Tschoner A, Engl J, Rettenbacher M, Edlinger M, Kaser S, Tatarczyk T, Effenberger M, Patsch J R, Fleischhacker W W, Ebenbichler C F
Department of Internal Medicine I, Medical University Innsbruck, Innsbruck, Austria.
Pharmacopsychiatry. 2009 Jan;42(1):29-34. doi: 10.1055/s-0028-1100425. Epub 2009 Jan 19.
Due to the association of second generation antipsychotics (SGAs) with weight gain and alterations of glucose and lipid homeostasis, we aimed to group six commonly prescribed SGAs into classes of differing risks.
Twenty-eight patients meeting the criteria for a diagnosis of schizophrenic disorder according to ICD-10 were assigned to monotherapy with olanzapine, clozapine, quetiapine, amisulpride, ziprasidone or risperidone. The levels of glucose and lipid metabolism were assessed before and after 28 days of treatment.
Based on cluster analysis, olanzapine and clozapine were found to constitute a high-risk group for metabolic dysregulation while amisulpride, quetiapine, risperidone and ziprasidone could be assigned to a non-high-risk group. Subjects from the high-risk group displayed significant weight gain with concomitant increases of HOMA-IR, levels of insulin, total cholesterol, TG, LDL-C and leptin. No significant changes were observed in the non-high-risk group.
The results of this study support the conclusion of the Consensus Development Conference on Antipsychotic Drugs and Obesity and Diabetes that certain SGAs are associated with a higher risk for weight gain, insulin resistance and dyslipidemia.
由于第二代抗精神病药物(SGA)与体重增加以及葡萄糖和脂质稳态改变有关,我们旨在将六种常用的SGA分为不同风险类别。
根据ICD-10符合精神分裂症障碍诊断标准的28例患者被分配接受奥氮平、氯氮平、喹硫平、氨磺必利、齐拉西酮或利培酮单药治疗。在治疗28天前后评估葡萄糖和脂质代谢水平。
基于聚类分析,发现奥氮平和氯氮平构成代谢失调的高风险组,而氨磺必利、喹硫平、利培酮和齐拉西酮可归为非高风险组。高风险组的受试者体重显著增加,同时伴有HOMA-IR、胰岛素水平、总胆固醇、甘油三酯、低密度脂蛋白胆固醇和瘦素水平升高。非高风险组未观察到显著变化。
本研究结果支持抗精神病药物与肥胖和糖尿病共识发展会议的结论,即某些SGA与体重增加、胰岛素抵抗和血脂异常的较高风险相关。