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Maternal perinatal depression and child brain structure at 2-3 years in a South African birth cohort study

  • Jennifer A. Pellowski*
  • , Catherine J. Wedderburn
  • , Nynke A. Groenewold
  • , Annerine Roos
  • , Sivenesi Subramoney
  • , Nadia Hoffman
  • , Jean Paul Fouche
  • , Shantanu H. Joshi
  • , Roger P. Woods
  • , Katherine L. Narr
  • , Heather J. Zar
  • , Kirsten A. Donald
  • , Dan J. Stein
  • *Corresponding author for this work
  • Brown University
  • University of Cape Town
  • London School of Hygiene and Tropical Medicine
  • University of California at Los Angeles

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Maternal perinatal depression is associated with risk of adverse child developmental outcomes and differences in offspring brain structure. Evidence from low- and middle-income countries is lacking as is an investigation of antenatal, postnatal, and persistent depression in the same sample. In a South African birth cohort, we investigated the effect of antenatal and postpartum maternal depressive symptoms on offspring brain structure at 2–3 years of age. Magnetic resonance imaging was performed, extracting cortical thickness and surface areas in frontal cortex regions of interest and subcortical volumes using FreeSurfer software. Maternal depressive symptoms were measured using the Edinburgh Postpartum Depression Scale and the Beck Depression Inventory II antenatally and at 6–10 weeks, 6 months, 12 months, and 18 months postpartum and analyzed dichotomously and continuously. Linear regressions were used controlling for child age, sex, intracranial volume, maternal education, age, smoking, alcohol use and HIV. 146 children were included with 38 (37%) exposed to depressive symptoms antenatally and 44 (35%) exposed postnatally. Of these, 16 (13%) were exposed to both. Postpartum, but not antenatal, depressive symptoms were associated with smaller amygdala volumes in children (B = −74.73, p = 0.01). Persistent maternal depressive symptoms across pregnancy and postpartum were also independently associated with smaller amygdala volumes (B = −78.61, p = 0.047). Differences in amygdala volumes among children exposed to postnatal as well as persistent maternal depressive symptomatology underscore the importance of identifying women at-risk for depression during the entire perinatal period.

Original languageEnglish
Article number96
JournalTranslational Psychiatry
Volume13
Issue number1
DOIs
StatePublished - Dec 2023
Externally publishedYes

Funding

FundersFunder number
National Research Foundation of Korea
Medical Research Council
UK Government’s Newton Fund
SA NRF
Carnegie Corporation of New York
National Research Foundation
National Institute on Alcohol Abuse and AlcoholismR21AA023887, R01 AA026834-01
Wellcome Trust203525, 203525/Z/16/Z
Bill and Melinda Gates FoundationOPP 1017641
National Institute of Mental HealthK01MH112443
Academy of Medical Sciences NewtonNAF002/1001
Collaborative Initiative on Fetal Alcohol Spectrum DisordersU24 AA014811
US Brain and Behavior Foundation24467

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being
    2. SDG 5 - Gender Equality
      SDG 5 Gender Equality

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