Evidence map›Paper›PMID 39405349›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Brighter nights and darker days predict higher mortality risk: A prospective analysis of personal light exposure in >88,000 individuals.

Daniel P Windred, Angus C Burns, Jacqueline M Lane, Patrick Olivier, Martin K Rutter, Richa Saxena, Andrew J K Phillips, Sean W Cain

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

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

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  12. Minimal Mimics and Maps of Natural Light for Mammals.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  13. Article
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  15. Physiologically-relevant light exposure and light behaviour in Switzerland and Malaysia.Journal of exposure science & environmental epidemiology · 2026
    Observational
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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

8 authors.

Daniel P WindredFlinders Health and Medical Research Institute (Sleep Health), Flinders University, Bedford Park, SA 5042, Australia.ORCID 0000-0002-7461-7498
Angus C BurnsDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115.
Jacqueline M LaneDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115.
Patrick OlivierAction Lab, Department of Human-Centred Computing, Faculty of Information Technology, Monash University, Melbourne, VIC 3800, Australia.
Martin K RutterCentre for Biological Timing, Division of Endocrinology, Diabetes & Gastroenterology, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester M13 9PL, United Kingdom.
Richa SaxenaDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115.
Andrew J K Phillips *Flinders Health and Medical Research Institute (Sleep Health), Flinders University, Bedford Park, SA 5042, Australia.ORCID 0000-0003-1156-7056
Sean W Cain *Flinders Health and Medical Research Institute (Sleep Health), Flinders University, Bedford Park, SA 5042, Australia.

Funding

Australian Government Research Training Program NANIHR Manchester Biomedical Research Centre NA
6 · The paper itself

Abstract

Light enhances or disrupts circadian rhythms, depending on the timing of exposure. Circadian disruption contributes to poor health outcomes that increase mortality risk. Whether personal light exposure predicts mortality risk has not been established. We therefore investigated whether personal day and night light, and light patterns that disrupt circadian rhythms, predicted mortality risk. UK Biobank participants (N = 88,905, 62.4 ± 7.8 y, 57% female) wore light sensors for 1 wk. Day and night light exposures were defined by factor analysis of 24-h light profiles. A computational model of the human circadian pacemaker was applied to model circadian amplitude and phase from light data. Cause-specific mortality was recorded in 3,750 participants across a mean (±SD) follow-up period of 8.0 ± 1.0 y. Individuals with brighter day light had incrementally lower all-cause mortality risk (adjusted-HR ranges: 0.84 to 0.90 [50 to 70th light exposure percentiles], 0.74 to 0.84 [70 to 90th], and 0.66 to 0.83 [90 to 100th]), and those with brighter night light had incrementally higher all-cause mortality risk (aHR ranges: 1.15 to 1.18 [70 to 90th], and 1.21 to 1.34 [90 to 100th]), compared to individuals in darker environments (0 to 50th percentiles). Individuals with lower circadian amplitude (aHR range: 0.90 to 0.96 per SD), earlier circadian phase (aHR range: 1.16 to 1.30), or later circadian phase (aHR range: 1.13 to 1.20) had higher all-cause mortality risks. Day light, night light, and circadian amplitude predicted cardiometabolic mortality, with larger hazard ratios than for mortality by other causes. Findings were robust to adjustment for age, sex, ethnicity, photoperiod, and sociodemographic and lifestyle factors. Minimizing night light, maximizing day light, and keeping regular light-dark patterns that enhance circadian rhythms may promote cardiometabolic health and longevity.

Indexed as

Circadian RhythmLightAgedFemaleHumansMaleMiddle AgedMortalityProspective StudiesRisk FactorsUnited Kingdomcardiometaboliccircadian disruptionlight at nightlight sensorlongevity

Identifiers

PMID39405349
PMCPMC11513964

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.