Evidence map›Paper›PMID 38965555›Full record

ArticleBMC biology2024

DNA methylation of exercise-responsive genes differs between trained and untrained men.

Carla Geiger, Maria Needhamsen, Eric B Emanuelsson, Jessica Norrbom, Karen Steindorf, Carl Johan Sundberg, Stefan M Reitzner, Malene E Lindholm

Abstract read
In one paragraph

Article in BMC biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

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

  1. Pooled it
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  7. Epigenetic Modulation of the ACE System Underlies the Slow Aerobic Muscle Phenotype and Metabolic Exercise Response.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  8. Article
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  20. Omics Sciences in Regular Physical Activity.International journal of molecular sciences · 2025
    Review
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.

Carla GeigerDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Maria NeedhamsenDepartment of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Eric B EmanuelssonDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Jessica NorrbomDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Karen SteindorfDivision of Physical Activity, Prevention and Cancer, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Carl Johan SundbergDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Stefan M Reitzner *Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Malene E Lindholm *Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. malenel@stanford.edu.ORCID http://orcid.org/0000-0002-5763-7833

Funding

Centrum för idrottsforskning B2021-0022Centrum för idrottsforskning FO2022-0005Centrum för idrottsforskning P2023-0128Vetenskapsrådet 2018-02932
6 · The paper itself

Abstract

backgroundPhysical activity is well known for its multiple health benefits and although the knowledge of the underlying molecular mechanisms is increasing, our understanding of the role of epigenetics in long-term training adaptation remains incomplete. In this intervention study, we included individuals with a history of > 15 years of regular endurance or resistance training compared to age-matched untrained controls performing endurance or resistance exercise. We examined skeletal muscle DNA methylation of genes involved in key adaptation processes, including myogenesis, gene regulation, angiogenesis and metabolism.

resultsA greater number of differentially methylated regions and differentially expressed genes were identified when comparing the endurance group with the control group than in the comparison between the strength group and the control group at baseline. Although the cellular composition of skeletal muscle samples was generally consistent across groups, variations were observed in the distribution of muscle fiber types. Slow-twitch fiber type genes MYH7 and MYL3 exhibited lower promoter methylation and elevated expression in endurance-trained athletes, while the same group showed higher methylation in transcription factors such as FOXO3, CREB5, and PGC-1α. The baseline DNA methylation state of those genes was associated with the transcriptional response to an acute bout of exercise. Acute exercise altered very few of the investigated CpG sites.

conclusionsEndurance- compared to resistance-trained athletes and untrained individuals demonstrated a different DNA methylation signature of selected skeletal muscle genes, which may influence transcriptional dynamics following a bout of acute exercise. Skeletal muscle fiber type distribution is associated with methylation of fiber type specific genes. Our results suggest that the baseline DNA methylation landscape in skeletal muscle influences the transcription of regulatory genes in response to an acute exercise bout.

Indexed as

DNA MethylationExerciseMuscle, SkeletalResistance TrainingAdultEpigenesis, GeneticHumansMalePhysical EnduranceDNA methylationEnzymatic methyl sequencingEpigenomicsExerciseGene expressionTraining

Identifiers

PMID38965555
PMCPMC11225400

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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.