Evidence map›Paper›PMID 35861824›Full record

ArticleJournal of the American Heart Association2022

Candidate Plasma Biomarkers to Detect Anthracycline-Related Cardiomyopathy in Childhood Cancer Survivors: A Case Control Study in the Dutch Childhood Cancer Survivor Study.

Jan M Leerink, Elizabeth A M Feijen, Perry D Moerland, Esmee C de Baat, Remy Merkx, Helena J H van der Pal, Wim J E Tissing, Marloes Louwerens, Marry M van den Heuvel-Eibrink, A Birgitta Versluys and 13 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Article
  5. Cardiotoxicity induced by traditional chemotherapy: mechanisms and mitigation strategies.Apoptosis : an international journal on programmed cell death · 2026
    Review
  6. 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

23 authors at 8 institutions in 3 countries.

Jan M LeerinkDepartment of Cardiology, Amsterdam Cardiovascular Sciences Amsterdam University Medical Center, University of Amsterdam, Heart Center Amsterdam The Netherlands.ORCID 0000-0002-9413-8478
Elizabeth A M FeijenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Perry D MoerlandBioinformatics Laboratory, Department of Epidemiology and Data Science Amsterdam University Medical Center, University of Amsterdam Amsterdam The Netherlands.
Esmee C de BaatPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Remy MerkxDepartment of Medical Imaging Radboud University Medical Center Nijmegen The Netherlands.ORCID 0000-0002-9853-7257
Helena J H van der PalPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Wim J E TissingPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Marloes LouwerensDepartment of Internal Medicine Leiden University Medical Center Leiden The Netherlands.ORCID 0000-0002-6748-3540
Marry M van den Heuvel-EibrinkPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.ORCID 0000-0002-7760-879X
A Birgitta VersluysPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Folkert W AsselbergsDivision of Heart and Lungs, Department of Cardiology University Medical Center Utrecht Utrecht The Netherlands.ORCID 0000-0002-1692-8669
Arjan SammaniDivision of Heart and Lungs, Department of Cardiology University Medical Center Utrecht Utrecht The Netherlands.ORCID 0000-0002-5557-9342
Arco J TeskeDivision of Heart and Lungs, Department of Cardiology University Medical Center Utrecht Utrecht The Netherlands.
Elvira C van DalenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.ORCID 0000-0002-8886-6532
Margriet van der Heiden-van der LooPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Eline van Dulmen-den BroederDepartment of Pediatric Oncology Amsterdam University Medical Center, Vrije Universiteit Amsterdam The Netherlands.
Andrica C H de VriesPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Livia KapustaDepartment of Pediatric Cardiology Amalia Children's Hospital, Radboud University Medical Center Nijmegen The Netherlands.
Jacqueline LoonenDepartment of Hematology Radboud University Medical Center Nijmegen The Netherlands.
Yigal M PintoDepartment of Cardiology, Amsterdam Cardiovascular Sciences Amsterdam University Medical Center, University of Amsterdam, Heart Center Amsterdam The Netherlands.
Leontien C M KremerPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.ORCID 0000-0001-7422-3248
Annelies M C Mavinkurve-GroothuisPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Wouter E M KokDepartment of Cardiology, Amsterdam Cardiovascular Sciences Amsterdam University Medical Center, University of Amsterdam, Heart Center Amsterdam The Netherlands.ORCID 0000-0002-7789-6285
Princess Máxima Center · NLUniversity Medical Center Utrecht · NLAmsterdam University Medical Centers · NLRadboud University Nijmegen · NLErasmus MC · NLLeiden University Medical Center · NLUniversity Medical Center Groningen · NLUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Plasma biomarkers may aid in the detection of anthracycline-related cardiomyopathy (ACMP). However, the currently available biomarkers have limited diagnostic value in long-term childhood cancer survivors. This study sought to identify diagnostic plasma biomarkers for ACMP in childhood cancer survivors. Methods and Results We measured 275 plasma proteins in 28 ACMP cases with left ventricular ejection fraction <45%, 29 anthracycline-treated controls with left ventricular ejection fraction ≥53% matched on sex, time after cancer, and anthracycline dose, and 29 patients with genetically determined dilated cardiomyopathy with left ventricular ejection fraction <45%. Multivariable linear regression was used to identify differentially expressed proteins. Elastic net model, including clinical characteristics, was used to assess discrimination of proteins diagnostic for ACMP. NT-proBNP (N-terminal pro-B-type natriuretic peptide) and the inflammatory markers CCL19 (C-C motif chemokine ligands 19) and CCL20, PSPD (pulmonary surfactant protein-D), and PTN (pleiotrophin) were significantly upregulated in ACMP compared with controls. An elastic net model selected 45 proteins, including NT-proBNP, CCL19, CCL20 and PSPD, but not PTN, that discriminated ACMP cases from controls with an area under the receiver operating characteristic curve (AUC) of 0.78. This model was not superior to a model including NT-proBNP and clinical characteristics (AUC=0.75;

Indexed as

Cancer SurvivorsCardiomyopathiesCardiomyopathy, DilatedNeoplasmsAnthracyclinesAntibiotics, AntineoplasticBiomarkersCase-Control StudiesChildHumansNatriuretic Peptide, BrainPeptide FragmentsStroke VolumeVentricular Function, LeftAnthracyclinesAntibiotics, AntineoplasticBiomarkersNatriuretic Peptide, BrainPeptide Fragmentsanthracycline‐related cardiomyopathybiomarkerscancer therapy–related cardiac dysfunctioncardio‐oncologychemokine ligandschildhood cancer survivors

Identifiers

PMID35861824
PMCPMC9707839
OpenAlexW4285085284

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.