Evidence map›Paper›PMID 40427452›Full record

ReviewAntioxidants (Basel, Switzerland)2025

Redox-Driven Epigenetic Modifications in Sperm: Unraveling Paternal Influences on Embryo Development and Transgenerational Health.

Aron Moazamian, Fabrice Saez, Joël R Drevet, Robert John Aitken, Parviz Gharagozloo

Abstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

5 authors.

Aron MoazamianEVALSEM, GReD Institute, CRBC, Faculté de Médecine, Université Clermont Auvergne, 28 Place Henri Dunant, 6300 Clermont-Ferrand, France.ORCID 0000-0002-1291-4390
Fabrice SaezEVALSEM, GReD Institute, CRBC, Faculté de Médecine, Université Clermont Auvergne, 28 Place Henri Dunant, 6300 Clermont-Ferrand, France.ORCID 0000-0001-9570-3777
Joël R DrevetEVALSEM, GReD Institute, CRBC, Faculté de Médecine, Université Clermont Auvergne, 28 Place Henri Dunant, 6300 Clermont-Ferrand, France.ORCID 0000-0003-3077-6558
Robert John AitkenPriority Research Centre for Reproductive Science, University of Newcastle, Newcastle 2308, Australia.ORCID 0000-0002-9152-156X
Parviz GharagozlooCellOxess Biotechnology, Research & Development, Ewing, NJ 08638, USA.ORCID 0000-0003-3955-3297

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male-factor infertility accounts for nearly half of all infertility cases, and mounting evidence points to oxidative stress as a pivotal driver of sperm dysfunction, genetic instability, and epigenetic dysregulation. In particular, the oxidative DNA lesion 8-hydroxy-2'-deoxyguanosine (8-OHdG) has emerged as a central mediator at the interface of DNA damage and epigenetic regulation. We discuss how this lesion can disrupt key epigenetic mechanisms such as DNA methylation, histone modifications, and small non-coding RNAs, thereby influencing fertilization outcomes, embryo development, and offspring health. We propose that the interplay between oxidative DNA damage and epigenetic reprogramming is further exacerbated by aging in both the paternal and maternal germlines, creating a "perfect storm" that increases the risk of heritable (epi)mutations. The consequences of unresolved oxidative lesions can thus persist beyond fertilization, contributing to transgenerational health risks. Finally, we explore the promise and potential pitfalls of antioxidant therapy as a strategy to mitigate sperm oxidative damage. While antioxidant supplementation may hold significant therapeutic value for men with subfertility experiencing elevated oxidative stress, a careful, personalized approach is essential to avoid reductive stress and unintended epigenetic disruptions. Recognizing the dual role of oxidative stress in shaping both the genome and the epigenome underscores the need for integrating redox biology into reproductive medicine, with the aim of improving fertility treatments and safeguarding the health of future generations.

Indexed as

8-hydroxy-2′-deoxyguanosine (8-OHdG)embryo developmentepigeneticsmale infertilityoxidative stresssperm DNA damagetransgenerational health

Identifiers

PMID40427452
PMCPMC12108309

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.