N Engl J Med. 2012 Jun 14;366(24):2247-56. doi: 10.1056/NEJMoa1109333. Epub 2012 Apr 29.
Despite the increasing prevalence of type 2 diabetes in youth, there are few data to guide treatment. We compared the efficacy of three treatment regimens to achieve durable glycemic control in children and adolescents with recent-onset type 2 diabetes.
Eligible patients 10 to 17 years of age were treated with metformin (at a dose of 1000 mg twice daily) to attain a glycated hemoglobin level of less than 8% and were randomly assigned to continued treatment with metformin alone or to metformin combined with rosiglitazone (4 mg twice a day) or a lifestyle-intervention program focusing on weight loss through eating and activity behaviors. The primary outcome was loss of glycemic control, defined as a glycated hemoglobin level of at least 8% for 6 months or sustained metabolic decompensation requiring insulin.
Of the 699 randomly assigned participants (mean duration of diagnosed type 2 diabetes, 7.8 months), 319 (45.6%) reached the primary outcome over an average follow-up of 3.86 years. Rates of failure were 51.7% (120 of 232 participants), 38.6% (90 of 233), and 46.6% (109 of 234) for metformin alone, metformin plus rosiglitazone, and metformin plus lifestyle intervention, respectively. Metformin plus rosiglitazone was superior to metformin alone (P=0.006); metformin plus lifestyle intervention was intermediate but not significantly different from metformin alone or metformin plus rosiglitazone. Prespecified analyses according to sex and race or ethnic group showed differences in sustained effectiveness, with metformin alone least effective in non-Hispanic black participants and metformin plus rosiglitazone most effective in girls. Serious adverse events were reported in 19.2% of participants.
Monotherapy with metformin was associated with durable glycemic control in approximately half of children and adolescents with type 2 diabetes. The addition of rosiglitazone, but not an intensive lifestyle intervention, was superior to metformin alone. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases and others; TODAY ClinicalTrials.gov number, NCT00081328.).
尽管 2 型糖尿病在青少年中的发病率不断上升,但指导治疗的相关数据却很少。我们比较了三种治疗方案在实现新近诊断的 2 型糖尿病患儿和青少年持久血糖控制方面的疗效。
10 至 17 岁的合格患者接受二甲双胍(剂量为每日 2 次,每次 1000mg)治疗,使糖化血红蛋白水平低于 8%,然后随机分配继续接受二甲双胍单药治疗或二甲双胍联合罗格列酮(每日 2 次,每次 4mg)或重点通过饮食和活动行为减轻体重的生活方式干预方案。主要结局是失去血糖控制,定义为 6 个月内糖化血红蛋白水平至少为 8%或持续代谢失代偿需要胰岛素治疗。
在 699 名随机分配的参与者中(确诊 2 型糖尿病的平均持续时间为 7.8 个月),在平均 3.86 年的随访中,有 319 名(45.6%)达到了主要结局。失败率分别为二甲双胍单药组 51.7%(120/232 名参与者)、二甲双胍联合罗格列酮组 38.6%(90/233 名)和二甲双胍联合生活方式干预组 46.6%(109/234 名)。二甲双胍联合罗格列酮优于二甲双胍单药组(P=0.006);二甲双胍联合生活方式干预组介于两者之间,但与二甲双胍单药组或二甲双胍联合罗格列酮组无显著差异。根据性别、种族或民族进行的预设分析显示,在持续疗效方面存在差异,二甲双胍单药组对非西班牙裔黑人参与者的效果最差,而二甲双胍联合罗格列酮组对女孩的效果最好。19.2%的参与者报告了严重不良事件。
二甲双胍单药治疗可使大约一半的 2 型糖尿病儿童和青少年实现持久的血糖控制。与二甲双胍单药治疗相比,添加罗格列酮而非强化生活方式干预更有效。(由国家糖尿病、消化和肾脏疾病研究所和其他机构资助;TODAY 临床试验。gov 编号,NCT00081328。)