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Reduced amygdala serotonin transporter binding in posttraumatic stress disorder
James W Murrough1, Yiyun Huang, Jian Hu
1Mood and Anxiety Disorders Program, Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA.
Biological Psychiatry
|August 23, 2011
Summary
Posttraumatic stress disorder (PTSD) is linked to reduced serotonin transporter (5-HTT) availability in the amygdala. This finding supports a neurobiological model of PTSD involving altered threat detection and fear learning.
Area of Science:
- Neuroscience
- Psychiatry
- Radiochemistry
Background:
- The amygdala plays a crucial role in stress response regulation.
- Dysfunctional serotonin transporter (5-HTT) and amygdala activity are implicated in posttraumatic stress disorder (PTSD) pathophysiology.
- Previous studies have not evaluated 5-HTT in humans with PTSD.
Purpose of the Study:
- To investigate amygdala 5-HTT expression in individuals with PTSD using positron emission tomography (PET).
- To test the hypothesis that PTSD patients exhibit reduced amygdala 5-HTT availability.
- To explore the relationship between amygdala 5-HTT binding and anxiety/depression symptom severity.
Main Methods:
- PET scans were performed on 15 participants with PTSD and 15 healthy controls (HC).
- A selective 5-HTT radiotracer, [(11)C]AFM, was used to measure 5-HTT binding potential (BP(ND)).
- Resting-state scans were conducted to assess amygdala 5-HTT availability.
Main Results:
- PTSD group showed significantly reduced amygdala [(11)C]AFM BP(ND) compared to HC (16.3% reduction).
- The left amygdala exhibited a more pronounced reduction in [(11)C]AFM BP(ND) in the PTSD group (20.5% reduction).
- Amygdala [(11)C]AFM BP(ND) was inversely correlated with Hamilton Rating Scale for Anxiety and Montgomery-Åsberg Depression Rating Scale scores.
Conclusions:
- Reduced amygdala 5-HTT binding is observed in individuals with PTSD.
- These findings support a translational neurobiological model of PTSD.
- Dysregulated 5-HTT signaling in the amygdala may contribute to threat detection and fear learning deficits in PTSD.
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