Department of Public Health & Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
J Clin Psychopharmacol. 2011 Dec;31(6):705-11. doi: 10.1097/JCP.0b013e318234ee84.
Schizophrenic patients have a high prevalence of metabolic adversities. Previous studies have suggested some candidate genes for obesity- and metabolic-related traits, including the insulin-induced gene (INSIG2), melanocortin 4 receptor gene (MC4R), and leptin and leptin receptor genes (LEP and LEPR). We aimed to investigate the associations between these genes and metabolic disturbances in patients with schizophrenia in Taiwan.
Patients with a diagnosis of schizophrenia or schizoaffective disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, were recruited from 36 community psychiatric rehabilitation centers or hospitals in Taipei. A total of 650 subjects were enrolled, and 577 were included in the genetic analyses. The anthropometric (body mass index, waist circumference [WC], and blood pressure) and biochemical measurements (fasting plasma glucose, insulin, triglyceride, high-density lipoprotein cholesterol, and Homeostasis Model of Assessment - Insulin Resistance index [HOMA-IR]) were assessed. Seven loci in the 4 genes were genotyped using standard TaqMan assays. Genetic association analyses were conducted for binary and quantitative measurements of the previously mentioned traits. Obese patients with schizophrenia exhibited more metabolic disturbances than nonobese patients.
Our data showed that INSIG2 was significantly associated with fasting plasma glucose (for rs17587100, P < 0.0001), MC4R was associated with WC (for rs2229616, P = 0.005), and LEP was associated with body mass index and WC (for rs7799039, P < 0.01). In addition, these loci showed suggestive associations with traits including high-density lipoprotein cholesterol and triglyceride, metabolic syndrome, insulin level, and HOMA-IR index (P = 0.05). In addition to the effect from antipsychotic medications and an unhealthy lifestyle, genetic factors also contribute to the high prevalence of obesity and metabolic disturbances in patients with schizophrenia, especially genes involved in metabolic-related pathways.
精神分裂症患者的代谢异常发生率较高。先前的研究表明,一些与肥胖和代谢相关特征的候选基因,包括胰岛素诱导基因(INSIG2)、黑素皮质素 4 受体基因(MC4R)以及瘦素和瘦素受体基因(LEP 和 LEPR)。我们旨在探讨这些基因与台湾精神分裂症患者代谢紊乱之间的关系。
根据《精神障碍诊断与统计手册》第四版,从台北的 36 家社区精神康复中心或医院招募被诊断为精神分裂症或分裂情感障碍的患者。共招募了 650 名受试者,其中 577 名纳入了遗传分析。对人体测量学(体重指数、腰围[WC]和血压)和生化指标(空腹血糖、胰岛素、甘油三酯、高密度脂蛋白胆固醇和稳态模型评估-胰岛素抵抗指数[HOMA-IR])进行评估。使用标准 TaqMan 检测法对 4 个基因中的 7 个位点进行基因分型。对上述特征的二元和定量测量进行遗传关联分析。患有精神分裂症的肥胖患者表现出更多的代谢紊乱。
我们的数据表明,INSIG2 与空腹血糖显著相关(对于 rs17587100,P<0.0001),MC4R 与 WC 相关(对于 rs2229616,P=0.005),LEP 与体重指数和 WC 相关(对于 rs7799039,P<0.01)。此外,这些位点与高密度脂蛋白胆固醇和甘油三酯、代谢综合征、胰岛素水平和 HOMA-IR 指数等特征呈提示性关联(P=0.05)。除了抗精神病药物和不健康的生活方式的影响外,遗传因素也导致精神分裂症患者肥胖和代谢紊乱的高发,尤其是与代谢相关途径相关的基因。