Department of Internal Medicine/Endocrinology and Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX.
Institute of Cardiovascular Science, University College London, London, U.K.
Diabetes Care. 2024 Aug 1;47(8):1360-1369. doi: 10.2337/dc24-0764.
To evaluate the cardiovascular effects of semaglutide by baseline glycated hemoglobin (HbA1c) and change in HbA1c in a prespecified analysis of Semaglutide Effects on Cardiovascular Outcomes in People With Overweight or Obesity (SELECT).
In SELECT, people with overweight or obesity and atherosclerotic cardiovascular disease without diabetes were randomized to weekly semaglutide 2.4 mg or placebo. The primary end point of first major adverse cardiovascular event (MACE) (cardiovascular mortality, nonfatal myocardial infarction, or stroke) was reduced by 20% with semaglutide versus placebo. Analysis of outcomes included first MACE, its individual components, expanded MACE (cardiovascular mortality, nonfatal myocardial infarction, or stroke; coronary revascularization; or hospitalization for unstable angina), a heart failure composite (heart failure hospitalization or urgent medical visit or cardiovascular mortality), coronary revascularization, and all-cause mortality by baseline HbA1c subgroup and categories of HbA1c change (<-0.3, -0.3 to 0.3, and >0.3 percentage points) from baseline to 20 weeks using the intention-to-treat principle with Cox proportional hazards.
Among 17,604 participants (mean age 61.6 years, 72.3% male), baseline HbA1c was <5.7% for 33.5%, 5.7% to <6.0% for 34.6%, and 6.0% to <6.5% for 31.9%. Cardiovascular risk reduction with semaglutide versus placebo was not shown to be different across baseline HbA1c groups and was consistent with that of the overall study for all end points, except all-cause mortality. Cardiovascular outcomes were also consistent across subgroups of HbA1c change.
In people with overweight or obesity and established atherosclerotic cardiovascular disease but not diabetes, semaglutide reduced cardiovascular events irrespective of baseline HbA1c or change in HbA1c. Thus, semaglutide is expected to confer cardiovascular benefits in people with established atherosclerotic cardiovascular disease who are normoglycemic at baseline and/or in those without HbA1c improvements.
通过基线糖化血红蛋白(HbA1c)和 HbA1c 变化对超重或肥胖人群的 semaglutide 对心血管结局的影响(SELECT)的预设分析,评估 semaglutide 的心血管效应。
在 SELECT 中,患有超重或肥胖症和无糖尿病的动脉粥样硬化性心血管疾病的患者被随机分配接受每周 2.4mg semaglutide 或安慰剂治疗。与安慰剂相比,semaglutide 使主要不良心血管事件(MACE)(心血管死亡率、非致死性心肌梗死或中风)的首要终点降低了 20%。结局分析包括首要 MACE、其各个组成部分、扩展 MACE(心血管死亡率、非致死性心肌梗死或中风;冠状动脉血运重建术;或不稳定型心绞痛住院治疗)、心力衰竭复合(心力衰竭住院或紧急医疗就诊或心血管死亡率)、冠状动脉血运重建术和全因死亡率,按基线 HbA1c 亚组和基线至 20 周时 HbA1c 变化(<-0.3、-0.3 至 0.3 和 >0.3 个百分点)类别进行分类,采用意向治疗原则,使用 Cox 比例风险进行分析。
在 17604 名参与者(平均年龄 61.6 岁,72.3%为男性)中,基线 HbA1c<5.7%占 33.5%,5.7%至<6.0%占 34.6%,6.0%至<6.5%占 31.9%。与安慰剂相比,semaglutide 降低心血管风险的效果在不同基线 HbA1c 组之间没有差异,除全因死亡率外,与整个研究的所有终点结果一致。HbA1c 变化的亚组之间的心血管结局也一致。
在超重或肥胖且患有已确诊的动脉粥样硬化性心血管疾病但无糖尿病的患者中,semaglutide 降低了心血管事件,无论基线 HbA1c 或 HbA1c 变化如何。因此,semaglutide 有望为基线时已确诊的动脉粥样硬化性心血管疾病且血糖正常的患者和/或 HbA1c 改善的患者带来心血管获益。