Lamberti J Steven, Costea G Oana, Olson David, Crilly John F, Maharaj Kumar, Tu Xin, Groman Adrienne, Dietz Marci B, Bushey Margaret P, Olivares Telva, Wiener Karen
Department of Psychiatry, University of Rochester Medical Center, Rochester, NY 14642, USA.
J Clin Psychiatry. 2005 Jul;66(7):900-6. doi: 10.4088/jcp.v66n0713.
Treatment with antipsychotic drugs has been associated with increased risk for developing diabetes mellitus. Recent consensus statements suggest that clozapine may pose an especially high risk. The purpose of this study is to examine the prevalence and clinical-demographic correlates of diabetes among outpatients with DSM-IV-diagnosed schizophrenia or schizoaffective disorder receiving clozapine.
One hundred one outpatients receiving clozapine at the University of Rochester Department of Psychiatry, Rochester, N.Y., were evaluated between September 2002 and September 2003. Demographic data were collected from medical records, and body mass index (BMI) and body fat measurements were conducted. Diagnosis of diabetes was established through review of medical records and fasting blood glucose testing. Associations between clinical and demographic variables and diabetes were examined using t tests, Fisher exact tests, and logistic regression.
Mean (SD) age of patients was 40.4 (9.5) years, and 79% were white. Mean (SD) dose and duration of clozapine treatment were 426 (164) mg/day and 5.7 (3.6) years, respectively. Point prevalence of diabetes was 25.7%. Mean (SD) BMI was 32.6 (8.0) kg/m(2), and mean (SD) body fat was 34.0% (11.0%). Logistic regression revealed significant associations between diabetes and nonwhite race/ethnicity and family history of diabetes (p = .02 and .002, respectively). No significant associations were found between diabetes prevalence and BMI or body fat.
Patients receiving clozapine are at substantial risk for developing diabetes, although the level of risk relative to other antipsychotic medications has not been fully determined. Clinicians should monitor all severely mentally ill patients receiving antipsychotic drugs for diabetes, with closer monitoring of patients with established demographic risk factors.
使用抗精神病药物治疗与患糖尿病风险增加有关。最近的共识声明表明氯氮平可能带来特别高的风险。本研究的目的是调查接受氯氮平治疗的、被诊断为DSM-IV精神分裂症或分裂情感性障碍的门诊患者中糖尿病的患病率及其临床人口统计学相关因素。
2002年9月至2003年9月期间,对纽约州罗切斯特市罗切斯特大学精神病学系的101名接受氯氮平治疗的门诊患者进行了评估。从病历中收集人口统计学数据,并测量体重指数(BMI)和体脂。通过查阅病历和空腹血糖检测确定糖尿病诊断。使用t检验、Fisher精确检验和逻辑回归分析临床和人口统计学变量与糖尿病之间的关联。
患者的平均(标准差)年龄为40.4(9.5)岁,79%为白人。氯氮平治疗的平均(标准差)剂量和疗程分别为426(164)毫克/天和5.7(3.6)年。糖尿病的点患病率为25.7%。平均(标准差)BMI为32.6(8.0)千克/平方米,平均(标准差)体脂为34.0%(11.0%)%。逻辑回归显示糖尿病与非白人种族/族裔以及糖尿病家族史之间存在显著关联(p值分别为0.02和0.002)。未发现糖尿病患病率与BMI或体脂之间存在显著关联。
接受氯氮平治疗的患者患糖尿病的风险很高,尽管相对于其他抗精神病药物的风险水平尚未完全确定。临床医生应监测所有接受抗精神病药物治疗的重症精神病患者是否患有糖尿病,对具有既定人口统计学风险因素的患者进行更密切的监测。