Evidence map›Paper›PMID 42886706›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Altered sperm DNA methylation provides an epigenetic route from overweight and older men to intergenerational disease transmission.

Mathieu Schulz, Xiaojian Shao, Romain Lambrot, Christine Lafleur, Donovan Chan, Marie-Charlotte Dumargne, Amanda J MacFarlane, Sergey Moskovtsev, Guillaume Bourque, Tomi Pastinen and 4 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. 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

14 authors.

Mathieu Schulz *Department of Pathology and Cell Biology, University of Montreal Hospital Research Center, Montreal, QC H2X 0A9, Canada.ORCID 0000-0003-0373-4264
Xiaojian Shao *Digital Technologies Research Center, National Research Council of Canada, Ottawa, ON K1A 0R6, Canada.ORCID 0000-0002-3044-621X
Romain LambrotDepartment of Pathology and Cell Biology, University of Montreal Hospital Research Center, Montreal, QC H2X 0A9, Canada.
Christine LafleurDepartment of Pathology and Cell Biology, University of Montreal Hospital Research Center, Montreal, QC H2X 0A9, Canada.
Donovan ChanChild Health and Human Development Program, Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.
Marie-Charlotte DumargneCenter for Basic Metabolic Research, University of Copenhagen, Copenhagen DK-2200, Denmark.ORCID 0000-0001-7009-9104
Amanda J MacFarlaneNutrition Research Division, Health Canada, Ottawa, Ottawa, ON K1A 0K9, Canada.ORCID 0000-0002-3208-3483
Sergey MoskovtsevCReATe Fertility Clinic Center, Toronto, ON M5G 1N8, Canada.
Guillaume BourqueMcGill Genome Center, Department of Human Genetics, McGill University, Montreal, QC H3A 0G1, Canada.ORCID 0000-0002-3933-9656
Tomi PastinenMcGill Genome Center, Department of Human Genetics, McGill University, Montreal, QC H3A 0G1, Canada.
Clifford LibrachCReATe Fertility Clinic Center, Toronto, ON M5G 1N8, Canada.
Hope WeilerNutrition Research Division, Bureau of Nutritional Sciences, Food and Nutrition Directorate, Health Products and Food Branch, Health Canada, Ottawa K1A 0K9, Canada.
Jacquetta TraslerChild Health and Human Development Program, Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.
Sarah KimminsDepartment of Pathology and Cell Biology, University of Montreal Hospital Research Center, Montreal, QC H2X 0A9, Canada.ORCID 0000-0002-0168-7233

Funding

Canadian Institutes of Health Research (CIHR) 148425Canadian Institutes of Health Research (CIHR) 180414Canadian Institutes of Health Research (CIHR) 191775Canadian Institutes of Health Research (CIHR) 341268Canadian Institutes of Health Research (CIHR) 358654
6 · The paper itself

Abstract

The occurrence of childhood neurodevelopmental disorders has been steadily increasing for decades, yet we have little understanding of modes of inheritance implicated in these diseases. Epidemiology studies have revealed an association between an elevated paternal Body Mass Index (BMI) and age as factors implicated in increased risk for neurodevelopmental disorders in children. Epigenetic regulation of gene expression by DNA methylation at cytosines is susceptible to environmental, diet, and lifestyle changes. Yet, whether a man's BMI and age influence the sperm methylome and potentially impact offspring development remains unresolved. Using MethylC capture sequencing, we identified over 38,000 differentially methylated CpGs in the sperm of men with an elevated BMI, with overlap occurring in regions associated with advanced paternal age. These were enriched for neural gene and disease ontologies. Differentially methylated regions localized to transposable elements that can act as active enhancers during human zygotic genome activation, and at gene promoters for early lineage specification. These results suggest that sperm methylome alterations that are linked to an elevated BMI may influence key embryonic transcriptional processes, notably those associated with trophectoderm and placental development.

Indexed as

DNA MethylationEpigenetic MemoryNeurodevelopmental DisordersOverweightPaternal AgePaternal InheritanceSpermatozoaAgingBody Mass IndexDNA-Cytosine MethylasesEmbryonic DevelopmentEpigenomicsHumansMaleDNA-Cytosine MethylasesDNA methylationEpigeneticssperm

Identifiers

PMID42886706
PMCPMC13684213

What OpenQuestion 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 OpenQuestion graph.