Evidence map›Paper›PMID 37993201›Full record

ArticleJournal of the American College of Cardiology2023

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

Javed Butler, Steen Z Abildstrøm, Barry A Borlaug, Melanie J Davies, Dalane W Kitzman, Mark C Petrie, Sanjiv J Shah, Subodh Verma, Walter P Abhayaratna, Vijay Chopra and 14 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of the American College of Cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT04788511. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
15.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04788511 phase3completed

Effect of Semaglutide 2.4 mg Once Weekly on Function and Symptoms in Subjects With Obesity-related Heart Failure With Preserved Ejection Fraction

Ran2021Enrolled529Registered outcomes15Posted comparisons2ConditionsObesityArmsPlacebo (semaglutide), semaglutide
PMID 37622681PMID 37635157other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 19 institutions in 13 countries.

Javed ButlerBaylor Scott and White Research Institute, Dallas, Texas, USA; University of Mississippi, Jackson, Mississippi, USA. Electronic address: butlzih@gmail.com.
Steen Z AbildstrømNovo Nordisk, Søborg, Denmark.
Barry A BorlaugDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Melanie J DaviesDiabetes Research Centre, University of Leicester, Leicester, United Kingdom; National Institute for Health and Care Research, Leicester Biomedical Research Centre, Leicester, United Kingdom.
Dalane W KitzmanDepartment of Cardiovascular Medicine and Section on Geriatrics and Gerontology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Mark C PetrieSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.
Sanjiv J ShahDivision of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Subodh VermaDivision of Cardiac Surgery, Li Ka Shing Knowledge Institute of St Michael's Hospital, Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.
Walter P AbhayaratnaCollege of Health and Medicine, the Australian National University, Canberra, Australian Capital Territory, Canberra, Australia.
Vijay ChopraMax Super Specialty Hospital, New Delhi, India.
Justin A EzekowitzUniversity of Alberta, Edmonton, Alberta, Canada.
Michael FuSection of Cardiology, Department of Medicine, Sahlgrenska University Hospital-Ostra, Gothenburg, Sweden.
Hiroshi ItoDepartment of General Internal Medicine 3, Kawasaki Medical School, Okayama, Japan.
Małgorzata LelonekDepartment of Noninvasive Cardiology, Medical University of Lodz, Lodz, Poland.
Julio NúñezHospital Clínico Universitario de Valencia, INCLIVA, Universitat de Valencia, Valencia, Spain; CIBER Cardiovascular, Valencia, Spain.
Eduardo PernaInstituto de Cardiologia J. F. Cabral, Corrientes, Argentina.
Morten SchouDepartment of Cardiology, Herlev-Gentofte Hospital, University of Copenhagen, Herlev, Denmark.
Michele SenniASST Papa Giovanni XXIII, Bergamo, Italy.
Peter van der MeerDepartment of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Dirk von LewinskiMedical University of Graz, Graz, Austria.
Dennis WolfCardiology and Angiology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Rebecca L AltschulNovo Nordisk, Søborg, Denmark.
Søren RasmussenNovo Nordisk, Søborg, Denmark.
Mikhail N KosiborodDepartment 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.
Novo Nordisk (Denmark) · DKAustralian National University · AUCentro de Investigación Biomédica en Red · ESGentofte Hospital · DKKawasaki Medical School · JPMax Super Speciality Hospital · INMayo Clinic in Arizona · USMedical University of Graz · ATMedical University of Lodz · PLNIHR Leicester Biomedical Research Centre · GBNorthwestern University · USOspedale Papa Giovanni XXIII · ITSahlgrenska University Hospital · SEUniversity of Alberta · CAUniversity of Glasgow · GBUniversity of Groningen · NLUniversity of Mississippi · USUniversity of Toronto · CAWake Forest University · US

Funding

Physical Rehabilitation for Older Patients with Acute HFpEF-The REHAB-HFpEF TrialR01AG078153 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KITZMAN, DALANE W · 2022 to 2025
$26.6M
REHAB-HF: A Trial of Rehabilitation Therapy in Older Acute Heart Failure PatientsR01AG045551 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KITZMAN, DALANE W · 2014 to 2018
$6.8M
Exercise Intolerance in Older HFPEF PatientsR01AG018915 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KITZMAN, DALANE W · 2001 to 2019
$5.2M
Wake Forest Atrium HeartShare Clinical CenterU01HL160272 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DALANE W KITZMAN · 2021 to 2026
$2.3M
Repurposing of Metormin for Older Patients with HFpEFU01AG076928 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KITZMAN, DALANE W, YADAV, HARIOM · 2022 to 2024
$2.3M
NHLBI NIH HHS U01 HL160272NIA NIH HHS R01 AG018915NIA NIH HHS R01 AG045551NIA NIH HHS R01 AG078153NIA NIH HHS U01 AG076928
6 · The paper itself

Abstract

backgroundMany therapies for heart failure (HF) have shown differential impact across the spectrum of left ventricular ejection fraction (LVEF).

objectivesIn 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.

methodsSTEP-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).

resultsAt 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.

conclusionsIn 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).

Indexed as

Heart FailureHumansObesitySemaglutideStroke VolumeVentricular Function, LeftSemaglutidefunctional statusGLP-1 receptor agonistsHFpEFobesitysemaglutidesymptoms

Identifiers

PMID37993201
PMCPMC11185158
OpenAlexW4387455980

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Texttitle and abstract
LicenceCC BY-NC-ND
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.