4.3 Article

Longitudinal brain volume changes in major depressive disorder

期刊

JOURNAL OF NEURAL TRANSMISSION
卷 125, 期 10, 页码 1433-1447

出版社

SPRINGER WIEN
DOI: 10.1007/s00702-018-1919-8

关键词

Gray matter volume; Major depressive disorder; Amygdala; Thalamus; Number of depressive episodes; Gray matter volume normalization

资金

  1. German Research Foundation (DFG) [KR 3822/2-1, FOR2107 DA1151/5-1, DA1151/5-2, SFB-TRR58]
  2. Interdisciplinary Center for Clinical Research (IZKF) of the medical faculty of Munster [Dan3/012/17]
  3. University Medical Center Giessen and Marburg (UKGM) [11/2010]
  4. Von-Behring-Rontgen-Foundation [61-0030]
  5. [FOR 2107]
  6. [KI 588/14-1]

向作者/读者索取更多资源

Patients with major depressive disorder (MDD) exhibit gray matter volume (GMV) reductions in limbic regions. Clinical variablessuch as the number of depressive episodesseem to affect volume alterations. It is unclear whether the observed cross-sectional GMV abnormalities in MDD change over time, and whether there is a longitudinal relationship between GMV changes and the course of disorder. We investigated T1 structural MRI images of 54 healthy control (HC) and 37 MDD patients in a 3-Tesla-MRI with a follow-up interval of 3years. The Cat12 toolbox was used to analyze longitudinal data (p<0.05, FWE-corrected, whole-brain analysis; flexible factorial design). Interaction effects indicated increasing GMV in MDD in the bilateral amygdala, and decreasing GMV in the right thalamus between T1 and T2. Further analyses comparing patients with a mild course of disorder (MCD; 0-1 depressive episode during the follow-up) to patients with a severe course of disorder (SCD; >1 depressive episode during the follow-up) revealed increasing amygdalar volume in MCD. Our study confirms structural alterations in limbic regions in MDD patients and an association between these impairments and the course of disorder. Thus, we assume that the reported volumetric alterations in the left amygdala (i.e. volumetric normalization) are reversible and apparently driven by the clinical phenotype. Hence, these results support the assumption that the severity and progression of disease influences amygdalar GMV changes in MDD or vice versa.

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