SchizophreniaInterpersonal Functioning & Social ConnectednessMDMA

MDMA for the Treatment of Negative Symptoms in Schizophrenia

This review argues that MDMA‑assisted therapy is a promising novel approach for treating negative symptoms of schizophrenia, drawing on MDMA’s prosocial, empathogenic and metaplastic effects to target deficits for which there are currently no FDA‑approved treatments. It synthesises recent evidence suggesting MDMA may be safe and potentially effective and outlines safety considerations and putative mechanisms of action.

Authors

  • Arnovitz, M. D.
  • Spitzberg, A. J.
  • Davani, A. J.

Published

Journal of Clinical Medicine
individual Study

Abstract

The profound economic burden of schizophrenia is due, in part, to the negative symptoms of the disease, which can severely limit daily functioning. There is much debate in the field regarding their measurement and classification and there are no FDA-approved treatments for negative symptoms despite an abundance of research. 3,4-Methylenedioxy methamphetamine (MDMA) is a schedule I substance that has emerged as a novel therapeutic given its ability to enhance social interactions, generate empathy, and induce a state of metaplasticity in the brain. This review provides a rationale for the use of MDMA in the treatment of negative symptoms by reviewing the literature on negative symptoms, their treatment, MDMA, and MDMA-assisted therapy. It reviews recent evidence that supports the safe and potentially effective use of MDMA to treat negative symptoms and concludes with considerations regarding safety and possible mechanisms of action.

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Research Summary of 'MDMA for the Treatment of Negative Symptoms in Schizophrenia'

Editorial

βBlossom's Take

This review is useful because it brings MDMA into a question that has been relatively neglected in the psychedelic revival, namely negative symptoms in schizophrenia. The argument is speculative, but it is a reasonable piece of the evidence base because it connects MDMA’s prosocial effects and metaplasticity to a symptom cluster with very limited treatment options.

Study Details

Cited By (3)

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112 cited
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