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辅助倍他司汀治疗对慢性精神分裂症患者脂质代谢的影响:一项随机双盲安慰剂对照研究

 

Authors Bai L, Liang W, Wang Y, Fan N, zhang Q, Bian Y, Yang F

Received 9 October 2022

Accepted for publication 27 January 2023

Published 27 February 2023 Volume 2023:19 Pages 453—460

DOI https://doi.org/10.2147/NDT.S392770

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Yuping Ning

Objective: This study aims to explore the ability of betahistine to inhibit weight gain and abnormal lipid metabolism in patients with chronic schizophrenia.
Methods: A comparison study of betahistine or placebo therapy was conducted for 4 weeks in 94 patients with chronic schizophrenia, who were randomly divided into two groups. Clinical information and lipid metabolic parameters were collected. Positive and Negative Syndrome Scale (PANSS) was used to assess psychiatric symptoms. Treatment Emergent Symptom Scale (TESS) was used to evaluate treatment-related adverse reactions. The differences in lipid metabolic parameters before and after treatment between the two groups were compared.
Results: Repeated measures analysis of variance (ANOVA) revealed that after 4 weeks of betahistine/placebo treatment, the interaction effect of time and group was statistically significant on low-density lipoprotein cholesterol (F = 6.453, = 0.013) and waist-to-hip ratio (F = 4.473, = 0.037), but did not reveal any significant interaction effect of time and group on weight, body mass index or other lipid metabolic parameters, as well as the time main effect and group main effect (all > 0.05). Betahistine had no significant impact on PANSS, and no side effects related to betahistine were detected.
Conclusion: Betahistine may delay metabolic abnormalities in patients with chronic schizophrenia. It does not affect the efficacy of the original antipsychotics. Thus, it provides new ideas for the treatment of metabolic syndrome in patients with chronic schizophrenia.
Keywords: schizophrenia, lipid metabolism, betahistine, histamine, H3-receptor antagonist