Psychophysiology, volume 60, issue 10

Risk for internalizing symptom development in young children: Roles of child parasympathetic reactivity and maternal depression and anxiety exposure in early life

Kelsey M. Quigley 1, 2
Carter R. Petty 3
Anne Elizabeth Sidamon Eristoff 4
Margaret Modico 4
CHARLES A. NELSON 1, 2, 5
Michelle Bosquet Enlow 4, 6
Publication typeJournal Article
Publication date2023-05-10
Journal: Psychophysiology
scimago Q1
SJR1.303
CiteScore6.8
Impact factor2.9
ISSN00485772, 14698986, 15405958
PubMed ID:  37162341
Neurology
General Neuroscience
Neuropsychology and Physiological Psychology
Biological Psychiatry
Experimental and Cognitive Psychology
Cognitive Neuroscience
Developmental Neuroscience
Endocrine and Autonomic Systems
Abstract

Intergenerational transmission of internalizing disorders (anxiety and depression) is well documented, but the responsible pathways are underspecified. One possible mechanism is via programming of the child's parasympathetic nervous system (PNS). For example, maternal depression and anxiety, via multiple pathways, may heighten child PNS reactivity, which has been linked to increased risk for internalizing disorders. Heightened PNS reactivity also may sensitize a child to their environment, increasing the vulnerability to developing psychopathology when exposed to stressors, such as maternal psychopathology. In a prospective longitudinal study of mother–child dyads (N = 446), we examined relations among maternal depression and anxiety symptoms when children were infants and aged 3 and 5 years, child respiratory sinus arrythmia (RSA) reactivity (measure of PNS reactivity) at 3 years, and child internalizing symptoms at age 5 years. Consistent with an adaptive calibration perspective, analyses tested the roles of child RSA reactivity as both a mediator and a moderator of associations between maternal and child symptoms. Greater child RSA reactivity in response to a fearful video predicted higher internalizing symptoms among children exposed to higher levels of maternal depression or anxiety symptoms at age 5 years (moderation effects). Child RSA reactivity did not mediate relations between maternal depression or anxiety symptoms in infancy and child internalizing symptoms at age 5 years. The results suggest that heightened PNS reactivity may represent a biological vulnerability to stressful environments early in life: When coupled with maternal depression or anxiety exposure, child PNS reactivity may promote the development of internalizing psychopathology in early childhood.

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