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首页> 外文期刊>Diabetes care >Efficacy and Safety of Liraglutide Versus Placebo as Add-on to Glucose-Lowering Therapy in Patients With Type 2 Diabetes and Moderate Renal Impairment ( LIRA-RENAL): A Randomized Clinical Trial
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Efficacy and Safety of Liraglutide Versus Placebo as Add-on to Glucose-Lowering Therapy in Patients With Type 2 Diabetes and Moderate Renal Impairment ( LIRA-RENAL): A Randomized Clinical Trial

机译:利拉鲁肽与安慰剂作为降糖治疗2型糖尿病和中度肾功能不全患者(LIRA-RENAL)的疗效和安全性:一项随机临床试验

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OBJECTIVE Renal impairment in type 2 diabetes limits available glucose-lowering treatment options. This trial was conducted to establish the efficacy and safety of liraglutide as an add-on to existing glucose-lowering medications in patients with inadequately controlled type 2 diabetes and moderate renal impairment. RESEARCH DESIGN AND METHODS In this 26-week, double-blind trial, 279 patients with HbA(1c) 7-10%, BMI 20-45 kg/m(2), and moderate renal impairment (estimated glomerular filtration rate [eGFR] 30-59 mL/min/1.73 m(2); MDRD) were randomized (1: 1) to once-daily liraglutide 1.8 mg (n = 140) or placebo (n = 139). RESULTS The estimated treatment difference in HbA1c from baseline to week 26 was 20.66% (-7.25 mmol/mol) (95% CI -0.90 to 0.43 [-9.82 to -4.69]), P < 0.0001). Fasting plasma glucose decreased more with liraglutide (-1.22 mmol/L [-22.0 mg/dL]) than with placebo (-0.57 mmol/L [-10.3 mg/dL], P = 0.036). There was a greater reduction in body weight with liraglutide (-2.41 kg) than with placebo (-1.09 kg, P = 0.0052). No changes in renal function were observed (eGFR relative ratio to baseline: -1% liraglutide, +1% placebo; estimated treatment ratio [ETR] 0.98, P = 0.36). The most common adverse events were gastrointestinal (GI) adverse effects (liraglutide, 35.7%; placebo, 17.5%). No difference in hypoglycemic episodes was observed between treatment groups (event rate/100 patient-years of exposure: liraglutide, 30.47; placebo, 40.08; P = 0.54). The estimated ratio to baseline for lipase was 1.33 for liraglutide and 0.97 for placebo (ETR 1.37, P < 0.0001). CONCLUSIONS Liraglutide did not affect renal function and demonstrated better glycemic control, with no increase in hypoglycemia risk but with higher withdrawals due to GI adverse events than placebo in patients with type 2 diabetes and moderate renal impairment.
机译:目的2型糖尿病的肾脏损害限制了可用的降糖治疗选择。进行该试验的目的是确定在控制不充分的2型糖尿病和中度肾功能不全患者中,利拉鲁肽作为现有降糖药物的附加疗效和安全性。研究设计和方法在这个为期26周的双盲试验中,有279例HbA(1c)为7-10%,BMI为20-45 kg / m(2)和中度肾功能不全(估计肾小球滤过率[eGFR])的患者将30-59 mL / min / 1.73 m(2); MDRD)随机(1:1)分配给每天一次的利拉鲁肽1.8 mg(n = 140)或安慰剂(n = 139)。结果从基线到第26周,HbA1c的估计治疗差异为20.66%(-7.25 mmol / mol)(95%CI -0.90至0.43 [-9.82至-4.69]),P <0.0001)。利拉鲁肽(-1.22 mmol / L [-22.0 mg / dL])的空腹血糖下降幅度大于安慰剂(-0.57 mmol / L [-10.3 mg / dL],P = 0.036)。利拉鲁肽(-2.41千克)比安慰剂(-1.09千克,P = 0.0052)减轻的体重更大。没有观察到肾功能的变化(eGFR与基线的相对比率:-1%利拉鲁肽,+ 1%安慰剂;估计治疗比率[ETR] 0.98,P = 0.36)。最常见的不良反应是胃肠道(GI)不良反应(利拉鲁肽35.7%;安慰剂17.5%)。治疗组之间降血糖发作无差异(事件发生率/ 100患者-年暴露:利拉鲁肽30.47;安慰剂40.08; P = 0.54)。利拉鲁肽的脂肪酶与基线的估计比率为1.33,安慰剂为0.97(ETR 1.37,P <0.0001)。结论对于2型糖尿病和中度肾功能不全的患者,利拉鲁肽未影响肾脏功能,并显示出更好的血糖控制,低血糖风险没有增加,但由于胃肠道不良事件导致的撤药率高于安慰剂。

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