4.5 Article

White Matter Correlates of Adolescent Depression: Structural Evidence for Frontolimbic Disconnectivity

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jaac.2014.04.021

关键词

Adolescent major depression; white matter; diffusion tensor imaging; uncinate fasciculus; emotion regulation

资金

  1. National Institute of Mental Health [NIMH: R01MH085734, R01MH085734-02S1, R01MH085734-05S1, 5K01MH097978-02]
  2. Brain and Behavior Research Foundation
  3. Center of Excellence in Stress and Mental Health
  4. Veteran's Affairs Merit Grant

向作者/读者索取更多资源

Objective: Despite the significant prevalence of adolescent depression, little is known about the neuroanatomical basis of this disorder. Functional dysregulation in frontolimbic circuitry has been suggested as a key neural correlate of adult and adolescent depression impeding emotional regulation. However, less is known about whether this dysregulation is overlaid on impaired white matter microstructure. Guided by neuroimaging findings, we test the a priori, hypotheses that adolescent depression is associated with alterations in white matter microstructure in the uncinate fasciculus (UF) and cingulum bundles. Method: Diffusion tensor magnetic resonance imaging (DTI) data were obtained on 52 unmedicated adolescents with major depressive disorder (MDD) and 42 matched controls. We calculated fractional anisotropy (FA), radial diffusivity (RD), and axial diffusivity (AD) for bilateral UF and cingulum. We also completed a voxelwise comparison of participants with depression and control participants using tract-based spatial statistics (TBSS). Results: Adolescents with depression had significantly lower FA and higher RD in bilateral UF; no significant differences were observed in cingulum. TBSS results additionally revealed lower FA values in the white matter associated with the limbic cortical striatal thalamic circuit, corpus callosum, and anterior and superior corona radiata. Conclusion: Unmedicated adolescent depression is associated with reduced fractional anisotropy in emotion regulatory networks, which may underlie the functional differences in frontolimbic circuitry characterizing depressive disorder. Given the relatively recent onset of depression in our sample, our findings in the context of the current literature provide preliminary evidence that reduced fractional anisotropy in the UF could be a predisposing risk factor for depression.

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