Gray matter volume reduction in orbitofrontal cortex correlated with plasma glial cell line-derived neurotrophic

Yifan Wu1, Lingtao Kong1, Anqi Yang1

  • 1Department of Psychiatry, The First Hospital of China Medical University, Shenyang, China.

Neuroimage. Clinical
|February 5, 2023
PubMed
Abstract

Insights

Major depressive disorder (MDD) is linked to reduced gray matter volume (GMV). Higher plasma glial cell line-derived neurotrophic factor (GDNF) in MDD patients correlates with this GMV reduction, suggesting GDNF

Area of Science:

  • Neuroscience
  • Psychiatry
  • Biomarker Research

Background:

  • Major Depressive Disorder (MDD) is a severe mental health condition associated with reduced gray matter volume (GMV).
  • The exact pathogenesis of MDD is not fully understood, but neurotrophic factors are implicated in its development.
  • Plasma glial cell line-derived neurotrophic factor (GDNF) is a potential biomarker for MDD activity and progression.

Purpose of the Study:

  • To investigate the correlation between plasma GDNF levels and GMV alterations in MDD patients.
  • To compare GDNF levels and GMV in MDD patients versus healthy controls (HCs).

Main Methods:

  • Studied 54 MDD patients and 48 HCs.
  • Utilized Analysis of Variance (ANOVA) to assess whole-brain GMV differences between groups.
  • Controlled for covariates including ethnicity, handedness, age, and gender; applied Gaussian random-field (GRF) correction.

Main Results:

  • MDD patients exhibited significantly reduced GMV in the right inferior orbitofrontal cortex (OFC) compared to HCs.
  • Plasma GDNF levels were significantly higher in the MDD group than in the HC group.
  • In MDD patients, higher GDNF levels positively correlated with GMV reduction in the right inferior OFC; HCs showed a negative correlation.

Conclusions:

  • Elevated GDNF in MDD may represent a compensatory response to neural damage.
  • Neuroinflammatory processes might impede the neural repair effects of increased GDNF in MDD.
  • Plasma GDNF may serve as a potential biomarker reflecting GMV changes in MDD.

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