Evidence map›Paper›PMID 39675927›Full record

ArticleJournal of sleep research2025

Daily rhythm in DNA methylation and the effect of total sleep deprivation.

Antti-Jussi Ämmälä, Thomas P M Hancox, Fan Qiuyu, Alexandra Lahtinen, Sonja Sulkava, Victoria L Revell, Katrin Ackermann, Manfred Kayser, Debra J Skene, Tiina Paunio

Abstract read
In one paragraph

Article in Journal of sleep research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

10 authors.

Antti-Jussi ÄmmäläSleepwell Program and Department of Psychiatry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-1355-194X
Thomas P M HancoxSchool of Biosciences, University of Birmingham, Birmingham, UK.
Fan QiuyuDepartment of Public Health and Welfare, Population Health Unit, National Institute of Health and Welfare, Helsinki, Finland.
Alexandra LahtinenDepartment of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.
Sonja SulkavaSleepwell Program and Department of Psychiatry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Victoria L RevellSurrey Sleep Research Centre, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Katrin AckermannEaStCHEM School of Chemistry, Biomedical Sciences Research Complex, and Centre of Magnetic Resonance, University of St Andrews, St Andrews, UK.ORCID 0000-0003-1632-0503
Manfred KayserDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
Debra J SkeneSection of Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Tiina PaunioSleepwell Program and Department of Psychiatry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-5560-0666

Funding

Academy of Finland 357643Biotechnology and Biological Sciences Research Council BB/I019405/1Finska LäkaresällskapetNetherlands Forensic Institute 018741
6 · The paper itself

Abstract

Numerous hormones and genes exhibit diurnal 24-hr rhythms that can also be affected by sleep deprivation. Here we studied diurnal rhythms in DNA methylation under a 24-hr sleep/wake cycle and a subsequent 29 hr of continual wakefulness (1 night of sleep deprivation). Fifteen healthy men (19-35 years) spent 3 days/nights in a sleep laboratory: (1) adaptation; (2) baseline; (3) total sleep deprivation day/night. DNA methylation was analysed from peripheral blood leukocytes, collected every 3 hr for 45 hr (starting at 15:00 hours) during the baseline period and the total sleep deprivation period. Epigenome-wide DNA methylation variation was assessed with the Infinium MethylationEPIC v2.0 Beadchip kit. Rhythm analysis was performed separately for the baseline and the total sleep deprivation time-series data. Pairwise analysis between diurnal samples and sleep deprivation samples at the same timepoint was also carried out to detect differentially methylated positions related to sleep deprivation. Of all DNA methylation sites, 14% exhibited a diurnal rhythm in methylation on the baseline day/night that was altered by sleep deprivation. During sleep deprivation, the number of differentially methylated positions increased towards the end of the sleep deprivation period, with a dominating pattern of hypomethylation. Among differentially methylated positions, an enrichment of genes related to the FAS immune response pathway was detected. In conclusion, DNA methylation exhibits diurnal rhythmicity, and this time-of-day variation needs to be considered when studying DNA methylation as a biomarker in biomedical studies. In addition, the observed DNA methylation changes under wakefulness might serve as a mediator of sleep deprivation-related immune response alterations.

Indexed as

Circadian RhythmDNA MethylationSleep DeprivationAdultHumansMaleWakefulnessYoung Adultdiurnal rhythmsDNA methylationepigeneticsimmune responsesleep deprivation

Identifiers

PMID39675927
PMCPMC12215246

What Socratic holds

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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 Socratic graph.