Evidence map›Paper›PMID 36527292›Full record

ArticlePsychiatry and clinical neurosciences2023

Circadian rest-activity rhythm and longitudinal brain changes underlying late-life cognitive decline.

So Yeon Jeon, Min Soo Byun, Dahyun Yi, Gijung Jung, Jun-Young Lee, Yu Kyeong Kim, Chul-Ho Sohn, Koung Mi Kang, Yu Jin Lee, Dong Young Lee and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 13 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

11 authors at 4 institutions in 2 countries.

So Yeon JeonDepartment of Psychiatry, Chungnam National University Hospital, Daejeon, Republic of Korea.
Min Soo ByunDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Dahyun YiInstitute of Human Behavioral Medicine, Medical Research Centre, Seoul National University, Seoul, South Korea.
Gijung JungDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Jun-Young LeeDepartment of Neuropsychiatry, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea.
Yu Kyeong KimDepartment of Nuclear Medicine, SMG-SNU Boramae Medical Center, Seoul, South Korea.
Chul-Ho SohnDepartment of Radiology, Seoul National University College of Medcine, Seoul, South Korea.
Koung Mi KangDepartment of Radiology, Seoul National University Hospital, Seoul, South Korea.
Yu Jin LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-5195-2579
Dong Young LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8976-8320
KBASE Research Group
Seoul National University · KRSeoul National University Hospital · KRSNUH SMG-SNU Boramae Medical Center · KRChungnam National University · KR

Funding

KBASE2: Korean Brain Aging Study, Longitudinal Endophenotypes and Systems BiologyU01AG072177 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LEE, DONG YOUNG, NHO, KWANGSIK TIMOTHY · 2021 to 2025
$11.2M
NIA NIH HHS U01 AG072177
6 · The paper itself

Abstract

aimThe neurobiological substrates underlying the relationship of circadian rest-activity rhythm (RAR) alteration with accelerated late-life cognitive decline are not clearly understood. In the present study, the longitudinal relationship of objectively measured circadian RAR with in vivo Alzheimer disease (AD) pathologies and cerebrovascular injury was investigated in older adults without dementia.

methodsThe present study included 129 participants without dementia who participated in the KBASE (Korean Brain Aging Study for Early Diagnosis and Prediction of Alzheimer's Disease) cohort. All participants underwent actigraphy at baseline and two consecutive [

resultsDelayed acrophase at baseline was significantly associated with greater annualized decline of AD-CM over a 2-year period, but not with that of other neuroimaging measures. In contrast, other circadian RAR parameters at baseline had no association with annualized change of any neuroimaging measures. Annualized decline of AD-CM was also significantly positively associated with the annual change in MMSE scores. Furthermore, a mediation analysis showed that greater reduction in AD-CM mediated the effect of delayed acrophase at baseline on faster decline of MMSE score.

conclusionThe findings indicate that delayed acrophase in late life may cause or predict hypometabolism at AD-signature brain regions, which underlies cognitive decline in the near future.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAmyloid beta-PeptidesBrainHumansLongitudinal StudiesMagnetic Resonance ImagingNeuroimagingPositron-Emission TomographyAmyloid beta-PeptidesAlzheimer diseasecognitive declineneurodegenerationolder adultsrest-activity rhythm

Identifiers

PMID36527292
PMCPMC10360409
OpenAlexW4311822750

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.