Evidence map›Paper›PMID 41569429›Full record

Trial reportCirculation. Heart failure2026

Association Between the 2022 AHA/ACC/HFSA Heart Failure Staging and Cardiovascular and Kidney Outcomes in Patients With Diabetes and Kidney Disease: A Post Hoc Analysis of the SCORED Randomized Controlled Trial.

Ayodele Odutayo, Deepak L Bhatt, Vikas S Sridhar, Michael Szarek, Christopher P Cannon, Lawrence A Leiter, Darren K McGuire, Julia B Lewis, Renato D Lopes, Benjamin M Scirica and 9 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Circulation. Heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Ayodele OdutayoSunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, ON, Canada (A.O.).ORCID 0000-0001-8619-5010
Deepak L BhattMount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY (D.L.B.).ORCID 0000-0002-1278-6245
Vikas S SridharUniversity Health Network (A.O., V.S.S., J.A.U., D.Z.I.C.), University of Toronto, ON, Canada.ORCID 0000-0001-7947-1822
Michael SzarekUniversity of Colorado Anschutz Medical Campus, Aurora (M.S.).ORCID 0000-0002-0046-0264
Christopher P CannonDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (C.P.C., B.M.S.).ORCID 0000-0003-4596-2791
Lawrence A LeiterUniversity of Toronto, ON, Canada (A.O., V.S.S., L.A.L., S.V., D.Z.I.C.).ORCID 0000-0002-1040-6229
Darren K McGuireUniversity of Texas Southwestern Medical Center and Parkland Health and Hospital System, Dallas (D.K.M.).ORCID 0000-0002-6412-7989
Julia B LewisVanderbilt University Medical Center, Nashville, TN (J.B.L.).ORCID 0000-0002-1530-7115
Renato D LopesDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC (R.D.L.).ORCID 0000-0003-2999-4961
Benjamin M SciricaDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (C.P.C., B.M.S.).ORCID 0000-0002-7093-7048
Kausik K RayDepartment of Primary Care and Public Health, Imperial Centre for Cardiovascular Disease Prevention, Imperial College London, United Kingdom (K.K.R.).ORCID 0000-0003-0508-0954
Michael J DaviesLexicon Pharmaceuticals Inc, The Woodlands, TX (M.J.D., P.B., M.G.).ORCID 0009-0008-4941-0883
Phillip BanksLexicon Pharmaceuticals Inc, The Woodlands, TX (M.J.D., P.B., M.G.).ORCID 0009-0001-7333-8374
Manon GirardLexicon Pharmaceuticals Inc, The Woodlands, TX (M.J.D., P.B., M.G.).ORCID 0009-0007-9254-6033
Subodh VermaUniversity of Toronto, ON, Canada (A.O., V.S.S., L.A.L., S.V., D.Z.I.C.).ORCID 0000-0002-4018-8533
Jacob A UdellUniversity Health Network (A.O., V.S.S., J.A.U., D.Z.I.C.), University of Toronto, ON, Canada.ORCID 0000-0001-7402-9584
Bertram PittUniversity of Michigan, Ann Arbor (B.P.).ORCID 0000-0001-7703-0345
Ph Gabriel StegAssistance Publique-Hôpitaux de Paris, Hôpital Bichat, INSERM U-1148, Université Paris-Cité, France (P.G.S.).ORCID 0000-0001-6896-2941
David Z I CherneyUniversity Health Network (A.O., V.S.S., J.A.U., D.Z.I.C.), University of Toronto, ON, Canada.ORCID 0000-0003-4164-0429

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 2022 American Heart Association/American College of Cardiology/Heart Failure Society of America heart failure (HF) classification incorporates cardiac biomarkers to identify early risk of HF. The HF stages may also guide the prognosis and management of cardiovascular and kidney-related events.

methodsSCORED (Effect of Sotagliflozin on Cardiovascular and Renal Events in Patients With Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk) was a randomized trial in diabetes with kidney disease comparing sotagliflozin versus placebo on cardiovascular death, HF hospitalizations, and urgent HF visits. SCORED participants were grouped by HF stage post hoc. Stage A: no HF, normal biomarkers (NT-proBNP [N-terminal pro-B-type natriuretic peptide] <125 pg/mL; high sensitivity cardiac troponin T [hs-cTnT] <14 ng/L), and normal cardiac structure/function. Stage B (pre-HF): no HF but elevated NT-proBNP, hs-cTnT, or abnormal cardiac structure/function. Stage C/D: symptomatic HF. End points include the primary composite (cardiovascular death and HF-related events), major adverse cardiovascular events, and kidney-related composites (≥50% decline in estimated glomerular filtration rate, kidney failure, or kidney death). Using competing-risk proportional hazards models, we examined the association between HF stage and these end points, and the effect of sotagliflozin versus placebo by HF stage.

resultsThere were 741 patients (7%) in stage A, 6560 (62%) in stage B (pre-HF), and 3283 (31%) in stage C/D (established HF). The median NT-proBNP and hs-cTnT increased with HF stage. Increasing HF stage was associated with a 2- to 4-fold increase in the primary outcome/major adverse cardiovascular events in the placebo group. The kidney-specific composite was 5-fold higher in stage B (pre-HF) versus stage A but similar in stages B and C/D. The effect of sotagliflozin versus placebo was similar, irrespective of HF stage (primary outcome: hazard ratio, 0.74 [95% CI, 0.63-0.88];

conclusionsIncreasing HF stage is associated with a higher risk of HF, major adverse cardiovascular events, and kidney events. Asymptomatic stage B (pre-HF) increased cardiovascular and renal events by >2- and 5-fold, respectively. The benefits of sotagliflozin are consistent, irrespective of HF stage.

Indexed as

Diabetes Mellitus, Type 2GlycosidesHeart FailureSodium-Glucose Transporter 2 InhibitorsAgedBiomarkersFemaleHumansMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsPyransRisk FactorsSeverity of Illness IndexTreatment OutcomeBiomarkersGlycosidesNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)PyransSodium-Glucose Transporter 2 Inhibitorssotagliflozinbiomarkerscoronary artery diseaseheart failurehypertrophyrenal insufficiency

Identifiers

PMID41569429
PMCPMC12986030

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.