Associations between prenatal, childhood, and adolescent stress and variations in white-matter properties in young men
Jensen, Sarah K.G.; Pangelinan, Melissa; Bjo¨rnholm, Lassi; Klasnja, Anja; Leemans, Alexander; Drakesmith, Mark; Evans, C. J.; Barker, Edward D.; Paus, Tomásˇ
(2018) NeuroImage, volume 182, pp. 389 - 397
(Article)
Abstract
Objective: Previous studies have shown that both pre- and post-natal adversities, the latter including exposures to stress during childhood and adolescence, explain variation in structural properties of white matter (WM) in the brain. While previous studies have examined effects of independent stress exposures within one developmental period, such as childhood,
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we examine effects of stress across development using data from a prospective longitudinal study. More specifically, we ask how stressful events during prenatal development, childhood, and adolescence relate to variation in WM properties in early adulthood in young men recruited from a birth cohort. Method: Using data from 393 mother-son pairs from a community-based birth cohort from England (Avon Longitudinal Study of Parents and Children), we examined how stressful life events relate to variation in different structural properties of WM in the corpus callosum and across the whole brain in early adulthood in men aged 18-21 years. We distinguish between stress occurring during three developmental periods: a) prenatal maternal stress, b) postnatal stress within the first four years of life, c) stress during adolescence (age 12-16 years). To obtain a comprehensive quantification of variation in WM, we assess structural properties of WM using four different measures, namely fractional anisotropy (FA), mean diffusivity (MD), magnetization transfer ratio (MTR) and myelin water fraction (MWF). Results: The developmental model shows that prenatal stress is associated with lower MTR and MWF in the genu and/or splenium of the corpus callosum, and with lower MTR in global (lobar) WM. Stress during early childhood is associated with higher MTR in the splenium, and stress during adolescence is associated with higher MTR in the genu and lower MD in the splenium. We see no associations between postnatal stress and variation in global (lobar) WM. Conclusions: The current study found evidence for independent effects of stress on WM properties during distinct neurodevelopmental periods. We speculate that these independent effects are due to differences in the developmental processes unfolding at different developmental time points. We suggest that associations between prenatal stress and WM properties may relate to abnormalities in neurogenesis, affecting the number and density of axons, while postnatal stress may interfere with processes related to myelination or radial growth of axons. Potential consequences of prenatal glucocorticoid exposure should be considered in obstetric care.
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Keywords: Adversity, DTI, MTR, MWF, Stress, White matter, Prenatal Exposure Delayed Effects, Humans, Child, Preschool, Corpus Callosum/diagnostic imaging, Infant, Male, White Matter/diagnostic imaging, Pregnancy, Young Adult, Adult Survivors of Child Adverse Events, Adolescent, Stress, Psychological, Adult, Female, Child, Longitudinal Studies, Diffusion Tensor Imaging/methods, Neurology, Cognitive Neuroscience, Review, Journal Article, Research Support, Non-U.S. Gov't
ISSN: 1053-8119
Publisher: Academic Press Inc.
Note: Funding Information: We are extremely grateful to the families who took part in this study and the ALSPAC team, including midwifes, interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses. We also acknowledge The UK Medical Research Council , the Wellcome Trust (Grant ref: 102215/2/13/2 ), and the University of Bristol for providing support for The Avon Longitudinal Study of Parents and Children. Funding Information: The UK Medical Research Council and the Wellcome Trust (Grant ref: 092731 ) and the University of Bristol provide core support for ALSPAC. This paper was supported by grants from the National Institutes of Health ( R01MH085772 to T Paus; R01HD068437 to ED Barker) and Canadian Institutes of Health Research ( MOP125892 to T Paus). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The research of A.L. is supported by VIDI Grant 639.072.411 from the Netherlands Organization for Scientific Research (NWO) . None of the authors report any conflicts of interest. Publisher Copyright: © 2017 Elsevier Inc. Copyright: Copyright 2018 Elsevier B.V., All rights reserved.
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