Evidence map›Paper›PMID 28784649›Full record

ArticleJournal of the American Heart Association2017

Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure.

Zhen-Yu Zhang, Susana Ravassa, Esther Nkuipou-Kenfack, Wen-Yi Yang, Shona M Kerr, Thomas Koeck, Archie Campbell, Tatiana Kuznetsova, Harald Mischak, Sandosh Padmanabhan and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-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

15 citing papers in PubMed, 40 citations in OpenAlex.

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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

13 authors at 6 institutions in 5 countries.

Zhen-Yu ZhangStudies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Belgium.
Susana RavassaProgram of Cardiovascular Diseases, Centre for Applied Medical Research, Navarra Institute for Health Research, University of Navarra, Pamplona, Spain.
Esther Nkuipou-KenfackMosaiques Diagnostics and Therapeutics AG, Hanover, Germany.
Wen-Yi YangStudies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Belgium.
Shona M KerrGeneration Scotland, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, United Kingdom.
Thomas KoeckMosaiques Diagnostics and Therapeutics AG, Hanover, Germany.
Archie CampbellGeneration Scotland, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, United Kingdom.
Tatiana KuznetsovaStudies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Belgium.
Harald MischakMosaiques Diagnostics and Therapeutics AG, Hanover, Germany.
Sandosh PadmanabhanInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Anna F DominiczakInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Christian DellesInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Jan A StaessenStudies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Belgium jan.staessen@med.kuleuven.be ja.staessen@maastrichtuniversity.nl.
KU Leuven · BEMosaiques Diagnostics and Therapeutics (Germany) · DEUniversity of Glasgow · GBCentro de Investigación en Red en Enfermedades Cardiovasculares · ESMRC Institute of Genetics and Molecular Medicine · GBUniversity of Edinburgh · GB

Funding

European Research Council 294713Medical Research Council MR/N005813/1
6 · The paper itself

Abstract

backgroundDetection of preclinical cardiac dysfunction and prognosis of left ventricular heart failure (HF) would allow targeted intervention, and appears to be the most promising approach in its management. Novel biomarker panels may support this approach and provide new insights into the pathophysiology. METHODS AND

resultsA retrospective comparison of urinary proteomic profiles generated by mass spectrometric analysis from 49 HF patients, 36 patients who progressed to HF within 2.6±1.6 years, and 192 sex- and age-matched controls who did not progress to HF enabled identification of 96 potentially HF-specific peptide biomarkers. Based on these 96 peptides, the classifier called Heart Failure Predictor (HFP) was established by support vector machine modeling. The incremental prognostic value of HFP was subsequently evaluated in urine samples from 175 individuals with asymptomatic diastolic dysfunction from an independent population cohort. Within 4.8 years, 17 of these individuals progressed to overt HF. The area under receiver-operating characteristic curve was 0.70 (95% CI, 0.56-0.82);

conclusionsHFP is a novel biomarker derived from the urinary proteome and might serve as a sensitive tool to improve risk stratification, patient management, and understanding of the pathophysiology of HF.

Indexed as

Decision Support TechniquesAgedArea Under CurveAsymptomatic DiseasesBiomarkersDisease ProgressionEuropeFemaleHeart FailureHumansIncidenceMaleMass SpectrometryMiddle AgedPeptidesPredictive Value of TestsBiomarkersPeptidesbiomarkerheart failureproteomicsrisk stratification

Identifiers

PMID28784649
PMCPMC5586413
OpenAlexW2742592217

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.