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Change in Negative Affective Bias following a Single Ketamine Treatment for Treatment-Resistant Depression

Anna J. Harvey, Stevan Nikolin, Nicholas Chand, William Flanney, Liyi Tan, Adriano Moffa, Colleen K. Loo, Donel M. Martin

Depression and Anxiety August 19, 2023 DOI: 10.1155/2023/3371272

Summary

AI-generated from the abstract

A single dose of ketamine, compared to an active control (midazolam), did not produce significant changes in most measures of emotional or cognitive processing in people with treatment-resistant depression one day after treatment. However, participants who received ketamine showed a significant improvement on a test of negative processing bias, though this improvement was not significantly linked to changes in depressive symptoms. The study was small and exploratory, and larger trials are needed to confirm the finding.

Study at a glance

Characteristics Randomized double-blind controlled study with an active control Peer reviewed
Sample size 44
Population Participants with treatment-resistant major depressive disorder and healthy controls
Interventions racemic ketamine hydrochloride midazolam hydrochloride
Duration Single treatment, assessments one day after treatment
Citations 4
Key finding A single ketamine treatment significantly improved negative processing bias on the Scrambled Sentence Task, but this improvement was not significantly associated with symptom change.

Abstract

Ketamine has recently emerged as a highly effective new treatment for people with treatment-resistant depression with rapid antidepressant effects. However, these effects are often short lasting, and the potential cognitive mechanisms underlying the therapeutic effects, such as effects on emotional processing bias, remain poorly understood. In the present study, we explored potential changes in emotional and cognitive processing following a single treatment of subcutaneous ketamine in a randomised double-blind controlled study with an active control. Participants with treatment-resistant major depressive disorder (MDD) were recruited from a single site from the Ketamine for Adult Depression Study (KADS Trial) and were randomly assigned to receive racemic ketamine hydrochloride ( n = 10 ) or midazolam hydrochloride ( n = 11 ) in a 1 : 1 ratio. A healthy control sample ( n = 23 ) was recruited to attend a single experimental session without any treatment. All MDD participants completed mood ratings and cognitive assessments prior to and one day after a single randomised treatment. The results showed no significant differences in performance changes after treatment across the majority of emotion-related (i.e., Emotional Stroop Task, Affective Go/No-Go Task) and cognitive (Ruff 2 and 7 Selective Attention Test, Controlled Word Association Test) outcome measures. Participants who received ketamine showed a significant improvement in a negative processing bias test (i.e., The Scrambled Sentence Task; Cohen’s d = .67 , p = .016 ), which was not significantly associated with improvement in psychological symptoms ( r = − .662 , p = .074 ). The results from this exploratory study suggest that a single ketamine treatment may modulate negative affective bias. Limitations to this study included the small sample size and lack of follow-up. Future larger trials are required to confirm this finding.

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