Cardiovascular and mortality benefits of sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide 1 receptor agonists as third-step glucose-lowering medicine in patients with type 2 diabetes: a retrospective cohort analysis

IF 3.7 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM BMJ Open Diabetes Research & Care Pub Date : 2024-05-01 DOI:10.1136/bmjdrc-2023-003792
Thomas A McCormick, Jason Kramer, Elizabeth G Liles, Qiana Amos, John P Martin, John L Adams
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Abstract

Introduction Studies have found that sodium-glucose cotransporter 2 inhibitors (SGLT2) and glucagon-like peptide 1 receptor agonists (GLP1) have cardiovascular benefits for patients with type 2 diabetes (DM2) and atherosclerotic cardiovascular disease (ASCVD), chronic kidney disease (CKD), or heart failure (HF). The literature does not provide evidence specifically for patients with these conditions who are adding one of these medicines to two glucose-lowering medications (ie, as “third-step” therapy). We explored the effects of different third-step medications on cardiovascular outcomes in patients with diabetes and these comorbid conditions. Specifically, we compared third-step SGLT2 or GLP1 to third-step dipeptidyl peptidase-4 inhibitors (DPP4), insulin, or thiazolidinediones (TZD). Research design and methods We assembled a retrospective cohort of adults at five Kaiser Permanente sites with DM2 and ASCVD, CKD, or HF, initiating third-step treatment between 2016 and 2020. Propensity score weighted Poisson models were used to calculate adjusted rate ratios (ARRs) for all-cause mortality, incident major adverse cardiovascular event (MACE), and incident HF hospitalization in patients initiating SGLT2 or GLP1 compared with DPP4, insulin, or TZD. Results We identified 27 542 patients initiating third-step treatment with one or more of these conditions (19 958 with ASCVD, 14 577 with CKD, and 3919 with HF). ARRs for GLP1 and SGLT2 versus DPP4, insulin, and TZD in the patient subgroups ranged between 0.22 and 0.55 for all-cause mortality, 0.38 and 0.81 for MACE, and 0.46 and 1.05 for HF hospitalization. Many ARRs were statistically significant, and all significant ARRs showed a benefit (ARR <1) for GLP1 or SGLT2 when compared with DPP4, insulin, or TZD. Conclusions Third-step SGLT2 and GLP1 are generally associated with a benefit for these outcomes in these patient groups when compared with third-step DPP4, insulin, or TZD. Our results add to evidence of a cardiovascular benefit of SGLT2 and GLP1 and could inform clinical guidelines for choosing third-step diabetes treatment. No data are available.
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钠-葡萄糖共转运体-2 抑制剂和胰高血糖素样肽 1 受体激动剂作为 2 型糖尿病患者第三步降糖药对心血管和死亡率的益处:回顾性队列分析
导言 研究发现,钠-葡萄糖共转运体 2 抑制剂 (SGLT2) 和胰高血糖素样肽 1 受体激动剂 (GLP1) 对患有 2 型糖尿病 (DM2) 和动脉粥样硬化性心血管疾病 (ASCVD)、慢性肾脏疾病 (CKD) 或心力衰竭 (HF) 的患者的心血管有益。文献中没有专门针对这些患者在两种降糖药物基础上加用其中一种药物(即 "第三步 "疗法)的证据。我们探讨了不同的第三步药物对糖尿病和这些合并症患者心血管预后的影响。具体而言,我们将第三步 SGLT2 或 GLP1 与第三步二肽基肽酶-4 抑制剂 (DPP4)、胰岛素或噻唑烷二酮类药物 (TZD) 进行了比较。研究设计与方法 我们在五个 Kaiser Permanente 医疗点收集了 2016 年至 2020 年期间开始接受第三步治疗的患有 DM2 和 ASCVD、CKD 或 HF 的成人回顾性队列。与 DPP4、胰岛素或 TZD 相比,我们使用倾向得分加权泊松模型计算了开始接受 SGLT2 或 GLP1 治疗的患者的全因死亡率、主要不良心血管事件 (MACE) 发生率和 HF 住院发生率的调整率比 (ARR)。结果 我们确定了 27 542 名患有一种或多种上述疾病并开始接受第三步治疗的患者(其中 19 958 人患有 ASCVD,14 577 人患有 CKD,3919 人患有 HF)。在患者亚组中,GLP1 和 SGLT2 相对于 DPP4、胰岛素和 TZD 的 ARR 分别为:全因死亡率 0.22 至 0.55,MACE 0.38 至 0.81,HF 住院率 0.46 至 1.05。与 DPP4、胰岛素或 TZD 相比,GLP1 或 SGLT2 的许多 ARR 均具有统计学意义,且所有显著的 ARR 均显示 GLP1 或 SGLT2 有获益(ARR <1)。结论 与第三阶段 DPP4、胰岛素或 TZD 相比,第三阶段 SGLT2 和 GLP1 通常对这些患者群体的这些结果有益。我们的研究结果增加了 SGLT2 和 GLP1 对心血管有益的证据,可为选择第三步糖尿病治疗的临床指南提供参考。暂无数据。
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来源期刊
BMJ Open Diabetes Research & Care
BMJ Open Diabetes Research & Care Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
9.30
自引率
2.40%
发文量
123
审稿时长
18 weeks
期刊介绍: BMJ Open Diabetes Research & Care is an open access journal committed to publishing high-quality, basic and clinical research articles regarding type 1 and type 2 diabetes, and associated complications. Only original content will be accepted, and submissions are subject to rigorous peer review to ensure the publication of high-quality — and evidence-based — original research articles.
期刊最新文献
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