Evidence map›Paper›PMID 34784296›Full record

ArticleJCI insight2021

Heterogeneity in the links between sleep arousals, amyloid-β, and cognition.

Daphne O Chylinski, Maxime Van Egroo, Justinas Narbutas, Martin Grignard, Ekaterina Koshmanova, Christian Berthomier, Pierre Berthomier, Marie Brandewinder, Eric Salmon, Mohamed Ali Bahri and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
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

9 citing papers in PubMed, 20 citations in OpenAlex.

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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

16 authors at 2 institutions in 3 countries.

Daphne O ChylinskiGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Maxime Van EgrooGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Justinas NarbutasGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Martin GrignardGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Ekaterina KoshmanovaGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Christian BerthomierPhysip SA, Paris, France.
Pierre BerthomierPhysip SA, Paris, France.
Marie BrandewinderPhysip SA, Paris, France.
Eric SalmonGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Mohamed Ali BahriGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Christine BastinGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Fabienne ColletteGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Christophe PhillipsGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Pierre MaquetGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Vincenzo MutoGIGA-Cyclotron Research Centre-In Vivo Imaging and.
Gilles VandewalleGIGA-Cyclotron Research Centre-In Vivo Imaging and.
STMicroelectronics (United Kingdom) · GBUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDTight relationships between sleep quality, cognition, and amyloid-β (Aβ) accumulation, a hallmark of Alzheimer's disease (AD) neuropathology, have been shown. Sleep arousals become more prevalent with aging and are considered to reflect poorer sleep quality. However, heterogeneity in arousals has been suggested while their associations with Aβ and cognition are not established.METHODSWe recorded undisturbed night-time sleep with EEG in 101 healthy individuals aged 50-70 years, devoid of cognitive and sleep disorders. We classified spontaneous arousals according to their association with muscular tone increase (M+/M-) and sleep stage transition (T+/T-). We assessed cortical Aβ burden over earliest affected regions via PET imaging and assessed cognition via neuropsychological testing.RESULTSArousal types differed in their oscillatory composition in θ (4-8 Hz) and β (16-30 Hz) EEG bands. Furthermore, T+M- arousals, interrupting sleep continuity, were positively linked to Aβ burden (P = 0.0053, R²β* = 0.08). By contrast, more prevalent T-M+ arousals, upholding sleep continuity, were associated with lower Aβ burden (P = 0.0003, R²β* = 0.13), and better cognition, particularly over the attentional domain (P < 0.05, R²β* ≥ 0.04).CONCLUSIONContrasting with what is commonly accepted, we provide empirical evidence that arousals are diverse and differently associated with early AD-related neuropathology and cognition. This suggests that sleep arousals, and their coalescence with other brain oscillations during sleep, may actively contribute to the beneficial functions of sleep and constitute markers of favorable brain and cognitive health trajectories.TRIAL REGISTRATIONEudraCT 2016-001436-35.FUNDINGFRS-FNRS Belgium (FRSM 3.4516.11), Actions de Recherche Concertées Fédération Wallonie-Bruxelles (SLEEPDEM 17/27-09), ULiège, and European Regional Development Fund (Radiomed Project).

Indexed as

Genetic HeterogeneitySleep QualityAgedAmyloid beta-PeptidesArousalCognitionFemaleHumansMaleMiddle AgedSleepAmyloid beta-PeptidesAgingAlzheimer diseaseNeuroscience

Identifiers

PMID34784296
PMCPMC8783672
OpenAlexW3213678320

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.