Beneficial adjunctive effects of the 5HT3 receptor antagonist ondansetron on symptoms, function and cognition in early phase schizophrenia in a double-blind, 2 × 2 factorial design, randomised controlled comparison with simvastatin

Author:

Chaudhry Imran B1234,Husain Muhammad Omair56,Khoso Ameer B3,Kiran Tayyeba3,Husain Muhammad Ishrat56,Qurashi Inti7,Rahman Raza Ur2,Mehmood Nasir3,Drake Richard48,Husain Nusrat489,Deakin Bill48ORCID

Affiliation:

1. Department of Psychiatry, Dow University of Health Sciences, Karachi, Pakistan

2. Ziauddin University Hospital, Karachi, Pakistan

3. Pakistan Institute of Living and Learning, Karachi, Pakistan

4. Division of Psychology and Mental Health, School of Health Sciences, University of Manchester, Manchester, UK

5. Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada

6. Temerty Faculty of Medicine, Department of Psychiatry, University of Toronto, Toronto, ON, Canada

7. Faculty of Health and Life Sciences, University of Liverpool, Merseyside, UK

8. Manchester Academic Health Science Centre, Manchester, UK

9. Mersey Care NHS Foundation Trust, Liverpool, Merseyside, UK

Abstract

Background: Variable benefits have been reported from the adjunctive use of simvastatin and the 5HT3 receptor antagonist, ondansetron, in patients with schizophrenia. We investigated their independent efficacy and possible synergy to improve negative symptoms of schizophrenia within a single trial. Methods: A 6-month, randomised, double-blind, placebo-controlled trial with a 4-arm, 2 × 2 factorial design, in three centres in Pakistan. In total, 303 people with stable treated schizophrenia aged 18–65 were randomly allocated to add-on ondansetron, simvastatin, both or neither. The primary outcome was a Positive and Negative Syndrome Scale (PANSS) negative score at 3 and 6 months. Results: Mixed model analysis and analysis of covariance revealed no main effects of simvastatin or ondansetron but a significant negative interaction between them ( p = 0.03); when given alone, both drugs significantly reduced negative symptoms compared to placebo but they were ineffective in combination. Individual treatment effects versus placebo were −1.9 points (95%CIs −3.23, −0.49; p = 0.01) for simvastatin and −1.6 points for ondansetron (95%CIs −3.00, −0.14; p = 0.03). Combined treatment significantly increased depression and side effects. In those with less than the median 5 years of treatment, ondansetron improved all PANSS subscales, global functioning measures and verbal learning and fluency, whereas simvastatin did not. Conclusion: Small improvement in negative symptoms on simvastatin and ondansetron individually are not synergistic in combination in treating negative symptoms of schizophrenia. Ondansetron showed broad efficacy in patients on stable antipsychotic treatment within 5 years of illness. The findings suggest that ondansetron should be evaluated in patients at risk of psychosis or early in treatment.

Funder

Stanley Medical Research Institute

Publisher

SAGE Publications

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