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Semaglutide and NT-proBNP in Obesity-Related HFpEF: Insights From the STEP-HFpEF Program.
Petrie, Mark C; Borlaug, Barry A; Butler, Javed; Davies, Melanie J; Kitzman, Dalane W; Shah, Sanjiv J; Verma, Subodh; Jensen, Thomas Jon; Einfeldt, Mette Nygaard; Liisberg, Karoline; Perna, Eduardo; Sharma, Kavita; Ezekowitz, Justin A; Fu, Michael; Melenovský, Vojtech; Ito, Hiroshi; Lelonek, Malgorzata; Kosiborod, Mikhail N.
Afiliação
  • Petrie MC; School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.
  • Borlaug BA; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Butler J; Baylor Scott and White Research Institute, Dallas, Texas, USA; Department of Medicine, University of Mississippi, Jackson, Mississippi, USA.
  • Davies MJ; Diabetes Research Centre, University of Leicester, Leicester, United Kingdom; NIHR Leicester Biomedical Research Centre, Leicester, United Kingdom.
  • Kitzman DW; Department of Cardiovascular Medicine and Section on Geriatrics and Gerontology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Shah SJ; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Verma S; Division of Cardiac Surgery, Li Ka Shing Knowledge Institute of St Michael's Hospital, Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.
  • Jensen TJ; Novo Nordisk A/S, Søborg, Denmark.
  • Einfeldt MN; Novo Nordisk A/S, Søborg, Denmark.
  • Liisberg K; Novo Nordisk A/S, Søborg, Denmark.
  • Perna E; Instituto de Cardiología de Corrientes J. F. Cabral, Corrientes, Argentina.
  • Sharma K; Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Ezekowitz JA; University of Alberta, Edmonton, Alberta, Canada.
  • Fu M; Section of Cardiology, Department of Medicine, Sahlgrenska University Hospital-Ostra, Gothenburg, Sweden.
  • Melenovský V; Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Ito H; Department of General Internal Medicine 3, Kawasaki Medical School, Okayama, Japan.
  • Lelonek M; Department of Noninvasive Cardiology, Medical University of Lodz, Lodz, Poland.
  • Kosiborod MN; Department of Cardiovascular Disease, Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA. Electronic address: mkosiborod@saint-lukes.org.
J Am Coll Cardiol ; 84(1): 27-40, 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38819334
ABSTRACT

BACKGROUND:

The glucagon-like peptide-1 receptor agonist, semaglutide, improved health status and reduced body weight in patients with obesity-related heart failure (HF) with preserved ejection fraction (HFpEF) in the STEP-HFpEF (Semaglutide Treatment Effect in People with Obesity and HFpEF) program. Whether benefits were due to mechanical unloading or effects on HF pathobiology is uncertain.

OBJECTIVES:

This study sought to determine if semaglutide 2.4 mg reduced N-terminal pro-B-type natriuretic peptide (NT-proBNP) in patients with obesity-related HFpEF and compare treatment responses by baseline NT-proBNP.

METHODS:

This was a prespecified secondary analysis of pooled data from 2 double-blind, placebo-controlled, randomized trials (STEP-HFpEF [Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity] and STEP-HFpEF DM [Research Study to Look at How Well Semaglutide Works in People Living With Heart Failure, Obesity and Type 2 Diabetes]) testing effects of semaglutide in patients with obesity-related HFpEF. The main outcomes were change in NT-proBNP at 52 weeks and change in the dual primary endpoints of Kansas City Cardiomyopathy Questionnaire Clinical Summary Score and body weight by baseline NT-proBNP.

RESULTS:

In total, 1,145 patients were randomized. Semaglutide compared with placebo reduced NT-proBNP at 52 weeks (estimated treatment ratio 0.82; 95% CI 0.74-0.91; P = 0.0002). Improvements in health status were more pronounced in those with higher vs lower baseline NT-proBNP (estimated difference tertile 1 4.5 points, 95% CI 0.8-8.2; tertile 2 6.2 points, 95% CI 2.4-10.0; tertile 3 11.9 points, 95% CI 8.1-15.7; P interaction = 0.02; baseline NT-proBNP as a continuous variable P interaction = 0.004). Reductions in body weight were consistent across baseline NT-proBNP levels (P interaction = 0.21).

CONCLUSIONS:

In patients with obesity-related HFpEF, semaglutide reduced NT-proBNP. Participants with higher baseline NT-proBNP had a similar degree of weight loss but experienced larger reductions in HF-related symptoms and physical limitations with semaglutide than those with lower NT-proBNP.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Volume Sistólico / Peptídeo Natriurético Encefálico / Peptídeos Semelhantes ao Glucagon / Insuficiência Cardíaca / Obesidade Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Volume Sistólico / Peptídeo Natriurético Encefálico / Peptídeos Semelhantes ao Glucagon / Insuficiência Cardíaca / Obesidade Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido