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Occupancy of serotonin transporters in the amygdala by paroxetine in association with attenuation of left amygdala activation by negative faces in major depressive disorder
Affiliation:1. Department of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany;2. Department of Psychiatry and Psychotherapy, Charité – Universitätsmedizin Berlin, Berlin, Germany;3. Department of Neurology, University of Lübeck, Lübeck, Germany;4. Department of Psychiatry and Psychotherapy, Medical Center, University of Freiburg, Faculty of Medicine, University of Freiburg, Germany;5. Center for Psychosocial Medicine, Heidelberg University, Heidelberg, Germany;6. Department of Psychiatry and Psychotherapy, CBASP Center of Competence, University of Bonn, Bonn, Germany;7. Department of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany;8. Center for Psychosocial Medicine, Agaplesion Diakonieklinikum Rotenburg, Rotenburg, Germany;9. Department of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany
Abstract:
Amygdala hyperactivation in major depressive disorder (MDD) might be attenuated by selective serotonin reuptake inhibitors (SSRIs), but the working mechanism remains unclear. We hypothesized that higher amygdala serotonin transporter (SERT) occupancy by paroxetine results in greater attenuation of amygdala activation by negative facial expressions in MDD patients. We treated fifteen MDD patients (22–55 years) with paroxetine 20–50 mg/day. After 6 and 12 weeks, we quantified (1) clinical response (≥50% decrease in Hamilton Depression Rating Scale (HDRS), (2) SERT occupancy in both amygdala measured by repeated [123I]β-CIT single photon emission computed tomography (SPECT), and (3) amygdala activation when viewing fearful and angry (negative) faces with repeated functional MRI scans. Response rates were 4/15 and 9/15 at 6 and 12 weeks, respectively. Attenuation of left amygdala activation was associated with amygdala SERT occupancy (P=0.006) and response (P=0.015). This association may provide a rationale for decreased limbic activity seen during treatment of MDD. It might also explain the rapid decrease in negative attentional bias and amygdala activation caused by SSRIs.
Keywords:Major depressive disorder  Amygdala  Paroxetine  Serotonin transporter  Single photon emission computed tomography  Functional magnetic resonance imaging
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