Neurocognitive effects of subanesthetic serial ketamine infusions in treatment resistant depression

• Published in: Journal of affective disorders Vol. 333; pp. 161 - 171
• Main Authors: Zavaliangos-Petropulu, Artemis, McClintock, Shawn M., Khalil, Jacqueline, Joshi, Shantanu H., Taraku, Brandon, Al-Sharif, Noor B., Espinoza, Randall T., Narr, Katherine L.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.07.2023
• Subjects: Adult; Antidepressant; Antidepressive Agents - adverse effects; Cognition; Depression; Depressive Disorder, Treatment-Resistant - drug therapy; Humans; Infusions, Intravenous; Ketamine; Ketamine - adverse effects; Middle Aged; Neurocognitive; Treatment; Treatment Outcome; Antidepressant; Ketamine; Treatment; TRD; Depression; Cognition; MDD; HDRS; TP; Neurocognitive
• ISSN: 0165-0327; 1573-2517
• DOI: 10.1016/j.jad.2023.04.015

Ketamine treatment prompts a rapid antidepressant response in treatment-resistant depression (TRD). We performed an exploratory investigation of how ketamine treatment in TRD affects different cognitive domains and relates to antidepressant response. Patients with TRD (N = 66; 30 M/35F; age = 39.5 ± 11.1 years) received four ketamine infusions (0.5 mg/kg). Neurocognitive function and depressive symptoms were assessed at baseline, 24 h after the first and fourth ketamine infusion, and 5 weeks following end of treatment. Mixed effect models tested for changes in seven neurocognitive domains and antidepressant response, with post-hoc pairwise comparisons between timepoints, including follow-up. Relationships between change in neurocognitive function and antidepressant response over the course of treatment were tested with Pearson's correlation and mediation analyses. Associations between baseline neurocognitive performance and antidepressant response were tested with Pearson's correlation. Significant improvements in inhibition, working memory, processing speed, and overall fluid cognition were observed after the first and fourth ketamine infusion. Improvements in processing speed and overall fluid cognition persisted through follow-up. Significant improvements in depressive symptoms reverted towards baseline at follow-up. Baseline working memory and change in inhibition were moderately correlated with antidepressant response, however, improvements in neurocognitive performance were statistically independent from antidepressant response. Antidepressant ketamine leads to improved neurocognitive function, which persist for at least 5 weeks. Neurocognitive improvements observed appear independent of antidepressant response, suggesting ketamine may target overlapping but distinct functional brain systems. Limitations Research investigating repeated serial ketamine treatments is important to determine cognitive safety. This study is a naturalistic design and does not include placebo. •Improvements in neurocognitive function observed 24 h after first and fourth ketamine infusion•Improvements in processing speed and global fluid cognitive function through 5-week follow-up•Change in neurocognitive function independent from antidepressant response