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Hippocampal subfield volumes in mood disorders
B Cao1, I C Passos2, B Mwangi1
1Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Molecular Psychiatry
|January 25, 2017
Summary
Bipolar disorder (BD) is linked to reduced hippocampal subfield volumes, particularly in bipolar I disorder (BD-I). Illness progression and manic episodes worsen these volume reductions in specific brain areas.
Area of Science:
- Neuroscience
- Psychiatry
- Neuroimaging
Background:
- Hippocampal volume abnormalities are linked to mood disorders.
- The hippocampus comprises distinct subfields (e.g., CA1-4, dentate gyrus) where mood disorder mechanisms may be localized.
- Investigating subfield-specific changes is crucial for understanding mood disorders.
Purpose of the Study:
- To examine in vivo hippocampal subfield volumes in bipolar disorder (BD) and major depressive disorder (MDD).
- To determine if specific subfields are differentially affected in BD and MDD.
- To explore the relationship between hippocampal subfield volumes and illness progression in BD.
Main Methods:
- Utilized a state-of-the-art hippocampal segmentation technique.
- Compared hippocampal subfield volumes between healthy subjects, patients with BD, and patients with MDD.
- Analyzed correlations between subfield volumes, illness duration, and manic episode count in BD patients.
Main Results:
- Patients with BD showed reduced volumes in left CA4, granule cell layer (GCL), molecular layer (ML), and bilateral hippocampal tail compared to healthy subjects and MDD patients.
- Volume reductions were most severe in bipolar I disorder (BD-I).
- In BD-I, increased illness duration correlated with reduced volumes in right CA1, ML, and subiculum. Manic episodes correlated with reduced volumes in bilateral CA2/3, CA4, and hippocampal tail.
Conclusions:
- Hippocampal subfields are more affected in BD-I than in BD-II or MDD.
- Manic episodes have a progressive, localized impact on CA2/3, CA4, and the hippocampal tail in BD-I.
- These findings highlight the specific neuroanatomical changes associated with different mood disorders and illness progression.

