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Effectiveness of Liraglutide and Lixisenatide in the Treatment of Type 2 Diabetes: Real-World Evidence from The Health Improvement Network (THIN) Database in the United Kingdom

机译:利拉鲁肽和利西拉肽治疗2型糖尿病的有效性:来自英国健康改善网络(THIN)数据库的真实证据

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IntroductionThe glucagon-like peptide-1 receptor agonists liraglutide and lixisenatide are effective at reducing glycated hemoglobin (HbA1c) levels in patients with type 2 diabetes mellitus (T2DM). Although liraglutide has demonstrated superior efficacy in head-to-head clinical trials, real-world evidence of comparative effectiveness is lacking. This observational study aimed to assess the effectiveness of liraglutide versus lixisenatide in UK clinical practice. MethodsElectronic medical records from The Health Improvement Network (THIN) UK primary care database were analyzed. Patients aged ≥18?years, diagnosed with T2DM, and prescribed liraglutide or lixisenatide between 01 May 2013 and 31 December 2015 were included in the study. Adjusted linear regression models compared the difference in mean change in HbA1c, body mass index (BMI), and systolic blood pressure (SBP) after 12-month follow-up. The proportion of patients achieving glycemic control (HbA1c 1%; and weight reduction ≥3% within 12?months were determined. Cox proportional hazards modeling was used to evaluate the effect of treatment on time to achieving HbA1c and weight reduction targets. Healthcare resource use (HCRU) (GP, secondary care, hospitalizations) was compared using analysis of covariance. ResultsThe primary outcome was assessed in 579 liraglutide and 213 lixisenatide new users. Fully adjusted linear regression indicated that liraglutide reduced HbA1c significantly more than lixisenatide (mean treatment difference ?0.30; 95% CI ?0.56, ?0.04; p =?0.025). Compared to lixisenatide, liraglutide recipients were 2.5 times more likely to achieve HbA1c p =?0.0002). Liraglutide users were also more likely to achieve HbA1c p p 1% HbA1c reduction (HR 1.29; p =?0.0002). BMI and SBP reductions were greater for the liraglutide group but results were not significant. HCRU was comparable between treatment groups. ConclusionThese results from the THIN database indicate that liraglutide treatment provided better outcomes related to glycemic control. FundingNovo Nordisk.
机译:简介胰高血糖素样肽1受体激动剂利拉鲁肽和利西拉来可有效降低2型糖尿病(T2DM)患者的糖化血红蛋白(HbA1c)水平。尽管利拉鲁肽在头对头临床试验中已显示出优异的疗效,但仍缺乏现实世界中比较疗效的证据。这项观察性研究旨在评估利拉鲁肽与利西拉来在英国临床实践中的有效性。方法分析来自英国健康改善网络(THIN)初级保健数据库的电子病历。该研究纳入了年龄≥18岁,诊断为T2DM并在2013年5月1日至2015年12月31日期间开具利拉鲁肽或利西拉来的患者。校正的线性回归模型比较了12个月的随访后HbA1c,体重指数(BMI)和收缩压(SBP)的平均变化的差异。确定在12个月内达到血糖控制(HbA1c 1%;体重减轻≥3%)的患者比例;使用Cox比例风险模型评估治疗在达到HbA1c和减轻体重目标的时间上的效果。结果使用579个利拉鲁肽和213个新的利西拉肽新使用者评估了主要结局,完全调整的线性回归表明利拉鲁肽对HbA1c的抑制作用明显大于利西拉肽(平均治疗差异? 0.30; 95%CI≤0.56,≤0.04; p =≤0.025)。与利西拉来相比,利拉鲁肽接受者达到HbA1c的可能性高2.5倍,p =≤0.0002)。利拉鲁肽的使用者也更有可能实现HbA1c p p 1%HbA1c降低(HR 1.29; p =?0.0002)。利拉鲁肽组的BMI和SBP降低更大,但结果并不显着。 HCRU在治疗组之间具有可比性。结论THIN数据库的这些结果表明,利拉鲁肽治疗可提供更好的与血糖控制相关的结果。资金Novo Nordisk。

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