Guo Fangjian, Garvey W Timothy
Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX
Center for Interdisciplinary Research in Women's Health, University of Texas Medical Branch, Galveston, TX.
Diabetes Care. 2017 Jul;40(7):856-862. doi: 10.2337/dc17-0088. Epub 2017 Apr 28.
To assess the ability of medication-assisted weight loss to prevent diabetes as a function of the baseline weighted Cardiometabolic Disease Staging (CMDS) score.
We pooled data from 3,040 overweight and obese participants in three randomized controlled trials-CONQUER, EQUIP, and SEQUEL-assessing efficacy and safety of phentermine/topiramate extended release (ER) for weight loss. In these double-blind phase III trials, overweight/obese adult patients were treated with a lifestyle intervention and randomly assigned to placebo versus once-daily oral phentermine/topiramate ER. The weighted CMDS score was calculated using baseline quantitative clinical data including waist circumference, blood glucose, blood pressure, and blood lipids. Incident diabetes was defined based on serial measures of fasting glucose, 2-h oral glucose tolerance test glucose, and/or HbA.
The absolute decrease in 1-year diabetes incidence rates in subjects treated with medication versus placebo was greatest in those with high-risk CMDS scores at baseline (10.43-6.29%), intermediate in those with moderate CMDS risk (4.67-2.37%), and small in the low-risk category (1.51-0.67%). The number of participants needed to treat to prevent one new case of diabetes over a 56-week period was 24, 43, and 120 in those with baseline CMDS scores of ≥60, 30-59, and 0-29, respectively.
Numbers needed to treat to prevent one case of type 2 diabetes are markedly lower in patients with high-risk scores. CMDS can be used to quantify risk of diabetes in overweight/obese individuals and predict the effectiveness of weight-loss therapy to prevent diabetes.
评估药物辅助减肥预防糖尿病的能力,该能力作为基线加权心脏代谢疾病分期(CMDS)评分的函数。
我们汇总了三项随机对照试验(CONQUER、EQUIP和SEQUEL)中3040名超重和肥胖参与者的数据,这些试验评估了缓释苯丁胺/托吡酯(ER)减肥的疗效和安全性。在这些双盲III期试验中,超重/肥胖成年患者接受生活方式干预,并随机分配接受安慰剂或每日一次口服苯丁胺/托吡酯ER治疗。使用包括腰围、血糖、血压和血脂在内的基线定量临床数据计算加权CMDS评分。根据空腹血糖、2小时口服葡萄糖耐量试验血糖和/或糖化血红蛋白的系列测量结果定义新发糖尿病。
与安慰剂相比,接受药物治疗的受试者1年糖尿病发病率的绝对降低在基线CMDS评分高风险者中最大(10.43%-6.29%),在中度CMDS风险者中次之(4.67%-2.37%),在低风险类别中最小(1.51%-0.67%)。在基线CMDS评分≥60、30-59和0-29的受试者中,在56周期间预防一例新糖尿病病例所需治疗的参与者人数分别为24、43和120。
预防一例2型糖尿病所需治疗的人数在高风险评分患者中明显更低。CMDS可用于量化超重/肥胖个体患糖尿病的风险,并预测减肥治疗预防糖尿病的有效性。