Evidence map›Paper›PMID 27798759›Full record

Trial reportJournal of cardiovascular translational research2016

Soluble ST2 and Risk of Arrhythmias, Heart Failure, or Death in Patients with Mildly Symptomatic Heart Failure: Results from MADIT-CRT.

Hicham Skali, Robert Gerwien, Timothy E Meyer, James V Snider, Scott D Solomon, Craig M Stolen

Abstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of cardiovascular translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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.

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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Myocardial-alternation index (MMI) is correlated with soluble suppression of tumorigenecity-2 (sST2) in patients with ischemic cardiomyopathy.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2025
    Article
  5. Review
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  7. Article
  8. Review
  9. Article
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  11. Review
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  13. Article
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  15. Article
  16. IL-33/ST2 Axis in Organ Fibrosis.Frontiers in immunology · 2018
    Review
  17. 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

6 authors at 3 institutions in 1 country.

Hicham SkaliCardiovascular Division, Brigham and Women's Hospital, 75 Francis St., Boston, MA, 02115, USA. hskali@post.harvard.edu.
Robert GerwienCritical Diagnostics, San Diego, CA, USA.
Timothy E MeyerBoston Scientific, St. Paul, MN, USA.
James V SniderCritical Diagnostics, San Diego, CA, USA.
Scott D SolomonCardiovascular Division, Brigham and Women's Hospital, 75 Francis St., Boston, MA, 02115, USA.
Craig M StolenBoston Scientific, St. Paul, MN, USA. craig.stolen@bsci.com.
Boston Scientific (United States) · USBrigham and Women's Hospital · USCritical Innovations (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble ST2 is an established biomarker of heart failure (HF) progression. Data about its prognostic implications in patients with mildly symptomatic HF eligible to receive cardiac resynchronization therapy defibrillators (CRT-D) are limited. In a cohort of 684 patients enrolled in Multicenter Automated Defibrillator Implantation Trial (MADIT)-CRT, levels of soluble ST2 (sST2) were serially assessed at baseline and 1 year (n = 410). In multivariable-adjusted models, elevated baseline sST2 was associated with an increased risk of death, death or HF, and death or ventricular arrhythmia (VA) even when adjusting for baseline brain natriuretic protein (BNP) levels. In addition, patients with lower baseline sST2 levels had greater risk reduction with CRT-D (p = 0.006). Serial assessment revealed increased risk of VA and death or VA (HR per 10 % increase in sST2 1.11 (1.04-1.20), p = 0.004). Among patients with mildly symptomatic HF and eligibility for CRT-D, baseline and serial assessments sST2 may provide important information for risk stratification.

Indexed as

AgedArrhythmias, CardiacBiomarkersCardiac Resynchronization TherapyDefibrillators, ImplantableDisease ProgressionElectric CountershockFemaleHeart FailureHumansInterleukin-1 Receptor-Like 1 ProteinKaplan-Meier EstimateMaleMiddle AgedMultivariate AnalysisNatriuretic Peptide, BrainBiomarkersIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinNatriuretic Peptide, BrainArrhythmiaBiomarkerCardiac resynchronization therapy (CRT)Heart failureImplantable cardioverter defibrillator (ICD)PrognosisST2Sudden cardiac death

Identifiers

PMID27798759
OpenAlexW2542064944

What OpenQuestion holds

Textmetadata
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.