Suvisaari Jaana M, Saarni Samuli I, Perälä Jonna, Suvisaari Janne V J, Härkänen Tommi, Lönnqvist Jouko, Reunanen Antti
Department of Mental Health and Alcohol Research, National Public Health Institute, Helsinki, Finland.
J Clin Psychiatry. 2007 Jul;68(7):1045-55. doi: 10.4088/jcp.v68n0711.
To determine the prevalence of metabolic syndrome and investigate its components in individuals with psychotic disorders and individuals using antipsychotic medication in a general population study.
The study population was a nationally representative, 2-stage cluster sample of 8028 persons aged 30 years or over from Finland. The field work for this study took place between September 2000 and June 2001. Laboratory and other measurements related to metabolic syndrome were taken in a health examination. We used the Structured Clinical Interview for DSM-IV (SCID-I) and case note data when making diagnostic assessments according to DSM-IV-TR criteria. Metabolic syndrome was diagnosed according to Adult Treatment Panel III criteria. Subjects who had not fasted the required 4 hours were excluded from the analysis. Prevalences of metabolic syndrome, adjusting for age, sex, and hours of fasting, were estimated by calculating predicted marginals, evaluated at 8 hours of fasting.
The prevalence estimates of metabolic syndrome were 36.2% (SE = 7.3), 41.4% (SE = 6.3), and 25.0% (SE = 8.6) among subjects with schizophrenia, other nonaffective psychosis, and affective psychosis, respectively, compared with 30.1% (SE = 0.8) in subjects without psychotic disorders. Subjects with schizophrenia had significantly lower high-density lipoprotein cholesterol and higher tri-glyceride and glucose levels and larger waist circumference, but also lower systolic blood pressure, than the remaining study population (all p values < .05). While all markers of metabolic syndrome were elevated among subjects with other nonaffective psychotic disorders, only the difference in waist circumference was statistically significant (p < .05). The prevalence of metabolic syndrome was significantly elevated among users of high-potency (52.1% [SE = 6.6]; p < .001) but not low-potency (39.0% [SE = 6.9]) and atypical (23.4% [SE = 10.8]) antipsychotic medication.
Nonaffective psychotic disorders are associated with abdominal obesity and glucose and lipid abnormalities. Regular monitoring and active treatment of metabolic abnormalities are essential in this patient population.
在一项普通人群研究中,确定精神障碍患者及使用抗精神病药物者代谢综合征的患病率,并调查其组成成分。
研究人群为来自芬兰的8028名30岁及以上人群的具有全国代表性的两阶段整群样本。本研究的现场工作于2000年9月至2001年6月进行。在健康检查中进行了与代谢综合征相关的实验室及其他测量。根据《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)标准进行诊断评估时,我们使用了《精神疾病诊断与统计手册》第四版(DSM-IV)的结构化临床访谈和病例记录数据。代谢综合征根据成人治疗小组第三次报告(ATP III)标准进行诊断。未禁食所需4小时的受试者被排除在分析之外。通过计算预测边际值估计代谢综合征的患病率,并根据8小时禁食情况进行评估,同时对年龄、性别和禁食时间进行了校正。
精神分裂症患者、其他非情感性精神病患者和情感性精神病患者中代谢综合征的患病率估计分别为36.2%(标准误=7.3)、41.4%(标准误=6.3)和25.0%(标准误=8.6),而无精神障碍的受试者中这一比例为30.1%(标准误=0.8)。与其余研究人群相比,精神分裂症患者的高密度脂蛋白胆固醇显著降低,甘油三酯和血糖水平升高,腰围增大,但收缩压较低(所有p值<0.05)。虽然其他非情感性精神病患者的所有代谢综合征指标均升高,但只有腰围差异具有统计学意义(p<0.05)。高效能抗精神病药物使用者中代谢综合征的患病率显著升高(52.1%[标准误=6.6];p<0.001),而低效能(39.0%[标准误=6.9])和非典型(23.4%[标准误=10.8])抗精神病药物使用者中则未升高。
非情感性精神病与腹部肥胖以及糖脂异常有关。对该患者群体进行代谢异常的定期监测和积极治疗至关重要。