Evidence map›Paper›PMID 39699681›Full record

SynthesisEuropean radiology2025

Diagnostic and prognostic value of quantitative cardiac magnetic resonance imaging biomarkers in systemic lupus erythematosus: a systematic review and meta-analysis.

Lévi-Dan Azoulay, Nadjia Kachenoura, Samia Boussouar, Etienne Charpentier, Alain Giron, Thomas Broussaud, Zahir Amoura, Alban Redheuil

Abstract readSystematic ReviewMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Lévi-Dan AzoulaySorbonne Université, Laboratoire d'Imagerie Biomédicale, Inserm, CNRS, Paris, France. levi-dan.azoulay@inserm.fr.ORCID http://orcid.org/0000-0001-7266-8614
Nadjia KachenouraSorbonne Université, Laboratoire d'Imagerie Biomédicale, Inserm, CNRS, Paris, France.
Samia BoussouarSorbonne Université, Assistance Publique-Hôpitaux de Paris, Unité d'Imagerie Cardiovasculaire et Thoracique (ICT), Institut de Cardiologie, Hôpital Pitié-Salpêtrière, Paris, France.
Etienne CharpentierSorbonne Université, Assistance Publique-Hôpitaux de Paris, Unité d'Imagerie Cardiovasculaire et Thoracique (ICT), Institut de Cardiologie, Hôpital Pitié-Salpêtrière, Paris, France.
Alain GironSorbonne Université, Laboratoire d'Imagerie Biomédicale, Inserm, CNRS, Paris, France.
Thomas BroussaudSorbonne Université, Assistance Publique-Hôpitaux de Paris, Service de Radiologie, Hôpital Pitié-Salpêtrière, Paris, France.
Zahir AmouraSorbonne Université, Assistance Publique-Hôpitaux de Paris, Service de Médecine Interne 2, Centre National de Référence du Lupus, Hôpital Pitié-Salpêtrière, Paris, France.
Alban RedheuilSorbonne Université, Laboratoire d'Imagerie Biomédicale, Inserm, CNRS, Paris, France.

Funding

Poste d'Accueil Inserm (PhD scholarship from the French National Institute of Health and Medical Research). None
6 · The paper itself

Abstract

objectivesThe aim of this study was to compare CMR imaging biomarkers between SLE patients and matched controls. MATERIALS AND

methodsElectronic databases were systematically searched from inception until November 2023. All studies reporting CMR imaging data in SLE patients were included. PRISMA guidelines were followed, and risk of bias was assessed using the Newcastle-Ottawa Quality Assessment Scale. CMR findings of SLE patients were compared to that of matched controls. Clinical features associated with CMR biomarkers were collected in a qualitative analysis.

resultsA total of 64 studies were included in the systematic review pooling 3304 individuals including 1870 SLE patients. Of these, 19 case-control studies were included in the comparative meta-analysis (1576 individuals, including 884 SLE patients). Compared to controls, left ventricular (LV) ejection fraction (62% vs. 64%, p = 0.001) and indexed end-diastolic volume (77 vs. 72 mL/m

conclusionsWhile CMR-assessed ventricular function and volumes only slightly differed in SLE patients when compared to controls, myocardial tissue characterization parameters were significantly modified and associated with disease activity. KEY POINTS: Question What are the diagnostic and prognostic values of cardiac magnetic resonance (CMR) quantitative parameters in systemic lupus erythematosus (SLE) patients? Findings Myocardial tissue characterization parameters are significantly altered in SLE patients and associated with disease activity. Clinical relevance CMR imaging demonstrates subclinical cardiac alterations in systemic lupus erythematosus patients. Additional studies are required to further demonstrate the prognostic value of CMR in SLE.

Indexed as

Lupus Erythematosus, SystemicMagnetic Resonance ImagingBiomarkersHumansPrognosisBiomarkersLupus erythematosus, SystemicMagnetic resonance imagingMeta-analysisSystematic review

Identifiers

What OpenQuestion holds

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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.