Adjunctive Garcinia mangostana Linn. (Mangosteen) Pericarp for Schizophrenia: A 24-Week Double-blind, Randomized, Placebo Controlled Efficacy Trial: Péricarpe d’appoint Garcinia mangostana Linn (mangoustan) pour la schizophrénie : un essai d’efficacité de 24 semaines, à double insu, randomisé et contrôlé par placebo

Author:

Turner Alyna12ORCID,Baker Andrea3,Dean Olivia M.14,Walker Adam J.1,Dodd Seetal156,Cotton Susan M.67,Scott James G.389,Kavanagh Bianca E.1ORCID,Ashton Melanie M.1ORCID,Brown Ellie167,McGrath John J.31011ORCID,Berk Michael14567ORCID

Affiliation:

1. Deakin University, IMPACT—the Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Barwon Health, Geelong, Australia

2. School of Medicine and Public Health, Faculty of Health and Medicine, The University of Newcastle, Callaghan, New South Wales, Australia

3. Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Wacol, Australia

4. Florey Institute for Neuroscience and Mental Health, University of Melbourne, Parkville, Australia

5. Department of Psychiatry, University of Melbourne, Royal Melbourne Hospital, Parkville, Australia

6. Centre for Youth Mental Health, The University of Melbourne, Parkville, Australia

7. Orygen, Parkville, Australia

8. Metro North Mental Health Service, Herston, Queensland, Australia

9. Mental Health Programme, QIMRBerghofer Medical Research Institute, Herston, Queensland, Australia

10. Queensland Brain Institute, University of Queensland, St Lucia, Australia

11. National Centre for Register-based Research, Aarhus BSS, Aarhus University, Aarhus V, Denmark

Abstract

Objectives: Garcinia mangostana Linn. (“mangosteen”) pericarp contains bioactive compounds that may target biological pathways implicated in schizophrenia. We conducted a double-blind randomized placebo-controlled trial evaluating the efficacy of adjunctive mangosteen pericarp, compared to placebo, in the treatment of schizophrenia. Methods: People diagnosed with schizophrenia or schizoaffective disorder ( Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition), recruited across 2 sites (Brisbane and Victoria, Australia), were randomized to receive 24 weeks of adjunctive mangosteen pericarp (1,000 mg/day) or matched placebo. The primary outcome measure was the Positive and Negative Symptom Scale total score. Secondary outcomes included positive and negative symptoms, general psychopathology, clinical global severity and improvement, participant reported overall improvement, depressive symptoms, functioning, quality of life, and safety data at 24 and 28 weeks (4 weeks postdiscontinuation). Data were collected from July 2016 to February 2019. Results: Baseline assessments were conducted on 148 people (mangosteen = 74, placebo = 74); data analyses were conducted on 136 (92%) participants with postbaseline data. The treatment group had significantly higher symptom severity compared to placebo, and both groups significantly improved on all symptom, functioning, and quality of life measures over time. No between-group differences were found for the rate of change between baseline and 24 or 28 weeks. Conclusion: Despite promising preclinical and clinical work, our results do not support mangosteen pericarp extract as an adjunctive treatment for schizophrenia or schizoaffective disorder.

Funder

Stanley Medical Research Institute

Publisher

SAGE Publications

Subject

Psychiatry and Mental health

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