Liakopoulou Paraskevi, Liakos Aris, Vasilakou Despoina, Athanasiadou Eleni, Bekiari Eleni, Kazakos Kyriakos, Tsapas Apostolos
Clinical Research and Evidence-Based Medicine Unit, Second Medical Department, Aristotle University Thessaloniki, Thessaloniki, Greece.
Third Medical Department, Aristotle University Thessaloniki, Thessaloniki, Greece.
Endocrine. 2017 Jun;56(3):485-494. doi: 10.1007/s12020-017-1293-6. Epub 2017 Apr 12.
Basal insulin controls primarily fasting plasma glucose but causes hypoglycaemia and weight gain, whilst glucagon like peptide 1 receptor agonists induce weight loss without increasing risk for hypoglycaemia. We conducted a systematic review and meta-analysis of randomised controlled trials to investigate the efficacy and safety of fixed ratio combinations of basal insulin with glucagon like peptide 1 receptor agonists.
We searched Medline, Embase, and the Cochrane Library as well as conference abstracts up to December 2016. We assessed change in haemoglobin A, body weight, and incidence of hypoglycaemia and gastrointestinal adverse events.
We included eight studies with 5732 participants in the systematic review. Switch from basal insulin to fixed ratio combinations with a glucagon like peptide 1 receptor agonist was associated with 0.72% reduction in haemoglobin A [95% confidence interval -1.03 to -0.41; I = 93%] and 2.35 kg reduction in body weight (95% confidence interval -3.52 to -1.19; I = 93%), reducing also risk for hypoglycaemia [odds ratio 0.70; 95% confidence interval 0.57 to 0.86; I = 85%] but increasing incidence of nausea (odds ratio 6.89; 95% confidence interval 3.73-12.74; I = 79%). Similarly, switching patients from treatment with a glucagon like peptide 1 receptor agonist to a fixed ratio combination with basal insulin was associated with 0.94% reduction in haemoglobin A (95% confidence interval -1.11 to -0.77) and an increase in body weight by 2.89 kg (95% confidence interval 2.17-3.61).
Fixed ratio combinations of basal insulin with glucagon like peptide 1 receptor agonists improve glycaemic control whilst balancing out risk for hypoglycaemia and gastrointestinal side effects.
基础胰岛素主要控制空腹血糖,但会导致低血糖和体重增加,而胰高血糖素样肽-1受体激动剂可诱导体重减轻且不会增加低血糖风险。我们对随机对照试验进行了系统评价和荟萃分析,以研究基础胰岛素与胰高血糖素样肽-1受体激动剂固定比例联合用药的疗效和安全性。
我们检索了截至2016年12月的Medline、Embase、Cochrane图书馆以及会议摘要。我们评估了糖化血红蛋白、体重的变化以及低血糖和胃肠道不良事件的发生率。
我们在系统评价中纳入了8项研究,共5732名参与者。从基础胰岛素转换为与胰高血糖素样肽-1受体激动剂的固定比例联合用药与糖化血红蛋白降低0.72%相关[95%置信区间-1.03至-0.41;I²=93%],体重减轻2.35千克(95%置信区间-3.52至-1.19;I²=93%),同时也降低了低血糖风险[比值比0.70;95%置信区间0.57至0.86;I²=85%],但恶心发生率增加(比值比6.89;95%置信区间3.73 - 12.74;I²=79%)。同样,将患者从胰高血糖素样肽-1受体激动剂治疗转换为与基础胰岛素的固定比例联合用药与糖化血红蛋白降低0.94%相关(95%置信区间-1.11至-0.77),体重增加2.89千克(95%置信区间2.17 - 3.61)。
基础胰岛素与胰高血糖素样肽-1受体激动剂的固定比例联合用药可改善血糖控制,同时平衡低血糖风险和胃肠道副作用。