Salivary DNA methylation and pubertal development in adolescents

Individuals differ in when and how quickly they experience puberty, and these differences in pubertal development are associated with lifelong health and mortality. We conducted sex-specific epigenome-wide association analyses of salivary DNA-methylation (DNAm) samples from ~ 3500 adolescents and identified 373 DNAm sites significantly associated with pubertal age, pace of pubertal development, and/or onset of early puberty by age 9. These DNAm signals converged with results from previous genomic and transcriptomic studies of puberty and with pan-mammalian epigenomic studies of age. Genomic annotations and trait enrichment results implicate child maltreatment and toxicant exposures as relevant for puberty. We developed a novel DNAm biomarker of pubertal age that was consistently associated with earlier age at menarche across three adolescent cohorts. Saliva DNAm is sensitive to signatures of pubertal development and suggests molecular links between reproductive maturation and both embryonic development and biological aging across species.

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Publication Details

Journal
Scientific Reports
Published
2025-10-15
DOI
https://doi.org/10.1038/s41598-025-19588-1
Citations
1
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.81

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article

Salivary DNA methylation and pubertal development in adolescents

Yayouk E. Willems, Elisabeth B. Binder, Laurel Raffington, Darina Czamara et al.
1 citations
Scientific Reports
Epigenetics and DNA Methylation
0.81
article

Salivary DNA methylation and pubertal development in adolescents

Yayouk E. Willems, Elisabeth B. Binder, Laurel Raffington, Darina Czamara, K. Paige Harden, Lisa Schneper, Joshua A. Goode, Bastian Mönkediek, Elliot M. Tucker–Drob, Colter Mitchell, Abby J. deSteiguer, Daniel A. Notterman, Alicia M. Schowe, Charlotte K. L. Pahnke, Andreas J. Forstner, T. Smith
article en
1 citations

Abstract

Individuals differ in when and how quickly they experience puberty, and these differences in pubertal development are associated with lifelong health and mortality. We conducted sex-specific epigenome-wide association analyses of salivary DNA-methylation (DNAm) samples from ~ 3500 adolescents and identified 373 DNAm sites significantly associated with pubertal age, pace of pubertal development, and/or onset of early puberty by age 9. These DNAm signals converged with results from previous genomic and transcriptomic studies of puberty and with pan-mammalian epigenomic studies of age. Genomic annotations and trait enrichment results implicate child maltreatment and toxicant exposures as relevant for puberty. We developed a novel DNAm biomarker of pubertal age that was consistently associated with earlier age at menarche across three adolescent cohorts. Saliva DNAm is sensitive to signatures of pubertal development and suggests molecular links between reproductive maturation and both embryonic development and biological aging across species.

Scientific ReportsVol. 15(1)
University of Bonn (DE), Forschungszentrum Jülich (DE), Princeton University (US), Bielefeld University (DE), University of Michigan (US), University Hospital Bonn (DE), Max Planck Institute for Human Development (DE), Max Planck Institute of Psychiatry (DE), Ludwig-Maximilians-Universität München (DE), The University of Texas at Austin (US)
University of Texas at Austin, National Institutes of Health, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Openalex Percentile: Top 23%
Epigenetics and DNA Methylation
0.81
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