Effects of oral semaglutide on cardiovascular outcomes in individuals with type 2 diabetes and established atherosclerotic cardiovascular disease and/or chronic kidney disease: Design and baseline characteristics of SOUL, a randomized trial

被引:84
作者
McGuire, Darren K. [1 ,2 ]
Busui, Rodica P. [3 ]
Deanfield, John [4 ]
Inzucchi, Silvio E. [5 ]
Mann, Johannes F. E. [6 ,7 ]
Marx, Nikolaus [8 ]
Mulvagh, Sharon L. [9 ]
Poulter, Neil [10 ]
Engelmann, Mads D. M. [11 ]
Hovingh, G. Kees [11 ]
Ripa, Maria Sejersten [11 ]
Gislum, Mette [11 ]
Brown-Frandsen, Kirstine [11 ]
Buse, John B. [12 ]
机构
[1] Univ Texas Southwestern Med Ctr, Dallas, TX USA
[2] Parkland Hlth & Hosp Syst, Dallas, TX USA
[3] Univ Michigan, Dept Internal Med Metab Endocrinol & Diabet, Ann Arbor, MI USA
[4] UCL, Inst Cardiovasc Sci, London, England
[5] Yale Sch Med, Sect Endocrinol, New Haven, CT USA
[6] KfH Kidney Ctr, Munich, Germany
[7] Friedrich Alexander Univ Erlangen, Erlangen, Germany
[8] Rhein Westfal TH Aachen, Univ Hosp Aachen, Dept Internal Med 1, Aachen, Germany
[9] Dalhousie Univ, Dept Med, Div Cardiol, Halifax, NS, Canada
[10] Imperial Coll London, Imperial Clin Trials Unit, London, England
[11] Novo Nord AS, Soborg, Denmark
[12] Univ N Carolina, Sch Med, Chapel Hill, NC USA
关键词
cardiovascular disease; GLP-1; randomized trial; semaglutide; type; 2; diabetes; MORTALITY; MELLITUS; STROKE;
D O I
10.1111/dom.15058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: To describe the design of the SOUL trial (Semaglutide cardiOvascular oUtcomes triaL) and the baseline clinical data of its participants. Materials and methods: In SOUL, the effects of oral semaglutide, the first oral glucagon-like peptide-1 receptor agonist, on the risk of cardiovascular (CV) events in individuals with type 2 diabetes and established atherosclerotic CV disease (ASCVD) and/or chronic kidney disease (CKD) will be assessed. SOUL is a randomized, double-blind, parallel-group, placebo-controlled CV outcomes trial comparing oral semaglutide (14 mg once daily) with placebo, both in addition to standard of care, in individuals aged >= 50 years with type 2 diabetes and evidence of ASCVD (coronary artery disease [CAD], cerebrovascular disease, symptomatic peripheral arterial disease [PAD]) and/or CKD (estimated glomerular filtration rate <60 mL/min/1.73 m(2)). The primary outcome is time from randomization to first occurrence of a major adverse CV event (MACE; a composite of CV death, nonfatal myocardial infarction or nonfatal stroke). This event-driven trial will continue until 1225 first adjudication-confirmed MACEs have occurred. Enrolment has been completed. Results: Overall, 9650 participants were enrolled between June 17, 2019 and March 24, 2021 (men 71.1%, White ethnicity 68.9%, mean age 66.1 years, diabetes duration 15.4 years, body mass index 31.1 kg/m(2), glycated haemoglobin 63.5 mmol/mol [8.0%]). The most frequently used antihyperglycaemic medications at baseline were metformin (75.7%), insulin and insulin analogues (50.5%), sulphonylureas (29.1%), sodium-glucose cotransporter-2 inhibitors (26.7%) and dipeptidyl peptidase-4 inhibitors (23.0%). At randomization, 70.7% of participants had CAD, 42.3% had CKD, 21.1% had cerebrovascular disease and 15.7% had symptomatic PAD (categories not mutually exclusive). Prevalent heart failure was reported in 23.0% of participants. Conclusion: SOUL will provide evidence regarding the CV effects of oral semaglutide in individuals with type 2 diabetes and established ASCVD and/or CKD.
引用
收藏
页码:1932 / 1941
页数:10
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