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Published on: August 2, 2021
Striatal circuit function is associated with prior self-harm in remitted major depression.
William R Marchand1, James N Lee, Susanna Johnson
1George E. Wahlen Veterans Affairs Medical Center, 500 Foothill Drive, Salt Lake City, UT 84148, USA; University of Utah, 201 Presidents Circle, Salt Lake City, UT 84112, USA.
Individuals with a history of self-harm show altered striatal circuit function in major depression. This dysfunction in striatal and cortical midline circuits may persist even in remission, indicating potential trait pathology for suicide risk.
Area of Science:
- Neuroscience
- Psychiatry
- Neuroimaging
Background:
- Suicide risk neurobiology is not fully understood.
- Recurrent major depression (RMD) involves complex neural processes.
- Previous research suggests striatal circuit involvement in self-harm.
Purpose of the Study:
- Investigate the association between self-harm history and striatal circuit function in remitted RMD.
- Identify aberrant functional connectivity in the striatal-motor circuit.
- Explore if striatal and cortical midline circuit dysfunction persists in euthymic RMD patients.
Main Methods:
- Functional magnetic resonance imaging (fMRI) with a motor activation paradigm.
- Analysis of functional connectivity in 20 unmedicated RMD subjects and 21 controls.
- Correlational analyses to link functional connectivity with self-harm history.
Main Results:
- A significant association was found between self-harm history and striatal-motor circuit functional connectivity.
- Remitted RMD patients showed decreased functional connectivity in striatal and cortical midline circuits compared to controls.
- Striatal circuit dysfunction was previously linked to self-harm in a depressive episode.
Conclusions:
- Striatal circuit function is critically implicated in the neurobiology of suicide and self-harm risk in RMD.
- Persistent dysfunction in striatal and cortical midline circuits during euthymia suggests trait pathology in RMD.
- These findings highlight potential neural markers for suicide risk assessment.
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