Evidence map›Paper›PMID 41814477›Full record

ArticleJournal of sleep research2026

Chronotype and All-Cause Mortality in US Middle-Aged and Older Adults: Results From the NHANES.

Zhuozhi Lin, Matthew J Reid, Anis Davoudi, Paul Nestadt, Jacek Urbanek, Junrui Di, Vadim Zipunnikov, Darlynn M Rojo-Wissar, Adam P Spira

Abstract read
In one paragraph

Article in Journal of sleep research, 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

9 authors.

Zhuozhi LinDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0002-1729-3538
Matthew J ReidDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0001-8540-7069
Anis DavoudiJohns Hopkins Center on Aging and Health, Johns Hopkins University, Baltimore, Maryland, USA.
Paul NestadtDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Jacek UrbanekJohns Hopkins Center on Aging and Health, Johns Hopkins University, Baltimore, Maryland, USA.
Junrui DiDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Vadim ZipunnikovJohns Hopkins Center on Aging and Health, Johns Hopkins University, Baltimore, Maryland, USA.
Darlynn M Rojo-WissarDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Adam P SpiraDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

Funding

Project 3: Isolating food insecurity to understand childhood health outcomes and biological mechanisms of riskP20GM139767 · NIGMS · MIRIAM HOSPITAL · PI KayLoni L. Olson · 2021 to 2026
$14.6M
PSYCHIATRIC EPIDEMIOLOGY TRAINING PROGRAMT32MH014592 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HEATHER E VOLK, Peter P. Zandi · 1985 to 2026
$8.5M
Research Training in Childhood Stress, Trauma, and ResilienceT32HD101392 · NICHD · MIRIAM HOSPITAL · PI PARADE, STEPHANIE HART, STROUD, LAURA R · 2020 to 2024
$1.7M
National Institute of Child Health and Human Development T32HD101392NICHD NIH HHS T32 HD101392NIGMS NIH HHS P20 GM139767NIGMS NIH HHS P20GM139767NIMH NIH HHS 5T32MH014592-39NIMH NIH HHS T32 MH014592
6 · The paper itself

Abstract

We examined the association between behavioural chronotype estimates and all-cause mortality in a nationally representative sample of middle-aged and older adults. We studied 2261 participants aged ≥ 50 years from the National Health and Nutrition Examination Survey (NHANES) who wore an ActiGraph on their hip for 7 days and were instructed to remove it for sleep. We estimated the average midpoint of time-in-bed (TIB) on weekends and categorised participants based on two sets of chronotype cutoffs. Chronotype I was defined as follows: intermediate-type I (≥ 3:30 AM and ≤ 4:30 AM), early-type I (≥ 11:00 PM and < 3:30 AM) and late-type I (> 4:30 AM and ≤ 11:00 AMm). In chronotype definition II, we expanded the intermediate category by 1 h on each side. We examined associations between chronotype and all-cause mortality in three age groups (50-65, n = 1055; 66-80, n = 895; 81+, n = 311) using survey-weighted Cox models. Six-hundred-fifty deaths occurred. Following adjustment for age, sex, race/ethnicity, poverty income ratio, BMI, smoking and drinking status, comorbidities and average TIB, among participants aged 81+, late-type I was associated with 123% greater mortality risk (HR = 2.23, 95% CI = 1.33, 3.74) versus intermediate-type I. Among participants aged 50-65, late-type II was associated with a 107% greater mortality risk (HR = 2.07, 95% CI = 1.09, 3.91) versus intermediate-type II. Findings suggest, in adults 50-65 and those aged 81+, that compared to individuals with intermediate chronotype, those with late chronotype have a higher risk of all-cause mortality; however, these associations may differ as a function of the temporal boundaries by which late chronotype is defined.

Indexed as

ChronotypeCircadian RhythmMortalityActigraphyAgedAged, 80 and overCause of DeathFemaleHumansMaleMiddle AgedNutrition SurveysProportional Hazards ModelsSleepUnited States24‐h rhythmbiological clockschronotypecircadian clockcircadian rhythmeveningnessmortalitysleepsleeping habits

Identifiers

PMID41814477
PMCPMC13217418

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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.