Evidence map›Paper›PMID 36747201›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance2023

Prognostic value of cardiovascular magnetic resonance T1 mapping and extracellular volume fraction in nonischemic dilated cardiomyopathy.

Farah Cadour, Morgane Quemeneur, Loic Biere, Erwan Donal, Zakarya Bentatou, Jean-Christophe Eicher, François Roubille, Alain Lalande, Roch Giorgi, Stanislas Rapacchi and 20 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02352129 (Prognostic Value of Myocardial Fibrosis Quantified Using CMR in Patient With Dilated Cardiomyopathy), which is not on this map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing 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.

NCT02352129 nacompletednot on this map

Prognostic Value of Myocardial Fibrosis Quantified Using CMR in Patient With Dilated Cardiomyopathy

TypeinterventionalSponsorAssistance Publique Hopitaux De MarseilleRan2011 to 2017Enrolled262ConditionsCardiomyopathy, DilatedArmsCMR using T1 mapping technique
3 · Its place in the literature

Who cites it

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

  1. Pooled it
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  12. A prognostically meaningful definition of non-dilated left ventricular cardiomyopathy.The international journal of cardiovascular imaging · 2025
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  13. Observational
  14. Article
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  17. Tissue characterization using cardiac magnetic resonance imaging and response to cardiac resynchronization therapy.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    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

30 authors.

Farah CadourCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Morgane QuemeneurCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Loic BiereDepartment of Cardiology, University Hospital of Angers, 49000, Angers, France.
Erwan DonalDepartment of Cardiology, Inserm, LTSI-UMR 1099, CHU Rennes, Univ Rennes, 35000, Rennes, France.
Zakarya BentatouCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Jean-Christophe EicherCardiology Department, University Hospital François Mitterrand, Dijon, France.
François RoubillePhyMedExp, INSERM, CNRS, Cardiology Department, INI-CRT, CHU de Montpellier, Université de Montpellier, Montpellier, France.
Alain LalandeImViA Laboratory, University of Burgundy, 7 Bld Jeanne d'arc, 21000, Dijon, France.
Roch GiorgiAPHM, INSERM, IRD, SESSTIM, Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, ISSPAM, Hop Timone, BioSTICBiostatistique et Technologies de l'Information et de la Communication, Aix Marseille Univ, Marseille, France.
Stanislas RapacchiCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Sébastien CortaredonaIRD, AP-HM, SSA, VITROME, Aix Marseille Univ, Marseille, France.
Farouk TradiCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Axel BartoliCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Serge WilloteauxUMR CNRS 6015-INSERMU1083, Institut Mitovasc, University of Angers, 49000, Angers, France.
François DelahayeDepartment of Cardiology, Hospices civils de Lyon, 69002, Lyon, France.
Stephanie M BieneDepartment of Radiology, CH d'Annecy, 74370, Annecy, France.
Lionel ManginDepartment of Cardiology, CH d'Annecy, 74370, Annecy, France.
Nadine FerrierDepartment of Cardiology, CH de Vichy, 03207, Vichy, France.
Jean-Nicolas DacherDepartment of Radiology, UNIROUEN, Inserm U1096, CHU de Rouen, 76000, Rouen, France.
Fabrice BauerINSERM U 1096, Cardiovascular Surgery Department, Pulmonary Hypertension and Advanced Heart Failure Clinic, Rouen University Hospital, Rouen, France.
Guillaume LeurentDepartment of Cardiology, Inserm, LTSI-UMR 1099, CHU Rennes, Univ Rennes, 35000, Rennes, France.
Pierre-Axel LentzDepartment of Radiology, University Hospital Pontchaillou, Rennes, France.
Hélène KovacsikDepartement of Cardiovascular Imaging, Chu Montpellier, Montpellier, France.
Pierre CroisilleDepartment of Radiology, University Hospital Saint-Etienne, Saint-Étienne, France.
Franck ThunyUnit of Heart Failure and Valvular Heart Diseases, Inserm 1263, Inrae 1260, Department of Cardiology, North Hospital, Assistance Publique - Hôpitaux de Marseille, Centre for CardioVascular and Nutrition Research (C2VN), University Mediterranean Center of Cardio-Oncology, Aix-Marseille University, Marseille, France.
Monique BernardCNRS, CRMBM, Aix-Marseille University, Marseille, France. monique.bernard@univ-amu.fr.ORCID 0000-0002-3179-8698
Maxime GuyeCNRS, CRMBM, Aix-Marseille University, Marseille, France.
Alain FurberDepartment of Cardiology, University Hospital of Angers, 49000, Angers, France.
Gilbert HabibCardiology Department, IRD, APHM, MEPHI, IHU-Méditerranée Infection, APHM, La Timone Hospital, Aix Marseille Univ, Marseille, France.
Alexis JacquierCNRS, CRMBM, Aix-Marseille University, Marseille, France.

Funding

PHRC PHRC 2011-A00887-34
6 · The paper itself

Abstract

backgroundHeart failure- (HF) and arrhythmia-related complications are the main causes of morbidity and mortality in patients with nonischemic dilated cardiomyopathy (NIDCM). Cardiovascular magnetic resonance (CMR) imaging is a noninvasive tool for risk stratification based on fibrosis assessment. Diffuse interstitial fibrosis in NIDCM may be a limitation for fibrosis assessment through late gadolinium enhancement (LGE), which might be overcome through quantitative T1 and extracellular volume (ECV) assessment. T1 and ECV prognostic value for arrhythmia-related events remain poorly investigated. We asked whether T1 and ECV have a prognostic value in NIDCM patients.

methodsThis prospective multicenter study analyzed 225 patients with NIDCM confirmed by CMR who were followed up for 2 years. CMR evaluation included LGE, native T1 mapping and ECV values. The primary endpoint was the occurrence of a major adverse cardiovascular event (MACE) which was divided in two groups: HF-related events and arrhythmia-related events. Optimal cutoffs for prediction of MACE occurrence were calculated for all CMR quantitative values.

resultsFifty-eight patients (26%) developed a MACE during follow-up, 42 patients (19%) with HF-related events and 16 patients (7%) arrhythmia-related events. T1 Z-score (p = 0.008) and global ECV (p = 0.001) were associated with HF-related events occurrence, in addition to left ventricular ejection fraction (p < 0.001). ECV > 32.1% (optimal cutoff) remained the only CMR independent predictor of HF-related events occurrence (HR 2.15 [1.14-4.07], p = 0.018). In the arrhythmia-related events group, patients had increased native T1 Z-score and ECV values, with both T1 Z-score > 4.2 and ECV > 30.5% (optimal cutoffs) being independent predictors of arrhythmia-related events occurrence (respectively, HR 2.86 [1.06-7.68], p = 0.037 and HR 2.72 [1.01-7.36], p = 0.049).

conclusionsECV was the sole independent predictive factor for both HF- and arrhythmia-related events in NIDCM patients. Native T1 was also an independent predictor in arrhythmia-related events occurrence. The addition of ECV and more importantly native T1 in the decision-making algorithm may improve arrhythmia risk stratification in NIDCM patients. Trial registration NCT02352129. Registered 2nd February 2015-Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT02352129.

Indexed as

Cardiomyopathy, DilatedHeart FailureContrast MediaFibrosisGadoliniumHumansMagnetic Resonance Imaging, CineMagnetic Resonance SpectroscopyMyocardiumPredictive Value of TestsPrognosisProspective StudiesStroke VolumeVentricular Function, LeftContrast MediaGadoliniumCardiac magnetic resonanceExtracellular volume (ECV)Late gadolinium enhancementMyocardial fibrosisNative T1Nonischemic dilated cardiomyopathyPrognostic value

Identifiers

PMID36747201
PMCPMC9900939

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Registered trials

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.