Evidence map›Paper›PMID 40008512›Full record

ArticleJournal of the American Heart Association2025

Extracellular Matrix Proteins Improve Risk Prediction in Patients Undergoing Transcatheter Aortic Valve Replacement.

Felicitas Boeckling, Tina Rasper, Lukas Zanders, Graziella Pergola, Sebastian Cremer, Silvia Mas-Peiro, Mariuca Vasa-Nicotera, David Leistner, Stefanie Dimmeler, Badder Kattih

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Molecular Mechanisms of Cardiac Adaptation After Device Deployment.Journal of cardiovascular development and disease · 2025
    Review
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

10 authors.

Felicitas BoecklingInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.
Tina RasperInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.
Lukas ZandersInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.
Graziella PergolaInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.
Sebastian CremerInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.
Silvia Mas-PeiroGerman Centre for Cardiovascular Research, Berlin Partner Site Frankfurt Rhine-Main Frankfurt Germany.ORCID 0000-0002-3828-8180
Mariuca Vasa-NicoteraGerman Centre for Cardiovascular Research, Berlin Partner Site Frankfurt Rhine-Main Frankfurt Germany.
David LeistnerDepartment of Cardiology Goethe University Frankfurt, University Hospital Frankfurt Germany.ORCID 0000-0002-4351-420X
Stefanie DimmelerInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.ORCID 0000-0002-1045-2436
Badder KattihInstitute for Cardiovascular Regeneration, Goethe University Frankfurt am Main Germany.ORCID 0000-0003-1324-5536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiac fibrosis is common in patients with severe aortic stenosis and an independent predictor of death. Therefore, we examined the additional value of circulating fibrosis markers as a putative biomarker platform to identify patients with aortic stenosis undergoing transcatheter aortic valve replacement (TAVR) who are at a higher risk of death.

methodsIn this study, 2-year survival analyses were conducted in 378 consecutive patients undergoing TAVR to evaluate the association between fibrosis marker and risk of adverse long-term outcome. Implementation of fibrosis marker into TAVR risk stratification was tested by a machine-learning algorithm.

resultsAmong 20 circulating fibrosis markers involved in pathological extracellular matrix remodeling, high tissue inhibitor of metalloproteinase-1 (TIMP-1) levels independently predicted risk of death in univariable (hazard ratio, 5.0 [95% CI, 2.6-9.7];

conclusionsCirculating TIMP-1 is an independent predictor of reduced 2-year overall survival in patients undergoing TAVR. Combined with high-sensitivity cardiac troponin T, circulating TIMP-1 should be incorporated into risk stratification to identify patients undergoing TAVR who are at a higher risk of death.

Indexed as

Aortic ValveAortic Valve StenosisExtracellular Matrix ProteinsTissue Inhibitor of Metalloproteinase-1Transcatheter Aortic Valve ReplacementAgedAged, 80 and overBiomarkersFemaleFibrosisHumansMachine LearningMalePredictive Value of TestsRetrospective StudiesRisk AssessmentBiomarkersExtracellular Matrix ProteinsTIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1biomarkerECMhs‐cTnTTAVR, TAVI, aortic stenosisTIMP‐1

Identifiers

PMID40008512
PMCPMC12132695

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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.