Evidence map›Paper›PMID 40325979›Full record

ArticleJournal of Alzheimer's disease : JAD2025

Sleep disturbances and disorders in the memory clinic: Self-report, actigraphy, and polysomnography.

Aaron Lam, Dexiao Kong, Angela L D'Rozario, Catriona Ireland, Rebekah M Ahmed, Zoe Menczel Schrire, Loren Mowszowski, Johannes Michaelian, Ron R Grunstein, Sharon L Naismith

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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  6. Article
  7. Review
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

10 authors.

Aaron LamHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0001-6087-3565
Dexiao KongHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0002-1717-5929
Angela L D'RozarioWoolcock Institute of Medical Research, Macquarie University, Macquarie Park, NSW, Australia.ORCID 0000-0001-8564-796X
Catriona IrelandHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.
Rebekah M AhmedHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.
Zoe Menczel SchrireHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0001-9903-0899
Loren MowszowskiHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0002-7534-5017
Johannes MichaelianHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0001-5683-8222
Ron R GrunsteinWoolcock Institute of Medical Research, Macquarie University, Macquarie Park, NSW, Australia.
Sharon L NaismithHealthy Brain Ageing Program, The Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.ORCID 0000-0001-9076-2778

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundSleep disturbances are common in dementia but rarely studied in memory clinics.ObjectiveIn a memory clinic setting we aimed to (1) identify rates of obstructive sleep apnea (OSA), abnormal sleep duration, circadian phase shift, insomnia, poor sleep quality, and REM sleep behavior disorder (RBD); (2) assess concordance between self-reported and actigraphy-derived measures; investigate associations between sleep disturbances; and (3) neuropsychological performance and (4) cognitive status.MethodsAdults over 50 at a memory clinic between 2009-2024 were included. OSA was assessed via polysomnography and prior history. Sleep duration and circadian phase were measured by self-report and actigraphy. Self-report questionnaires evaluated insomnia, sleep quality, and RBD. Global cognition, processing speed, memory, and executive function were assessed. Analysis of Covariance and multinomial logistic regression examined the impact of OSA, sleep duration, insomnia, and sleep quality on cognition and cognitive status.Results1234 participants (Mage 67.2, 46%M) were included. 75.3% had OSA, while 12.7% were previously diagnosed. Insomnia affected 12.0%, 54.3% had poor sleep quality, and 14.2% endorsed RBD symptoms. Self-reported short (30.5%) and long (10.2%) sleep exceeded actigraphy rates (8.5% and 5.1%) with poor concordance between measures. OSA was linked to impaired global cognition and memory (p < 0.05). Prolonged sleep predicted deficits in global cognition, processing speed, memory, and executive function and a higher risk of aMCI (all p < 0.05). Poor sleep quality was linked to better memory (p < 0.05).ConclusionsDespite discrepancies between self-reported and objective prevalence rates, sleep disturbances are highly prevalent in memory clinics and impact cognition, necessitating further examination.

Indexed as

ActigraphyMemory DisordersPolysomnographySelf ReportSleep Wake DisordersAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeuropsychological TestsSleep QualityagingAlzheimer's diseasecircadian rhythmdementiamild cognitive impairmentREM sleep behavior disordersleep apnea

Identifiers

PMID40325979
PMCPMC12231846

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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.