Quetiapine Extended Release Open-Label Treatment Associated Changes in Amygdala Activation and Connectivity in Anxious Depression: An fMRI Study
Journal of Clinical Psychopharmacology, ISSN: 1533-712X, Vol: 36, Issue: 6, Page: 562-571
2016
- 17Citations
- 52Captures
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Metrics Details
- Citations17
- Citation Indexes17
- 17
- CrossRef13
- Captures52
- Readers52
- 52
Article Description
Background: This study investigated extended release quetiapine (quetiapine XR) associated changes in functional MRI (fMRI) measures of task-induced amygdalar activation and resting state connectivity in anxious unipolar major depressive disorder (AMDD). Methods: Anxious unipolar major depressive disorder patients (n = 15) (17-item Hamilton Depression Rating Scale (HAM-D) >18 and Hamilton Anxiety Scale (HAM-A) >18) and closely matched healthy control (HC) subjects were compared at baseline for task induced amygdala activation and resting state connectivity on fMRI. Subsequently, AMDD patients were treated for 8 weeks with open-label quetiapine XR. Weekly HAM-D and HAM-A ratings were obtained, and the fMRI scan was repeated at weeks 2 and 8. Changes in fMRI measures were calculated using repeated-measures analysis of variance and correlation with decrease in HAM-D and HAM-A scores was examined. Results At baseline, AMDD compared with HC exhibited increased task-induced left amygdalar activation (P = 0.05 clusterwise corrected) and decreased resting state amygdala-cortical and amygdala-pons connectivity (P < 0.05 clusterwise corrected). Quetiapine XR treatment was associated with significant decrease in HAM-D (df = 1,28; female [F] = 39; P = 0.001) and HAM-A scores (df = 1,28; F = 55; P = 0.001). The AMDD group showed increased amygdala-cortical connectivity (P < 0.05 [clusterwise corrected]) at week 2, which was maintained at week 8. At week 8, additional areas showed increased connectivity including insula and putamen. At 8 weeks, decrease in HAM-D scores correlated with increase in amygdala-mid cingulate and amygdala-cuneus connectivity (P = 0.05 [clusterwise corrected]). Decrease in HAM-A scores correlated with increase in amygdala-cuneus and parietal cortex connectivity (P = 0.05 [clusterwise corrected]). Limitations Small sample-size, open-label single-arm design, HC only tested at baseline, focused only on amygdala. Conclusions: Quetiapine XR effects in the treatment of AMDD are associated with modulation of amygdala connectivity.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84992156990&origin=inward; http://dx.doi.org/10.1097/jcp.0000000000000600; http://www.ncbi.nlm.nih.gov/pubmed/27768670; https://journals.lww.com/00004714-201612000-00006; http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:landingpage&an=00004714-201612000-00006; https://dx.doi.org/10.1097/jcp.0000000000000600; https://journals.lww.com/psychopharmacology/Abstract/2016/12000/Quetiapine_Extended_Release_Open_Label_Treatment.6.aspx
Ovid Technologies (Wolters Kluwer Health)
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