Details zur Publikation

Kategorie Textpublikation
Referenztyp Zeitschriften
DOI 10.1038/s41380-023-02010-5
Volltext Shareable Link
Titel (primär) Epigenome-wide meta-analysis of prenatal maternal stressful life events and newborn DNA methylation
Autor Kotsakis Ruehlmann, A.; Sammallahti, S.; Cortés Hidalgo, A.P.; Bakulski, K.M.; Binder, E.B.; Campbell, M.L.; Caramaschi, D.; Cecil, C.; Colicino, E.; Cruceanu, C.; Czamara, D.; Dieckmann, L.; Dou, J.; Felix, J.F.; Frank, J.; Håberg, S.E.; Herberth, G. ORCID logo ; Hoang, T.T.; Houtepen, L.C.; Hüls, A.; Koen, N.; London, S.J.; Magnus, M.C.; Mancano, G.; Mulder, R.H.; Page, C.M.; Räikkönen, K.; Röder, S. ORCID logo ; Schmidt, R.J.; Send, T.S.; Sharp, G.; Stein, D.J.; Streit, F.; Tuhkanen, J.; Witt, S.H.; Zar, H.J.; Zenclussen, A.C.; Zhang, Y.; Zillich, L.; Wright, R.; Lahti, J.; Brunst, K.J.
Quelle Molecular Psychiatry
Erscheinungsjahr 2023
Department IMMU
Band/Volume 28
Seite von 5090
Seite bis 5100
Sprache englisch
Topic T9 Healthy Planet
Abstract Prenatal maternal stressful life events are associated with adverse neurodevelopmental outcomes in offspring. Biologic mechanisms underlying these associations are largely unknown, but DNA methylation likely plays a role. This meta-analysis included twelve datasets from ten pregnancy cohorts (N=5,496) within the international Pregnancy and Childhood Epigenetics consortium to examine maternal stressful life events during pregnancy and DNA methylation in cord blood. Children whose mothers reported higher levels of cumulative maternal stressful life events during pregnancy exhibited differential methylation of cg26579032 in ALKBH3. Stressor-specific domains of conflict with family/friends, abuse (physical, sexual, and emotional), and death of a close friend/relative were also associated with differential methylation of CpGs in APTX, MyD88, and both UHRF1 and SDCCAG8, respectively; these genes are implicated in neurodegeneration, immune and cellular functions, regulation of global methylation levels, metabolism, and schizophrenia risk. Thus, differences in DNA methylation at these loci may provide novel insights into potential mechanisms of neurodevelopment in offspring.
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Kotsakis Ruehlmann, A., Sammallahti, S., Cortés Hidalgo, A.P., Bakulski, K.M., Binder, E.B., Campbell, M.L., Caramaschi, D., Cecil, C., Colicino, E., Cruceanu, C., Czamara, D., Dieckmann, L., Dou, J., Felix, J.F., Frank, J., Håberg, S.E., Herberth, G., Hoang, T.T., Houtepen, L.C., Hüls, A., Koen, N., London, S.J., Magnus, M.C., Mancano, G., Mulder, R.H., Page, C.M., Räikkönen, K., Röder, S., Schmidt, R.J., Send, T.S., Sharp, G., Stein, D.J., Streit, F., Tuhkanen, J., Witt, S.H., Zar, H.J., Zenclussen, A.C., Zhang, Y., Zillich, L., Wright, R., Lahti, J., Brunst, K.J. (2023):
Epigenome-wide meta-analysis of prenatal maternal stressful life events and newborn DNA methylation
Mol. Psychiatr. 28 , 5090 - 5100 10.1038/s41380-023-02010-5