Skip to content

Acute and long-term effects of repeated ketamine infusions in treatment-resistant depression and associated metabolite changes.

Hitoshi Sakurai, Daiki Setoyama, Takahiro A Kato, Hisateru Tachimori, Masami Murao, Yasuyuki Matsumoto, Teruo Tada, Yayoi Imamura, Hiroyuki Seki, Takashi Tsuboi, Hiroyuki Uchida, Koichiro Watanabe

Psychiatry and Clinical Neurosciences July 15, 2025 DOI: 10.1111/pcn.13870 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Open-label study Peer reviewed
Sample size 30
Population Patients with treatment-resistant depression
Intervention Ketamine
Dose 0.5 mg/kg
Duration 2-week intervention, 12-month follow-up
Topics Depression Ketamine Esketamine
Keywords 3‐hydroxybutyrate Metabolomics Treatment‐resistant depression Depression treatment Biomarkers Personalized medicine
Citations 1
Key points Early increases in 3-hydroxybutyrate levels predicted antidepressant response to repeated ketamine infusions, but sustained remission was achieved in only a minority of patients.

Abstract

This study aims to investigate the acute and sustained antidepressant effects of repeated ketamine infusions in patients with treatment-resistant depression (TRD), and to identify early metabolomic changes predictive of treatment outcomes using metabolome analyses. This open-label study investigated the effects of four intravenous ketamine infusions (0.5 mg/kg) administered over 2 weeks in 30 patients with TRD. Clinical outcomes, including the Montgomery-Åsberg Depression Rating Scale (MADRS), were evaluated at baseline, 1-2 h after each infusion, and monthly during a 12-month follow-up. Plasma levels of 11 depression-associated metabolites were measured at baseline and 1.5-2 h after the first infusion. A general linear model was employed to analyze the association between metabolite changes after the first infusion and the MADRS score percent improvements after the fourth infusion and at 12 months. Remission was defined as a MADRS score of ≤10. All participants completed the four infusions. The MADRS score decreased from 30.6 ± 6.1 at baseline to 20.3 ± 11.5 after the fourth infusion, with a remission rate of 26.7%. At 12 months, 13.3% of participants remained in remission. Changes in 3-hydroxybutyrate levels after the first infusion predicted the MADRS score percent improvements after the fourth infusion (β = 1.35, 95% CI: 0.41-2.30, P = 0.005) and at 12 months (β = 1.38, 95% CI: 0.37-2.39, P = 0.007). While repeated ketamine infusions demonstrated rapid antidepressant effects, sustained remission was achieved in a minority of patients with TRD. 3-Hydroxybutyrate may serve as a biomarker for predicting treatment response. These findings underscore the potential for individualized strategies using ketamine infusions. jRCTs031210648 (Japan Registry of Clinical Trials).

Comparable studies

Other non-randomized and open-label trials on ketamine for depression, most cited first.

Study Year Design Participants
Rapid Resolution of Suicidal Ideation After a Single Infusion of anN-Methyl-D-Aspartate Antagonist in Patients With Treatment-Resistant Major Depressive Disorder Subjects with DSM-IV-diagnosed treatment-resistant major depressive disorder 2010 Open-label trial n = 33
Esketamine Nasal Spray Plus Oral Antidepressant in Patients With Treatment-Resistant Depression Adults (≥ 18 years) with treatment-resistant depression 2020 Phase 3, open-label, multicenter, long-term study n = 802
Intravenous arketamine for treatment-resistant depression: open-label pilot study Humans with treatment-resistant depression 2020 Open-label pilot trial n = 7
A Phase 2 Open Label Study of Efficacy, Safety, and Tolerability of SLS-002 (Intranasal Racemic Ketamine) in Adults with MDD at Imminent Risk of Suicide. Hospitalized patients with Major Depressive Disorder and acute suicidal ideation and... 2024 Open label study n = 17
Ketamine Safety and Tolerability in Clinical Trials for Treatment-Resistant Depression Participants with DSM-IV-defined major depressive disorder and treatment-resistant... 2014 Pooled analysis of three clinical trials n = 97

Explore topics

By condition and practice