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ISSN Approved Journal || eISSN: 2582-8185 || CODEN: IJSRO2 || Impact Factor 8.2 || Google Scholar and CrossRef Indexed

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Research and review articles are invited for publication in January 2026 (Volume 18, Issue 1)

Interest of Cardiac MRI in the Etiological Diagnosis of Dilated Cardiomyopathies: About 45 Cases

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  • Interest of Cardiac MRI in the Etiological Diagnosis of Dilated Cardiomyopathies: About 45 Cases

Nadia LOUDIYI 1, *, Siham BELLOUIZE 2, Achraf ZAIMI 1, Mohamed MALKI 1, Najat MOUINE 1 and Atif BENYASS 1

1 Department of Cardiology, Military Instruction Hospital Mohammed V, Rabat, Morocco. 

2 Department of Cardiovascular Surgery, Military Instruction Hospital Mohammed V Rabat, Morocco.

Research Article

International Journal of Science and Research Archive, 2025, 17(01), 686-690

Article DOI: 10.30574/ijsra.2025.17.1.2779

DOI url: https://doi.org/10.30574/ijsra.2025.17.1.2779

Received on 03September 2025; revised on 11 October 2025; accepted on 13 October 2025

Dilated cardiomyopathies (DCM) represent a heterogeneous group of disorders characterized by dilation and systolic impairment of the left or both ventricles. Identifying the underlying etiology is crucial for guiding management, assessing prognosis, and orienting therapeutic strategies. Cardiac magnetic resonance imaging (CMR) plays a central role thanks to its morphological, functional, and tissue characterization capabilities.

Objective: To evaluate the contribution of CMR in the etiological identification of dilated cardiomyopathies.

Methods: A retrospective study was conducted on 45 patients with echocardiographically documented DCM who underwent cardiac MRI.

Results: CMR provided accurate assessment of ventricular function and chamber dilation. Analysis of late gadolinium enhancement (LGE) and mapping sequences contributed to distinguishing ischemic causes (15 cases) from non-ischemic forms (30 cases: myocarditis, idiopathic/genetic DCM, infiltrative etiologies). MRI also provided prognostic insights by characterizing the extent and distribution of myocardial fibrosis.

Conclusion: Cardiac MRI is an essential tool in the etiological diagnosis of DCM, allowing better therapeutic orientation and risk stratification.

Cardiac MRI; Dilated cardiomyopathie ; Etiology; Myocardial fibrosis; Tissue characterization 

https://journalijsra.com/sites/default/files/fulltext_pdf/IJSRA-2025-2779.pdf

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Nadia LOUDIYI, Siham BELLOUIZE, Achraf ZAIMI, Mohamed MALKI, Najat MOUINE and Atif BENYASS. Interest of Cardiac MRI in the Etiological Diagnosis of Dilated Cardiomyopathies: About 45 Cases. International Journal of Science and Research Archive, 2025, 17(01), 686-690. Article DOI: https://doi.org/10.30574/ijsra.2025.17.1.2779.

Copyright © 2025 Author(s) retain the copyright of this article. This article is published under the terms of the Creative Commons Attribution Liscense 4.0

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