Department of Psychiatry, Seoul National Hospital, Seoul, Republic of Korea.
Psychiatry Investig. 2015 Apr;12(2):242-8. doi: 10.4306/pi.2015.12.2.242. Epub 2015 Mar 18.
Atypical antipsychotic (AAP) treatment is associated with weight gain and metabolic disturbances such as dyslipidemia and dysglycemia. The metabolic disturbances are usually considered to develop secondary to weight gain. We performed the comparison of metabolic disturbances of three AAP group with different risk of metabolic side effect after adjusting for body mass to investigate whether any metabolic disturbances develop independently from body mass index (BMI).
This cross-sectional study included 174 subjects with schizophrenia who were on 1) monotherapy with clozapine (CL), olanzapine (OL), or quetiapine (QT) (n=61), 2) monotherapy with risperidone (RSP) (n=89), or 3) monotherapy with aripiprizole (ARP), or ziprasidone (ZPS) (n=24) more than 1 year. Association between the prevalence of metabolic disturbances and groups were analysed using logistic regression after adjusting confounding variables including BMI. Analysese of covariance were used to compare the AAP groups in terms of the levels of metabolic parameters.
There were significant differences among groups in terms of the prevalence of hypertriglyceridemia (p=0.015), low HDL-cholesterol (p=0.017), and hyperglycemia (p=0.022) after adjusting for BMI. Triglyceride level (p=0.014) and the ratio of triglyceride to HDL-cholesterol (p=0.004) were significantly different among groups after adjusting for BMI.
In conclusion, metabolic disturbances are significantly different in AAP groups even after adjusting BMI. AAPs may have direct effect on metabolic parameters. Blood lipid and glucose levels should be monitored regularly regardless of whether patients tend to gain weight.
非典型抗精神病药物(AAP)治疗与体重增加和代谢紊乱有关,如血脂异常和血糖异常。这些代谢紊乱通常被认为是体重增加的继发结果。我们对三组 AAP 患者进行了比较,这三组患者的代谢紊乱风险不同,且在调整体重后存在代谢副作用,以调查是否存在任何与体重指数(BMI)无关的代谢紊乱。
这项横断面研究共纳入 174 例精神分裂症患者,他们接受了 1)氯氮平(CL)、奥氮平(OL)或喹硫平(QT)单药治疗(n=61),2)利培酮(RSP)单药治疗(n=89),或 3)阿立哌唑(ARP)或齐拉西酮(ZPS)单药治疗(n=24)超过 1 年。采用逻辑回归分析,调整包括 BMI 在内的混杂变量后,分析代谢紊乱的发生率与各组之间的关系。采用协方差分析比较各组间代谢参数水平。
调整 BMI 后,各组间的高甘油三酯血症(p=0.015)、低高密度脂蛋白胆固醇(p=0.017)和高血糖症(p=0.022)的患病率存在显著差异。调整 BMI 后,各组间的甘油三酯水平(p=0.014)和甘油三酯与高密度脂蛋白胆固醇比值(p=0.004)存在显著差异。
总之,即使调整 BMI 后,AAP 组之间的代谢紊乱仍存在显著差异。AAP 可能对代谢参数有直接影响。无论患者是否有体重增加的趋势,都应定期监测血脂和血糖水平。