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Functional Dysconnectivity of Frontal Cortex to Striatum Predicts Ketamine Infusion Response in Treatment-Resistant Depression

Authors :
Ya Mei Bai
Mu Hong Chen
Tung Ping Su
Wei Chen Lin
Shih-Jen Tsai
Cheng Ta Li
Wan Chen Chang
Pei Chi Tu
Wen Sheng Huang
Source :
International Journal of Neuropsychopharmacology
Publication Year :
2020
Publisher :
Oxford University Press (OUP), 2020.

Abstract

Background Frontostriatal disconnectivity plays a crucial role in the pathophysiology of major depressive disorder. However, whether the baseline functional connectivity of the frontostriatal network could predict the treatment outcome of low-dose ketamine infusion remains unknown. Methods In total, 48 patients with treatment-resistant depression were randomly divided into 3 treatment groups (a single-dose 40-minute i.v. infusion) as follows: 0.5 mg/kg ketamine, 0.2 mg/kg ketamine, and saline placebo infusion. Patients were subsequently followed-up for 2 weeks. Resting-state functional magnetic resonance imaging was performed for each patient before infusion administration. In addition, the baseline frontostriatal functional connectivity of patients with treatment-resistant depression was also compared with that of healthy controls. Results Compared with the healthy controls, patients with treatment-resistant depression had a decreased functional connectivity in the frontostriatal circuits, especially between the right superior frontal cortex and executive region of the striatum and between the right paracingulate cortex and rostral-motor region of the striatum. The baseline hypoconnectivity of the bilateral superior frontal cortex to the executive region of the striatum was associated with a greater reduction of depression symptoms after a single 0.2-mg/kg ketamine infusion. Conclusion Reduced connectivity of the superior frontal cortex to the striatum predicted the response to ketamine infusion among patients with treatment-resistant depression.

Details

ISSN :
14695111 and 14611457
Volume :
23
Database :
OpenAIRE
Journal :
International Journal of Neuropsychopharmacology
Accession number :
edsair.doi.dedup.....32305b7616d75e8eb914dbe60fbb9553
Full Text :
https://doi.org/10.1093/ijnp/pyaa056