Psychiatry Investig.  2022 Sep;19(9):703-711. 10.30773/pi.2022.0100.

Association Between the C4 Binding Protein Level and White Matter Integrity in Major Depressive Disorder

Affiliations
  • 1Department of Psychiatry, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea
  • 2Department of Biomedical Sciences, Korea University College of Medicine, Seoul, Republic of Korea
  • 3Brain Convergence Research Center, Korea University Anam Hospital, Seoul, Republic of Korea
  • 4Bertis R&D Division, Bertis Inc., Seongnam, Republic of Korea

Abstract


Objective
Considerable evidence suggests that neuroinflammation plays an important role in the pathophysiology of major depressive disorder (MDD). However, the relationship between serum C4 binding protein (C4BP) and white matter (WM) tract integrity in MDD has not been investigated.
Methods
We obtained diffusion tensor images of 44 patients with MDD and 44 healthy controls and performed TRActs Constrained by UnderLying Anatomy (TRACULA) analysis to assess WM tract integrity. Serum C4-binding protein alpha chain (C4BPA) and C4- binding protein beta chain (C4BPB) levels were measured and in-between group comparisons were obtained. The correlation between serum C4BP levels and WM tract integrity was examined.
Results
In comparison to healthy controls, both serum C4BPA and C4BPB were higher in MDD. Also, fractional anisotropy (FA) was increased in the left cingulum-angular bundle (CAB) in MDD, but not healthy controls (HCs). A significant correlation was found between serum C4BP and FA levels in the right cingulum-cingulate gyrus bundle (CCG) in MDD.
Conclusion
This study is the first to investigate the correlation between serum C4BP levels and WM tract integrity in MDD. We identified an increase in WM integrity in the left CAB region in MDD. Furthermore, serum C4BP levels were higher in MDD, and this finding correlated with increased WM integrity in the right CCG region.

Keyword

Major depressive disorder; Complement; C4 binding protein; Neuroinflammation; White matter tract integrity
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