Literature DB >> 27578495

Impaired Frontal-Limbic White Matter Maturation in Children at Risk for Major Depression.

Yuwen Hung1, Zeynep M Saygin1, Joseph Biederman2,3, Dina Hirshfeld-Becker2, Mai Uchida2,3, Oliver Doehrmann1, Michelle Han1, Xiaoqian J Chai1, Tara Kenworthy3, Pavel Yarmak4, Schuyler L Gaillard5, Susan Whitfield-Gabrieli1, John D E Gabrieli1,2,5,6.   

Abstract

Depression is among the most common neuropsychiatric disorders. It remains unclear whether brain abnormalities associated with depression reflect the pathological state of the disease or neurobiological traits predisposing individuals to depression. Parental history of depression is a risk factor that more than triples the risk of depression. We compared white matter (WM) microstructure cross-sectionally in 40 children ages 8-14 with versus without parental history of depression (At-Risk vs. Control). There were significant differences in age-related changes of fractional anisotropy (FA) between the groups, localized in the anterior fronto-limbic WM pathways, including the anterior cingulum and the genu of the corpus callosum. Control children exhibited typical increasing FA with age, whereas At-Risk children exhibited atypical decreasing FA with age in these fronto-limbic regions. Furthermore, dorsal cingulate FA significantly correlated with depressive symptoms for At-Risk children. The results suggest maturational WM microstructure differences in mood-regulatory neurocircuitry that may contribute to neurodevelopmental risk for depression. The study provides new insights into neurodevelopmental susceptibility to depression and related disabilities that may promote early preventive intervention approaches.
© The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  anterior cingulate; diffusion tensor imaging; frontal–limbic connectivity; major depression

Mesh:

Year:  2017        PMID: 27578495      PMCID: PMC6411032          DOI: 10.1093/cercor/bhw250

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


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