Evidence map›Paper›PMID 41659073›Full record

ArticlemedRxiv : the preprint server for health sciences2026

REM Sleep is Associated with Cognition and Biomarkers Longitudinally in Older Adults Across the Alzheimer Disease Continuum.

Valentina Pinilla Manriquez, Era M Laho, Stephanie A Marvin, Yazmeen Usman, Michael J Properzi, Kailee A Palmgren, Yiwen Rao, Wai-Ying Wendy Yau, Gretchen Reynolds, Keith A Johnson and 9 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Valentina Pinilla ManriquezDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Era M LahoDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Stephanie A MarvinDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Yazmeen UsmanDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Michael J ProperziDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Kailee A PalmgrenDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Yiwen RaoDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Wai-Ying Wendy YauDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Gretchen ReynoldsDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Keith A JohnsonDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Rachel BuckleyDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.ORCID 0000-0002-5356-5537
Dorene RentzDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Rebecca AmariglioDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Susan RedlineDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Shaun PurcellDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.ORCID 0000-0002-7402-5812
Reisa A SperlingDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.
Ina DjonlagicHarvard Medical School, Boston, MA, USA.
Jasmeer P ChhatwalDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.ORCID 0000-0002-7792-1698
Stephanie A SchultzDepartment of Neurology, Massachusetts General Brigham, Boston, MA, USA.

Funding

Vascular factors, physical activity, and inflammation as modulators of neurodegenerative and cognitive trajectories (Project 2)P01AG036694 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Hyun-Sik Yang · 2010 to 2026
$50.2M
Linking Sleep Disruption to Tau Accumulation and Network Dysregulation in Early Alzheimer's DiseaseR01AG062667 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI CHHATWAL, JASMEER P · 2019 to 2024
$4.2M
Elevated systolic blood pressure, body mass index, and amyloid as drivers of tau and cognitive decline in preclinical Alzheimers disease: critical windows in mid- to late-lifeK23AG084868 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Wai-Ying Wendy Yau · 2024 to 2026
$587k
Identifying variations in gamma-secretase function that are critical determinants of clinical and biomarker progression of Autosomal Dominant Alzheimer's disease: From mechanism to clinical trialsK01AG084816 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Stephanie Schultz · 2024 to 2026
$387k
NIA NIH HHS K01 AG084816NIA NIH HHS K23 AG084868NIA NIH HHS P01 AG036694NIA NIH HHS R01 AG062667
6 · The paper itself

Abstract

Sleep disturbances represent a potentially modifiable risk factor for Alzheimer disease (AD). The extent to which changes in rapid eye movement (REM) sleep are related to the accumulation of AD pathology and brain tissue loss is not well understood. In the current study, ninety-four individuals 74 clinically unimpaired [CU] and 20 clinically impaired [CI]) underwent polysomnography (PSG), cognitive assessments, and neuroimaging. Cross-sectional and longitudinal models examined the associations between PSG outcomes of interest (percentage of sleep period spent in REM [%REM] and REM latency) and pre-clinical Alzheimer's cognitive composite-5 (PACC5) scores, entorhinal tau-positron emission tomography (PET; 18F-flortaucipir), cerebral amyloid-PET (11C-Pittsburgh Compound B; PiB), AD signature cortical thickness, and hippocampal volume, after adjusting for covariates. Across CU and CI individuals, less time spent in REM sleep and prolonged REM latency were associated with poorer cognition after adjusting for age, sex, and years of education. Additionally, these factors were associated with a greater AD pathologic burden after adjusting for age and sex. Longitudinal data, spanning up to 16 years, demonstrated that the rate of change in cognition and AD biomarkers in the time preceding PSG assessment was also strongly associated with REM characteristics. Our findings highlight the potentially bidirectional relationship between the accumulation of AD pathology and the disruption of REM sleep. Future studies are needed to better understand the longitudinal relationship between sleep characteristics, AD progression, and cognitive decline, and to assess the potential of sleep-focused interventions to alter the course of AD clinical, cognitive, and pathological progression.

Identifiers

PMID41659073
PMCPMC12879712

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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.