Developmental epigenomic effects of maternal financial problems

Holuka; C.; Menta; G.; Caro; J.C.; Vögele; C.; D'Ambrosio; C.; Turner; J.D.

Keywords: Aging; ALSPAC; biological pathways; DNA methylation; epigenome, wide association studies; financial issues; Pace of Ageing

Abstract

Early-life adversity as neglect or low socioeconomic status is associated with negative physical/mental health outcomes and plays an important role in health trajectories through life. The early-life environment has been shown to be encoded as changes in epigenetic markers that are retained for many years. We investigated the effect of maternal major financial problems (MFP) and material deprivation (MD) on their children’s epigenome in the Avon Longitudinal Study of Parents and Children (ALSPAC) cohort. Epigenetic aging, measured with epigenetic clocks, was weakly accelerated with increased MFP. In subsequent EWAS, MFP, and MD showed strong, independent programing effects on children’s genomes. MFP in the period from birth to age seven was associated with genome-wide epigenetic modifications on children’s genome visible at age 7 and partially remaining at age 15. These results support the hypothesis that physiological processes at least partially explain associations between early-life adversity and health problems later in life. Both maternal stressors (MFP/MD) had similar effects on biological pathways, providing preliminary evidence for the mechanisms underlying the effects of low socioeconomic status in early life and disease outcomes later in life. Understanding these associations is essential to explain disease susceptibility, overall life trajectories and the transition from health to disease. © The Author(s), 2024.

Más información

Título según WOS: Developmental epigenomic effects of maternal financial problems
Título según SCOPUS: Developmental epigenomic effects of maternal financial problems
Título de la Revista: Development and Psychopathology
Volumen: 37
Número: 2
Editorial: Cambridge University Press
Fecha de publicación: 2025
Página de inicio: 1004
Página final: 1017
Idioma: English
DOI:

10.1017/S095457942400083X

Notas: ISI, SCOPUS