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Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials

  • Authors:
    • Shan Gao
    • Ling Fan
    • Zhigang Yu
    • Xingxing Xie
  • View Affiliations / Copyright

    Affiliations: Department of Pharmacy, Chengdu Second People's Hospital, Chengdu, Sichuan 618000, P.R. China, Department of Good Clinical Practice, Yaan People's Hospital, Yaan, Sichuan 625000, P.R. China, Department of Pharmacy, Yaan People's Hospital, Yaan, Sichuan 625000, P.R. China
    Copyright: © Gao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 91
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    Published online on: April 11, 2024
       https://doi.org/10.3892/br.2024.1779
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Abstract

Lurasidone is an atypical anti‑psychotic approved by the US Food and Drug Administration. It is mainly used to treat schizophrenia in adults through its antagonistic action on dopamine and 5‑hydroxytryptamine receptors. The present study systematically assessed the efficacy and safety of lurasidone in the treatment of schizophrenia. Clinical, double‑blind, parallel, randomized controlled trials (RCTs) of lurasidone in the treatment of schizophrenia were retrieved from PubMed\Medline, EBSCO, Embase, Cochrane Library, OVID, Web of Science and related clinical trial registration websites up to May 2023. A total of two investigators independently screened the included references and evaluated their quality. RevMan 5.3 software was used for meta‑analysis of each measure outcome. The present systematic review was registered in PROSPERO (ID=CRD42018108178). A total of eight RCTs were included in the present study, including a total of 2,456 patients with schizophrenia. All eight references were randomized, double‑blind and parallel control trials. All eight references were evaluated as high quality. The meta‑analysis results demonstrated that there were no significant change in total Positive and Negative Syndrome Scale (PANSS) score, Clinical Global Impression of Severity (CGI‑S) score and Montgomery‑Asberg Depression Rating Scale (MADRS) between the 40 mg lurasidone group and the placebo group (P>0.05). However, as the dosage increased, the 80, 120 and 160 mg lurasidone groups had significant changes in total PANSS score, CGI‑S score and MADRS Compared with placebo (P<0.05), although changes in MADRS in the 120 mg lurasidone group were not statistically significant (P>0.05). In terms of safety, the changes in the incidence of agitation in the 40 mg lurasidone group (P<0.05), vomiting in the 80 mg group (P<0.05) and akathisia in the 160 mg group (P<0.05) were statistically significant and there were also statistically significant changes in the incidence of akathisia, nausea, somnolence and extrapyramidal disorder among the 40, 80 and 120 mg lurasidone groups (P<0.05); No statistically significant changes in the in the incidence of other adverse reactions (P>0.05). In conclusion, existing evidence suggests that the initial dose of lurasidone for schizophrenia can be adjusted to 80 mg. As the condition aggravates, the dose can be incrementally increased to 160 mg. A dose of 160 mg lurasidone is recommended as the most efficacious and safe dose for acute schizophrenia and the risk of occurrence of akathisia, nausea, somnolence and extrapyramidal disorder is still high when lurasidone is administered at a dose of 80‑120 mg. The dose should be promptly adjusted or the drug should be withdrawn if the aforementioned adverse reactions worsen. Multi‑center, high‑quality and long‑term clinical RCTs influenced by the included references are still necessary to support the aforementioned conclusions.
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Copy and paste a formatted citation
Spandidos Publications style
Gao S, Fan L, Yu Z and Xie X: Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials. Biomed Rep 20: 91, 2024.
APA
Gao, S., Fan, L., Yu, Z., & Xie, X. (2024). Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials. Biomedical Reports, 20, 91. https://doi.org/10.3892/br.2024.1779
MLA
Gao, S., Fan, L., Yu, Z., Xie, X."Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials". Biomedical Reports 20.6 (2024): 91.
Chicago
Gao, S., Fan, L., Yu, Z., Xie, X."Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials". Biomedical Reports 20, no. 6 (2024): 91. https://doi.org/10.3892/br.2024.1779
Copy and paste a formatted citation
x
Spandidos Publications style
Gao S, Fan L, Yu Z and Xie X: Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials. Biomed Rep 20: 91, 2024.
APA
Gao, S., Fan, L., Yu, Z., & Xie, X. (2024). Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials. Biomedical Reports, 20, 91. https://doi.org/10.3892/br.2024.1779
MLA
Gao, S., Fan, L., Yu, Z., Xie, X."Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials". Biomedical Reports 20.6 (2024): 91.
Chicago
Gao, S., Fan, L., Yu, Z., Xie, X."Efficacy and safety of lurasidone for schizophrenia: A systematic review and meta‑analysis of eight short‑term, randomized, double‑blind, placebo‑controlled clinical trials". Biomedical Reports 20, no. 6 (2024): 91. https://doi.org/10.3892/br.2024.1779
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