1981-LB:模拟塞马鲁肽 2.4 mg 对患有动脉粥样硬化性心血管疾病且体重指数≥27 kg/m2 的美国患者的影响

IF 6.2 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Diabetes Pub Date : 2024-06-21 DOI:10.2337/db24-1981-lb
MADS FAURBY, MICHAEL G. NANNA, JOSHUA C. TOLIVER, QUAN V. DOAN, ALASDAIR D. HENRY, THOMAS SCASSELLATI SFORZOLINI, ALINA LEVINE, ANTHONY FABRICATORE, AZADEH S. HOUSHMAND-OEREGAARD, ANN MARIE NAVAR
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The 10-year rate of recurrent MACE events was estimated based on the SMART2 risk calculator. The potential treatment effect of semaglutide 2.4 mg on the number of MACE events in this population was estimated using results from the SELECT trial. As of 2023, 6,161,981 US adults met SELECT inclusion criteria (mean age 67.2 ± 9.9 years, 43.6% female, mean BMI 32.6 ± 5.0 kg/m2). Based on SMART2, an estimated 2,529,310 individuals (41.0%) will experience at least one MACE event in the next 10 years, with the total number of events estimated at 3,064,993. Of these, 497,631 MACE events could be avoided with semaglutide 2.4 mg treatment (Table). The possible therapeutic impact of semaglutide 2.4 mg on eligible US adults is substantial, with the potential to prevent nearly half a million CV events and deaths over the next 10 years. Disclosure M. Faurby: Employee; Novo Nordisk. M.G. Nanna: Consultant; Merck & Co., Inc., HeartFlow, Inc. J.C. Toliver: Employee; Novo Nordisk. Q.V. Doan: Consultant; Novo Nordisk, Daiichi Sankyo, Akebia Therapeutics, Inc., AbbVie Inc. A.D. Henry: Consultant; Novo Nordisk. T. Scassellati Sforzolini: Consultant; Novo Nordisk. A. Levine: Consultant; Novo Nordisk. A. Fabricatore: Employee; Novo Nordisk. Stock/Shareholder; Novo Nordisk. A.S. Houshmand-Oeregaard: Employee; Novo Nordisk. Stock/Shareholder; Eli Lilly and Company, Novo Nordisk A/S. A. Navar: Consultant; ESPERION Therapeutics, Inc. Research Support; ESPERION Therapeutics, Inc. Consultant; Amgen Inc. Research Support; Amgen Inc., Bristol-Myers Squibb Company. Consultant; Bristol-Myers Squibb Company, Janssen Pharmaceuticals, Inc., Merck & Co., Inc., Bayer Inc., Novartis Pharmaceuticals Corporation, Novo Nordisk, Pfizer Inc., New Amsterdam, Boehringer-Ingelheim, Eli Lilly and Company, Silence Therapeutics. 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引用次数: 0

摘要

SELECT 试验表明,对于患有动脉粥样硬化性心血管疾病(ASCVD)和超重/肥胖(体重指数≥27 kg/m2)的成年人,使用 2.4 mg semaglutide 可将主要不良心血管事件(MACE)的风险降低 20%。我们的目标是量化这种治疗方法对美国人口的潜在影响。美国国家健康与检查调查(NHANES)数据用于描述符合 SELECT 试验标准的美国人口特征:BMI≥27 kg/m2、年龄≥45岁、ASCVD、无糖尿病,并根据2023年的人口普查预测确定了潜在的候选治疗人数。根据 SMART2 风险计算器估算了 10 年的复发性 MACE 事件发生率。根据 SELECT 试验的结果,估算出 semaglutide 2.4 mg 对该人群中 MACE 事件数量的潜在治疗效果。截至 2023 年,共有 6161981 名美国成年人符合 SELECT 纳入标准(平均年龄为 67.2 ± 9.9 岁,43.6% 为女性,平均体重指数为 32.6 ± 5.0 kg/m2)。根据SMART2,估计有2,529,310人(41.0%)将在未来10年内经历至少一次MACE事件,事件总数估计为3,064,993起。其中,497,631 例 MACE 事件可通过使用 2.4 mg semaglutide 治疗而避免(表)。在未来 10 年内,塞马鲁肽 2.4 毫克对符合条件的美国成年人可能产生的治疗影响是巨大的,有可能避免近 50 万例心血管事件和死亡。披露 M. Faurby:诺和诺德公司雇员。M.G. Nanna:默克公司、HeartFlow公司顾问。J.C. Toliver:诺和诺德公司员工:诺和诺德公司员工。Q.V. Doan:顾问;诺和诺德公司、第一三共公司、Akebia Therapeutics 公司、艾伯维公司。A.D. Henry:诺和诺德公司顾问T. Scassellati Sforzolini:诺和诺德公司顾问A. Levine:诺和诺德公司顾问A. Fabricatore:员工; 诺和诺德诺和诺德公司股票/股东。A.S. Houshmand-Oeregaard:诺和诺德员工。股票/股东;礼来公司、诺和诺德公司。A. Navar:顾问;ESPERION Therapeutics, Inc.研究支持;ESPERION Therapeutics, Inc.顾问;Amgen Inc.研究支持;安进公司、百时美施贵宝公司。顾问;百时美施贵宝公司、杨森制药公司、默克公司、拜耳公司、诺华制药公司、诺和诺德公司、辉瑞公司、新阿姆斯特丹公司、勃林格殷格翰公司、礼来公司、Silence Therapeutics。资助诺和诺德公司
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1981-LB: Modeling the Impact of Semaglutide 2.4 mg in U.S. Patients with Atherosclerotic Cardiovascular Disease and BMI ≥27 kg/m2
The SELECT trial demonstrated a 20% risk reduction in major adverse cardiovascular events (MACE) with semaglutide 2.4 mg in adults with atherosclerotic cardiovascular disease (ASCVD) and overweight/obesity (BMI ≥27 kg/m2). We aimed to quantify the potential population impact of this treatment in the US. National Health and Examination Survey (NHANES) data were used to characterize the US population meeting SELECT trial criteria: BMI ≥27 kg/m2, age ≥45 years, ASCVD, and no diabetes, with the number of potential treatment candidates determined using 2023 census projections. The 10-year rate of recurrent MACE events was estimated based on the SMART2 risk calculator. The potential treatment effect of semaglutide 2.4 mg on the number of MACE events in this population was estimated using results from the SELECT trial. As of 2023, 6,161,981 US adults met SELECT inclusion criteria (mean age 67.2 ± 9.9 years, 43.6% female, mean BMI 32.6 ± 5.0 kg/m2). Based on SMART2, an estimated 2,529,310 individuals (41.0%) will experience at least one MACE event in the next 10 years, with the total number of events estimated at 3,064,993. Of these, 497,631 MACE events could be avoided with semaglutide 2.4 mg treatment (Table). The possible therapeutic impact of semaglutide 2.4 mg on eligible US adults is substantial, with the potential to prevent nearly half a million CV events and deaths over the next 10 years. Disclosure M. Faurby: Employee; Novo Nordisk. M.G. Nanna: Consultant; Merck & Co., Inc., HeartFlow, Inc. J.C. Toliver: Employee; Novo Nordisk. Q.V. Doan: Consultant; Novo Nordisk, Daiichi Sankyo, Akebia Therapeutics, Inc., AbbVie Inc. A.D. Henry: Consultant; Novo Nordisk. T. Scassellati Sforzolini: Consultant; Novo Nordisk. A. Levine: Consultant; Novo Nordisk. A. Fabricatore: Employee; Novo Nordisk. Stock/Shareholder; Novo Nordisk. A.S. Houshmand-Oeregaard: Employee; Novo Nordisk. Stock/Shareholder; Eli Lilly and Company, Novo Nordisk A/S. A. Navar: Consultant; ESPERION Therapeutics, Inc. Research Support; ESPERION Therapeutics, Inc. Consultant; Amgen Inc. Research Support; Amgen Inc., Bristol-Myers Squibb Company. Consultant; Bristol-Myers Squibb Company, Janssen Pharmaceuticals, Inc., Merck & Co., Inc., Bayer Inc., Novartis Pharmaceuticals Corporation, Novo Nordisk, Pfizer Inc., New Amsterdam, Boehringer-Ingelheim, Eli Lilly and Company, Silence Therapeutics. Funding Novo Nordisk, Inc.
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来源期刊
Diabetes
Diabetes 医学-内分泌学与代谢
CiteScore
12.50
自引率
2.60%
发文量
1968
审稿时长
1 months
期刊介绍: Diabetes is a scientific journal that publishes original research exploring the physiological and pathophysiological aspects of diabetes mellitus. We encourage submissions of manuscripts pertaining to laboratory, animal, or human research, covering a wide range of topics. Our primary focus is on investigative reports investigating various aspects such as the development and progression of diabetes, along with its associated complications. We also welcome studies delving into normal and pathological pancreatic islet function and intermediary metabolism, as well as exploring the mechanisms of drug and hormone action from a pharmacological perspective. Additionally, we encourage submissions that delve into the biochemical and molecular aspects of both normal and abnormal biological processes. However, it is important to note that we do not publish studies relating to diabetes education or the application of accepted therapeutic and diagnostic approaches to patients with diabetes mellitus. Our aim is to provide a platform for research that contributes to advancing our understanding of the underlying mechanisms and processes of diabetes.
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