Larsen Julie R, Svensson Camilla K, Vedtofte Louise, Jakobsen Mathilde Lund, Jespersen Hans Søe, Jakobsen Michelle I, Koyuncu Kamuran, Schjerning Ole, Nielsen Jimmi, Ekstrøm Claus T, Holst Jens J, Correll Christoph U, Vilsbøll Tina, Fink-Jensen Anders
Psychiatric Centre Copenhagen, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Center for Diabetes Research, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
CNS Spectr. 2019 Aug;24(4):441-452. doi: 10.1017/S1092852918001311. Epub 2018 Dec 31.
To assess the prevalence of prediabetes and metabolic abnormalities among overweight or obese clozapine- or olanzapine-treated schizophrenia patients, and to identify characteristics of the schizophrenia group with prediabetes.
A cross-sectional study assessing the presence of prediabetes and metabolic abnormalities in schizophrenia clozapine- or olanzapine-treated patients with a body mass index (BMI) ≥27 kg/m2. Procedures were part of the screening process for a randomized, placebo-controlled trial evaluating liraglutide vs placebo for improving glucose tolerance. For comparison, an age-, sex-, and BMI-matched healthy control group without psychiatric illness and prediabetes was included. Prediabetes was defined as elevated fasting plasma glucose and/or impaired glucose tolerance and/or elevated glycated hemoglobin A1c.
Among 145 schizophrenia patients (age = 42.1 years; males = 59.3%) on clozapine or olanzapine (clozapine/olanzapine/both: 73.8%/24.1%/2.1%), prediabetes was present in 69.7% (101 out of 145). While schizophrenia patients with and without prediabetes did not differ regarding demographic, illness, or antipsychotic treatment variables, metabolic abnormalities (waist circumference: 116.7±13.7 vs 110.1±13.6 cm, P = 0.007; triglycerides: 2.3±1.4 vs 1.6±0.9 mmol/L, P = 0.0004) and metabolic syndrome (76.2% vs 40.9%, P<0.0001) were significantly more pronounced in schizophrenia patients with vs without prediabetes. The age-, sex-, and BMI-matched healthy controls had significantly better glucose tolerance compared to both groups of patients with schizophrenia. The healthy controls also had higher levels of high-density lipoprotein compared to patients with schizophrenia and prediabetes.
Prediabetes and metabolic abnormalities were highly prevalent among the clozapine- and olanzapine-treated patients with schizophrenia, putting these patients at great risk for later type 2 diabetes and cardiovascular disease. These results stress the importance of identifying and adequately treating prediabetes and metabolic abnormalities among clozapine- and olanzapine-treated patients with schizophrenia.
评估超重或肥胖的接受氯氮平或奥氮平治疗的精神分裂症患者中糖尿病前期和代谢异常的患病率,并确定患有糖尿病前期的精神分裂症患者群体的特征。
一项横断面研究,评估体重指数(BMI)≥27kg/m²的接受氯氮平或奥氮平治疗的精神分裂症患者中糖尿病前期和代谢异常的情况。这些程序是一项随机、安慰剂对照试验筛查过程的一部分,该试验评估利拉鲁肽与安慰剂对改善糖耐量的作用。为作比较,纳入了一个年龄、性别和BMI匹配的无精神疾病和糖尿病前期的健康对照组。糖尿病前期定义为空腹血糖升高和/或糖耐量受损和/或糖化血红蛋白A1c升高。
在145例接受氯氮平或奥氮平治疗的精神分裂症患者(年龄 = 42.1岁;男性 = 59.3%)中(氯氮平/奥氮平/两者都用:73.8%/24.1%/2.1%),69.7%(145例中的101例)存在糖尿病前期。虽然有和没有糖尿病前期的精神分裂症患者在人口统计学、疾病或抗精神病药物治疗变量方面没有差异,但代谢异常(腰围:116.7±13.7 vs 110.1±13.6cm,P = 0.007;甘油三酯:2.3±1.4 vs 1.6±0.9mmol/L,P = 0.0004)和代谢综合征(76.2% vs 40.9%,P<0.0001)在有糖尿病前期的精神分裂症患者中比没有糖尿病前期的患者更明显。年龄、性别和BMI匹配的健康对照组的糖耐量明显优于两组精神分裂症患者。与患有精神分裂症和糖尿病前期的患者相比,健康对照组的高密度脂蛋白水平也更高。
在接受氯氮平和奥氮平治疗的精神分裂症患者中,糖尿病前期和代谢异常非常普遍,使这些患者面临后期患2型糖尿病和心血管疾病的巨大风险。这些结果强调了识别和适当治疗接受氯氮平和奥氮平治疗的精神分裂症患者中的糖尿病前期和代谢异常的重要性。