A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

A new blood based epigenetic age predictor for adolescents and young adults




TekijätAanes Håvard., Bleka Øyvind, Dahlberg Pål S., Carm Kristina T., Lehtimäki Terho, Raitakari Olli, Kähönen Mika, Hurme Mikko, Rolseth Veslemøy

KustantajaNature Research

Julkaisuvuosi2023

JournalScientific Reports

Tietokannassa oleva lehden nimiScientific Reports

Artikkelin numero2303

Vuosikerta13

Numero1

DOIhttps://doi.org/10.1038/s41598-023-29381-7

Verkko-osoitehttps://www.nature.com/articles/s41598-023-29381-7

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/179124878


Tiivistelmä

Children have special rights for protection compared to adults in our society. However, more than 1/4 of children globally have no documentation of their date of birth. Hence, there is a pressing need to develop biological methods for chronological age prediction, robust to differences in genetics, psychosocial events and physical living conditions. At present, DNA methylation is the most promising biological biomarker applied for age assessment. The human genome contains around 28 million DNA methylation sites, many of which change with age. Several epigenetic clocks accurately predict chronological age using methylation levels at age associated GpG-sites. However, variation in DNA methylation increases with age, and there is no epigenetic clock specifically designed for adolescents and young adults. Here we present a novel age Predictor for Adolescents and Young Adults (PAYA), using 267 CpG methylation sites to assess the chronological age of adolescents and young adults. We compared different preprocessing approaches and investigated the effect on prediction performance of the epigenetic clock. We evaluated performance using an independent validation data set consisting of 18-year-old individuals, where we obtained a median absolute deviation of just below 0.7 years. This tool may be helpful in age assessment of adolescents and young adults. However, there is a need to investigate the robustness of the age predictor across geographical and disease populations as well as environmental effects.


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Last updated on 2025-27-03 at 21:49