kost J Voss T, et al Randomized trial of verubecestat for prodromal Alzheimer’s disease. N Engl J Med. 2019; 380: 1408- 1420. 30970186 PMC6776078 source
- Not checked yetcites [34] Henley D Raghavan N Sperling R Aisen P Raman R Romano G Preliminary results of a trial of atabecestat in preclinical Alzheimer’s disease. N Engl J Med. 2019; 380: 1483- 1485. 30970197 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“APH-1105 is delivered intranasally and is assessed in mild to moderate AD.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Etazolate is currently evaluated in animal studies for its preventive effect in post-traumatic stress disorder.49”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [49] Alzoubi KH Al Subeh ZY Khabour OF Molecular targets for the interactive effect of etazolate during post-traumatic stress disorder: role of oxidative stress, BDNF and histones. Behav Brain Res. 2019; 369:111930. 31047921
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Aβ42 is the most aggregation-prone form and has the tendency to cluster into oligomers.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Etazolate (EHT0202) stimulates the nonamyloidogenic α-secretase pathway acting as a selective modulator of GABA receptors.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [48] Vellas B Sol O Snyder PJ, et al EHT0202 in Alzheimer’s disease: a 3-month, randomized, placebo-controlled, double-blind study. Curr Alzheimer Res. 2011; 8: 203- 212. 21222604 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The KLVFF compound that mainly prevents the aggregation of Aβ42 and can also dissolve the oligomerics to a limited extend is the final compound 18, which is resilient in proteolytic decomposition.51”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [51] Stark T Lieblein T Pohland M, et al Peptidomimetics that inhibit and partially reverse the aggregation of Aβ1-42. Biochemistry. 2017; 56: 4840- 4849. 28841311 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“A phase 2 clinical trial in patients with AD did not provide evidence to support a clinical benefit of ELND005 while severe toxicity issues (infections) forced the cessation of the study.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [50] Salloway S Sperling R Keren R, et al; ELND005-AD201 Investigators. A phase 2 randomized trial of ELND005, scyllo-inositol, in mild to moderate Alzheimer disease. Neurology. 2011; 77: 1253- 1262. 21917766 PMC3179648 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Aβ38 is soluble, present in the vasculature of patients with sporadic and familial AD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“This fact is probably responsible for recent failures in clinical trials with γ-secretase inhibitors: semagacestat29 was associated with worsening of activities in daily leaving and increased rates of infections and skin cancer, avagacestat41 was associated with higher rate of cognitive decline and adverse dose-limiting effects (skin cancer) and tarenflurbil which showed low brain penetration.42”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [29] Doody RS Raman R Farlow M, et al A phase 3 trial of semagacestat for treatment of Alzheimer’s disease. N Engl J Med. 2013; 369: 341- 350. 23883379 source
- Not checked yetcites [41] Coric V Salloway S van Dyck CH, et al Targeting prodromal Alzheimer disease with avagacestat: a randomized clinical trial. JAMA Neurol. 2015; 72: 1324- 1333. 26414022 source
- Not checked yetcites [42] Muntimadugu E Dhommati R Jain A Challa VG Shaheen M Khan W Intranasal delivery of nanoparticle encapsulated tarenflurbil: a potential brain targeting strategy for Alzheimer’s disease. Eur J Pharm Sci. 2016; 92: 224- 234. 27185298
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“KLVFF is a peptide sequence that resembles the hydrophobic central part of the Aβ and gradually replaces natural polypeptides.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [51] Stark T Lieblein T Pohland M, et al Peptidomimetics that inhibit and partially reverse the aggregation of Aβ1-42. Biochemistry. 2017; 56: 4840- 4849. 28841311 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Major sites of γ-secretase cleavage usually occur in positions 40 and 42 of Aβ, thus Aβ40 and Aβ42 oligomers are the main products of the sequential APP cleavage, as the amyloidogenic pathway is favored in neurons because of the greater plentifulness of BACE1.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Aβ40 usually constitutes more than 50% of total detected Aβ.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Restricted, nowadays, knowledge assumes that α-secretase activation is promoted through the phosphatidylinositol 3-kinase (PI3K)/Akt pathway and may be through γ-aminobutyric acid (GABA) receptor signaling; thus, agents that activate the PI3K/Akt pathway or act as selective GABA receptor modulators are suggested as potential therapeutic drugs for AD.47,48”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [47] Cho WH Park JC Kim DH, et al ID1201, the ethanolic extract of the fruit of Melia toosendan ameliorates impairments in spatial learning and reduces levels of amyloid beta in 5XFAD mice. Neurosci Lett. 2014; 583: 170- 175. 25281546 source
- Not checked yetcites [48] Vellas B Sol O Snyder PJ, et al EHT0202 in Alzheimer’s disease: a 3-month, randomized, placebo-controlled, double-blind study. Curr Alzheimer Res. 2011; 8: 203- 212. 21222604 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
In the paper
“Aβ40 is somewhat aggregation-prone and it is mostly found in the cerebral vasculature as a main component of “cerebral amyloid angiopathy.””
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“All agents showed significant and dose-dependent result of reducing CSF Aβ42, but without cognitive or functional benefit while many of them were poorly tolerated and some of them failed in subjects with prodromal AD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [46] Panza F Lozupone M Solfrizzi V, et al BACE inhibitors in clinical development for the treatment of Alzheimer’s disease. Expert Rev Neurother. 2018; 18: 847- 857. 30277096
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Unluckily, concerning γ-secretase, in addition to APP, this particular enzyme acts on many other substances and cleaves different transmembrane proteins. Notch receptor 1, which is essential for control of normal cell differentiation and communication, is among them.5”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [5] Yiannopoulou KG Papageorgiou SG Current and future treatments for Alzheimer’s disease. Ther Adv Neurol Disord. 2013; 6: 19- 33. 23277790 PMC3526946 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“ID1201 is a fruit extract of melia toosendan and also induces α-secretase activation. It is evaluated in mild AD.47”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [47] Cho WH Park JC Kim DH, et al ID1201, the ethanolic extract of the fruit of Melia toosendan ameliorates impairments in spatial learning and reduces levels of amyloid beta in 5XFAD mice. Neurosci Lett. 2014; 583: 170- 175. 25281546 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Consequently, it is possible that effective AD immunotherapies must be able to simultaneously target both ptau and Aβ pathologies.56”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [56] Wisniewski T Goñi F Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015; 85: 1162- 1176. 25789753 PMC4366618 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, Aβ-targeted strategies seem promising if used very early in the progression of the disease, before the presence of any symptoms; thus, they are developed in current trials in preclinical AD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“CAD106 is an active Aβ immunotherapeutic agent, is studied in preclinical AD under the umbrella of the Alzheimer prevention initiative generation program, which comprises 2 phase 3 studies that evaluate simultaneously the safety and efficacy of CAD106 and umibecestat in asymptomatic individuals at risk of developing AD (60-75 years of age, APOE4 homozygotes, or APOE4 heterozygotes with elevated Am”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [45] Lopez Lopez C Tariot PN Caputo A, et al The Alzheimer’s Prevention Initiative Generation Program: study design of two randomized controlled trials for individuals at risk for clinical onset of Alzheimer’s disease. Alzheimers Dement; 5: 216- 227. PMC6562315 31211217 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“A metal protein–attenuating compound, PBT2, has recently progressed in phase 2 AD treatment trials, as it demonstrated promising efficacy data in preclinical studies.54”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [54] Krishnan HS Bernard-Gauthier V Placzek MS Metal protein-attenuating compound for PET neuroimaging: synthesis and preclinical evaluation of [11C]PBT2. Mol Pharm. 2018; 15: 695- 702. 29298483
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Antigen-presenting cells present the immunogens to B cells. Use of Ab or ptau peptides will produce antibodies to Ab or ptau epitopes, respectively. Use of pBri will produce antibodies to both Aβ and ptau epitopes.56”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [56] Wisniewski T Goñi F Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015; 85: 1162- 1176. 25789753 PMC4366618 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“ABvac40 is evaluated in a phase 2 study, as the first active vaccine against the C-terminal end of Aβ40.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [59] Lopez Lopez C Tariot PN Caputo A, et al The Alzheimer’s Prevention Initiative Generation Program: study design of two randomized controlled trials for individuals at risk for clinical onset of Alzheimer’s disease. Alzheimers Dement. 2019; 12: 216- 227. PMC6562315 31211217 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“ABri is a rare hereditary amyloidosis associated with a mutation that results in the production of a highly amyloidogenic protein with a unique carboxyl terminus that has no homology to any other human protein.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [57] Goñi F Herline K Peyser D, et al Immunomodulation targeting of both Aβ and tau pathological conformers ameliorates Alzheimer’s disease pathology in TgSwDI and 3xTg mouse models. J Neuroinflammation. 2013; 10: 150. 24330773 PMC3878790
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“In a 3-month phase 2 study, PBT2 succeeded in a 13% reduction of CSF Aβ and an executive function improvement in a dose-related pattern in patients with early AD.55”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [55] Villemagne VL Rowe CC Barnham KJ, et al A randomized, exploratory molecular imaging study targeting amyloid β with a novel 8-OH quinoline in Alzheimer’s disease: the PBT2-204 IMAGINE study. Alzheimers Dement. 2017; 3: 622- 635. PMC5702880 29201996
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“GV1001 peptide (tertomotide) was previously studied as a vaccine against various cancers, whereas now it is evaluated in a phase 2 study for AD.60”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [60] Lacosta AM Pascual-Lucas M Pesini P, et al Safety, tolerability and immunogenicity of an active anti-Aβ40 vaccine (ABvac40) in patients with Alzheimer’s disease: a randomised, double-blind, placebocontrolled, phase I trial. Alzheimers Res Ther. 2018; 10: 12. 29378651 PMC5789644 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Immunotherapeutic approaches have dominated in the past 15 years with negative results until now.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [56] Wisniewski T Goñi F Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015; 85: 1162- 1176. 25789753 PMC4366618 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“UB-311, a synthetic peptide used as Aβ vaccine, has been advanced into an ongoing phase 2 study in patients with mild and moderate AD. In phase 1, it induced a 100% responder rate in patients with AD. The usual adverse effects were swelling in the injection site and agitation. A slower cognitive decline rate was observed in patients with mild AD.62”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [62] Hull M Sadowsky C Arai H, et al Long-term extensions of randomized vaccination trials of ACC-001 and QS-21 in mild to moderate Alzheimer’s disease. Curr Alzheimer Res. 2017; 14: 696- 708. 28124589 PMC5543567 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Monoclonal Abs to Ab, ptau, or b sheet epitopes are systemically and adequately for BBB penetration infused. As antibodies cross the BBB, they act to clear, degrade, or alternatively disaggregate or neutralize their targets.56”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [56] Wisniewski T Goñi F Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015; 85: 1162- 1176. 25789753 PMC4366618 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Furthermore, the design of the studies became more specific and targeted: the characteristics of amyloid-related imaging abnormalities were associated with the dose of antibodies and APOε4 genotyping, higher dosing necessity was recognized, and accurate measures for specific targets, such as reduction of Aβ plaque burden on amyloid PET, were required.10”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [10] Atri A Current and future treatments in Alzheimer’s disease. Semin Neurol. 2019; 39: 227- 240. 30925615 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The pBri peptide corresponds to this terminus and induces an immune response that recognizes Aβ and ptau.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [57] Goñi F Herline K Peyser D, et al Immunomodulation targeting of both Aβ and tau pathological conformers ameliorates Alzheimer’s disease pathology in TgSwDI and 3xTg mouse models. J Neuroinflammation. 2013; 10: 150. 24330773 PMC3878790
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“ACC-001 (vanutide cridificar), an Aβ vaccine, was studied in phase 2a extension studies in subjects with mild to moderate AD. It was administered with QS-21 adjuvant. Long-term therapy with this combination was very well tolerated and produced the highest anti-Aβ IgG titers compared with other regimens.61”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [61] Kim H Seo EH Lee SH Kim BJ The telomerase-derived anticancer peptide vaccine GV1001 as an extracellular heat shock protein-mediated cell-penetrating peptide. Int J Mol Sci. 2016; 17: E2054. PMC5187854 27941629
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Strict inclusion criteria were applied, such as biomarker proof of “amyloid positivity” and enrollment of individuals with preclinical stages of the disease.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“A phase 1 study was conducted with patients with mild to moderate AD aged 50 to 85 years. Neither incident vasogenic edema nor microhemorrhages were identified. Specific anti-Aβ40 antibodies were developed in the 92% of the individuals receiving injections of ABvac40.59”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [59] Lopez Lopez C Tariot PN Caputo A, et al The Alzheimer’s Prevention Initiative Generation Program: study design of two randomized controlled trials for individuals at risk for clinical onset of Alzheimer’s disease. Alzheimers Dement. 2019; 12: 216- 227. PMC6562315 31211217 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“and crenezumab,70 gantenerumab, and solanezumab71 in studies for preclinical or at-risk populations”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [70] Logovinsky V Satlin A Lai R, et al Safety and tolerability of BAN2401–a clinical study in Alzheimer’s disease with a protofibril selective Aβ antibody. Alzheimers Res Ther. 2016; 8: 14. 27048170 PMC4822297
- Not checked yetcites [68] Sevigny J Chiao P Bussière T, et al The antibody aducanumab reduces Aβ plaques in Alzheimer’s disease. Nature. 2016; 537: 50- 56. 27582220 source
- Not checked yetcites [71] Yang T Dang Y Ostaszewski B, et al Target engagement in an Alzheimer trial: crenezumab lowers amyloid β oligomers in cerebrospinal fluid. Ann Neurol. 2019; 86: 215- 224. 31168802 PMC6771589 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Eleven of them are studied in phase 3: 3 cognitive intensifiers and 8 acting on BPSD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Twenty symptomatic agents are in phase 2: 14 cognitive intensifiers and 6 acting on BPSD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Only 1 agent with tau-related mechanism is evaluated in phase 2/3, whereas 10 agents that target tau as one of their mechanisms are evaluated in phase 2, and 5 more agents with tau-related mechanism are assessed in phase 1 studies.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“NPT088 reduced Aβ and ptau aggregates and improved cognition in aged Tg2576 mice.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [77] Levenson JM Schroeter S Carroll JC, et al NPT088 reduces both amyloid-β and tau pathologies in transgenic mice. Alzheimers Dement. 2016; 2: 141- 155. PMC5651359 29067301
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“patients treated with ANAVEX 2-73 had high levels of 2 gut microbiota families, Ruminococcaceae and Porphyromonadaceae, which were associated with improved activities of daily living.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [81] Parmentier F Etcheto A Missling CU, et al Exploring Gut Microbiota as a Source of Potential Biomarkers: Initial Results from the ANAVEX®2-73 Alzheimer’s Disease Clinical Study [O4-02-04]. AAIC; 2019 http://www.arianapharma.com/wp-content/uploads/2019/07/Anavex-Microbiota-Presentation-AAIC-July-2019-FINAL-1.pdf.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“There are also 2 cognitive intensifiers being studied in phase 1.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The quote only partly states this claim.
In the paper
“A monotherapy trial with MB on mild and moderate AD (NCT00515333) has demonstrated some clinical benefit in moderate, but not mild AD.82”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [82] Wischik CM Staff RT Wischik DJ, et al Tau aggregation inhibitor therapy: an exploratory phase 2 study in mild or moderate Alzheimer’s disease. J Alzheimers Dis. 2015; 44: 705- 720. 25550228 source
boostedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the first completed phase 3 trial of IVIg as a treatment for AD demonstrated good tolerability but lack of efficacy of the agent on clinical stability or delay of cognitive or functional decline of participants with mild and moderate AD.74”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [74] Schwarz AJ Sundell KL Charil A, et al Magnetic resonance imaging measures of brain atrophy from the EXPEDITION3 trial in mild Alzheimer’s disease. Alzheimers Dement. 2019; 5: 328- 337. PMC6675941 31388559
boosted- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“TNF-α signaling has been proved to exacerbate both Aβ aggregation and tau phosphorylation in vivo,90”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [90] Alam Q Alam MZ Mushtaq G, et al Inflammatory process in Alzheimer’s and Parkinson’s diseases: central role of cytokines. Curr Pharm Des. 2016; 22: 541- 548. 26601965
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“AGB101 (low-dose extended-release levetiracetam) is an SV2A modulator that is assessed in a phase 3 clinical trial as a repurposed agent (approved for use in another indication, not epilepsy but MCI due to AD).”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Overall, there are 33 symptomatic agents in current trials: 19 agents aim to improve cognition and 14 target BPSD.”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“COR388 targets a periodontal pathogen acting as bacterial protease inhibitor that reduces neuroinflammation and consequently hippocampal degeneration and is currently assessed in a phase 3 clinical trial (NCT03823404).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“NDX-1017 is an hepatocyte growth factor with the role to regenerate neurons, which is studied in a phase 1 clinical trial (NCT03298672).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“BHV4157 (troriluzole) is a glutamate modulator that reduces synaptic levels of glutamate and is assessed in a phase 3 clinical trial (NCT03605667).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Losartan plus amlodipine plus atorvastatin plus exercise is a combination repurposed agent suggested to succeed significant reduction of the vascular risk capable of preserving cognitive function. It is assessed in a phase 3 clinical trial (NCT02913664).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Masitinib acts on mast cells as a selective tyrosine kinase inhibitor and a modulator of neuroinflammation. It is assessed in a phase 3 clinical trial (NCT01872598).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“AstroStem is currently assessed in a phase 2 study (NCT03117738), whereas hMSCs (human mesenchymal stem cells) treatment is assessed in a phase 1 study (NCT02600130).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Candesartan, an angiotensin receptor blocker; formoterol, a β2 adrenergic receptor agonist; and intranasal insulin glulisine, which rises brain insulin signaling, are currently studied in phase 2 clinical trials (NCT02646982, NCT02500784, NCT02503501, respectively), whereas intranasal insulin aspart is assessed in a phase 1 clinical study.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Icosapent ethyl is the eicosapentaenoic acid (EPA) omega-3 fatty acid in a purified form. It is supposed to protect neurons from disease pathology and is assessed in a phase 3 clinical trial (NCT02719327).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“There are also 2 biologics and 24 small molecules with neuroprotection as one of their mechanisms4 assessed in phase 2 clinical studies and 8 small molecules in phase 1 clinical trials.4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Elderberry Juice improves the mitochondrial function acting as powerful antioxidant rich in anthocyanins (NCT02414607) and GRF6019, a human plasma protein fraction administered with infusions, based on the hypothesis that brain neuroinflammation can be counteracted by young blood parabiosis (NCT03520998, NCT03765762).4”
§ Current and Future Treatments in Alzheimer Disease: An Update > Current Landscape in Treatment Research for AD > Currently studied DMTs for AD
What the sources say
- Not checked yetcites [4] Cummings J Lee G Ritter A Sabbagh M Zhong K Alzheimer’s disease drug development pipeline: 2019. Alzheimers Dement. 2019; 5: 272- 293. PMC6617248 31334330 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Donepezil, galantamine, and rivastigmine are the cholinesterase inhibitors that are most frequently prescribed [102,103,104,105,106].”
From Recent Advances in Therapeutics for the Treatment of Alzheimer’s Disease (2024) · cites this paper as [102]
In the citing paper
“Monotherapy has shown beneficial effects in the short and long term in patients with moderate to severe AD, improving their quality of life, cognition, and behavioral and psychological symptoms of neurodegenerative diseases [33,34]”
From Multi-Target Mechanisms of Phytochemicals in Alzheimer’s Disease: Effects on Oxidative Stress, Neuroinflammation and Protein Aggregation (2022) · cites this paper as [34]
In the citing paper
“In fact, in preclinical models, decreasing tau protein levels via ASO strategies185,186 and recently by engineered zinc-finger transcription factors187 was shown to be durable and to reverse tau pathology.”
From PROTAC targeted protein degraders: the past is prologue (2022) · cites this paper as [186]
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Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Current and Future Treatments in Alzheimer Disease: An Update > References
“45. Lopez Lopez C Tariot PN Caputo A, et al The Alzheimer’s Prevention Initiative Generation Program: study design of two randomized controlled trials for individuals at risk for clinical onset of Alzheimer’s disease. Alzheimers Dement; 5: 216- 227. PMC6562315 31211217”
§ Current and Future Treatments in Alzheimer Disease: An Update > References
“59. Lopez Lopez C Tariot PN Caputo A, et al The Alzheimer’s Prevention Initiative Generation Program: study design of two randomized controlled trials for individuals at risk for clinical onset of Alzheimer’s disease. Alzheimers Dement. 2019; 12: 216- 227. PMC6562315 31211217”
Citations
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- Savolainen-Peltonen H, 2019, BMJ, 364
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- Yiannopoulou KG, 2009, Primary Psychiatry, 16, 29
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Cited by
Sorted by citations
Items 101–200 of 964
Rodrigues, R. O., Shin, S.-R., & Bañobre-López, M. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02720-0 · Cited by 44
“…(NDs) include a broad category of brain diseases caused by progressive death of neuron cells with the decline of brain function, including Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease, amyotrophic lateral sclerosis (ALS), the degeneration of a diseased brain [5].”
BackgroundSmall-molecule theranostics in Alzheimer's disease
Sarabia‐Vallejo, Á., López‐Alvarado, P., & Menéndez, J. C. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115382 · Cited by 48
Monoclonal Antibody Therapy in Alzheimer’s Disease
Neațu, M., Covaliu, A., Ioniță, I., Jugurt, A., Davidescu, E. I., & Popescu, B. O. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics16010060 · Cited by 46
“…disease is notably higher in individuals who are aged over 65 years, and the probability of AD development experiences an exponential growth with advancing age, doubling approximately every five years thereafter, impacting 3% of individuals aged 65–75 and 32% of those aged above 84 years [6,11–15].”
BackgroundAlzheimer’s Disease: The Past, Present, and Future of a Globally Progressive Disease
Vejandla, B., Savani, S., Appalaneni, R., Veeravalli, R. S., & Gude, S. S. (2024) · Cureus · doi:10.7759/cureus.51705 · Cited by 50
Sethi, P., Bhaskar, R., Singh, D. K. K., Gupta, S., Han, S. S., Avinash, D., Abomughaid, M. M., Koul, A., Rani, B., Ghosh, S., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102411 · Cited by 44
Pereira, T. D. M. C., Côco, L. Z., Ton, A. M. M., Meyrelles, S. S., Campos‐Toimil, M., Campagnaro, B. P., & Vasquez, E. C. (2021) · Antioxidants · doi:10.3390/antiox10111845 · Cited by 47
“Dementia in AD is a progressive, global, and irreversible decline in cognitive functions mainly in elderly patients [227,248].”
BackgroundThe Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease
Mohammad Shehata, I., Masood, W., Nemr, N., Anderson, A., Bhusal, K., Edinoff, A. N., Cornett, E. M., Kaye, A. M., & Kaye, A. D. (2022) · Neurology International · doi:10.3390/neurolint14020025 · Cited by 41
“However, the drug pimavanserin is a serotonin receptor antagonist that may soon receive approval by the FDA to treat AD-related psychosis [22].”
BackgroundInfluentialNeurotechnological Approaches to the Diagnosis and Treatment of Alzheimer’s Disease
Ning, S., Jorfi, M., Patel, S. R., Kim, D. Y., & Tanzi, R. E. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.854992 · Cited by 43
Webberley, T. S., Masetti, G., Bevan, R. J., Kerry-Smith, J., Jack, A. A., Michael, D. R., Thomas, S., Glymenaki, M., Li, J., McDonald, J. A. K., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.843105 · Cited by 46
“Ageing is the strongest risk factor for AD and there is currently no cure for established disease, only strategies to slow progression and alleviate symptom severity (Yiannopoulou and Papageorgiou, 2020).”
BackgroundKumar, A., Kashyap, S., Mazahir, F., et al. (2024) · Drug Discovery Today · doi:10.1016/j.drudis.2024.104164 · Cited by 41
Newer Therapeutic Approaches in Treating Alzheimer’s Disease: A Comprehensive Review
Sree, R. R., Kalyan, M., Anand, N., Mani, S., Gorantla, V. R., Sakharkar, M. K., Song, B., & Chidambaram, S. B. (2025) · ACS Omega · doi:10.1021/acsomega.4c05527 · Cited by 45
Antidepressants in Alzheimer’s Disease: A Focus on the Role of Mirtazapine
Correia, A. S., & Vale, N. (2021) · Pharmaceuticals · doi:10.3390/ph14090930 · Cited by 42
Optogenetics: implications for Alzheimer’s disease research and therapy
Mirzayi, P., Shobeiri, P., Kalantari, A., Perry, G. L., & Rezaei, N. (2022) · Molecular Brain · doi:10.1186/s13041-022-00905-y · Cited by 45
“Conventional AD treatments AD treatment remains symptomatic without changing the disease prognosis, and there is no definitive cure available for it, which could slow the disease progression and mitigate cognitive and memory impairments [141, 142].”
BackgroundMusumeci, T., Benedetto, G. D., Carbone, C., Bonaccorso, A., Amato, G., Faro, M. J. L., Burgaletto, C., Puglisi, G., Bernardini, R., & Cantarella, G. (2022) · Biomedicines · doi:10.3390/biomedicines10050985 · Cited by 41
“Current available Food and Drug Administration (FDA)-approved pharmacotherapies for AD provide only symptomatic relief without any disease-modifying potential [13,14].”
BackgroundBowirrat, A. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12111817 · Cited by 46
Talebi, M., Kakouri, E., Talebi, M., Tarantilis, P. Α., Farkhondeh, T., İlgün, S., Pourbagher‐Shahri, A. M., & Samarghandian, S. (2021) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2021.1923479 · Cited by 41
Ohno, S., Chen, Y., Sakamaki, H., Matsumaru, N., Yoshino, M., & Tsukamoto, K. (2021) · Journal of Medical Economics · doi:10.1080/13696998.2021.1880801 · Cited by 38
Metabolomic and lipidomic signatures in autosomal dominant and late‐onset Alzheimer's disease brains
Novotny, B. C., Fernández, M. V., Wang, C., Budde, J., Bergmann, K., Eteleeb, A. M., Bradley, J. L., Webster, C., Ebl, C., Norton, J. B., et al. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12800 · Cited by 42
“The Super Pathways represented in the ADAD-associated metabolites were amino acids (48 metabolites), carbohydrates (12), cofactors and vitamins (9), energy (2), lipid (30), nucleotide (12), peptide (12), and xenobiotics (6).”
Reiss, A. B., Raphael, D. D. L., Chin, N. A., & Sinha, V. (2022) · AIMS Public Health · doi:10.3934/publichealth.2022047 · Cited by 40
“Over the years, research has been gradually revealing that early detection of cognitive change can help to extend the longevity of the patient and enhance the quality of life for those who are eventually diagnosed with a cognitive disease and their family caregivers [24].”
BackgroundWang, Y., Li, Q., Li, X., Zhao, Y., Wang, C., Xue, C., Wang, Y., & Zhang, T. (2023) · Marine Drugs · doi:10.3390/md21070410 · Cited by 39
“Alzheimer’s has a long incubation period of 15 to 20 years, but current treatments only improve symptoms [4,5].”
BackgroundThe Alzheimer’s Knowledge Base: A Knowledge Graph for Alzheimer Disease Research
Romano, J. D., Truong, V. Q., Kumar, R., Venkatesan, M., Graham, B. E., Hao, Y., Matsumoto, N., Li, X., Wang, Z. P., Ritchie, M. D., et al. (2023) · Journal of Medical Internet Research · doi:10.2196/46777 · Cited by 40
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Nallasamy, P., Sivamaruthi, B. S., Chaiyasut, C., & Suganthy, N. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13030299 · Cited by 41
“Failure in current therapeutic strategies for AD therapy is due to the blood–brain barrier (BBB), which blocks the entry of drugs into the central nervous system (CNS) [37].”
BackgroundElmaidomy, A. H., Abdelmohsen, U. R., Alsenani, F., Aly, H. F., Shams, S. G. E., Younis, E. A., Ahmed, K. A., Sayed, A. M., Owis, A. I., Afifi, N., et al. (2022) · RSC Advances · doi:10.1039/d2ra01340a · Cited by 38
RetractedBittner, N., Funk, C. S. M., Schmidt, A., Bermpohl, F., Brandl, E. J., Algharably, E. A. E., Kreutz, R. H., & Riemer, T. (2023) · Drugs & Aging · doi:10.1007/s40266-023-01065-x · Cited by 49
“The acetylcholinesterase Extended author information available on the last page of the article inhibitors (AChEIs) donepezil, rivastigmine, and galan-tamine are approved by the US Food and Drug Administration as well as the European Medicines Agency for the treatment of mild-to-moderate AD [6, 7].”
BackgroundEmerging therapeutic developments in neurodegenerative diseases: A clinical investigation
Kumar, D., Ashraf, G. M., Bilgrami, A. L., & Hassan, M. I. (2022) · Drug Discovery Today · doi:10.1016/j.drudis.2022.06.005 · Cited by 39
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“Inferior frontal gyrus (BA44) 13789 (263) 151 (3) 1.”
Rice bran, an off-shoot to newer therapeutics in neurological disorders
Behl, T., Kumar, S., Sehgal, A., Singh, S., Kumari, S., Brisc, M. C., Munteanu, M. A., Brisc, C., Buhaș, C. L., Pusta, C. T. J., et al. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111796 · Cited by 33
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Unraveling Alzheimer’s: the promise of aducanumab, lecanemab, and donanemab
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“As of now, a remedy for AD remains elusive, although there are available interventions designed to enhance symptoms [12, 13].”
BackgroundBhat, A. A., Moglad, E. H. O., Goyal, A., Afzal, M., Thapa, R., Almalki, W. H., Kazmi, I. A., Alzarea, S. I., Ali, H., Gaur, A., et al. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123056 · Cited by 38
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Recent Progress in Nanomedicine for the Diagnosis and Treatment of Alzheimer’s Diseases
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Alzheimer disease seen through the lens of sex and gender
Castro‐Aldrete, L., Einsiedler, M., Martínková, J., Depypere, H. T., Ang, T. F. A., Mielke, M. M., Sindi, S., Eyre, H. A., Au, R., Dimech, A. S., et al. (2025) · Nature Reviews Neurology · doi:10.1038/s41582-025-01071-0 · Cited by 46
“Conventional treatments for AD alleviate cognitive symptoms by targeting neurotransmitter signalling 192,193 .”
Senescent Microglia Represent a Subset of Disease-Associated Microglia in P301S Mice
Ng, P. Y., Zhang, C., Li, H., & Baker, D. J. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230109 · Cited by 38
“However, treatment options for these conditions remain largely targeted toward the alleviation of symptoms and not at the true treatment of the underlying disease-causing effects [4].”
Comprehensive Review of Nutraceuticals against Cognitive Decline Associated with Alzheimer’s Disease
Reza-Zaldívar, E. E., & Jacobo‐Velázquez, D. A. (2023) · ACS Omega · doi:10.1021/acsomega.3c04855 · Cited by 39
Drug Development for Alzheimer’s and Parkinson’s Disease: Where Do We Go Now?
Sequeira, L., Benfeito, S., Fernandes, C., Gaspar, A., Lima, I., Peixoto, J., Alves, C., Machado, C. S., Borges, F., & Chavarria, D. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16060708 · Cited by 37
“For instance, AChE inhibitors offer relatively short-lasting positive effects in AD patients [151] and display cholinomimetic actions on the gastrointestinal tract that result in diarrhea, nausea, and vomiting [152].”
BackgroundŠagud, M., Tudor, L., & Pivac, N. (2021) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2021.1906223 · Cited by 31
“Antidementia drugs are also associated with adverse events, such as weight loss induced by AChE inhibitors [7,10].”
BackgroundInfluentialIslam, M. T., Aktaruzzaman, M., Saif, A., Hasan, A. R., Sourov, M. M. H., Sikdar, B., Rehman, S., Tabassum, A., Abeed-Ul-Haque, S., Sakib, M. H., et al. (2024) · RSC Advances · doi:10.1039/d4ra05073h · Cited by 32
García‐Viñuales, S., Sciacca, M. F. M., Lanza, V., Santoro, A. M., Grasso, G., Tundo, G. R., Sbardella, D., Coletta, M., Grasso, G., Rosa, C. L., et al. (2021) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2021.105072 · Cited by 34
Queda, F., Calò, S., Gwizdała, K., Magalhães, J. D., Cardoso, S. M., Chaves, S., Piemontese, L., & Santos, M. A. (2021) · Molecules · doi:10.3390/molecules26061658 · Cited by 37
“Therefore, the identification of valid disease-modifying treatments for AD represents nowadays a very urgent and still unmet medical global problem [4,5].”
BackgroundBakrim, S., Aboulaghras, S., Menyiy, N. E., Omari, N. E., Assaggaf, H. M., Lee, L., Montesano, D., Gallo, M., Zengin, G., Al-Dhaheri, Y., et al. (2022) · Molecules · doi:10.3390/molecules27249043 · Cited by 34
“To slow disease development, treatment drugs are thought to interfere with the pathogenic stages that cause clinical symptoms, such as the creation of extracellular-amyloid plaques and intracellular neurofibrillary tangles [51].”
BackgroundFatima, I., Safdar, N., Akhtar, W., Munir, A., Saqib, S., Ayaz, A., Bahadur, S., Alrefaei, A. F., Ullah, F., & Zaman, W. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e15909 · Cited by 32
“The degenerating cholinergic neurons in the forebrain and other parts of the brain cause cognitive decline in AD that can be treated by increasing acetylcholine (ACh) levels in the brain [10].”
BackgroundIslamie, R., Myint, S. L. L., Rojanaratha, T., Ritthidej, G. C., Wanakhachornkrai, O., Wattanathamsan, O., & Rodsiri, R. (2023) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-023-04125-2 · Cited by 35
“AD treatment, including cholinesterase inhibitors and N-methyl-D-aspartate (NMDA) receptor antagonists, is limited to the symptomatic therapy [6].”
BackgroundRoles and Mechanisms of the Protein Quality Control System in Alzheimer’s Disease
Liu, Y., Ding, R., Xu, Z., Xue, Y., Zhang, D., Zhang, Y., Li, W., & Li, X. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010345 · Cited by 32
“It is predicted that the number of AD cases among the elderly will increase to 135 million by 2050 [123].”
BackgroundInfluentialApplications of Carbon Dots for the Treatment of Alzheimer’s Disease
Guo, F. W., Li, Q., Zhang, X., Liu, Y., Jiang, J., Cheng, S., Si, Y., Zhang, X., Liu, F., Li, Y., et al. (2022) · International Journal of Nanomedicine · doi:10.2147/ijn.s388030 · Cited by 33
“The BBB is a unique and complex multicellular structural barrier separating the central nervous system from the rest of the body, composed of a semi-permeable membrane of endothelial cells.(17) The BBB prevents viruses and most macromolecules from entering the CNS, shields the brain from blood-borne pathogens and othe…”
BackgroundTobeh, N. S., & Bruce, K. D. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1259012 · Cited by 35
Valizadeh, G., Elahi, R., Hasankhani, Z., Rad, H. S., & Shalbaf, A. (2024) · Archives of Computational Methods in Engineering · doi:10.1007/s11831-024-10176-6 · Cited by 35
Park, H. Y., Park, C. R., Suh, C. H., Shim, W. H., & Kim, S. J. (2021) · European Radiology · doi:10.1007/s00330-021-08227-8 · Cited by 33
“Early detection of AD has become important due to the advancement in disease-modifying treatments [3].”
BackgroundDesai, R. J., Mahesri, M., Lee, S. B., Varma, V. R., Loeffler, T., Schilcher, I., Gerhard, T., Segal, J. B., Ritchey, M. E., Horton, D. B., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac247 · Cited by 33
Dave, B. P., Shah, Y. B., Maheshwari, K. G., Mansuri, M. K. A., Prajapati, B., Postwala, H. I., & Chorawala, M. R. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01408-7 · Cited by 33
“Similarly, they should not be used if you experience active peptic ulcer, possess a history of gastrointestinal bleeding, or have uncontrolled seizures (Yiannopoulou and Papageorgiou 2020).”
BackgroundNanotechnology in the diagnostic and therapy for Alzheimer's disease
Panghal, A., & Flora, S. J. S. (2024) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2024.130559 · Cited by 31
Psychobiotics for Mitigation of Neuro‐Degenerative Diseases: Recent Advancements
Dhyani, P., Goyal, C., Dhull, S. B., Chauhan, A. K., Saharan, B. S., Harshita, Duhan, J. S., & Gökşen, G. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300461 · Cited by 30
Sighencea, M. G., Popescu, R. Ș., & Trifu, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212311 · Cited by 33
“…memantine [8] Kinase (GSK-3 β ) inhibitors Lithium chloride [1,8] Phosphodiesterase-4 inhibitors BPN14770 [8] Acetylation inhibitors Salsalate [3,8] Tau aggregation inhibitors Deoxyvasicinone analogs, methylthioninium derivatives [8,29] Tau deglycosylation inhibitors (GlcNAcase enzyme…”
InfluentialKang, N., Luan, Y., Jiang, Y., Cheng, W., Liu, Y., Su, Z., Liu, Y., & Tan, P. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.878631 · Cited by 31
“The burden of AD affects patients themselves, their families, and the social economy, costing an estimated US$1 trillion annually in the world (Livingston et al., 2020; Yiannopoulou and Papageorgiou, 2020).”
BackgroundThe Roles of the Amyloid Beta Monomers in Physiological and Pathological Conditions
Schreiner, T. G., Schreiner, O. D., Adam, M., & Popescu, B. O. (2023) · Biomedicines · doi:10.3390/biomedicines11051411 · Cited by 35
“Currently, there is no curative treatment and pharmacological therapeutic means unsatisfactorily improve the clinical symptoms and the patient’s quality of life [70].”
BackgroundGSK-3β dysregulation in aging: Implications for tau pathology and Alzheimer's disease progression
Rekha, A., Afzal, M., Babu, M. A., Menon, S. V., Nathiya, D., Supriya, S., Mishra, S. B., Gupta, S., Goyal, K., Rana, M., et al. (2025) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2025.104005 · Cited by 34
Advances in Drug Therapy for Alzheimer’s Disease
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Second Sphere Interactions in Amyloidogenic Diseases
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Bérard, C., Desgranges, S., Dumas, N., Novell, A., Larrat, B., Hamimed, M., Taulier, N., Estève, M., Corréard, F., & Contino-Pepin, C. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14071498 · Cited by 30
“Presently, in neurodegenerative diseases, such as Alzheimer’s or Parkinson’s disease, while approved drugs mainly alleviate symptoms temporarily without significantly altering disease progression, no new drug offers hope for a cure [1,2].”
BackgroundKalita, S., Bergman, H., Dubey, K. D., & Shaik, S. S. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c12305 · Cited by 29
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“Up until now, the current available approved therapeutics mainly target on the symptomatic treatments (Sivanandy et al., 2021; Yiannopoulou & Papageorgiou, 2020).”
BackgroundZhang, P., Hou, Y., Tu, W., Campbell, N. L., Pieper, A. A., Leverenz, J. B., Gao, S., Cummings, J. L., & Cheng, F. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12819 · Cited by 31
“viduals and AA individuals (Figure S1 in supporting information) that were: (1) ≥60 years old on the first day of enrollment; (2) continuously enrolled for≥3 years; and (3) had anMPR of ARBs>0.”
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“Consulting a healthcare professional before starting or stopping any medication is vital to ensure safety and effectiveness, tailoring treatment to individual health needs [29].”
BackgroundNaik, R. A., Mir, M. N., Malik, I. A., Bhardwaj, R., Alshabrmi, F. M., Mahmoud, M. A., Alhomrani, M., Alamri, A. S., Alsanie, W. F., Hjazi, A. M., et al. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl25551 · Cited by 29
Repositioning of Immunomodulators: A Ray of Hope for Alzheimer’s Disease?
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“AD is characterized by intracellular accumulation of phosphorylated tau proteins as neurofibrillary tangles (NFTs) and extracellular deposition of Aβ as neuritic plaques [1, 4, 5].”
BackgroundRecent Studies on Heterocyclic Cholinesterase Inhibitors Against Alzheimer's Disease
Tok, F. (2024) · Chemistry & Biodiversity · doi:10.1002/cbdv.202402837 · Cited by 30
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“AD persists as the most prominent form of dementia worldwide, being estimated to increase in the coming decades (Yiannopoulou and Papageorgiou, 2020).”
Kwak, M. G., Mao, L., Zheng, Z., Su, Y., Lure, F. Y. M., Li, J., & Initiative, A. D. N. (2025) · IEEE Transactions on Automation Science and Engineering · doi:10.1109/tase.2025.3556290 · Cited by 31
“Yet, the potential of these drugs to slow down disease progression is contingent upon early administration, ideally during the mild cognitive impairment (MCI) phase preceding AD dementia [3].”
Ghafoori, S., & Shalbaf, A. (2022) · International Journal of Computer Assisted Radiology and Surgery · doi:10.1007/s11548-022-02620-4 · Cited by 28
“Alzheimer’s disease is known to be the cause of dementia at old age for 60–80% of cases [1].”
BackgroundALNasser, M. N., Mellor, I. R., & Carter, W. G. (2022) · Molecules · doi:10.3390/molecules27154891 · Cited by 26
“In addition, these treatments can cause adverse side effects, including headaches, nausea, vomiting, diarrhoea, dizziness, confusion, and cardiac arrhythmias [25,29,30].”
BackgroundPhytomedicine for neurodegenerative diseases: The road ahead
Madhubala, D., Patra, A., Khan, M. R., & Mukherjee, A. K. (2024) · Phytotherapy Research · doi:10.1002/ptr.8192 · Cited by 29
“Currently, approximately 50 million people suffer from AD worldwide, and this number is expected to double every 5 years to reach 152 million by 2050 (Yiannopoulou & Papageorgiou, 2020).”
BackgroundCurrent Findings and Potential Mechanisms of KarXT (Xanomeline–Trospium) in Schizophrenia Treatment
Azargoonjahromi, A. (2024) · Clinical Drug Investigation · doi:10.1007/s40261-024-01377-9 · Cited by 30
Exploring Alzheimer's disease treatment: Established therapies and novel strategies for future care
Soni, U., Singh, K., Jain, D., & Pujari, R. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177520 · Cited by 28
Therapeutic Strategies Targeting Amyloid-β Receptors and Transporters in Alzheimer’s Disease
Lao, K., Zhang, R., Luan, J., Zhang, Y., & Gou, X. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-200851 · Cited by 25
“Since 2003, hundreds of studies based on A (cid:2) hypothesis have been processed, but none of them have been approved for AD treatment [115].”
Selenium-Derivative Compounds: A Review of New Perspectives in the Treatment of Alzheimer’s Disease
Barbosa, F. A. R., Canto, R. F. S., Teixeira, K. F., de Souza, A. S., de Oliveira, A. S., & Braga, A. L. (2022) · Current Medicinal Chemistry · doi:10.2174/0929867329666220224161454 · Cited by 26
New Drug Design Avenues Targeting Alzheimer’s Disease by Pharmacoinformatics-Aided Tools
Arrué, L., Cigna-Méndez, A., Barbosa, T., Borrego-Muñoz, P., Struve-Villalobos, S., Oviedo, V., Martínez-García, C., Sepúlveda-Lara, A., Millán, N., Montesinos, J. C. E. M., et al. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14091914 · Cited by 28
“However, they have the inconvenience of presenting some side effects such as gastrointestinal complications [70], muscle problems in anesthetized patients, slow heartbeat and fainting, as well as seizures [71].”
BackgroundThe Transcranial Light Therapy Improves Synaptic Plasticity in the Alzheimer’s Disease Mouse Model
Buendía, D., Guncay, T., Oyanedel, M., Lemus, M., Weinstein, A., Ardiles, Á. O., Marcos, J. L., Fernandes, A. B., Zângaro, R. A., & Muñoz, P. (2022) · Brain Sciences · doi:10.3390/brainsci12101272 · Cited by 26
“This may cause a deficit in synaptic transmission [21], leading to an impairment in synaptic plasticity (SP), which is the ability of neurons to modify the number, structure, and functions of synapses over time, including long-term potentiation (LTP) and long-term depression (LTD), among others [22].”
BackgroundSharma, P., & Singh, M. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121568 · Cited by 25
Beyond amyloid and tau: rethinking Alzheimer’s disease through less explored avenues
Gyimesi, M., Okolicsanyi, R. K., & Haupt, L. M. (2024) · Open Biology · doi:10.1098/rsob.240035 · Cited by 29
“Despite the wealth of new insights into the dysregulated processes underlying the appearance of toxic amyloid plaques and hyperphosphorylated tau protein, treatments targeting these continue to fail to cure AD, and offer only minimal symptomatic relief [6–10].”
BackgroundEpigenetic biomarkers in Alzheimer's disease: Diagnostic and prognostic relevance
Behl, T., Kyada, A., Roopashree, R., Nathiya, D., Arya, R., Kumar, M., Khalid, M., Gulati, M., Sachdeva, M., Fareed, M., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102556 · Cited by 31
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“Nevertheless, drugs approved by the food and drug administration (FDA), such as rivastigmine, galantamine, donepezil, memantine, and tacrine, have shown mild anti-Alzheimer’s effects [8].”
Recent advance on pleiotropic cholinesterase inhibitors bearing amyloid modulation efficacy
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Manipulation of the diet–microbiota–brain axis in Alzheimer’s disease
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“This includes Biogen’s antiAβ monoclonal antibody aducanumab, which was recently approved by the US Food and Drug Administration, aiming to remove amyloid protein depositions from the brains of patients at the expense of potential adverse effects (Ferrero et al., 2016; Yiannopoulou and Papageorgiou, 2020; Crosson et a…”
BackgroundProspective use of amniotic mesenchymal stem cell metabolite products for tissue regeneration
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“Additionally, Alzheimer’s therapies that have neuroprotective mechanisms and the use of antiinflammatory stem cell therapies and the growth factor NDX-1017 are currently under investigation [5, 6].”
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The elusive role of herpesviruses in Alzheimer’s disease: current evidence and future directions
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Metadata
- Authors
- Yiannopoulou, K. G., & Papageorgiou, S. G.
- Affiliations
- Henry Dunant Hospital (GR)
- National and Kapodistrian University of Athens (GR)
- Corresponding author
- Yiannopoulou, Konstantina G
- Venue
- Journal of Central Nervous System Disease
- Publisher
- SAGE Publications
- Published
- 2020-01
- Volume
- 12
- Pages
- 117957352090739
- ISSN
- 1179-5735 (ISSN-L)
- PMC
- PMC7050025
- OpenAlex
- W3007853567
- Semantic Scholar
- 35a37a9e5cb7e502b1d43a326dbbe0efe4d86057
- Cited by
- 966
- References
- 96
- Citations by year
- 2026: 122 · 2025: 171 · 2024: 214 · 2023: 204 · 2022: 136 · 2021: 93 · 2020: 26
- FWCI
- 14.69
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Central Nervous System Disease (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Pharmacology (medical) › Cholinesterase and Neurodegenerative Diseases
- Keywords
- Alzheimer's disease, disease-modifying therapy, cholinesterase inhibitors, memantine, amyloid plaques, neurofibrillary tangles, neuroprotection, anti-inflammatory therapy, growth factor therapy, stem cell therapy, biomarkers, precision medicine, clinical trial design
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