Department of Medicine, University of Padova, 35128 Padova, Italy; Division of Metabolic Diseases, Padova Hospital, 35128 Padova, Italy.
ULSS2 Diabetology Service, 31100 Treviso, Italy.
Metabolism. 2020 May;106:154190. doi: 10.1016/j.metabol.2020.154190. Epub 2020 Feb 25.
Real-word data on the head-to-head comparisons among glucagon-like peptide-1 receptor agonists (GLP-1RA) are scant. Therefore, we aimed to compare the effectiveness of dulaglutide versus liraglutide and exenatide once weekly (exeOW) in type 2 diabetic (T2D) patients under routine care.
This was a retrospective, multicenter, real-world study on patients with T2D (aged 18-80) initiating a GLP-1RA between 2010 and 2018 at specialist outpatient clinics. We compared the effectiveness of dulaglutide versus liraglutide and exeOW on the changes in HbA1c (primary outcome), body weight, blood pressure and fasting glucose (secondary outcomes). Average follow-up was 5.9 months. Channelling biases were addressed with propensity score matching or multivariable adjustment. Meta-analyses of observational studies, covering the same comparisons, are also presented.
849, 1371 and 198 patients were included in the dulaglutide, liraglutide and exeOW groups, respectively. The reduction of HbA1c was greater with dulaglutide than with liraglutide (-0.24 ± 0.08%; p = 0.003), and was confirmed in the meta-analysis of observational studies. In our study, dulaglutide showed similar effectiveness compared to exeOW. When these results were pooled with other observational studies, dulaglutide showed a greater reduction of HbA1c (-0.19%; p = 0.003) and body weight (-0.8 kg; p = 0.007).
In a real-world scenario, dulaglutide reduced HbA1c more than liraglutide. Conversely, we found similar effect of dulaglutide and exeOW, with statistical differences arising solely when results were meta-analysed with those from other observational studies. Lack of up-titration for liraglutide and higher discontinuation rate for exeOW likely influenced the estimated treatment difference.
关于胰高血糖素样肽-1 受体激动剂(GLP-1RA)头对头比较的真实世界数据很少。因此,我们旨在比较常规护理下,接受度拉鲁肽与利拉鲁肽和艾塞那肽每周一次(exeOW)治疗的 2 型糖尿病(T2D)患者的疗效。
这是一项回顾性、多中心、真实世界研究,纳入了 2010 年至 2018 年期间在专科门诊开始接受 GLP-1RA 治疗的 T2D(年龄 18-80 岁)患者。我们比较了度拉鲁肽与利拉鲁肽和 exeOW 对糖化血红蛋白(HbA1c,主要结局)、体重、血压和空腹血糖(次要结局)变化的影响。平均随访时间为 5.9 个月。采用倾向评分匹配或多变量调整来解决选择偏倚。还进行了涵盖相同比较的观察性研究的荟萃分析。
度拉鲁肽、利拉鲁肽和 exeOW 组分别纳入 849、1371 和 198 例患者。与利拉鲁肽相比,度拉鲁肽降低 HbA1c 的幅度更大(-0.24±0.08%;p=0.003),这在观察性研究的荟萃分析中得到了证实。在本研究中,度拉鲁肽与 exeOW 的疗效相似。当将这些结果与其他观察性研究合并时,度拉鲁肽降低 HbA1c 的幅度更大(-0.19%;p=0.003)和体重降幅更大(-0.8kg;p=0.007)。
在真实场景中,度拉鲁肽降低 HbA1c 的效果优于利拉鲁肽。相反,我们发现度拉鲁肽与 exeOW 的疗效相似,仅在对与其他观察性研究的结果进行荟萃分析时才出现统计学差异。利拉鲁肽未进行滴定以及 exeOW 的停药率较高可能影响了估计的治疗差异。