Lingvay Ildiko, Kirk Andreas R, Lophaven Søren, Wolden Michael L, Shubrook Jay H
Department of Internal Medicine/Endocrinology and Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Novo Nordisk A/S, Søborg, Denmark.
Diabetes Ther. 2021 Mar;12(3):879-896. doi: 10.1007/s13300-021-01010-4. Epub 2021 Feb 17.
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are highly effective for glycaemic control and weight loss in patients with type 2 diabetes (T2D). In this retrospective, observational study, we analysed glycated haemoglobin (HbA1c) and weight following switching to semaglutide from any other GLP-1 RA, using US electronic health records and prescription data.
Adults (≥ 18 years old) with T2D required at least one prescription for injectable semaglutide at index date (treatment switch), at least one prescription for any other GLP-1 RA in the previous 365 days, a baseline HbA1c and/or weight measurement in the 90 days pre-index and a follow-up measurement at 180 and 365 days post-index. HbA1c and weight cohorts were analysed separately using an ANCOVA model. Sensitivity analyses were conducted in patients with at least two prescriptions for pre-switch GLP-1 RA. A secondary analysis compared subgroups receiving different GLP-1 RAs pre-switch.
Patients with HbA1c (n = 710) and weight (n = 921) data had similar baseline characteristics. Significant reductions in HbA1c at 6 months (0.7%; 95% confidence interval [CI] - 0.8, - 0.6) were sustained at 12 months. Weight reductions were significant at 6 months (- 2.1 kg; 95% CI - 2.6, - 1.6) and greater at 12 months (- 2.8 kg; 95% CI - 3.9, - 1.8). These patterns were consistent with the two-prescription sensitivity analysis and independent of the pre-switch GLP-1 RA.
Switching to injectable semaglutide from any other GLP-1 RA was associated with significant improvements in glycaemic control and weight. Our findings support decision-making in clinical practice in patients with an indication to switch between GLP-1 RAs.
胰高血糖素样肽-1受体激动剂(GLP-1 RAs)对2型糖尿病(T2D)患者的血糖控制和体重减轻非常有效。在这项回顾性观察研究中,我们利用美国电子健康记录和处方数据,分析了从任何其他GLP-1 RA转换为司美格鲁肽后的糖化血红蛋白(HbA1c)和体重情况。
患有T2D的成年人(≥18岁)在索引日期(治疗转换)需要至少一张注射用司美格鲁肽的处方,在过去365天内需要至少一张任何其他GLP-1 RA的处方,在索引前90天进行基线HbA1c和/或体重测量,并在索引后180天和365天进行随访测量。使用协方差分析模型分别分析HbA1c和体重队列。对至少有两张转换前GLP-1 RA处方的患者进行敏感性分析。二次分析比较了转换前接受不同GLP-1 RA的亚组。
有HbA1c(n = 710)和体重(n = 921)数据的患者具有相似的基线特征。6个月时HbA1c显著降低(0.7%;95%置信区间[CI] -0.8,-0.6),并在12个月时持续。体重在6个月时显著减轻(-2.1 kg;95% CI -2.6,-1.6),在12个月时减轻更多(-2.8 kg;95% CI -3.9,-1.8)。这些模式与双处方敏感性分析一致,且与转换前的GLP-1 RA无关。
从任何其他GLP-1 RA转换为注射用司美格鲁肽与血糖控制和体重的显著改善相关。我们的研究结果支持有GLP-1 RA转换指征的患者在临床实践中的决策制定。