Semaglutide in Patients With Obesity and Heart Failure Across Mildly Reduced or Preserved Ejection Fraction

被引:19
|
作者
Butler, Javed [1 ,2 ]
Abildstrom, Steen Z. [3 ]
Borlaug, Barry A. [4 ]
Davies, Melanie J. [5 ,6 ]
Kitzman, Dalane W. [7 ,8 ]
Petrie, Mark C. [9 ]
Shah, Sanjiv J. [10 ]
Verma, Subodh [11 ]
Abhayaratna, Walter P. [12 ]
Chopra, Vijay [13 ]
Ezekowitz, Justin A. [14 ]
Fu, Michael [15 ]
Ito, Hiroshi [16 ]
Lelonek, Malgorzata [17 ]
Nunez, Julio [18 ,19 ]
Perna, Eduardo [20 ]
Schou, Morten [21 ]
Senni, Michele [22 ]
van der Meer, Peter [23 ]
Lewinski, Dirk von [24 ]
Wolf, Dennis [25 ]
Altschul, Rebecca L. [3 ]
Rasmussen, Soren [3 ]
Kosiborod, Mikhail N. [26 ]
机构
[1] Baylor Scott & White Res Inst, 3434 Live Oak St,Suite 501, Dallas, TX 75204 USA
[2] Univ Mississippi, Jackson, MS 39216 USA
[3] Novo Nordisk, Soborg, Denmark
[4] Mayo Clin, Dept Cardiovasc Med, Rochester, MN USA
[5] Univ Leicester, Diabet Res Ctr, Leicester, Leics, England
[6] Natl Inst Hlth & Care Res, Leicester Biomed Res Ctr, Leicester, Leics, England
[7] Wake Forest Sch Med, Dept Cardiovasc Med, Winston Salem, NC USA
[8] Wake Forest Sch Med, Sect Geriatr & Gerontol, Winston Salem, NC USA
[9] Univ Glasgow, Sch Cardiovasc & Metab Hlth, Glasgow City, Scotland
[10] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Cardiol, Chicago, IL USA
[11] Univ Toronto, St Michaels Hosp, Div Cardiac Surg, Li Ka Shing Knowledge Inst,Unity Hlth Toronto, Toronto, ON, Canada
[12] Australian Natl Univ, Coll Hlth & Med, Canberra, ACT, Australia
[13] Max Super Specialty Hosp, New Delhi, India
[14] Univ Alberta, Edmonton, AB, Canada
[15] Sahlgrens Univ Hosp, Dept Med, Sect Cardiol, Gothenburg, Sweden
[16] Kawasaki Med Sch, Dept Gen Internal Med 3, Okayama, Japan
[17] Med Univ Lodz, Dept Noninvas Cardiol, Lodz, Poland
[18] Univ Valencia, Hosp Clin Univ Valencia, INCLIVA, Valencia, Spain
[19] CIBER Cardiovasc, Valencia, Spain
[20] Inst Cardiol JF Cabral, Corrientes, Argentina
[21] Univ Copenhagen, Herlev Gentofte Hosp, Dept Cardiol, Herlev, Denmark
[22] ASST Papa Giovanni XXIII, Bergamo, Italy
[23] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[24] Med Univ Graz, Graz, Austria
[25] Univ Freiburg, Cardiol & Angiol, Med Ctr, Fac Med, Freiburg, Germany
[26] Univ Missouri Kansas City, Sch Med, St Lukes Mid Amer Heart Inst, Dept Cardiovasc Dis, Kansas City, MO USA
基金
美国国家卫生研究院;
关键词
functional status; GLP-1; receptor agonists; HFpEF; obesity; SPIRONOLACTONE; LIRAGLUTIDE; PHENOTYPE;
D O I
10.1016/j.jacc.2023.09.811
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Many therapies for heart failure (HF) have shown differential impact across the spectrum of left ventricular ejection fraction (LVEF).OBJECTIVES In this prespecified analysis, the authors assessed the effects of semaglutide across the baseline LVEF strata in patients with the obesity phenotype of HF with preserved ejection fraction (HFpEF) in the STEP-HFpEF (Semaglutide Treatment Effect in People with obesity and HFpEF) trial.METHODS STEP-HFpEF randomized 529 patients (263 semaglutide; 266 placebo). For this prespecified analysis, patients were categorized into 3 groups based on LVEF: 45% to 49% (n = 85), 50% to 59% (n = 215), and >= 60% (n = 229).RESULTS At 52 weeks, semaglutide improved the dual primary endpoints of Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (estimated treatment difference: EF [ejection fraction] 45%-49%: 5.0 points [95% CI: -2.7 to 12.8 points], EF 50%-59%: 9.8 points [95% CI: 5.0 to 14.6 points], and EF >= 60%: 7.4 points [95% CI: 2.8 to 12.0 points]; P interaction = 0.56) and body weight (EF: 45%-49%: -7.6 [95% CI: -10.7 to -4.4], EF 50%-59%: -10.6 [95% CI: -12.6 to -8.6] and EF >= 60%: -11.9 [95% CI: -13.8 to -9.9]; P interaction = 0.08), to a similar extent across LVEF categories. Likewise, LVEF did not influence the benefit of semaglutide on confirmatory secondary endpoints: 6-minute walk distance (P interaction = 0.19), hierarchal composite endpoint (P interaction = 0.43), and high-sensitivity C-reactive protein (P interaction = 0.26); or exploratory endpoint of N-terminal pro-brain natriuretic peptide (P interaction = 0.96). Semaglutide was well-tolerated across LVEF categories.CONCLUSIONS In patients with HFpEF and obesity, semaglutide 2.4 mg improved symptoms, physical limitations, and exercise function, and reduced inflammation and body weight to a similar extent across LVEF categories. These data support treatment with semaglutide in patients with the obesity phenotype of HFpEF regardless of LVEF. (Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity [STEP-HFpEF]; NCT04788511).
引用
收藏
页码:2087 / 2096
页数:10
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