Evidence map›Paper›PMID 36979791›Full record

ArticleBiomedicines2023

Circulating Biomarkers of Fibrosis Formation in Patients with Arrhythmogenic Cardiomyopathy.

Stephanie M van der Voorn, Mimount Bourfiss, Steven A Muller, Tolga Çimen, Ardan M Saguner, Firat Duru, Anneline S J M Te Riele, Carol Ann Remme, Toon A B van Veen

Open access · goldFull text read
In one paragraph

Article in Biomedicines, 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. Review
  3. Article
  4. Article
  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

9 authors at 4 institutions in 2 countries.

Stephanie M van der VoornDepartment of Medical Physiology, Division Heart & Lungs, University Medical Center Utrecht, 3584 CM Utrecht, The Netherlands.ORCID 0000-0003-0934-3491
Mimount BourfissDepartment of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.
Steven A MullerDepartment of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.ORCID 0000-0002-2674-8709
Tolga ÇimenDepartment of Cardiology, University Heart Center Zurich, University Hospital Zurich, CH-8091 Zurich, Switzerland.
Ardan M SagunerDepartment of Cardiology, University Heart Center Zurich, University Hospital Zurich, CH-8091 Zurich, Switzerland.ORCID 0000-0003-1896-0803
Firat DuruDepartment of Cardiology, University Heart Center Zurich, University Hospital Zurich, CH-8091 Zurich, Switzerland.ORCID 0000-0002-4748-0158
Anneline S J M Te RieleDepartment of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.ORCID 0000-0002-4694-4790
Carol Ann RemmeDepartment of Clinical and Experimental Cardiology, Heart Centre, Amsterdam UMC, Location Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.ORCID 0000-0003-0095-0084
Toon A B van VeenDepartment of Medical Physiology, Division Heart & Lungs, University Medical Center Utrecht, 3584 CM Utrecht, The Netherlands.
University Medical Center Utrecht · NLUniversity Hospital of Zurich · CHAmsterdam UMC Location University of Amsterdam · NLUniversity of Zurich · CH

Funding

Hartstichting CVON-eDETECT 2015-12Netherlands Federation of University Medical Centres CVON-eDETECT 2015-12Netherlands Organisation for Health Research and Development CVON-eDETECT 2015-12Royal Netherlands Academy of Arts and Sciences CVON-eDETECT 2015-12Swiss Heart Foundation FF17019 and FF21073Swiss National Science Foundation 160327USZ Foundation Dr. Wild GrantZonMW Off Road FUEL CARDIOMYOPATHY 2021
6 · The paper itself

Abstract

Arrhythmogenic cardiomyopathy (ACM) is a progressive inheritable disease which is characterized by a gradual fibro-(fatty) replacement of the myocardium. Visualization of diffuse and patchy fibrosis patterns is challenging using clinically applied cardiac imaging modalities (e.g., late gadolinium enhancement, LGE). During collagen synthesis and breakdown, carboxy-peptides are released into the bloodstream, specifically procollagen type-I carboxy-terminal propeptides (PICP) and collagen type-I carboxy-terminal telopeptides (ICTP). We collected the serum and EDTA blood samples and clinical data of 45 ACM patients (age 50.11 ± 15.53 years, 44% female), divided into 35 diagnosed ACM patients with a 2010 ARVC Task Force Criteria score (TFC) ≥ 4, and 10 preclinical variant carriers with a TFC < 4. PICP levels were measured using an enzyme-linked immune sorbent assay and ICTP levels with a radio immunoassay. Increased PICP/ICTP ratios suggest a higher collagen deposition. We found significantly higher PICP and PICP/ICTP levels in diagnosed patients compared to preclinical variant carriers (

Indexed as

arrhythmogenic cardiomyopathy (ACM)biomarkerscollagenfibrosis

Identifiers

PMID36979791
PMCPMC10045011
OpenAlexW4323569710

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read21
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.