Sleep Disturbances in Alzheimer’s and Parkinson’s Diseases
Open accessAbstract
Alzheimer's disease (AD) and Parkinson's disease (PD) are the two most common neurodegenerative disorders and exact a burden on our society greater than cardiovascular disease and cancer combined. While cognitive and motor symptoms are used to define AD and PD, respectively, patients with both disorders exhibit sleep disturbances including insomnia, hypersomnia and excessive daytime napping. The molecular basis of perturbed sleep in AD and PD may involve damage to hypothalamic and brainstem nuclei that control sleep-wake cycles. Perturbations in neurotransmitter and hormone signaling (e.g., serotonin, norepinephrine and melatonin) and the neurotrophic factor BDNF likely contribute to the disease process. Abnormal accumulations of neurotoxic forms of amyloid β-peptide, tau and α-synuclein occur in brain regions involved in the regulation of sleep in AD and PD patients, and are sufficient to cause sleep disturbances in animal models of these neurodegenerative disorders. Disturbed regulation of sleep often occurs early in the course of AD and PD, and may contribute to the cognitive and motor symptoms. Treatments that target signaling pathways that control sleep have been shown to retard the disease process in animal models of AD and PD, suggesting a potential for such interventions in humans at risk for or in the early stages of these disorders.
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?
In individuals with PD, sleep-wake symptoms often precede the development of motor or cognitive symptoms and may be useful as a diagnostic biomarker.
“In individuals with PD, these sleep–wake symptoms often precede the development of motor or cognitive symptoms and may even be useful as a diagnostic biomarker259,260”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [260]
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 154 · Cited by 102
- Authors
- Rothman, S. M., & Mattson, M. P.
- Affiliations
- National Institute on Aging (US)
- Corresponding author
- Rothman, Sarah M.
- Venue
- NeuroMolecular Medicine
- Published
- 2012-05-03
- Volume
- 14
- Issue
- 3
- Pages
- 194-204
- ISSN
- 1535-1084 (ISSN-L)
- 1559-1174
- PMC
- PMC4544709
- OpenAlex
- W2064833041
- Cited by
- 102
- References
- 154
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 13 · 2023: 5 · 2022: 5 · 2021: 6 · 2020: 9 · 2019: 2 · 2018: 8 · 2017: 4 · 2016: 5 · 2015: 12 · 2014: 11 · 2013: 9
- FWCI
- 5.25
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- NeuroMolecular Medicine (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (Z01AG000312)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Keywords
- sleep disorders, Alzheimer's disease, Parkinson's disease, insomnia, hypersomnia, excessive daytime sleepiness, sleep-wake regulation, hypothalamus, brainstem, serotonin, norepinephrine, melatonin, brain-derived neurotrophic factor, amyloid-beta, tau protein, alpha-synuclein, neurodegeneration, animal models
- MeSH terms
- Alzheimer Disease, Animals, Brain, Disease Models, Animal, Humans, Parkinson Disease, Sleep Wake Disorders
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