Melkersson K I, Hulting A L, Brismar K E
Department of Psychiatry, St Görans Hospital, Stockholm, Sweden.
J Clin Psychiatry. 2000 Oct;61(10):742-9. doi: 10.4088/jcp.v61n1006.
The aim of this study was to investigate the influence of the antipsychotic agent olanzapine on glucose-insulin homeostasis to explain possible mechanisms behind olanzapine-associated weight gain.
Fourteen patients on treatment with olanzapine (all meeting DSM-IV criteria for schizophrenia or related psychoses) were studied. Fasting blood samples for glucose, insulin, the growth hormone (GH)-dependent insulin-like growth factor I, and the insulin-dependent insulin-like growth factor binding protein-1 (IGFBP-1) were analyzed, as well as GH, leptin, and blood lipid levels and the serum concentrations of olanzapine and its metabolite N-desmethylolanzapine. In addition, body mass index (BMI) was calculated. Moreover, weight change during olanzapine treatment was determined.
Twelve of the 14 patients reported weight gain between 1 and 10 kg during a median olanzapine treatment time of 5 months, whereas data were not available for the other 2 patients. Eight patients (57%) had BMI above the normal limit. Eleven patients were normoglycemic, and 3 showed increased blood glucose values. Most patients (10/14; 71%) had elevated insulin levels (i.e., above the normal limit). Accordingly, the median value of IGFBP-1 was significantly lower for the patients in comparison with healthy subjects. Moreover, 8 (57%) of 14 patients had hyperleptinemia, 62% (8/13) had hypertriglyceridemia, and 85% (11/13) hypercholesterolemia. Weight change correlated positively to blood glucose levels and inversely to the serum concentration level of N-desmethylolanzapine. Additionally, the levels of blood glucose, triglycerides, and cholesterol correlated inversely to the serum concentration of N-desmethylolanzapine.
Olanzapine treatment was associated with weight gain and elevated levels of insulin, leptin, and blood lipids as well as insulin resistance, with 3 patients diagnosed to have diabetes mellitus. Both increased insulin secretion and hyprleptinemia may be mechanisms behind olanzapine-induced weight gain. Moreover, it is suggested that the metabolite N-desmethylolanzapine, but not olanzapine, has a normalizing effect on the metabolic abnormalities.
本研究旨在调查抗精神病药物奥氮平对葡萄糖 - 胰岛素稳态的影响,以解释奥氮平相关体重增加背后的可能机制。
对14名接受奥氮平治疗的患者(均符合精神分裂症或相关精神病的DSM - IV标准)进行了研究。分析了空腹血样中的葡萄糖、胰岛素、生长激素(GH)依赖性胰岛素样生长因子I以及胰岛素依赖性胰岛素样生长因子结合蛋白 - 1(IGFBP - 1),同时分析了GH、瘦素、血脂水平以及奥氮平及其代谢产物N - 去甲基奥氮平的血清浓度。此外,计算了体重指数(BMI)。而且,确定了奥氮平治疗期间的体重变化。
14名患者中有12名报告在奥氮平治疗的中位时间5个月内体重增加了1至10千克,而另外2名患者的数据不可用。8名患者(57%)的BMI高于正常范围。11名患者血糖正常,3名患者血糖值升高。大多数患者(10/14;71%)的胰岛素水平升高(即高于正常范围)。相应地,与健康受试者相比,患者的IGFBP - 1中位值显著更低。此外,14名患者中有8名(57%)患有高瘦素血症,62%(8/13)患有高甘油三酯血症,85%(11/13)患有高胆固醇血症。体重变化与血糖水平呈正相关,与N - 去甲基奥氮平的血清浓度水平呈负相关。此外,血糖、甘油三酯和胆固醇水平与N - 去甲基奥氮平的血清浓度呈负相关。
奥氮平治疗与体重增加、胰岛素、瘦素和血脂水平升高以及胰岛素抵抗有关,有3名患者被诊断患有糖尿病。胰岛素分泌增加和高瘦素血症可能都是奥氮平引起体重增加的机制。此外,提示代谢产物N - 去甲基奥氮平而非奥氮平对代谢异常具有正常化作用。