Evidence map›Paper›PMID 41369261›Full record

SynthesisEpigenetics2025

Strength of evidence for paternal influence on offspring epigenome in observational human studies: a systematic review and risk-of-bias appraisal for non-randomized exposures.

Ka Kei Sum, Mark A Burton, Cristina Garcia-Maurino Alcazar, Ai Ling Teh, Keith M Godfrey, Jonathan Yinhao Huang

Abstract readSystematic Review
In one paragraph

Synthesis in Epigenetics, 2025. 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

6 authors.

Ka Kei SumInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Mark A BurtonHuman Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK.
Cristina Garcia-Maurino AlcazarInstitute for Global Health, University College London, London, UK.
Ai Ling TehInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Keith M GodfreyHuman Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK.
Jonathan Yinhao HuangDepartment of Public Health Sciences, Thompson School of Social Work & Public Health, University of Hawai'i at Mānoa, Honolulu, Hawai'i, USA.

Funding

The Role of gp120 on Cardiovascular Disease in People Living with HIVU54MD007601 · NIMHD · UNIVERSITY OF HAWAII AT MANOA · PI Lee Ellen Buenconsejo-Lum, Jerris Robert Hedges · 2017 to 2026
$59.5M
Urgent Competitive Revision to Existing NIH Grants and Cooperative Agreements (Urgent Supplement - Clinical Trial Optional)U24MD015970 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI Sandra Perreira Chang, Elizabeth O. Ofili · 2020 to 2026
$20.6M
NIMHD NIH HHS U24 MD015970NIMHD NIH HHS U54 MD007601
6 · The paper itself

Abstract

Paternal influence on the offspring epigenome is difficult to interpret in observational human studies due to heterogeneous designs, causing varying susceptibility to bias and non-causal explanations. We conducted a systematic review (CRD42022302695) of paternal exposures before or during pregnancy in relation to the offspring epigenome, focusing on characteristics affecting causal interpretation and reproducibility. We searched three electronic databases for human studies published between 2003 and 2023. Eligible studies assessed paternal factors before or during pregnancy as exposures, and epigenetic mechanisms as outcomes. Risk of bias (RoB) was evaluated using ROBINS-E. The most frequently studied paternal factors were BMI/obesity (7), age (7), smoking (5), and socioeconomic status (SES) (4). All 28 studies assessed DNA methylation; two additionally explored miRNA expression. Most studies were rated 'high' or 'very high' RoB, primarily due to unclear exposure measurement and confounding. Findings showed limited overlap in CpG sites and genomic regions across studies. However, exposures that were stable (

Indexed as

Epigenesis, GeneticEpigenomePaternal ExposurePrenatal Exposure Delayed EffectsDNA MethylationFemaleHumansMaleObservational Studies as TopicPregnancycausal inferenceEpigeneticsmolecular epidemiologypaternal effects

Identifiers

PMID41369261
PMCPMC12897544

What OpenQuestion holds

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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.