Sensory processing deficits and related cortical pathological changes in Alzheimer’s disease
Open accessAbstract
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder primarily affecting cognitive functions. However, sensory deficits in AD start to draw attention due to their high prevalence and early onsets which suggest that they could potentially serve as diagnostic biomarkers and even contribute to the disease progression. This literature review examines the sensory deficits and cortical pathological changes observed in visual, auditory, olfactory, and somatosensory systems in AD patients, as well as in various AD animal models. Sensory deficits may emerge at the early stages of AD, or even precede the cognitive decline, which is accompanied by cortical pathological changes including amyloid-beta deposition, tauopathy, gliosis, and alterations in neuronal excitability, synaptic inputs, and functional plasticity. Notably, these changes are more pronounced in sensory association areas and superficial cortical layers, which may explain the relative preservation of basic sensory functions but early display of deficits of higher sensory functions. We propose that sensory impairment and the progression of AD may establish a cyclical relationship that mutually perpetuates each condition. This review highlights the significance of sensory deficits with or without cortical pathological changes in AD and emphasizes the need for further research to develop reliable early detection and intervention through sensory systems.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Eleven ROIs have nominally significant correlations with both behaviors, including key sensory regions (VCP, VCS, and MGD) linked to early symptoms of AD in humans.
“Eleven ROIs have nominally significant correlations with both behaviors (Supplementary Table 10), including key sensory regions (VCP, VCS, and MGD) linked to early symptoms of AD in humans71-74.”
From Magnetic resonance microscopy maps widespread effects of Alzheimer’s disease on brain structures and behavior in mice (2026) · cites this paper as [73]
The Introduction (page unavailable) says visual and auditory deficits can appear before cognitive decline in people with AD, and “Pathological changes in visual cortex” describes early changes in visual association areas. The paper does not establish the claimed link for each named region, particularly MGD. The eleven ROI correlations are attributed to the citing paper’s Supplementary Table 10, not to this source. (LLM, conf=0.82)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 174 · Cited by 49
Research works printed but not linked: 158
- Ahmad K. Peter H. Daniel E. Nichola Z. Lax J. R. Evangelia K. (2016). Analysis of primary visual cortex in dementia with lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinations. Acta Neuropathol. Commun. 4: 66. 10.1186/s40478-016-0334-3 27357212 PMC4928325 · DOI
- Alcantara-Gonzalez D. Chartampila E. Criscuolo C. Scharfman H. E. (2021). Early changes in synaptic and intrinsic properties of dentate gyrus granule cells in a mouse model of Alzheimer’s disease neuropathology and atypical effects of the cholinergic antagonist atropine. Neurobiol. Dis. 152: 105274. 10.1016/j.nbd.2021.105274 33484828 PMC7956160 · DOI
- Algamal M. Russ A. N. Miller M. R. Hou S. S. Maci M. Munting L. P. (2022). Reduced excitatory neuron activity and interneuron-type-specific deficits in a mouse model of Alzheimer’s disease. Commun. Biol. 5: 1323. 10.1038/s42003-022-04268-x 36460716 PMC9718858 · DOI · Paper page
- Ali F. Ali F. Baringer S. L. Neal A. Choi E. Y. Kwan A. C. (2019). Parvalbumin-Positive neuron loss and amyloid-β deposits in the frontal cortex of Alzheimer’s disease-related mice. J. Alzheimers Dis. 72 1323– 1339. 10.3233/jad-181190 31743995 PMC7123545 · DOI · Paper page
- Al-Otaibi M. Lessard-Beaudoin M. Castellano C. Gris D. Cunnane S. C. Graham R. K. (2020). Volumetric MRI demonstrates atrophy of the olfactory cortex in AD. Curr. Alzheimer Res. 17 904– 915. 10.2174/1567205017666201215120909 33327913 · DOI
- Armstrong R. A. (1996). Visual field defects in Alzheimer’s disease patients may reflect differential pathology in the primary visual cortex. Optom. Vis. Sci. 73 677– 682. 10.1097/00006324-199611000-00001 8950748 · DOI
- Attems J. Jellinger K. A. (2006). Olfactory tau pathology in Alzheimer disease and mild cognitive impairment. Clin. Neuropathol. 25 265– 271. 17140156
- Aylward A. Auduong P. Anderson J. S. Zielinski B. A. Wang A. Y. Weng C. (2020). Changes in the auditory association cortex in dementing illnesses. Otol. Neurotol. 41 1327– 1333. 10.1097/mao.0000000000002786 32810019 · DOI
- Baloyannis S. J. Costa V. Mauroudis I. Psaroulis D. Manolides S. L. Manolides L. S. (2007). Dendritic and spinal pathology in the acoustic cortex in Alzheimer’s disease: Morphological and morphometric estimation by Golgi technique and electron microscopy. Acta Otolaryngol. 127 351– 354. 10.1080/00016480601126986 17453452 · DOI
- Beach T. G. Beach T. G. Beach T. G. McGeer E. G. (1988). Lamina-specific arrangement of astrocytic gliosis and senile plaques in Alzheimer’s disease visual cortex. Brain Res. 463 357– 361. 10.1016/0006-8993(88)90410-6 3196922 · DOI
- Beach T. G. Beach T. G. Beach T. G. McGeer E. G. (1992). Senile plaques, amyloid β-protein, and acetylcholinesterase fibres: Laminar distributions in Alzheimer’s disease striate cortex. Acta Neuropathol. 83 292– 299. 10.1007/bf00296792 1373024 · DOI
- Beker S. Kellner V. Kerti L. Stern E. A. (2012). Interaction between amyloid-β pathology and cortical functional columnar organization. J. Neurosci. 32 11241– 11249. 10.1523/jneurosci.2426-12.2012 22895708 PMC3752077 · DOI
- Bero A. W. Yan P. Roh J. H. Cirrito J. R. Stewart F. R. Raichle M. E. (2011). Neuronal activity regulates the regional vulnerability to amyloid-β deposition. Nat. Neurosci. 14 750– 756. 10.1038/nn.2801 21532579 PMC3102784 · DOI · Paper page
- Braak H. Braak E. Kalus P. (1989). Alzheimer’s disease: Areal and laminar pathology in the occipital isocortex. Acta Neuropathol. 77 494– 506. 10.1007/bf00687251 2566255 · DOI
- Brewer A. A. Barton B. (2016). “ Changes in Visual Cortex in Healthy Aging and Dementia,” in Update on dementia, ed. Moretti D. (Rijeka: InTech), 10.5772/64562 · DOI
- Brückner G. Hausen D. Härtig W. Drlicek M. Arendt T. Brauer K. (1999). Cortical areas abundant in extracellular matrix chondroitin sulphate proteoglycans are less affected by cytoskeletal changes in Alzheimer’s disease. Neuroscience 92 791– 805. 10.1016/s0306-4522(99)00071-8 10426522 · DOI · Paper page
- Brun A. Gustafson L. (1976). Distribution of cerebral degeneration in Alzheimer’s disease. A clinico-pathological study. Arch. Psychiatr. Nervenkr. 223 15– 33. 10.1007/BF00367450 828039 · DOI · Paper page
- Bublak P. Redel P. Sorg C. Kurz A. Förstl H. Müller H. J. (2011). Staged decline of visual processing capacity in mild cognitive impairment and Alzheimer’s disease. Neurobiol. Aging 32 1219– 1230. 10.1016/j.neurobiolaging.2009.07.012 19713001 · DOI
- Buchanan H. Mackay M. Palmer K. Tothová K. Katsur M. Platt B. (2020). Synaptic loss, ER stress and neuro-inflammation emerge late in the lateral temporal cortex and associate with progressive tau pathology in Alzheimer’s disease. Mol. Neurobiol. 57 3258– 3272. 10.1007/s12035-020-01950-1 32514860 PMC7340653 · DOI
- Busche M. A. Konnerth A. (2015). Neuronal hyperactivity – A key defect in Alzheimer’s disease? Bioessays 37 624– 632. 10.1002/bies.201500004 25773221 · DOI · Paper page
- Busche M. A. Eichhoff G. Adelsberger H. Abramowski D. Wiederhold K. H. Haass C. (2008). Clusters of hyperactive neurons near amyloid plaques in a mouse model of Alzheimer’s disease. Science 321 1686– 1689. 10.1126/science.1162844 18802001 · DOI · Paper page
- Busche M. A. Wegmann S. Dujardin S. Commins C. Schiantarelli J. Klickstein N. (2019). Tau impairs neural circuits, dominating amyloid-β effects, in Alzheimer models in vivo. Nat. Neurosci. 22 57– 64. 10.1038/s41593-018-0289-8 30559471 PMC6560629 · DOI · Paper page
- Cancelli I. Cadore I. Merlino G. Valentinis L. Moratti U. Bergonzi P. (2006). Sensory gating deficit assessed by P50/Pb middle latency event related potential in Alzheimer’s disease. J. Clin. Neurophysiol. 23 421– 425. 10.1097/01.wnp.0000218991.99714.ee 17016152 · DOI
- Chen C. Wei J. Ma X. Xia B. Shakir N. Zhang J. K. (2022). Disrupted maturation of prefrontal layer 5 neuronal circuits in an Alzheimer’s mouse model of amyloid deposition. Neurosci. Bull. 39 881– 892. 10.1007/s12264-022-00951-5 36152121 PMC10264337 · DOI
- Claire M. (2019). Olfactory and other sensory impairments in Alzheimer disease. Nat. Rev. Neurol. 15 11– 24. 10.1038/s41582-018-0097-5 30532084 · DOI · Paper page
- Criscuolo C. Cerri E. Fabiani C. Capsoni S. Cattaneo A. Domenici L. (2018). The retina as a window to early dysfunctions of Alzheimer’s disease following studies with a 5xFAD mouse model. Neurobiol. Aging 67 181– 188. 10.1016/j.neurobiolaging.2018.03.017 29735432 · DOI
- Cronin-Golomb A. (1995). Vision in Alzheimer’s disease. Gerontologist 35 370– 376. 10.1093/geront/35.3.370 7622089 · DOI
- Cronin-Golomb A. Corkin S. Growdon J. (1995). Visual dysfunction predicts cognitive deficits in Alzheimer’s disease. Optom. Vis. Sci. 72 168– 176. 10.1097/00006324-199503000-00004 7609939 · DOI
- Cronin-Golomb A. Corkin S. Growdon J. H. (1987). “ Contrast sensitivity In Alzheimer’s disease,” in Annual Meeting Optical Society of America (1987), paper MC2, (Washington, DC: Optica Publishing Group), 10.1364/OAM.1987.MC2 · DOI
- Cronin-Golomb A. Corkin S. Rizzo J. F. Cohen J. G. Growdon J. H. Banks K. S. (1991). Visual dysfunction in Alzheimer’s disease: Relation to normal aging. Ann. Neurol. 29 41– 52. 10.1002/ana.410290110 1996878 · DOI
- Crowe S. E. Ellis-Davies G. C. R. (2014). Spine pruning in 5xFAD mice starts on basal dendrites of layer 5 pyramidal neurons. Brain Struct. Funct. 219 571– 580. 10.1007/s00429-013-0518-6 23417057 PMC4157364 · DOI
- Crutch S. J. Lehmann M. Schott J. M. Rabinovici G. D. Rossor M. N. Fox N. C. (2012). Posterior cortical atrophy. Lancet Neurol. 11 170– 178. 10.1016/S1474-4422(11)70289-7 22265212 PMC3740271 · DOI
- Deal J. A. Sharrett A. R. Albert M. S. Coresh J. Mosley T. H. Knopman D. (2015). Hearing impairment and cognitive decline: A pilot study conducted within the atherosclerosis risk in communities neurocognitive study. Am. J. Epidemiol. 181 680– 690. 10.1093/aje/kwu333 25841870 PMC4408947 · DOI
- Devanand D. P. Michaels-Marston K. S. Liu X. Pelton G. H. Padilla M. Marder K. (2000). Olfactory deficits in patients with mild cognitive impairment predict Alzheimer’s disease at follow-up. Am. J. Psychiatry 157 1399– 1405. 10.1176/appi.ajp.157.9.1399 10964854 · DOI
- Drzezga A. Grimmer T. Peller M. Wermke M. Siebner H. Rauschecker J. P. (2005). Impaired cross-modal inhibition in Alzheimer disease. PLoS Med. 2: e288. 10.1371/journal.pmed.0020288 16159306 PMC1216331 · DOI
- Duff K. McCaffrey R. J. Solomon G. S. (2002). The pocket smell test. J. Neuropsychiatry Clin. Neurosci. 14 197– 201. 10.1176/jnp.14.2.197 11983795 · DOI
- Duyckaerts C. Hauw J. J. Bastenaire F. Piette F. Piette F. Poulain C. (1986). Laminar distribution of neocortical senile plaques in senile dementia of the Alzheimer type. Acta Neuropathol. 70 249– 256. 10.1007/bf00686079 3766125 · DOI
- Esiri M. M. Pearson R. C. A. Powell T. P. S. (1986). The cortex of the primary auditory area in Alzheimer’s disease. Brain Res. 366 385– 387. 10.1016/0006-8993(86)91324-7 3697692 · DOI
- Esiri M. M. Pearson R. C. Steele J. E. Bowen D. M. Powell T. P. (1990). A quantitative study of the neurofibrillary tangles and the choline acetyltransferase activity in the cerebral cortex and the amygdala in Alzheimer’s disease. J. Neurol. Neurosurg. Psychiatry 53 161– 165. 10.1136/jnnp.53.2.161 2313304 PMC487958 · DOI
- Fernandez R. Kavcic V. Duffy C. J. (2007). Neurophysiologic analyses of low- and high-level visual processing in Alzheimer disease. Neurology 68 2066– 2076. doi: 17562827
- Festa E. K. Insler R. Z. Salmon D. P. Paxton J. L. Hamilton J. M. Heindel W. C. (2005). Neocortical disconnectivity disrupts sensory integration in Alzheimer’s disease. Neuropsychol. J. 19 728– 738. 10.1037/0894-4105.19.6.728 16351348 · DOI
- Frisoni G. B. Pievani M. Testa C. Sabattoli F. Bresciani L. Bonetti M. (2007). The topography of grey matter involvement in early and late onset Alzheimer’s disease. Brain 130 720– 730. 10.1093/brain/awl377 17293358 · DOI
- Gates G. A. Anderson M. L. Feeney M. McCurry S. M. Larson E. B. (2008). Central auditory dysfunction in older persons with memory impairment or Alzheimer dementia. Arch. Otolaryngol. Head Neck Surg. 134 771– 777. 10.1001/archotol.134.7.771 18645130 PMC2871110 · DOI
- Gates G. A. Beiser A. S. Rees T. S. D’Agostino R. B. Wolf P. A. (2002). Central auditory dysfunction may precede the onset of clinical dementia in people with probable Alzheimer’s disease. J. Am. Geriatr. Soc. 50 482– 488. 10.1046/j.1532-5415.2002.50114.x 11943044 · DOI
- Geneviève L. Rudolf K. (1994). Visual cortex in Alzheimer’s disease: Occurrence of neuronal death and glial proliferation, and correlation with pathological hallmarks. Neurobiol. Aging 15 29– 43. 10.1016/0197-4580(94)90142-2 8159261 · DOI
- Giannakopoulos P. Gold G. Duc M. Michel J. P. Hof P. R. Bouras C. (2000). Impaired processing of famous faces in Alzheimer’s disease is related to neurofibrillary tangle densities in the prefrontal and anterior cingulate cortex. Dement. Geriatr. Cogn. Disord. 11 336– 341. 10.1159/000017263 11044779 · DOI
- Gilbert C. D. (1983). Microcircuitry of the visual cortex. Annu. Rev. Neurosci. 6 217– 247. 10.1146/annurev.ne.06.030183.001245 6132585 · DOI
- Gilmore G. C. Whitehouse P. J. (1995). Contrast Sensitivity in Alzheimer’s Disease: A 1-year longitudinal analysis. Optom. Vis. Sci. 72: 83. 7753532
- Gilmore G. C. Wenk H. E. Naylor L. A. Koss E. (1994). Motion perception and Alzheimer’s disease. J. Gerontol. 49: 52. 10.1093/geronj/49.2.p52 8126359 · DOI
- Golden H. Nicholas J. Yong K. Downey L. Schott J. Mummery C. (2015). Auditory spatial processing in Alzheimer’s disease. Brain 138 189– 202. 10.1093/brain/awu337 25468732 PMC4285196 · DOI
- Goll J. C. Kim L. G. Ridgway G. R. Hailstone J. C. Lehmann M. Buckley A. H. (2012). Impairments of auditory scene analysis in Alzheimer’s disease. Brain J. Neurol. 135 190– 200. 10.1093/brain/awr260 22036957 PMC3267978 · DOI
- Golub J. Brickman A. Ciarleglio A. (2020). Association of subclinical hearing loss with cognitive performance. JAMA Otolaryngol. Head Neck Surg. 146 56– 57. 10.1001/jamaoto.2019.3375 31725853 PMC6865840 · DOI · Paper page
- Govindpani K. Turner C. Waldvogel H. J. Faull R. L. M. Kwakowsky A. (2020). Impaired expression of GABA signaling components in the Alzheimer’s disease middle temporal gyrus. Int. J. Mol. Sci. 21: 8704. 10.3390/ijms21228704 33218044 PMC7698927 · DOI
- Graff-Radford J. Yong K. X. X. Apostolova L. G. Bouwman F. H. Carrillo M. Dickerson B. C. (2021). New insights into atypical Alzheimer’s disease in the era of biomarkers. Lancet Neurol. 20 222– 234. 10.1016/S1474-4422(20)30440-3 33609479 PMC8056394 · DOI · Paper page
- Greicius M. D. Srivastava G. Reiss A. L. Menon V. (2004). Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: Evidence from functional MRI. Proc. Natl. Acad. Sci. U. S. A. 101 4637– 4642. 10.1073/pnas.0308627101 15070770 PMC384799 · DOI · Paper page
- Grienberger C. Rochefort N. L. Adelsberger H. Henning H. A. Hill D. N. Reichwald J. (2012). Staged decline of neuronal function in vivo in an animal model of Alzheimer’s disease. Nat. Commun. 3: 774. 10.1038/ncomms1783 22491322 PMC3337977 · DOI
- Griffiths T. D. Lad M. Kumar S. Holmes E. McMurray B. Maguire E. A. (2020). How can hearing loss cause dementia? Neuron 108 401– 412. 10.1016/j.neuron.2020.08.003 32871106 PMC7664986 · DOI
- Grothe M. J. Barthel H. Sepulcre J. Dyrba M. Sabri O. Teipel S. J. (2017). In vivo staging of regional amyloid deposition. Neurology 89 2031– 2038. 10.1212/WNL.0000000000004643 29046362 PMC5711511 · DOI · Paper page
- Guan Z. Z. Zhang X. Ravid R. Ravid R. Nordberg A. (2001). Decreased protein levels of nicotinic receptor subunits in the hippocampus and temporal cortex of patients with Alzheimer’s disease. J. Neurochem. 74 237– 243. 10.1046/j.1471-4159.2000.0740237.x 10617125 · DOI
- Hector A. Brouillette J. (2021). Hyperactivity induced by soluble amyloid-β oligomers in the early stages of Alzheimer’s disease. Front. Mol. Neurosci. 13: 600084. 10.3389/fnmol.2020.600084 33488358 PMC7817907 · DOI
- Hijazi S. Heistek T. S. Scheltens P. Neumann U. Shimshek D. R. Mansvelder H. D. (2020). Early restoration of parvalbumin interneuron activity prevents memory loss and network hyperexcitability in a mouse model of Alzheimer’s disease. Mol. Psychiatry 25 3380– 3398. 10.1038/s41380-019-0483-4 31431685 PMC7714697 · DOI · Paper page
- Holroyd S. Shepherd M. L. Downs J. H. (2000). Occipital atrophy is associated with visual hallucinations in Alzheimer’s disease. J. Neuropsychiatry Clin. Neurosci. 12 25– 28. 10.1176/jnp.12.1.25 10678508 · DOI
- Hoshi A. Tsunoda A. Yamamoto T. Yamamoto T. Tada M. Tada M. (2018). Altered expression of glutamate transporter-1 and water channel protein aquaporin-4 in human temporal cortex with Alzheimer’s disease. Neuropathol. Appl. Neurobiol. 44 628– 638. 10.1111/nan.12475 29405337 · DOI
- Huang J. Beach P. Bozoki A. Zhu D. C. (2021). Alzheimer’s disease progressively reduces visual functional network connectivity. J. Alzheimers Dis. Rep. 5 549– 562. 10.3233/ADR-210017 34514338 PMC8385433 · DOI
- Hwang J. Kim C. M. Kim J. E. Oh M. Oh J. S. Yoon Y. W. (2021). Clinical implications of amyloid-beta accumulation in occipital lobes in Alzheimer’s continuum. Brain Sci. 11: 1232. 10.3390/brainsci11091232 34573252 PMC8470691 · DOI
- Iliadou V. V. Bamiou D. E. Sidiras C. Moschopoulos N. P. Tsolaki M. Nimatoudis I. (2017). The use of the gaps-in-noise test as an index of the enhanced left temporal cortical thinning associated with the transition between mild cognitive impairment and Alzheimer’s disease. J. Am. Acad. Audiol. 28 463– 471. 10.3766/jaaa.16075 28534735 · DOI
- Iseri P. K. Altinaş O. Tokay T. Yüksel N. (2006). Relationship between cognitive impairment and retinal morphological and visual functional abnormalities in Alzheimer disease. J. Neuro Ophthalmol. Off. J. North Am. Neuro Ophthalmol. Soc. 26 18– 24. 10.1097/01.wno.0000204645.56873.26 16518161 · DOI
- Jack C. R. Lowe V. J. Senjem M. L. Weigand S. D. Kemp B. J. Shiung M. M. (2008). 11C PiB and structural MRI provide complementary information in imaging of Alzheimer’s disease and amnestic mild cognitive impairment. Brain J. Neurol. 131 665– 680. 10.1093/brain/awm336 18263627 PMC2730157 · DOI · Paper page
- Jessen F. Kucharski C. Fries T. Papassotiropoulos A. Hoenig K. Maier W. (2001). Sensory gating deficit expressed by a disturbed suppression of the P50 event-related potential in patients with Alzheimer’s disease. Am. J. Psychiatry 158 1319– 1321. 10.1176/appi.ajp.158.8.1319 11481170 · DOI
- Jiang F. Mishra S. R. Shrestha N. Ozaki A. Virani S. S. Bright T. (2023). Association between hearing aid use and all-cause and cause-specific dementia: An analysis of the UK Biobank cohort. Lancet Public Health 8 e329– e338. 10.1016/S2468-2667(23)00048-8 37062296 · DOI
- Katz B. Rimmer S. (1989). Ophthalmologic manifestations of Alzheimer’s disease. Surv. Ophthalmol. 34 31– 43. 10.1016/0039-6257(89)90127-6 2678551 · DOI
- Kaylegian K. Stebritz A. J. Weible A. P. Wehr M. (2019). 5XFAD mice show early onset gap detection deficits. Front. Aging Neurosci. 11: 66. 10.3389/fnagi.2019.00066 31001105 PMC6454034 · DOI · Paper page
- Kopeikina K. J. Hyman B. T. Spires-Jones T. L. (2012). Soluble forms of tau are toxic in Alzheimer’s disease. Transl. Neurosci. 3 223– 233. 10.2478/s13380-012-0032-y 23029602 PMC3460520 · DOI · Paper page
- Koronyo Y. Rentsendorj A. Mirzaei N. Regis G. C. Sheyn J. Shi H. (2023). Retinal pathological features and proteome signatures of Alzheimer’s disease. Acta Neuropathol. 145 409– 438. 10.1007/s00401-023-02548-2 36773106 PMC10020290 · DOI
- Kovács T. Cairns N. J. Lantos P. L. (1999). Beta-amyloid deposition and neurofibrillary tangle formation in the olfactory bulb in ageing and Alzheimer’s disease. Neuropathol. Appl. Neurobiol. 25 481– 491. 10.1046/j.1365-2990.1999.00208.x 10632898 · DOI
- Kuchibhotla K. V. Lattarulo C. R. Hyman B. T. Bacskai B. J. (2009). Synchronous hyperactivity and intercellular calcium waves in astrocytes in Alzheimer mice. Science 323 1211– 1215. 10.1126/science.1169096 19251629 PMC2884172 · DOI · Paper page
- Kunz M. Lautenbacher S. (2004). The impact of Alzheimer’s disease on the pain processing. Fortschr. Neurol. Psychiatr. 72 375– 382. 10.1055/s-2004-818389 15252751 · DOI
- Kurucu H. Colom-Cadena M. Davies C. Wilkins L. King D. Rose J. (2022). Inhibitory synapse loss and accumulation of amyloid beta in inhibitory presynaptic terminals in Alzheimer’s disease. Eur. J. Neurol. 29 1311– 1323. 10.1111/ene.15043 34331352 · DOI
- Kurylo D. D. Corkin S. Dolan R. Rizzo J. F. Parker S. W. Growdon J. H. (1994). Broad-band visual capacities are not selectively impaired in Alzheimer’s disease. Neurobiol. Aging 15 305– 311. 10.1016/0197-4580(94)90025-6 7936054 · DOI
- Kurylo D. Corkin S. Allard T. Zatorre R. Growdon J. (1993). Auditory function in Alzheimer’s disease. Neurology 43 1893– 1899. 10.1212/wnl.43.10.1893 8413944 · DOI
- Kwakowsky A. Guzmán B. C. F. Pandya M. Turner C. Waldvogel H. J. Waldvogel H. J. (2018). GABAA receptor subunit expression changes in the human Alzheimer’s disease hippocampus, subiculum, entorhinal cortex and superior temporal gyrus. J. Neurochem. 145 374– 392. 10.1111/jnc.14325 29485232 · DOI
- L’Esperance O. J. McGhee J. Davidson G. Smith A. S. Subramanian J. (2023). Functional connectivity favors hyperactivity leading to synapse loss in amyloidosis. Biorxiv [ Preprint]. 10.1101/2023.01.05.522900 36712054 PMC9881957 · DOI
- Lai M. K. P. Tsang S. W. Y. Alder J. T. Alder J. T. Keene J. Hope T. (2005). Loss of serotonin 5-HT2A receptors in the postmortem temporal cortex correlates with rate of cognitive decline in Alzheimer’s disease. Psychopharmacology 179 673– 677. 10.1007/s00213-004-2077-2 15551121 · DOI
- Leuba G. Kraftsik R. Saini K. (1998). Quantitative distribution of parvalbumin, calretinin, and calbindin D-28k immunoreactive neurons in the visual cortex of normal and Alzheimer cases. Exp. Neurol. 152 278– 291. 10.1006/exnr.1998.6838 9710527 · DOI
- Leuba G. Saini K. Zimmermann V. Giannakopoulos P. Bouras C. (2001). Mild amyloid pathology in the primary visual system of nonagenarians and centenarians. Dement. Geriatr. Cogn. Disord. 12 146– 152. 10.1159/000051249 11173888 · DOI
- Lewis D. Campbell M. Terry R. Morrison J. (1987). Laminar and regional distributions of neurofibrillary tangles and neuritic plaques in Alzheimer’s disease: A quantitative study of visual and auditory cortices. J. Neurosci. 7 1799– 1808. 10.1523/jneurosci.07-06-01799.1987 2439665 PMC6568896 · DOI · Paper page
- Liebscher S. Keller G. B. Goltstein P. M. Bonhoeffer T. Hübener M. (2016). Selective persistence of sensorimotor mismatch signals in visual cortex of behaving Alzheimer’s disease mice. Curr. Biol. 26 956– 964. 10.1016/j.cub.2016.01.070 27020746 · DOI
- Lin F. R. Metter E. J. Resnick S. M. Zonderman A. B. Ferrucci L. (2011). Hearing loss and incident dementia. JAMA Neurol. 68 214– 220. 10.1001/archneurol.2010.362 21320988 PMC3277836 · DOI
- Liu Y. Fang S. Liu L. M. Zhu Y. Li C. R. Chen K. (2020). Hearing loss is an early biomarker in APP/PS1 Alzheimer’s disease mice. Neurosci. Lett. 717: 134705. 10.1016/j.neulet.2019.134705 31870800 PMC7004828 · DOI
- Livingston G. Sommerlad A. Orgeta V. Costafreda S. G. Huntley J. Ames D. (2017). Dementia prevention, intervention, and care. Lancet 390 2673– 2734. 10.1016/S0140-6736(17)31363-6 28735855 · DOI · Paper page
- Maatuf Y. Stern E. A. Slovin H. (2016). Abnormal population responses in the somatosensory cortex of Alzheimer’s disease model mice. Sci. Rep. 6: 24560. 10.1038/srep24560 27079783 PMC4832196 · DOI
- Marquié M. Castilla-Martí M. Valero S. Martínez J. Sánchez D. Hernández I. (2019). Visual impairment in aging and cognitive decline: Experience in a Memory Clinic. Sci. Rep. 9: 8698. 10.1038/s41598-019-45055-9 31213626 PMC6581941 · DOI
- Martin-Ruiz C. Court J. A. Molnar E. Lee M. Gotti C. Mamalaki A. (2002). A4 but Not α3 and α7 nicotinic acetylcholine receptor subunits Are Lost from the temporal cortex in Alzheimer’s disease. J. Neurochem. 73 1635– 1640. 10.1046/j.1471-4159.1999.0731635.x 10501210 · DOI
- Masliah E. Terry R. D. Mallory M. Alford M. Hansen L. A. (1990). Diffuse plaques do not accentuate synapse loss in Alzheimer’s disease. Am. J. Pathol. 137 1293– 1297. 2124413 PMC1877714
- Mavroudis I. Fotiou D. Manani M. G. Njaou S. N. Frangou D. Costa V. (2011). Dendritic pathology and spinal loss in the visual cortex in Alzheimer’s disease: A golgi study in pathology. Int. J. Neurosci. 121 347– 354. 10.3109/00207454.2011.553753 21545306 · DOI
- McCool M. F. Varty G. B. Del Vecchio R. A. Kazdoba T. M. Parker E. M. Hunter J. C. (2003). Increased auditory startle response and reduced prepulse inhibition of startle in transgenic mice expressing a double mutant form of amyloid precursor protein. Brain Res. 994 99– 106. 10.1016/j.brainres.2003.09.025 14642453 · DOI
- McKee A. C. Au R. Cabral H. J. Kowall N. W. Seshadri S. Kubilus C. A. (2006). Visual association pathology in preclinical Alzheimer disease. J. Neuropathol. Exp. Neurol. 65 621– 630. 10.1097/00005072-200606000-00010 16783172 · DOI
- Meadowcroft M. D. Purnell C. J. Lu J. Wang J. Karunanayaka P. Yang Q. S. (2019). P4-304: 18f-Fdg-pet hyperactivity in Alzheimer’s disease primary olfactory cortex. Alzheimers Dement. 15 1407– 1407. 10.1016/j.jalz.2019.06.5072 · DOI
- Mendez M. Mendez M. Martin R. Smyth K. Whitehouse P. (1990). Complex visual disturbances in Alzheimer’s disease. Neurology 40 439– 443. 10.1212/wnl.40.3_part_1.439 2314585 · DOI
- Murty D. V. P. S. Shirhatti V. Ravishankar P. Ray S. (2018). Large visual stimuli induce two distinct gamma oscillations in primate visual cortex. J. Neurosci. Off. J. Soc. Neurosci. 38 2730– 2744. 10.1523/JNEUROSCI.2270-17.2017 29440388 PMC5852657 · DOI
- Na D. Zhang J. Beaulac H. J. Piekna-Przybylska D. Nicklas P. R. Kiernan A. E. (2023). Increased central auditory gain in 5xFAD Alzheimer’s disease mice as an early biomarker candidate for Alzheimer’s disease diagnosis. Front. Neurosci. 17: 1106570. 10.3389/fnins.2023.1106570 37304021 PMC10250613 · DOI
- Niraula S. Doderer J. J. Indulkar S. Berry K. P. Hauser W. L. L’Esperance O. J. (2023). Excitation-inhibition imbalance disrupts visual familiarity in amyloid and non-pathology conditions. Cell Rep. 42: 111946. 10.1016/j.celrep.2022.111946 36640331 PMC9939293 · DOI
- O’Leary T. P. Shin S. Fertan E. Dingle R. N. Almuklass A. Gunn R. K. (2017). Reduced acoustic startle response and peripheral hearing loss in the 5xFAD mouse model of Alzheimer’s disease. Genes Brain Behav. 16 554– 563. 10.1111/gbb.12370 28133939 · DOI
- Pache M. Smeets C. H. W. Gasio P. F. Savaskan E. Flammer J. Wirz-Justice A. (2003). Colour vision deficiencies in Alzheimer’s disease. Age Ageing 32 422– 426. 10.1093/ageing/32.4.422 12851187 · DOI
- Paciello F. Rinaudo M. Longo V. Cocco S. Conforto G. Pisani A. (2021). Auditory sensory deprivation induced by noise exposure exacerbates cognitive decline in a mouse model of Alzheimer’s disease. eLife 10: e70908. 10.7554/elife.70908 34699347 PMC8547960 · DOI
- Papanikolaou A. Rodrigues F. R. Holeniewska J. Phillips K. G. Saleem A. B. Solomon S. G. (2020). Plasticity in visual cortex is disrupted in a mouse model of tauopathy and neurodegeneration. Biorxiv [ Preprint]. 10.1101/2020.11.02.365767 PMC8776781 35058544 · DOI
- Papanikolaou A. Rodrigues F. R. Holeniewska J. Phillips K. G. Saleem A. B. Solomon S. G. (2022). Plasticity in visual cortex is disrupted in a mouse model of tauopathy. Commun. Biol. 5: 77. 10.1038/s42003-022-03012-9 35058544 PMC8776781 · DOI
- Peters C. A. Potter J. F. Scholer S. G. (1988). Hearing impairment as a predictor of cognitive decline in dementia. J. Am. Geriatr. Soc. 36 981– 986. 10.1111/j.1532-5415.1988.tb04363.x 3171050 · DOI
- Petrache A. L. Rajulawalla A. Shi A. Wetzel A. Saito T. Saido T. C. (2019). Aberrant excitatory-inhibitory synaptic mechanisms in entorhinal cortex microcircuits during the pathogenesis of Alzheimer’s disease. Cereb. Cortex 1991 1834– 1850. 10.1093/cercor/bhz016 30766992 PMC6418384 · DOI · Paper page
- Polo V. Rodrigo M. Garcia-Martin E. Otin S. Larrosa J. Fuertes M. (2017). Visual dysfunction and its correlation with retinal changes in patients with Alzheimer’s disease. Eye 31 1034– 1041. 10.1038/eye.2017.23 28282060 PMC5519267 · DOI
- Rafalowska J. Barcikowska M. Barcikowska M. Wen G. Y. Wen G. Y. Wen G. Y. (1988). Laminar distribution of neuritic plaques in normal aging, Alzheimer’s disease and Down’s syndrome. Acta Neuropathol. 77 21– 25. 10.1007/bf00688238 2977047 · DOI
- Rajendran L. Paolicelli R. C. (2018). Microglia-mediated synapse loss in Alzheimer’s disease. J. Neurosci. 38 2911– 2919. 10.1523/JNEUROSCI.1136-17.2017 29563239 PMC6596066 · DOI · Paper page
- Risacher S. L. Wudunn D. Pepin S. M. MaGee T. R. McDonald B. C. Flashman L. A. (2013). Visual contrast sensitivity in Alzheimer’s disease, mild cognitive impairment, and older adults with cognitive complaints. Neurobiol. Aging 34 1133– 1144. 10.1016/j.neurobiolaging.2012.08.007 23084085 PMC3545045 · DOI
- Risacher S. L. WuDunn D. Tallman E. F. West J. D. Gao S. Farlow M. R. (2020). Visual contrast sensitivity is associated with the presence of cerebral amyloid and tau deposition. Brain Commun. 2: fcaa019. 10.1093/braincomms/fcaa019 32309804 PMC7151662 · DOI
- Rizzo M. Nawrot M. (1998). Perception of movement and shape in Alzheimer’s disease. Brain 121 2259– 2270. 10.1093/brain/121.12.2259 9874479 · DOI
- Sadun A. A. Borchert M. DeVita E. Hinton D. R. Bassi C. J. (1987). Assessment of visual impairment in patients with Alzheimer’s disease. Am. J. Ophthalmol. 104 113– 120. 10.1016/0002-9394(87)90001-8 3618708 · DOI
- Salamone G. Di Lorenzo C. Mosti S. Lupo F. Cravello L. Palmer K. (2009). Color discrimination performance in patients with Alzheimer’s disease. Dement. Geriatr. Cogn. Disord. 27 501– 507. 10.1159/000218366 19451717 · DOI
- Sarant J. Harris D. Busby P. Maruff P. Schembri A. Lemke U. (2020). The effect of hearing aid use on cognition in older adults: Can we delay decline or even improve cognitive function? J. Clin. Med. 9: 254. 10.3390/jcm9010254 31963547 PMC7020090 · DOI
- Sartucci F. Borghetti D. Bocci T. Murri L. Orsini P. Porciatti V. (2010). Dysfunction of the magnocellular stream in Alzheimer’s disease evaluated by pattern electroretinograms and visual evoked potentials. Brain Res. Bull. 82 169– 176. 10.1016/j.brainresbull.2010.04.001 20385208 PMC3227554 · DOI
- Savioz A. Giannakopoulos P. Herrmann F. Klein W. L. Kovari E. V. Bouras C. (2016). A study of Aβ oligomers in the temporal cortex and cerebellum of patients with neuropathologically confirmed Alzheimer’s disease compared to aged controls. Neurodegener. Dis. 16 398– 406. 10.1159/000446283 27400224 · DOI
- Schlotterer G. Moscovitch M. Crapper-Mclachlan D. (1984). Visual processing deficits as assessed by spatial frequency contrast sensitivity and backward masking in normal ageing and Alzheimer’s disease. Brain 107 309– 324. 10.1093/brain/107.1.309 6697160 · DOI
- Selkoe D. J. (2002). Alzheimer’s disease is a synaptic failure. Science 298 789– 791. 10.1126/science.1074069 12399581 · DOI · Paper page
- Sichler M. E. Löw M. J. Schleicher E. M. Bayer T. A. Bouter Y. (2019). Reduced acoustic startle response and prepulse inhibition in the Tg4-42 model of Alzheimer’s disease. J. Alzheimers Dis. Rep. 3 269– 278. 10.3233/ADR-190132 31867566 PMC6918877 · DOI
- Silverman D. H. Small G. W. Chang C. Y. Lu C. S. Kung De Aburto M. A. Chen W. (2001). Positron emission tomography in evaluation of dementia: Regional brain metabolism and long-term outcome. JAMA 286 2120– 2127. 10.1001/jama.286.17.2120 11694153 · DOI
- Silverman S. E. Tran D. B. Zimmerman K. Feldon S. E. (1994). Dissociation between the detection and perception of motion in Alzheimer’s disease. Neurology 44 1814– 1814. 10.1212/wnl.44.10.1814 7936228 · DOI
- Sinha U. K. Hollen K. M. Rodriguez R. Miller C. A. (1993). Auditory system degeneration in Alzheimer’s disease. Neurology 43 779– 779. 10.1212/wnl.43.4.779 8469340 · DOI
- Smith B. C. D’Amico M. (2020). Sensory-based interventions for adults with dementia and Alzheimer’s disease: A scoping review. Occup. Ther. Health Care 34 171– 201. 10.1080/07380577.2019.1608488 31066598 · DOI
- Soula M. Martín-Ávila A. Zhang Y. Dhingra A. Nitzan N. Sadowski M. J. (2023). Forty-hertz light stimulation does not entrain native gamma oscillations in Alzheimer’s disease model mice. Nat. Neurosci. 26 570– 578. 10.1038/s41593-023-01270-2 36879142 PMC10839995 · DOI
- Stephen J. M. Montaño R. Donahue C. H. Adair J. C. Knoefel J. E. Qualls C. (2010). Somatosensory responses in normal aging, mild cognitive impairment, and Alzheimer’s disease. J. Neural Transm. 117 217– 225. 10.1007/s00702-009-0343-5 20013008 PMC2833105 · DOI
- Stevenson J. S. Clifton L. Kuźma E. Littlejohns T. J. (2022). Speech-in-noise hearing impairment is associated with an increased risk of incident dementia in 82,039 UK Biobank participants. Alzheimers Dement. 18 445– 456. 10.1002/alz.12416 34288382 · DOI
- Story D. Chan E. Munro N. Rossignol J. Dunbar G. L. (2019). Latency to startle is reduced in the 5xFAD mouse model of Alzheimer’s disease. Behav. Brain Res. 359 823– 827. 10.1016/j.bbr.2018.07.021 30055208 · DOI
- Strouse A. L. Hall J. W. I. Burger M. C. (1995). Central auditory processing in Alzheimer’s disease. Ear Hear. 16: 230. 7789674
- Styren S. D. Kamboh M. I. DeKosky S. T. (1998). Expression of differential immune factors in temporal cortex and cerebellum: The role of α-1-antichymotrypsin, apolipoprotein E, and reactive glia in the progression of Alzheimer’s disease. J. Comp. Neurol. 396 511– 520. 9651008
- Targa Dias Anastacio H. Matosin N. Ooi L. (2022). Neuronal hyperexcitability in Alzheimer’s disease: What are the drivers behind this aberrant phenotype? Transl. Psychiatry 12 1– 14. 10.1038/s41398-022-02024-7 35732622 PMC9217953 · DOI · Paper page
- Terry R. D. Masliah E. Salmon D. P. Butters N. Butters N. DeTeresa R. (1991). Physical basis of cognitive alterations in Alzheimer’s disease: Synapse loss is the major correlate of cognitive impairment. Ann. Neurol. 30 572– 580. 10.1002/ana.410300410 1789684 · DOI · Paper page
- Trick G. Trick L. Morris P. Wolf M. (1995). Visual field loss in senile dementia of the Alzheimer’s type. Neurology 45 68– 74. 10.1212/wnl.45.1.68 7824139 · DOI
- Tsuboi Y. Wszolek Z. K. Graff-Radford N. R. Cookson N. Dickson D. W. (2003). Tau pathology in the olfactory bulb correlates with Braak stage, Lewy body pathology and apolipoprotein epsilon4. Neuropathol. Appl. Neurobiol. 29 503– 510. 10.1046/j.1365-2990.2003.00453.x 14507342 · DOI
- Tsui K. C. Roy J. Chau S. C. Wong K. H. Shi L. Poon C. H. (2022). Distribution and inter-regional relationship of amyloid-beta plaque deposition in a 5xFAD mouse model of Alzheimer’s disease. Front. Aging Neurosci. 14: 964336. 10.3389/fnagi.2022.964336 35966777 PMC9371463 · DOI
- Uhlmann R. F. Larson E. B. Koepsell T. D. (1986). Hearing impairment and cognitive decline in senile dementia of the Alzheimer’s type. J. Am. Geriatr. Soc. 34 207– 210. 10.1111/j.1532-5415.1986.tb04204.x 3950288 · DOI
- Uylings H. B. M. de Brabander J. M. (2002). Neuronal changes in normal human aging and Alzheimer’s disease. Brain Cogn. 49 268– 276. 10.1006/brcg.2001.1500 12139954 · DOI
- Waller R. Mandeya M. Viney E. Simpson J. E. Wharton S. B. (2020). Histological characterization of interneurons in Alzheimer’s disease reveals a loss of somatostatin interneurons in the temporal cortex. Neuropathology 40 336– 346. 10.1111/neup.12649 32232904 · DOI
- Wang H. He J. Zhang R. Zhu S. Wang J. Kong L. (2012). Sensorimotor gating and memory deficits in an APP/PS1 double transgenic mouse model of Alzheimer’s disease. Behav. Brain Res. 233 237– 243. 10.1016/j.bbr.2012.05.007 22595040 · DOI
- Wang S. Wu C. (2021). Tau phosphorylation and cochlear apoptosis cause hearing loss in 3×Tg-AD mouse model of Alzheimer’s disease. Chin. J. Physiol. 64 61– 71. 10.4103/cjp.cjp_79_20 33938816 · DOI
- Weible A. P. Wehr M. (2022). Amyloid pathology in the central auditory pathway of 5XFAD mice appears first in auditory cortex. J. Alzheimers Dis. 89 1385– 1402. 10.3233/jad-220538 36031901 PMC10097438 · DOI
- Weible A. P. Stebritz A. J. Wehr M. (2020). 5XFAD mice show early-onset gap encoding deficits in the auditory cortex. Neurobiol. Aging 94 101– 110. 10.1016/j.neurobiolaging.2020.05.013 32599514 PMC7483957 · DOI
- Wesson D. W. Levy E. Nixon R. A. Wilson D. A. (2010). Olfactory dysfunction correlates with amyloid-β burden in an Alzheimer’s disease mouse model. J. Neurosci. 30 505– 514. 10.1523/JNEUROSCI.4622-09.2010 20071513 PMC2826174 · DOI · Paper page
- Wiesman A. I. Mundorf V. M. Casagrande C. C. Wolfson S. L. Johnson C. M. May P. E. (2021a). Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer’s disease spectrum. Ebiomedicine 73: 103638. 10.1016/j.ebiom.2021.103638 34689085 PMC8550984 · DOI
- Wiesman A. I. Murman D. L. May P. E. Schantell M. Wolfson S. L. Johnson C. M. (2021b). Visuospatial alpha and gamma oscillations scale with the severity of cognitive dysfunction in patients on the Alzheimer’s disease spectrum. Alzheimers Res. Ther. 13: 139. 10.1186/s13195-021-00881-w 34404472 PMC8369319 · DOI
- Wijk H. Berg S. Sivik L. Steen B. (1999). Colour discrimination, colour naming and colour preferences among individuals with Alzheimer’s disease. Int. J. Geriatr. Psychiatry 14 1000– 1005. 10607966
- Wood K. C. Blackwell J. M. Geffen M. N. (2017). Cortical inhibitory interneurons control sensory processing. Curr. Opin. Neurobiol. 46 200– 207. 10.1016/j.conb.2017.08.018 28938181 PMC5693245 · DOI
- Woodward M. R. Amrutkar C. V. Shah H. C. Benedict R. H. B. Rajakrishnan S. Doody R. S. (2017). Validation of olfactory deficit as a biomarker of Alzheimer disease. Neurol. Clin. Pract. 7 5– 14. 10.1212/CPJ.0000000000000293 28243501 PMC5310210 · DOI
- Wright A. L. Zinn R. Hohensinn B. Konen L. M. Beynon S. B. Tan R. P. (2013). Neuroinflammation and neuronal loss precede Aβ plaque deposition in the hAPP-J20 mouse model of Alzheimer’s disease. PLoS One 8: e59586. 10.1371/journal.pone.0059586 23560052 PMC3613362 · DOI
- Wu N. Rao X. Gao Y. Wang J. Xu F. (2013). Amyloid-β deposition and olfactory dysfunction in an Alzheimer’s disease model. J. Alzheimers Dis. 37 699– 712. 10.3233/JAD-122443 23948910 · DOI · Paper page
- Yamasaki T. Muranaka H. Kaseda Y. Mimori Y. Tobimatsu S. (2012). Understanding the pathophysiology of Alzheimer’s disease and mild cognitive impairment: A mini review on fMRI and ERP studies. Neurol. Res. Int. 2012: 719056. 10.1155/2012/719056 21773027 PMC3135099 · DOI
- Zaforas M. Rosa J. M. Alonso-Calviño E. Fernández-López E. Miguel-Quesada C. Oliviero A. (2021). Cortical layer-specific modulation of neuronal activity after sensory deprivation due to spinal cord injury. J. Physiol. 599 4643– 4669. 10.1113/JP281901 34418097 PMC9292026 · DOI
- Zatorre R. J. Belin P. Penhune V. B. (2002). Structure and function of auditory cortex: Music and speech. Trends Cogn. Sci. 6 37– 46. 10.1016/S1364-6613(00)01816-7 11849614 · DOI
- Zhang M. Zhong L. Han X. Xiong G. Xu D. Zhang S. (2021). Brain and retinal abnormalities in the 5xFAD mouse model of Alzheimer’s disease at early stages. Front. Neurosci. 15: 681831. 10.3389/fnins.2021.681831 34366774 PMC8343228 · DOI
- Zou Y. Lu D. Liu L. Zhang H. Zhou Y. (2016). Olfactory dysfunction in Alzheimer’s disease. Neuropsychiatr. Dis. Treat. 12 869– 875. 10.2147/NDT.S104886 27143888 PMC4841431 · DOI
- Authors
- Zhang, N. K., Zhang, S. K., Zhang, L. I., Tao, H. W., & Zhang, G.-W.
- Affiliations
- University of Southern California (US)
- Venue
- Frontiers in Aging Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2023-08-15
- Volume
- 15
- Pages
- 1213379-1213379
- ISSN
- 1663-4365 (ISSN-L)
- PMC
- PMC10464619
- OpenAlex
- W4385874589
- Cited by
- 49
- References
- 174
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 12
- FWCI
- 1.75
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Aging Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Alzheimer's Association (AARF-23-1148428)
- Cure Alzheimer's Fund
- National Institute for Health and Care Research
- National Institutes of Health
- National Institute of Mental Health (U01MH116990)
- National Eye Institute (R01EY019049)
- National Institute on Deafness and Other Communication Disorders (R01DC008983, R01DC020887)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- Alzheimer's disease, sensory processing deficits, cortical pathology, olfactory dysfunction, somatosensory impairment, amyloid-beta deposition, tauopathy, gliosis, neuronal excitability, synaptic plasticity, early diagnosis biomarkers, animal models of Alzheimer's disease
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review