Metabolic biomarkers of risperidone-induced weight gain in drug-naïve patients with schizophrenia

利培酮 体重增加 内科学 精神分裂症(面向对象编程) 抗精神病药 阿米必利 内分泌学 队列 前瞻性队列研究 医学 药理学 化学 精神科 体重
作者
Yuying Qiu,Yeqing Dong,Wei Sun,Gang Li,Mei Juan Li,Yongfu Zhao,Changyong Jiang,Jie Li
出处
期刊:Frontiers in Psychiatry [Frontiers Media]
卷期号:14 被引量:1
标识
DOI:10.3389/fpsyt.2023.1144873
摘要

Risperidone is a commonly prescribed antipsychotic drug with a potential side effect of weight gain. However, the pathophysiological mechanism is still poorly understood. Here, we sought to identify potential biomarkers of risperidone-induced weight gain by using a targeted metabolomics approach.We enrolled 30 subjects who received risperidone monotherapy for 8 weeks from a prospective longitudinal cohort study for drug-naïve schizophrenia patients. Plasma metabolites were measured by targeted metabolomics Biocrates MxP® Quant 500 Kit at baseline and 8-week follow-up.After 8 weeks of risperidone treatment, the levels of 48 differential metabolites were upregulated, including lysophosphatidylcholines (2), phosphatidylcholines (PC) (8), cholesteryl esters (CE) (3), and triglycerides (35), while 6 differential metabolites namely PC aa C38:6, methionine (Met), α-aminobutyric acid (AABA), TrpBetaine, CE (22:6), and Taurocholic acid (TCA) were downregulated. Interestingly, the reduction of PC aa C38:6, AABA and CE (22:6) was linearly related with increased BMI. Further multiple regression analysis showed that the changes of PC aa C38:6 and AABA were independent contributors of increased BMI. In addition, baseline levels of PC aa C36:5, CE (20:5) and AABA had positive relationships with the change of BMI.Our findings indicate phosphatidylcholines and amino acids may serve as biomarkers for risperidone-induced weight gain.

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