Molecular Psychiatry
September 7, 2022
Rebecca B Price, Nicholas Kissel, Andrew Baumeister et al.
80 citations
Ketamine given intravenously rapidly reduces depressive symptoms, with effects lasting at least a week. In an analysis of 17 randomized controlled trials with 809 participants, the benefit over placebo was larger for patients who had already failed two or more prior antidepressant trials. However, no patient-level clinical or demographic characteristics—such as age, sex, or diagnosis—could predict who would respond best, limiting the ability to personalize ketamine prescriptions. The findings confirm ketamine's broad effectiveness for depression but show that precision medicine approaches cannot yet guide treatment decisions.
Psychiatry and clinical psychopharmacology
August 11, 2025
Reinhard Janssen-Aguilar, Shakila Meshkat, Huda F Al-Shamali et al.
4 citations
Posttraumatic stress disorder (PTSD) is a severe condition that can be difficult to treat, prompting interest in innovative therapies. This systematic review of 94 studies evaluated interventional treatments including neuromodulation, rapid-acting pharmacotherapies like intravenous ketamine and esketamine, and psychedelic-assisted psychotherapies. Randomized controlled trials showed response rates ranging from 12.5% to 80% for transcranial magnetic stimulation, 17% to 67% for intravenous ketamine, and 50% to 87% for MDMA-assisted therapy. Most treatments were well tolerated with only mild, transient adverse effects. The review highlights variability in efficacy, safety, and tolerability across treatments, reflecting differences in patient populations, protocols, and comorbidities. While symptom improvement is observed, sustained efficacy varies, underscoring the need for maintenance strategies.
Journal of psychopharmacology (Oxford, England)
February 26, 2025
Sara de la Salle, Jennifer L Phillips, Pierre Blier et al.
3 citations
A sub-anesthetic dose of ketamine, an NMDAR antagonist, produces rapid antidepressant effects in treatment-resistant major depressive disorder. In 24 patients, ketamine reduced frontal mismatch negativity (MMN) amplitude, theta event-related oscillations, and source-localized frontal generator activity immediately and 2 hours after infusion, compared to midazolam. Larger reductions in MMN measures, particularly left frontal amplitude and theta oscillations, correlated with and predicted greater early and sustained symptom improvement on the Montgomery-Åsberg Depression Rating Scale. Baseline phase-locking factor also predicted sustained response. The findings suggest that acute NMDAR blockade reduces frontal MMN, and that MMN indices may serve as non-invasive biomarkers for predicting antidepressant response to glutamatergic agents.