Current Understanding on Psilocybin for Major Depressive Disorder: A Review Focusing on Clinical Trials.
Sheng-Min WangSunghwan KimWon-Seok ChoiHyun Kook LimYoung Sup WooChi-Un PaeWon-Myong BahkPublished in: Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology (2023)
Previous studies suggested effectiveness of psilocybin in the field of mental health. FDA designated psilocybin as a "breakthrough therapy" for the treatment of treatment-resistant depression (TRD) in 2018. This paper provided a review of psilocybin's potential role in treatment of depression by focusing on published clinical trials. Studies showed that psilocybin, an agonist on 5-HT 2A receptors, manifests antidepressant and anxiolytic effects by increasing glutamate transmission, reducing brain inflammation, decreasing default mode network activity. In terms of clinical trials, eleven studies (six open-label and five double blinded randomized clinical trials [DB-RCTs]) trials exploring psilocybin's impact on depression were found. Among open-label studies, a pilot study on TRD patients demonstrated significant reductions in depressive symptoms after two psilocybin sessions. Psilocybin also improved cognitive bias associated with depression. Extension studies confirmed sustained improvements and high remission rates. Among five DB-RCTs, two showed that psilocybin led to significant reductions in anxiety and depression in cancer patients, and the improvements sustained for over six months. In MDD, psilocybin showed rapid reductions in depression, with higher remission rates compared to escitalopram in a DB-RCT. Another DB-RCT showed that psilocybin induced higher decrease in depression around 6 hours after their administrations than placebo. The last DB-RCT showed that in patients with TRD, a single dose of psilocybin 25 mg, but not psilocybin 10 mg, resulted in superior antidepressant effect than psilocybin 1 mg. Overall, psilocybin showed promise in treating depression and anxiety, with notable safety profiles. Further research should explore optimal dosages and long-term effects.
Keyphrases
- major depressive disorder
- depressive symptoms
- clinical trial
- open label
- mental health
- sleep quality
- bipolar disorder
- randomized controlled trial
- case control
- end stage renal disease
- oxidative stress
- phase ii
- rheumatoid arthritis
- physical activity
- ejection fraction
- resting state
- phase iii
- combination therapy
- phase ii study
- peritoneal dialysis
- prognostic factors
- mental illness
- subarachnoid hemorrhage
- brain injury