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Striatal dopamine D2/3 receptor availability in treatment resistant depression
Bart P de Kwaasteniet1, Chedwa Pinto2, Henricus G Ruhé
1Department of Psychiatry, Academic Medical Center, Amsterdam, the Netherlands; Brain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands.
Plos One
|November 21, 2014
Summary
This study found no significant differences in dopamine D2/3 receptor availability in severe treatment-resistant depression (TRD) patients compared to healthy controls. Antipsychotics did not improve TRD symptoms despite occupying these receptors.
Area of Science:
- Neuroscience
- Psychiatry
- Radiology
Background:
- Dopamine agonists improve depressive symptoms in treatment-resistant depression (TRD), suggesting abnormal dopaminergic neurotransmission.
- Previous research has not investigated striatal dopamine D(2/3) receptor (D2/3R) binding in TRD patients.
Purpose of the Study:
- To investigate striatal D2/3R binding in severe TRD patients using [(123)I]IBZM SPECT.
- To compare D2/3R availability between TRD patients, TRD patients on antipsychotics (TRD AP), and healthy controls.
Main Methods:
- Utilized [(123)I]IBZM single photon emission computed tomography (SPECT) imaging.
- Included 6 severe TRD patients, 11 TRD AP patients, and 15 matched healthy controls.
Main Results:
- No significant difference in striatal D2/3R availability was observed between TRD patients and healthy controls (p = 0.75).
- TRD AP group showed significantly decreased D2/3R availability compared to TRD patients and controls (p<0.001), indicating antipsychotic occupancy.
- No clinical symptom differences were found between TRD AP and TRD patients, despite D2/3R occupancy.
Conclusions:
- This preliminary study does not support the hypothesis of altered dopaminergic transmission in severe TRD patients.
- Severe TRD patients do not appear to have large differences in striatal D2/3R availability.
- Atypical antipsychotics showed no clinical benefit in severe TRD patients, even with significant D2/3R occupancy.
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