Tarricone Ilaria, Casoria Michela, Gozzi Beatrice Ferrari, Grieco Daniela, Menchetti Marco, Serretti Alessandro, Ujkaj Manjola, Pastorelli Francesca, Berardi Domenico
Institute of Psychiatry, Bologna University, Viale C, Pepoli 5, 40123 Bologna, Italy.
BMC Psychiatry. 2006 Mar 16;6:11. doi: 10.1186/1471-244X-6-11.
Second generation antipsychotics (SGA) have demonstrated several advantages over first generation antipsychotics (FGA) in terms of positive, negative, cognitive, and affective symptoms and a lower propensity for extrapyramidal side effects. Despite these undeniable advantages, SGA have been associated with causing and exacerbating metabolic disorders, such as obesity, diabetes, and hyperlipidemia. This cross sectional study aimed to evaluate the metabolic risk factor profile associated with use of SGAs in comparison with non -treated control patients.
The study was carried out at a Community Mental Health Centre (CMHC) in Bologna. The study subjects were outpatients with serious mental disorders treated with SGA (clozapine, olanzapine, risperidone, quetiapine). A sample of adult men and women suffering from idiopathic hyperhydrosis, without psychiatric history or antipsychotic treatment, were randomly selected from outpatients of the Department of Neurology in Bologna as a reference group. We investigated differences among the treatment and reference groups for glycaemia, cholesterolaemia and triglyceridaemia levels.
The study sample was composed of 76 patients, 38 males and 38 females. The reference group was composed of 36 subjects, 19 females and 17 males. All patients treated with SGAs had higher mean glycaemia and triglyceridaemia and a significantly higher risk of receiving a diagnosis of hyperglycaemia and hypertriglyceridaemia than the reference group. We did not find any differences in mean glycaemia or mean triglyceridaemia levels among treatment groups. Patients with clozapine had a significantly higher mean BMI value and rate of obesity than patients treated with other SGAs.
The rate of obesity and metabolic disorders observed in this study were higher than the prevalence in the control group and similar to that previously reported in psychiatric samples; these findings imply per se that more attention should be paid to the metabolic condition of psychiatric patients. In line with the International Consensus Conferences we recommend that monitoring of weight, fasting plasma glucose, cholesterol and triglyceride levels be obtained in routine clinical practice with all antipsychotics.
与第一代抗精神病药物(FGA)相比,第二代抗精神病药物(SGA)在阳性、阴性、认知和情感症状方面已显示出若干优势,且锥体外系副作用的倾向较低。尽管有这些不可否认的优势,但SGA与引发和加剧代谢紊乱有关,如肥胖、糖尿病和高脂血症。这项横断面研究旨在评估与未治疗的对照患者相比,使用SGA相关的代谢风险因素概况。
该研究在博洛尼亚的一个社区心理健康中心(CMHC)进行。研究对象是接受SGA(氯氮平、奥氮平、利培酮、喹硫平)治疗的严重精神障碍门诊患者。从博洛尼亚神经病学系门诊患者中随机选取患有特发性多汗症、无精神病史或抗精神病药物治疗的成年男性和女性样本作为参照组。我们调查了治疗组和参照组在血糖、胆固醇血症和甘油三酯血症水平上的差异。
研究样本由76名患者组成,38名男性和38名女性。参照组由36名受试者组成,19名女性和17名男性。所有接受SGA治疗的患者的平均血糖和甘油三酯水平均高于参照组,且被诊断为高血糖和高甘油三酯血症的风险显著更高。我们未发现各治疗组之间在平均血糖或平均甘油三酯水平上存在任何差异。与接受其他SGA治疗的患者相比,服用氯氮平的患者的平均体重指数值和肥胖率显著更高。
本研究中观察到的肥胖率和代谢紊乱高于对照组的患病率,与先前在精神科样本中报告的患病率相似;这些发现本身意味着应更加关注精神科患者的代谢状况。根据国际共识会议,我们建议在常规临床实践中对所有抗精神病药物治疗的患者监测体重、空腹血糖、胆固醇和甘油三酯水平。