Schizophrenia Program, Massachusetts General Hospital, Boston, MA, USA.
J Clin Psychopharmacol. 2011 Oct;31(5):653-8. doi: 10.1097/JCP.0b013e31822bb573.
Few interventions have been successful to prevent or reverse the medical complications associated with antipsychotic agents in the schizophrenia population. In particular, no single agent can correct multiple metabolic abnormalities such as insulin resistance, hyperlipidemia, inflammation, obesity, and fat distribution. We now report a randomized placebo-controlled pilot study to examine the effects of ramelteon on obesity and metabolic disturbances among subjects with schizophrenia.
A double-blind, placebo-controlled, 8-week pilot trial was conducted, adding ramelteon 8 mg/d to stable outpatients with schizophrenia. Vital signs and anthropometric measurements, including height, weight, waist circumference, and body fat were assessed, and laboratory assays were tracked to monitor changes in metabolic markers.
Twenty-five subjects were randomly assigned to treatment with study drug or placebo, and 20 subjects were included in the final analysis. Ramelteon did not improve anthropometric measurements, glucose metabolism, and inflammatory markers. There was, however, a significant decrease in total cholesterol and ratio of cholesterol to high-density lipoprotein in the ramelteon group. Although the standard anthropometric measures did not show significant change, the dual-energy x-ray absorptiometry scan showed a trend toward reduction in fat in the abdominal and trunk areas with a moderate effect size.
Although ramelteon decreased cholesterol, treatment may have to be longer than 8 weeks and with a higher dose for maximal effect of ramelteon for body fat and lipid changes. Future studies are needed for patients with schizophrenia with a larger sample size to fully understand ramelteon's effects on abdominal adiposity and lipids.
很少有干预措施能够成功预防或逆转精神分裂症患者使用抗精神病药物相关的医学并发症。特别是,没有单一的药物可以纠正多种代谢异常,如胰岛素抵抗、血脂异常、炎症、肥胖和脂肪分布。我们现在报告一项随机安慰剂对照的初步研究,以检验雷美替胺对精神分裂症患者肥胖和代谢紊乱的影响。
进行了一项为期 8 周的双盲、安慰剂对照的初步试验,在稳定的精神分裂症门诊患者中添加雷美替胺 8 毫克/天。评估生命体征和人体测量学测量,包括身高、体重、腰围和体脂肪,并进行实验室检测以监测代谢标志物的变化。
25 名受试者被随机分配接受研究药物或安慰剂治疗,其中 20 名受试者纳入最终分析。雷美替胺并未改善人体测量学测量、葡萄糖代谢和炎症标志物。然而,雷美替胺组的总胆固醇和胆固醇与高密度脂蛋白的比值显著下降。尽管标准的人体测量指标没有显示出显著变化,但双能 X 线吸收法扫描显示腹部和躯干区域脂肪有减少的趋势,且效应量适中。
虽然雷美替胺降低了胆固醇,但治疗可能需要 8 周以上,并且需要更高的剂量,才能达到雷美替胺对体脂肪和脂质变化的最大效果。需要对更多的精神分裂症患者进行更大样本量的研究,以充分了解雷美替胺对腹部肥胖和脂质的影响。