Perez-Iglesias Rocio, Mata Ignacio, Pelayo-Teran Jose M, Amado Jose A, Garcia-Unzueta Maria T, Berja Ana, Martinez-Garcia Obdulia, Vazquez-Barquero Jose L, Crespo-Facorro Benedicto
Department of Psychiatry, Marques de Valdecilla University Hospital, Avda. Valdecilla s/n, 39008, University of Cantabria, Spain.
Schizophr Res. 2009 Feb;107(2-3):115-21. doi: 10.1016/j.schres.2008.09.028. Epub 2008 Nov 6.
This study examined the main metabolic side effects induced by antipsychotic treatment in a cohort of first episode drug-naïve subjects after the first year of treatment.
A randomized, open-label, prospective clinical trial was conducted. Participants were 164 consecutive subjects included in a first episode program and never treated with antipsychotic medication. Patients were assigned to haloperidol, olanzapine or risperidone. The main outcome measures were changes at 1 year in fasting glucose parameters (glucose, insulin levels and insulin resistance index) and changes in fasting lipid parameters (total cholesterol, triglycerides, LDL cholesterol, HDL cholesterol).
144 of the total sample were evaluated at 1 year. There was a statistically significant increase in the mean values of insulin levels, insulin resistance index, total cholesterol, LDL-cholesterol and triglycerides. No pathological values in fasting glucose plasma levels were found at baseline and there were no changes after 1 year. Weight gain was positively correlated with changes in insulin levels, insulin resistance index and triglyceride levels. We did not detect statistically significant differences between treatments in any of the parameters evaluated.
Fasting glycaemia and insulin concentrations at baseline do not support the hypothesis that schizophrenia is associated with an underlying abnormality in glucose metabolism. The changes in insulin and lipid parameters at 1 year seem to be related to the magnitude of weight gain. There were no significant differences between haloperidol, olanzapine and risperidone concerning metabolic adverse effects after the first year of treatment.
本研究调查了首次发作且未用过药的受试者在接受抗精神病药物治疗一年后出现的主要代谢副作用。
开展了一项随机、开放标签的前瞻性临床试验。参与者为164名连续纳入首次发作项目且从未接受过抗精神病药物治疗的受试者。患者被分配至接受氟哌啶醇、奥氮平或利培酮治疗。主要结局指标为1年后空腹血糖参数(血糖、胰岛素水平和胰岛素抵抗指数)的变化以及空腹血脂参数(总胆固醇、甘油三酯、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇)的变化。
共144名受试者在1年后接受了评估。胰岛素水平、胰岛素抵抗指数、总胆固醇、低密度脂蛋白胆固醇和甘油三酯的平均值出现了具有统计学意义的升高。基线时空腹血糖血浆水平未发现病理值,1年后也无变化。体重增加与胰岛素水平、胰岛素抵抗指数和甘油三酯水平的变化呈正相关。在评估的任何参数中,我们均未检测到不同治疗组之间存在统计学显著差异。
基线时的空腹血糖和胰岛素浓度不支持精神分裂症与潜在糖代谢异常相关的假说。1年后胰岛素和血脂参数的变化似乎与体重增加幅度有关。治疗一年后,氟哌啶醇、奥氮平和利培酮在代谢不良反应方面无显著差异。