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
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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