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根据 SELECT 试验,在美国有资格使用司美格鲁肽的人群中,心血管事件减少。

Cardiovascular event reduction among a US population eligible for semaglutide per the SELECT trial.

机构信息

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC; Department of Neurology, Duke University School of Medicine, Durham, NC.

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC; Duke Clinical Research Institute, Durham, NC.

出版信息

Am Heart J. 2024 Oct;276:110-114. doi: 10.1016/j.ahj.2024.05.007. Epub 2024 Jul 30.

Abstract

BACKGROUND

Our objective was to determine the number of major cardiovascular events (MACE, nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death) and deaths from any cause that could be prevented across varying nationwide uptake of semaglutide 2.4 mg SC weekly for the secondary prevention of cardiovascular disease.

METHODS

Using a nationally representative cross-sectional study of participants in the 2017-2018 and 2019-March 2020 cycles of the National Health and Nutrition Examination Survey in the U.S. (NHANES), we estimated the number of MACE and deaths from any cause potentially prevented over a four-year period among participants meeting SELECT trial inclusion criteria.

RESULTS

In a sample of n = 216 individuals (corresponding to 4,473,681 adults in the U.S. population) potentially eligible for this therapy, a total of 356,329 MACE and 232,808 all-cause mortality events were expected without semaglutide over 4 years and 35,633 MACE and 22,117 all-cause mortality events would be prevented with 50% uptake of semaglutide.

CONCLUSIONS

Approximately 4.5 million adults in the U.S. are forecasted to be eligible for semaglutide 2.4mg SC weekly therapy, with substantial impact on CVD and mortality if accessible and broadly used.

摘要

背景

我们的目的是确定在全国范围内不同程度使用每周皮下注射 2.4 毫克司美格鲁肽用于心血管疾病二级预防的情况下,可预防的主要心血管事件(MACE,非致死性心肌梗死、非致死性卒中和心血管死亡)和任何原因导致的死亡数量。

方法

我们使用美国 2017-2018 年和 2019 年 3 月至 2020 年全国健康和营养调查(NHANES)周期中参与者的全国代表性横断面研究,估计符合 SELECT 试验纳入标准的参与者在四年期间内可预防的 MACE 和任何原因导致的死亡数量。

结果

在 n = 216 名(相当于美国成年人人口的 4,473,681 人)有资格接受这种治疗的样本中,预计在没有司美格鲁肽的情况下,4 年内将发生 356,329 次 MACE 和 232,808 次全因死亡事件,而在司美格鲁肽使用率为 50%的情况下,将发生 35,633 次 MACE 和 22,117 次全因死亡事件。

结论

预计美国约有 450 万成年人有资格接受每周皮下注射 2.4 毫克司美格鲁肽治疗,如果这种治疗方法可获得且广泛使用,将对 CVD 和死亡率产生重大影响。

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