Cumulative risk exposure and child cellular aging in a Dutch low‐risk community sample

Abstract One of the proposed mechanisms linking childhood stressor exposure to negative mental and physical health outcomes in later life is cellular aging. In this prospective, longitudinal, and pre‐registered study, we examined the association between a cumulative pattern of childhood risk exposure from age 6 to age 10 (i.e., poor maternal mental health, parental relationship problems, family/friend death, bullying victimization, poor quality friendships) and change in two biomarkers of cellular aging (i.e., telomere length, epigenetic age) from age 6 to age 10 in a Dutch low‐risk community... Mehr ...

Verfasser: Beijers, Roseriet
ten Thije, Ilse
Bolhuis, Emma
O'Donnell, Kieran J.
Tollenaar, Marieke S.
Shalev, Idan
Hastings, Waylon J.
MacIsaac, Julia L.
Lin, David T. S.
Meaney, Michael
Kobor, Michael S.
Belsky, Jay
de Weerth, Carolina
Dokumenttyp: Artikel
Erscheinungsdatum: 2022
Reihe/Periodikum: Psychophysiology ; volume 60, issue 4 ; ISSN 0048-5772 1469-8986
Verlag/Hrsg.: Wiley
Schlagwörter: Experimental and Cognitive Psychology / Neuropsychology and Physiological Psychology / Biological Psychiatry / Cognitive Neuroscience / Developmental Neuroscience / Endocrine and Autonomic Systems / Neurology / General Neuroscience
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26690865
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://dx.doi.org/10.1111/psyp.14205

Abstract One of the proposed mechanisms linking childhood stressor exposure to negative mental and physical health outcomes in later life is cellular aging. In this prospective, longitudinal, and pre‐registered study, we examined the association between a cumulative pattern of childhood risk exposure from age 6 to age 10 (i.e., poor maternal mental health, parental relationship problems, family/friend death, bullying victimization, poor quality friendships) and change in two biomarkers of cellular aging (i.e., telomere length, epigenetic age) from age 6 to age 10 in a Dutch low‐risk community sample ( n = 193). We further examined the moderating effect of cortisol reactivity at age 6. Ordinary Least Squares regression analyses revealed no significant main effects of childhood risk exposure on change in cellular aging, nor a moderation effect of child cortisol reactivity. Secondary findings showed a positive correlation between telomere length and cortisol reactivity at age 6, warranting further investigation. More research in similar communities is needed before drawing strong conclusions based on the null results.