Evidence map›Paper›PMID 26008895›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2015

Endomyocardial expression of SDF-1 predicts mortality in patients with suspected myocarditis.

Christine S Zuern, Britta Walker, Martina Sauter, Malte Schaub, Madhumita Chatterjee, Karin Mueller, Dominik Rath, Sebastian Vogel, Roland Tegtmeyer, Peter Seizer and 6 more

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Article in Clinical research in cardiology : official journal of the German Cardiac Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

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  4. DPP4 Inhibition, NPYThe Journal of pharmacology and experimental therapeutics · 2020
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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

16 authors at 1 institution in 1 country.

Christine S ZuernDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany. christine.zuern@gmx.de.
Britta WalkerDepartment of Physiology, University of Tuebingen, Gmelinstr. 5, 72076, Tuebingen, Germany.
Martina SauterDepartment of Molecular Pathology, University of Tuebingen, Liebermeisterstr. 8, 72076, Tuebingen, Germany.
Malte SchaubDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Madhumita ChatterjeeDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Karin MuellerDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Dominik RathDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Sebastian VogelDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Roland TegtmeyerDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Peter SeizerDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Tobias GeislerDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
Reinhard KandolfDepartment of Molecular Pathology, University of Tuebingen, Liebermeisterstr. 8, 72076, Tuebingen, Germany.
Florian LangDepartment of Physiology, University of Tuebingen, Gmelinstr. 5, 72076, Tuebingen, Germany.
Karin KlingelDepartment of Molecular Pathology, University of Tuebingen, Liebermeisterstr. 8, 72076, Tuebingen, Germany.
Meinrad GawazDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany. meinrad.gawaz@med.uni-tuebingen.de.
Oliver BorstDepartment of Cardiology and Cardiovascular Medicine, University of Tuebingen, Otfried-Mueller-Str. 10, 72076, Tuebingen, Germany.
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRisk stratification in patients with suspected myocarditis is pivotal for optimizing therapy. Stromal cell-derived factor 1 (SDF-1) is an inflammatory chemokine expressed in the inflamed and failing myocardium. Therefore, we aimed to investigate whether endomyocardial expression of SDF-1 identifies high-risk patients with suspected myocarditis. METHODS AND

resultsWe prospectively enrolled 174 patients with non-ischemic HF who underwent endomyocardial biopsy for suspected myocarditis. Biopsies were analyzed using established histopathological and immunohistological criteria together with SDF-1 staining. SDF-1 was significantly enhanced in patients with inflammatory cardiomyopathy (65.4 % positive biopsies) as compared to patients with non-inflammatory cardiomyopathy (19.1 %, p < 0.001). SDF-1 expression levels correlated significantly with the degree of myocardial fibrosis (correlation coefficient r = 0.196; p = 0.010) since patients with severe myocardial fibrosis displayed high myocardial SDF-1 expression. During a mean follow-up of 27.5 months, 20 patients (11.5 %) died. The 4-year mortality rate was 26.0 % among the 92 SDF-1-positive patients vs. 9.5 % among the 82 SDF-1-negative patients (p = 0.001). On multivariable analysis which considered clinical (NYHA functional class, left ventricular ejection fraction), laboratory (brain natriuretic peptide, troponin I) and biopsy staining, SDF-1 was the strongest independent predictor of mortality (hazard ratio 6.1; 95 % confidence interval 1.4-27.5; p = 0.018). Subgroup analysis revealed SDF-1 as a predictor of mortality in both patients with inflammatory and non-inflammatory cardiomyopathy.

conclusionsEndomyocardial expression of SDF-1 is enhanced in inflammatory cardiomyopathy, positively correlates with myocardial fibrosis and identifies high-risk patients with suspected myocarditis.

Indexed as

AdultAgedBiopsyChemokine CXCL12FemaleFibrosisFollow-Up StudiesHumansInflammationMaleMiddle AgedMultivariate AnalysisMyocarditisMyocardiumProspective StudiesRiskChemokine CXCL12BiomarkerCardiomyopathyEndomyocardial biopsyMyocarditisSDF-1

Identifiers

PMID26008895
OpenAlexW415193906

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Registered trials

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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.