Evidence map›Paper›PMID 36627164›Full record

ArticleLife science alliance2023

Disease- and sex-specific differences in patients with heart valve disease: a proteome study.

Sarah Nordmeyer, Milena Kraus, Matthias Ziehm, Marieluise Kirchner, Marie Schafstedde, Marcus Kelm, Sylvia Niquet, Mariet Mathew Stephen, Istvan Baczko, Christoph Knosalla and 7 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Recent advances in omics-based research of mitral valve disease.Frontiers in cardiovascular medicine · 2026
    Review
  3. Article
  4. Review
  5. Article
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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

17 authors at 8 institutions in 4 countries.

Sarah NordmeyerDeutsches Herzzentrum der Charité - Medical Heart Center of Charité and German Heart Institute Berlin, Institute for Cardiovascular Computer-Assisted Medicine, Berlin, Germany snordmeyer@dhzb.de titus.kuehne@dhzb.de philipp.mertins@mdc-berlin.de.ORCID https://orcid.org/0000-0002-1111-2521
Milena KrausHasso Plattner Institute for Digital Engineering, Digital Health Center, University of Potsdam, Potsdam, Germany.ORCID https://orcid.org/0000-0002-4472-0427
Matthias ZiehmMax Delbrück Center for Molecular Medicine in the Helmholtz Association, Proteomics Platform, Berlin, Germany.ORCID https://orcid.org/0000-0001-7074-4054
Marieluise KirchnerMax Delbrück Center for Molecular Medicine in the Helmholtz Association, Proteomics Platform, Berlin, Germany.ORCID https://orcid.org/0000-0002-7049-534X
Marie SchafsteddeDeutsches Herzzentrum der Charité - Medical Heart Center of Charité and German Heart Institute Berlin, Institute for Cardiovascular Computer-Assisted Medicine, Berlin, Germany.ORCID https://orcid.org/0000-0002-4860-8010
Marcus KelmDeutsches Herzzentrum der Charité - Medical Heart Center of Charité and German Heart Institute Berlin, Institute for Cardiovascular Computer-Assisted Medicine, Berlin, Germany.
Sylvia NiquetMax Delbrück Center for Molecular Medicine in the Helmholtz Association, Proteomics Platform, Berlin, Germany.
Mariet Mathew StephenHasso Plattner Institute for Digital Engineering, Digital Health Center, University of Potsdam, Potsdam, Germany.
Istvan BaczkoDepartment of Pharmacology and Pharmacotherapy, Interdisciplinary Excellence Centre, University of Szeged, Szeged, Hungary.ORCID https://orcid.org/0000-0002-9588-0797
Christoph KnosallaGerman Center for Cardiovascular Research (DZHK), Partner Site Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-8127-5019
Matthieu-P SchapranowHasso Plattner Institute for Digital Engineering, Digital Health Center, University of Potsdam, Potsdam, Germany.ORCID https://orcid.org/0000-0001-6601-2942
Gunnar DittmarProteomics of Cellular Signaling, Luxembourg Institute of Health, Strassen, Luxembourg.ORCID https://orcid.org/0000-0003-3647-8623
Michael GotthardtGerman Center for Cardiovascular Research (DZHK), Partner Site Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0003-1788-3172
Martin FalckeMax Delbrück Center for Molecular Medicine, Mathematical Cell Physiology, Berlin, Germany.ORCID https://orcid.org/0000-0001-7137-1114
Vera Regitz-ZagrosekCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Titus KuehneDeutsches Herzzentrum der Charité - Medical Heart Center of Charité and German Heart Institute Berlin, Institute for Cardiovascular Computer-Assisted Medicine, Berlin, Germany snordmeyer@dhzb.de titus.kuehne@dhzb.de philipp.mertins@mdc-berlin.de.
Philipp MertinsGerman Center for Cardiovascular Research (DZHK), Partner Site Berlin, Berlin, Germany snordmeyer@dhzb.de titus.kuehne@dhzb.de philipp.mertins@mdc-berlin.de.ORCID https://orcid.org/0000-0002-2245-528X
Max Delbrück Center · DEHasso Plattner Institute · DEGerman Centre for Cardiovascular Research · DEHumboldt-Universität zu Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DELuxembourg Institute of Health · LUUniversity of Szeged · HUUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pressure overload in patients with aortic valve stenosis and volume overload in mitral valve regurgitation trigger specific forms of cardiac remodeling; however, little is known about similarities and differences in myocardial proteome regulation. We performed proteome profiling of 75 human left ventricular myocardial biopsies (aortic stenosis = 41, mitral regurgitation = 17, and controls = 17) using high-resolution tandem mass spectrometry next to clinical and hemodynamic parameter acquisition. In patients of both disease groups, proteins related to ECM and cytoskeleton were more abundant, whereas those related to energy metabolism and proteostasis were less abundant compared with controls. In addition, disease group-specific and sex-specific differences have been observed. Male patients with aortic stenosis showed more proteins related to fibrosis and less to energy metabolism, whereas female patients showed strong reduction in proteostasis-related proteins. Clinical imaging was in line with proteomic findings, showing elevation of fibrosis in both patient groups and sex differences. Disease- and sex-specific proteomic profiles provide insight into cardiac remodeling in patients with heart valve disease and might help improve the understanding of molecular mechanisms and the development of individualized treatment strategies.

Indexed as

Aortic Valve StenosisHeart Valve DiseasesMitral Valve InsufficiencyFemaleFibrosisHumansMaleProteomeProteomicsSex CharacteristicsVentricular RemodelingProteome

Identifiers

PMID36627164
PMCPMC9834574
OpenAlexW4315478617

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.