Evidence mapPaperPMID 37952180Full record

ArticleCirculation2024

Effects of Semaglutide on Symptoms, Function, and Quality of Life in Patients With Heart Failure With Preserved Ejection Fraction and Obesity: A Prespecified Analysis of the STEP-HFpEF Trial.

Mikhail N Kosiborod, Subodh Verma, Barry A Borlaug, Javed Butler, Melanie J Davies, Thomas Jon Jensen, Søren Rasmussen, Peter Erlang Marstrand, Mark C Petrie, Sanjiv J Shah and 6 more

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Circulation, 2024. 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 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
17.1field-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
NCT07738276 phase3not yet recruitingstarted 2026, after this paper: background citation

Evaluation of the Efficacy and Safety of Tirzepatide, a Dual GLP-1/GIP Agonist, on Functional Capacity in Reduced Ejection Fraction Heart Failure Patients With Obesity: A Double-Blinded Randomized Controlled Trial

Ran2026Enrolled60Registered outcomes27Posted comparisons0ConditionsHeart Failure and Reduced Ejection Fraction, Obesity & Overweight, TirzepatideArmsPlacebo, Tirzepatide
Open the trial in the graph
3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Guideline
  2. Pooled it
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  14. Improving the Analysis of KCCQ Endpoints in Heart Failure Clinical Trials.Therapeutic innovation & regulatory science · 2026
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 13 institutions in 7 countries.

Mikhail N KosiborodDepartment of Cardiovascular Disease, Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City School of Medicine (M.N.K.).ORCID 0000-0002-3750-9789
Subodh VermaDivision of Cardiac Surgery, Li Ka Shing Knowledge Institute of St Michael's Hospital, Unity Health Toronto, University of Toronto, ON, Canada (S.V.).ORCID 0000-0002-4018-8533
Barry A BorlaugDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN (B.A.B.).ORCID 0000-0001-9375-0596
Javed ButlerBaylor Scott and White Research Institute, Dallas, TX (J.B.).ORCID 0000-0001-7683-4720
Melanie J DaviesDiabetes Research Centre, University of Leicester, and NIHR Leicester Biomedical Research Centre, UK (M.J.D.).
Thomas Jon JensenNovo Nordisk A/S, Søborg, Denmark (T.J.J., S.R., P.E.M.).
Søren RasmussenNovo Nordisk A/S, Søborg, Denmark (T.J.J., S.R., P.E.M.).
Peter Erlang MarstrandNovo Nordisk A/S, Søborg, Denmark (T.J.J., S.R., P.E.M.).
Mark C PetrieSchool of Cardiovascular and Metabolic Health, University of Glasgow, UK (M.C.P.).ORCID 0000-0002-6333-9496
Sanjiv J ShahDivision of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL (S.J.S.).ORCID 0000-0002-5655-8201
Hiroshi ItoDepartment of General Internal Medicine 3, Kawasaki Medical School, Okayama, Japan (H.I.).
Morten SchouDepartment of Cardiology, Herlev-Gentofte Hospital, University of Copenhagen, Herlev, Denmark (M.S.).ORCID 0000-0002-4271-2466
Vojtěch MelenovskýInstitute for Clinical and Experimental Medicine-IKEM, Prague, Czech Republic (V.M.).ORCID 0000-0001-8921-7078
Walter AbhayaratnaCollege of Health and Medicine, The Australian National University, Canberra, Australia (W.A.).ORCID 0000-0002-4908-0641
Dalane W KitzmanDepartment of Internal Medicine, Sections of Cardiovascular Medicine and Geriatrics, Wake Forest University School of Medicine, Winston-Salem, NC (D.W.K.).ORCID 0009-0000-5274-0826
STEP-HFpEF Trial Committees and Investigators
Novo Nordisk (Denmark) · DKAustralian National University · AUInstitute of Clinical and Experimental Medicine · CZKawasaki Medical School · JPMayo Clinic · USNorthwestern University · USSaint Luke's Health System · USSt. Michael's Hospital · CAUniversity of Copenhagen · DKUniversity of Glasgow · GBUniversity of Leicester · GBUniversity of Mississippi · USWake Forest University · US

Funding

Wake Forest Claude D. Pepper OAIC - RenewalP30AG021332 · WAKE FOREST UNIVERSITY HEALTH SCIENCES · 2002 to 2025
$7.7M
Physical Rehabilitation for Older Patients with Acute HFpEF-The REHAB-HFpEF TrialR01AG078153 · WAKE FOREST UNIVERSITY HEALTH SCIENCES · 2025 to 2025
$6.8M
HeartShare DeCODE-HF: Data translation center to Combine Omics, Deep phenotyping, and Electronic health records for Heart Failure subtypes and treatment targetsU54HL160273 · NORTHWESTERN UNIVERSITY · 2025 to 2025
$3.3M
EXERCISE INTOLERANCE IN ELDERLY DIASTOLIC HEART FAILURER01AG018915 · WAKE FOREST UNIVERSITY HEALTH SCIENCES · 2001 to 2004
$1.4M
Pulmonary Hypertension in Left Heart DiseaseR01HL162828 · MAYO CLINIC ROCHESTER · 2025 to 2025
$790k
Pepper OAIC Coordinating CenterU24AG059624 · WAKE FOREST UNIVERSITY HEALTH SCIENCES · 2025 to 2025
$640k
Wake Forest Atrium HeartShare Clinical CenterU01HL160272 · WAKE FOREST UNIVERSITY HEALTH SCIENCES · 2025 to 2025
$529k
Mayo Clinic HeartShare Clinical CenterU01HL160226 · MAYO CLINIC ROCHESTER · 2025 to 2025
$281k
NHLBI NIH HHS R01 HL107577NHLBI NIH HHS R01 HL127028NHLBI NIH HHS R01 HL128526NHLBI NIH HHS R01 HL140731NHLBI NIH HHS R01 HL149423NHLBI NIH HHS R01 HL162828NHLBI NIH HHS U01 HL160226NHLBI NIH HHS U01 HL160272NHLBI NIH HHS U54 HL160273NIA NIH HHS P30 AG021332NIA NIH HHS R01 AG018915NIA NIH HHS R01 AG045551NIA NIH HHS R01 AG078153NIA NIH HHS U01 AG076928NIA NIH HHS U24 AG059624
6 · The paper itself

Abstract

backgroundPatients with heart failure (HF) with preserved ejection fraction (HFpEF) and obesity experience a high burden of symptoms and functional impairment, and a poor quality of life. In the STEP-HFpEF trial (Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity), once-weekly semaglutide 2.4 mg improved symptoms, physical limitations, and exercise function, and reduced inflammation and body weight. This prespecified analysis investigated the effects of semaglutide on the primary and confirmatory secondary end points across the range of the Kansas City Cardiomyopathy Questionnaire (KCCQ) scores at baseline and on all key summary and individual KCCQ domains.

methodsSTEP-HFpEF randomly assigned 529 participants with symptomatic HF, an ejection fraction of ≥45%, and a body mass index of ≥30 kg/m

resultsBaseline median KCCQ-CSS across tertiles was 37, 59, and 77 points, respectively. Semaglutide consistently improved primary end points across KCCQ tertiles 1 to 3 (estimated treatment differences [95% CI]: for KCCQ-CSS, 10.7 [5.4 to 16.1], 8.1 [2.7 to 13.4], and 4.6 [-0.6 to 9.9] points; for body weight, -11 [-13.2 to -8.8], -9.4 [-11.5 to -7.2], and -11.8 [-14.0 to -9.6], respectively;

conclusionsIn patients with HFpEF and obesity, semaglutide produced large improvements in HF-related symptoms, physical limitations, exercise function, inflammation, body weight, and N-terminal pro-brain natriuretic peptide, regardless of baseline health status. The benefits of semaglutide extended to all key KCCQ domains. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT04788511.

Indexed as

Glucagon-Like PeptidesHeart FailureQuality of LifeHumansInflammationNatriuretic Peptide, BrainObesitySemaglutideStroke VolumeGlucagon-Like PeptidesNatriuretic Peptide, BrainSemaglutidehealth statusheart failure, diastolicobesityquality of lifesemaglutideweight loss

Identifiers

PMID37952180
PMCPMC10782938
OpenAlexW4388609165

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.