Evidence map›Paper›PMID 39333449›Full record

ArticleGeroScience2025

Disruption of sleep macro- and microstructure in Alzheimer's disease: overlaps between neuropsychology, neurophysiology, and neuroimaging.

Anna Csilla Kegyes-Brassai, Robert Pierson-Bartel, Gergo Bolla, Anita Kamondi, Andras Attila Horvath

Abstract read
In one paragraph

Article in GeroScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Lower slow wave sleep and rapid eye movement sleep are associated with brain atrophy of Alzheimer's disease-vulnerable regions.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2025
    Article
  6. bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Anna Csilla Kegyes-BrassaiSchool of PhD Studies, Semmelweis University, Budapest, Hungary. kegyes.brassai.anna@gmail.com.
Robert Pierson-BartelFaculty of Medicine, Semmelweis University, Budapest, Hungary.
Gergo BollaSchool of PhD Studies, Semmelweis University, Budapest, Hungary.
Anita KamondiNeurocognitive Research Centre, Nyírő Gyula National Institute of Psychiatry, and Addictology, Budapest, Hungary.
Andras Attila HorvathNeurocognitive Research Centre, Nyírő Gyula National Institute of Psychiatry, and Addictology, Budapest, Hungary.

Funding

Magyar Tudományos Akadémia bo_78_20_2020Magyar Tudományos Akadémia Lendulet-2023_94National Research, Development and Innovation Office 146936National Research, Development and Innovation Office 2017-1.2.1-NKP-2017-00002National Research, Development and Innovation Office 2019-2.1.7-ERA-NET-2020-00006National Research, Development and Innovation Office NAP2022-I-9/2022National Research, Development and Innovation Office OTKA-K_23_ 146792National Research, Development and Innovation Office ÚNKP-22-2-III-BME-212
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the leading cause of dementia, often associated with impaired sleep quality and disorganized sleep structure. This study aimed to characterize changes in sleep macrostructure and K-complex density in AD, in relation to neuropsychological performance and brain structural changes. We enrolled 30 AD and 30 healthy control participants, conducting neuropsychological exams, brain MRI, and one-night polysomnography. AD patients had significantly reduced total sleep time (TST), sleep efficiency, and relative durations of non-rapid eye movement (NREM) stages 2 (S2), 3 (S3), and rapid eye movement (REM) sleep (p < 0.01). K-complex (KC) density during the entire sleep period and S2 (p < 0.001) was significantly decreased in AD. We found strong correlations between global cognitive performance and relative S3 (p < 0.001; r = 0.86) and REM durations (p < 0.001; r = 0.87). TST and NREM stage 1 (S1) durations showed a moderate negative correlation with amygdaloid and hippocampal volumes (p < 0.02; r = 0.51-0.55), while S3 and REM sleep had a moderate positive correlation with cingulate cortex volume (p < 0.02; r = 0.45-0.61). KC density strongly correlated with global cognitive function (p < 0.001; r = 0.66) and the thickness of the anterior cingulate cortex (p < 0.05; r = 0.45-0.47). Our results indicate significant sleep organization changes in AD, paralleling cognitive decline. Decreased slow wave sleep and KCs are strongly associated with cingulate cortex atrophy. Since sleep changes are prominent in early AD, they may serve as prognostic markers or therapeutic targets.

Indexed as

Alzheimer DiseaseSleepSleep Wake DisordersAgedAged, 80 and overBrainCase-Control StudiesFemaleHumansMagnetic Resonance ImagingMaleNeuroimagingNeuropsychological TestsPolysomnographySleep StagesAlzheimer’s diseaseCingulate cortexK-complexPolysomnographySleep

Identifiers

PMID39333449
PMCPMC12181553

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.