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Meta-analysis of Voxel-Based Neuroimaging Studies using Seed-based d Mapping with Permutation of Subject Images (SDM-PSI)
Published on: November 27, 2019
Reduced subgenual cingulate volumes in mood disorders: a meta-analysis
Tomas Hajek1, Jiri Kozeny, Miloslav Kopecek
1Department of Psychiatry, Dalhousie University, Halifax, NS. tomas.hajek@dal.ca
Subgenual cingulate (SGC) volumes are reduced in mood disorders, particularly unipolar depression. This SGC reduction, especially in the left hemisphere, may indicate a vulnerability marker for mood disorders, particularly in those with a family history.
Area of Science:
- Neuroscience
- Psychiatry
- Radiology
Background:
- The subgenual cingulate (SGC) plays a crucial role in mood regulation.
- Abnormalities in SGC function and structure are implicated in the pathophysiology of mood disorders.
Purpose of the Study:
- To conduct the first meta-analysis of subgenual cingulate (SGC) volumes in patients diagnosed with mood disorders.
- To investigate potential differences in SGC volume based on diagnosis (unipolar vs. bipolar) and family history.
Main Methods:
- A meta-analysis was performed on 10 volumetric magnetic resonance imaging (MRI) studies.
- Standardized differences between means (SDMs) and random effects models were utilized.
- Studies were subgrouped by diagnosis and family history to explore heterogeneity.
Main Results:
- Patients with mood disorders exhibited significantly reduced left and right SGC volumes compared to healthy controls.
- Significant SGC volume reductions were observed in unipolar depression but not in bipolar disorder.
- A positive family history of mood disorders was associated with a significant decrease in left SGC volume.
Conclusions:
- Evidence suggests left and right SGC volumetric reductions in mood disorder patients, most prominent in unipolar depression.
- The moderate effect size, particularly in subgroups with a positive family history, suggests SGC abnormalities may be an early vulnerability marker.
- Further research in unaffected high-risk individuals is needed to confirm the SGC's role as a primary vulnerability marker.
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