4.5 Article

Newborn white matter microstructure moderates the association between maternal postpartum depressive symptoms and infant negative reactivity

Journal

SOCIAL COGNITIVE AND AFFECTIVE NEUROSCIENCE
Volume 15, Issue 6, Pages 649-660

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/scan/nsaa081

Keywords

DTI; maternal depression; infancy; negative affect; susceptibility

Funding

  1. Alexander von Humboldt Foundation
  2. Emil Aaltonen Foundation
  3. Hospital District of South-Western Finland State Research Grants for Clinical Research
  4. Alfred Kordelin Foundation
  5. Turku University Foundation
  6. Sigrid Juselius Foundation
  7. Finnish Cultural Foundation
  8. Signe and Ane Gyllenberg Foundation
  9. Yrjo Jahnsson Foundation
  10. Brain and Behavior Research Foundation [19056]
  11. Academy of Finland Research Council for Health [308176, 253270, 264363, 134950]
  12. Academy of Finland Research Council for Culture and Society [2608063]
  13. Jane and Aatos Erkko Foundation

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Maternal postpartum depression is a prominent risk factor for aberrant child socioemotional development, but there is little understanding about the neural phenotypes that underlie infant sensitivity to maternal depression. We examined whether newborn white matter fractional anisotropy (FA), a measure of white matter maturity, moderates the association between maternal postpartum depressive symptoms and infant negative reactivity at 6 months. Participants were 80 mother-infant dyads participating in a prospective population-based cohort, and included families whose newborns underwent a magnetic resonance/diffusion tensor imaging scan at 2-5 weeks of age and whose mothers reported their own depressive symptoms at 3 and 6 months postpartum and infant negative emotional reactivity at 6 months. The whole-brain FA moderated the association between maternal depressive symptoms and mother-reported infant negative reactivity at 6 months after adjusting for the covariates. Maternal depressive symptoms were positively related to infant negative reactivity among infants with high or average FA in the whole brain and in corpus callosum and cingulum, but not among those with low FA. The link between maternal depressive symptoms and infant negative reactivity was moderated by newborn FA. The variation in white matter microstructure might play a role in child susceptibility to parental distress.

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