Ikramuddin Sayeed, Korner Judith, Lee Wei-Jei, Thomas Avis J, Connett John E, Bantle John P, Leslie Daniel B, Wang Qi, Inabnet William B, Jeffery Robert W, Chong Keong, Chuang Lee-Ming, Jensen Michael D, Vella Adrian, Ahmed Leaque, Belani Kumar, Billington Charles J
Department of Surgery, University of Minnesota, Minneapolis.
Division of Endocrinology, Department of Medicine, Columbia University Medical Center, New York, New York.
JAMA. 2018 Jan 16;319(3):266-278. doi: 10.1001/jama.2017.20813.
The Roux-en-Y gastric bypass is effective in achieving established diabetes treatment targets, but durability is unknown.
To compare durability of Roux-en-Y gastric bypass added to intensive lifestyle and medical management in achieving diabetes control targets.
DESIGN, SETTING, AND PARTICIPANTS: Observational follow-up of a randomized clinical trial at 4 sites in the United States and Taiwan, involving 120 participants who had a hemoglobin A1c (HbA1c) level of 8.0% or higher and a body mass index between 30.0 and 39.9 (enrolled between April 2008 and December 2011) were followed up for 5 years, ending in November 2016.
Lifestyle-intensive medical management intervention based on the Diabetes Prevention Program and LookAHEAD trials for 2 years, with and without (60 participants each) Roux-en-Y gastric bypass surgery followed by observation to year 5.
The American Diabetes Association composite triple end point of hemoglobin A1c less than 7.0%, low-density lipoprotein cholesterol less than 100 mg/dL, and systolic blood pressure less than 130 mm Hg at 5 years.
Of 120 participants who were initially randomized (mean age, 49 years [SD, 8 years], 72 women [60%]), 98 (82%) completed 5 years of follow-up. Baseline characteristics were similar between groups: mean (SD) body mass index 34.4 (3.2) for the lifestyle-medical management group and 34.9 (3.0) for the gastric bypass group and had hemoglobin A1c levels of 9.6% (1.2) and 9.6% (1.0), respectively. At 5 years, 13 participants (23%) in the gastric bypass group and 2 (4%) in the lifestyle-intensive medical management group had achieved the composite triple end point (difference, 19%; 95% CI, 4%-34%; P = .01). In the fifth year, 31 patients (55%) in the gastric bypass group vs 8 (14%) in the lifestyle-medical management group achieved an HbA1c level of less than 7.0% (difference, 41%; 95% CI, 19%-63%; P = .002). Gastric bypass had more serious adverse events than did the lifestyle-medical management intervention, 66 events vs 38 events, most frequently gastrointestinal events and surgical complications such as strictures, small bowel obstructions, and leaks. Gastric bypass had more parathyroid hormone elevation but no difference in B12 deficiency.
In extended follow-up of obese adults with type 2 diabetes randomized to adding gastric bypass compared with lifestyle and intensive medical management alone, there remained a significantly better composite triple end point in the surgical group at 5 years. However, because the effect size diminished over 5 years, further follow-up is needed to understand the durability of the improvement.
clinicaltrials.gov Identifier: NCT00641251.
Roux-en-Y胃旁路术在实现既定的糖尿病治疗目标方面是有效的,但疗效的持久性尚不清楚。
比较在强化生活方式和药物治疗基础上加用Roux-en-Y胃旁路术实现糖尿病控制目标的疗效持久性。
设计、地点和参与者:在美国和台湾的4个地点对一项随机临床试验进行观察性随访,纳入120名糖化血红蛋白(HbA1c)水平为8.0%或更高且体重指数在30.0至39.9之间的参与者(于2008年4月至2011年12月入组),随访5年,至2016年11月结束。
基于糖尿病预防计划和“展望”(LookAHEAD)试验进行强化生活方式和药物治疗干预2年,其中一组60名参与者接受Roux-en-Y胃旁路手术,另一组60名参与者不接受该手术,之后观察至第5年。
5年时达到美国糖尿病协会糖化血红蛋白低于7.0%、低密度脂蛋白胆固醇低于100mg/dL和收缩压低于130mmHg的复合三联终点。
最初随机分组的120名参与者(平均年龄49岁[标准差8岁],72名女性[60%])中,98名(82%)完成了5年随访。两组基线特征相似:生活方式-药物治疗组平均(标准差)体重指数为34.4(3.2),胃旁路术组为34.9(3.0),糖化血红蛋白水平分别为9.6%(1.2)和9.6%(1.0)。5年时,胃旁路术组13名参与者(23%)和生活方式-强化药物治疗组2名参与者(4%)达到复合三联终点(差异为19%;95%置信区间,4%-34%;P = 0.01)。在第5年,胃旁路术组31名患者(55%)与生活方式-药物治疗组8名患者(14%)的糖化血红蛋白水平低于7.0%(差异为41%;95%置信区间,19%-63%;P = 0.002)。胃旁路术比生活方式-药物治疗干预有更严重的不良事件,分别为66起和38起,最常见的是胃肠道事件和手术并发症,如狭窄、小肠梗阻和渗漏。胃旁路术导致甲状旁腺激素升高更多,但维生素B12缺乏无差异。
在对随机分配接受胃旁路术与单纯生活方式和强化药物治疗的肥胖2型糖尿病成年人进行的延长随访中,手术组在5年时的复合三联终点仍显著更好。然而,由于效应大小在5年中减小,需要进一步随访以了解改善效果的持久性。
clinicaltrials.gov标识符:NCT00641251。