4.6 Article

Effects of Antenatal Maternal Depressive Symptoms and Socio-Economic Status on Neonatal Brain Development are Modulated by Genetic Risk

期刊

CEREBRAL CORTEX
卷 27, 期 5, 页码 3080-3092

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhx065

关键词

amygdala; cortical thickness; depression; morphological shape; polygenic risk score

资金

  1. National Medical Research Council (NMRC) [NMRC/TCR/004-NUS/2008, NMRC/CBRG/0039/2013]
  2. Singapore Ministry of Education [MOE2012-T2-2-130]
  3. Hope for Depression Research Foundation
  4. Sackler Foundation
  5. National Institute of Health [R01 MH091351, R01 HD060628]
  6. ERA-NET NEURON [01EW1407A]
  7. Canadian Institutes for Advanced Research

向作者/读者索取更多资源

This study included 168 and 85 mother-infant dyads from Asian and United States of America cohorts to examine whether a genomic profile risk score for major depressive disorder (GPRS(MDD)) moderates the association between antenatal maternal depressive symptoms (or socio-economic status, SES) and fetal neurodevelopment, and to identify candidate biological processes underlying such association. Both cohorts showed a significant interaction between antenatal maternal depressive symptoms and infant GPRS(MDD) on the right amygdala volume. The Asian cohort also showed such interaction on the right hippocampal volume and shape, thickness of the orbitofrontal and ventromedial prefrontal cortex. Likewise, a significant interaction between SES and infant GPRS(MDD) was on the right amygdala and hippocampal volumes and shapes. After controlling for each other, the interaction effect of antenatal maternal depressive symptoms and GPRS(MDD) was mainly shown on the right amygdala, while the interaction effect of SES and GPRS(MDD) was mainly shown on the right hippocampus. Bioinformatic analyses suggested neurotransmitter/neurotrophic signaling, SNAp REceptor complex, and glutamate receptor activity as common biological processes underlying the influence of antenatal maternal depressive symptoms on fetal cortico-limbic development. These findings suggest gene-environment interdependence in the fetal development of brain regions implicated in cognitive-emotional function. Candidate biological mechanisms involve a range of brain region-specific signaling pathways that converge on common processes of synaptic development.

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