Effect of exenatide QW or placebo, both added to titrated insulin glargine, in uncontrolled type 2 diabetes: The DURATION-7 randomized study

被引:79
作者
Guja, Cristian [1 ,2 ]
Frias, Juan P. [3 ]
Somogyi, Aniko [4 ]
Jabbour, Serge [5 ]
Wang, Hui [6 ]
Hardy, Elise [6 ]
Rosenstock, Julio [7 ]
机构
[1] Carol Davila Univ Med & Pharm, Dept Diabet Nutr & Metab Dis, Bucharest, Romania
[2] Natl Inst Diabet Nutr & Metab Dis NC Paulescu, Bucharest, Romania
[3] Natl Res Inst, Los Angeles, CA USA
[4] Semmelweis Univ, Dept Internal Med 2, Budapest, Hungary
[5] Thomas Jefferson Univ, Div Endocrinol Diabet & Metab Dis, Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA
[6] AstraZeneca, Gaithersburg, MD USA
[7] Dallas Diabet Res Ctr Med City, Dallas, TX USA
关键词
exenatide once weekly; glucagon-like peptide-1 receptor agonist; insulin glargine; type; 2; diabetes; PEPTIDE-1 RECEPTOR AGONIST; FIXED-RATIO COMBINATION; ONCE-DAILY LIXISENATIDE; BASAL INSULIN; GLYCEMIC CONTROL; BOLUS INSULIN; THERAPY; PLUS; LIRAGLUTIDE; MANAGEMENT;
D O I
10.1111/dom.13266
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Aims To compare the efficacy and safety of adding the glucagon-like peptide-1 receptor agonist exenatide once weekly (QW) 2 mg or placebo among patients with type 2 diabetes who were inadequately controlled despite titrated insulin glargine (IG) metformin. Methods This multicentre, double-blind study ( identifier: NCT02229383) randomized (1:1) patients with persistent hyperglycaemia after an 8-week titration phase (glycated haemoglobin [HbA1c] 7.0%-10.5% [53-91 mmol/mol]) to exenatide QW or placebo. The primary endpoint was HbA1c change from baseline to week 28. Secondary endpoints included body weight, 2-hour postprandial glucose, and mean daily IG dose. Results Of 464 randomized patients (mean: age, 58 years; HbA1c, 8.5% [69 mmol/mol]; diabetes duration, 11.3 years), 91% completed 28 weeks. Exenatide QW + IG vs placebo + IG significantly reduced HbA1c (least-squares mean difference, -0.73% [-8.0 mmol/mol]; 95% confidence interval, -0.93%, -0.53% [-10.2, -5.8 mmol/mol]; P < .001; final HbA1c, 7.55% [59 mmol/mol] and 8.24% [67 mmol/mol], respectively); body weight (-1.50 kg; -2.17, -0.84; P < .001); and 2-hour postprandial glucose (-1.52 mmol/L [-27.5 mg/dL]; -2.15, -0.90 [-38.7, -16.2]; P < .001). Significantly more exenatide QW + IG-treated patients vs placebo + IG-treated patients reached HbA1c <7.0% (<53 mmol/mol) (32.5% vs 7.4%; P < .001); daily IG dose increased by 2 and 4 units, respectively. Gastrointestinal and injection-site adverse events were more frequent with exenatide QW + IG (15.1% and 7.8%, respectively) than with placebo + IG (10.8% and 3.0%, respectively); hypoglycaemia incidence was similar between the exenatide QW + IG (29.7%) and placebo + IG (29.0%) groups, with no major hypoglycaemic events. Conclusions Among patients with inadequate glycaemic control, exenatide QW significantly improved glucose control and decreased body weight, without increased hypoglycaemia or unexpected safety findings.
引用
收藏
页码:1602 / 1614
页数:13
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