4.7 Article

Modulation of the functional connectome in major depressive disorder by ketamine therapy

Journal

PSYCHOLOGICAL MEDICINE
Volume 52, Issue 13, Pages 2596-2605

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291720004560

Keywords

Functional connectivity; ketamine; major depression; salience network

Funding

  1. National Institute of Mental Health of the National Institutes of Health [MH110008, MH102743]
  2. Muriel Harris Chair in Geriatric Psychiatry
  3. UCLA Depression Grand Challenge

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This study found that subanesthetic ketamine infusion therapy can modify the functional connectome in patients with major depressive disorder (MDD), making it closer to the pattern seen in healthy controls. After treatment, there was a significant decrease in functional connectivity between the cerebellum and the salience network (SN). Additionally, patients who responded to treatment showed increased functional connectivity between the cerebellum and the striatum before treatment, which decreased after treatment.
Background Subanesthetic ketamine infusion therapy can produce fast-acting antidepressant effects in patients with major depression. How single and repeated ketamine treatment modulates the whole-brain functional connectome to affect clinical outcomes remains uncharacterized. Methods Data-driven whole brain functional connectivity (FC) analysis was used to identify the functional connections modified by ketamine treatment in patients with major depressive disorder (MDD). MDD patients (N = 61, mean age = 38, 19 women) completed baseline resting-state (RS) functional magnetic resonance imaging and depression symptom scales. Of these patients, n = 48 and n = 51, completed the same assessments 24 h after receiving one and four 0.5 mg/kg intravenous ketamine infusions. Healthy controls (HC) (n = 40, 24 women) completed baseline assessments with no intervention. Analysis of RS FC addressed effects of diagnosis, time, and remitter status. Results Significant differences (p < 0.05, corrected) in RS FC were observed between HC and MDD at baseline in the somatomotor network and between association and default mode networks. These disruptions in FC in MDD patients trended toward control patterns with ketamine treatment. Furthermore, following serial ketamine infusions, significant decreases in FC were observed between the cerebellum and salience network (SN) (p < 0.05, corrected). Patient remitters showed increased FC between the cerebellum and the striatum prior to treatment that decreased following treatment, whereas non-remitters showed the opposite pattern. Conclusion Results support that ketamine treatment leads to neurofunctional plasticity between distinct neural networks that are shown as disrupted in MDD patients. Cortico-striatal-cerebellar loops that encompass the SN could be a potential biomarker for ketamine treatment.

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