Evidence map›Paper›PMID 41716719›Full record

ArticleInternational journal of cardiology. Heart & vasculature2026

Staging of Fabry cardiomyopathy in clinical practice: an algorithm proposal.

Inês Fortuna, Janete Santos, Raquel Machado, André Lobo, Conceição Queirós, Cristina Gavina, Natália António, Patrícia Rodrigues, Ricardo Fontes-Carvalho, Sofia Correia and 2 more

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Article in International journal of cardiology. Heart & vasculature, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Inês FortunaFaculty of Medicine, University of Porto, Portugal.
Janete SantosFaculty of Medicine, University of Porto, Portugal.
Raquel MachadoFaculty of Medicine, University of Porto, Portugal.
André LoboULS Gaia e Espinho, Portugal.
Conceição QueirósCentro Hospitalar Tâmega e Sousa, Portugal.
Cristina GavinaULS de Matosinhos, Portugal.
Natália AntónioULS Coimbra, Portugal.
Patrícia RodriguesCentro Hospitalar Universitário de Santo António, Portugal.
Ricardo Fontes-CarvalhoULS Gaia e Espinho, Portugal.
Sofia CorreiaULS de Matosinhos, Portugal.
Giuseppe LimongelliDipartimento di Scienze Cardio-Toraciche e Respiratorie, Università della Campania "Luigi Vanvitelli", AORN Colli, Ospedale Monaldi, Naples, Italy.
Elisabete MartinsDepartment of Cardiology, Centro Hospitalar Universitário de São João, E.P.E., Porto, Portugal, Member of the European Reference Network for Rare, Low-Prevalence, or Complex Diseases of the Heart (ERN GUARD-Heart), Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Fabry disease (FD) is characterized by hypertrophic cardiomyopathy and early diagnosis is essential, considering the response to enzyme replacement or chaperone therapies. Recently, a new clinical staging for Fabry cardiomyopathy suggested five stages (0A, 0B, IA, IB, II, III), where the imaging characterization of hypertrophy and fibrosis are critical key items. Our study aimed to evaluate the applicability of the recent proposal of Meucci et al. 2024 in patients with FD, considering the last imaging cardiac evaluations. Methods: This retrospective observational study collected clinical data from patients diagnosed with FD. Staging system followed a hierarchical flowchart, staging patients based on LVEF, LGE, LV wall thickness, and other cardiac findings (symptoms, ECG/Echo/CMR abnormalities). Results: We included 53 FD patients. As cardiac magnetic resonance and echocardiogram parameters are essential to complete staging, the algorithm was fully applied to 44 patients. Among these patients, the majority (29,5%) were in the non-hypertrophic stage 0. In hypertrophic stage I, 27,2% of patients were classified according to the maximum wall thickness. The hypertrophic fibrotic stage II included 29,5% of the patients. Patients in stage III (13,6%) presented diffuse myocardial fibrosis ≥ 3 LV segments and/or impaired systolic function (LVEF < 50%). Conclusion: The staging scheme allows us to classify different stages of FD cardiomyopathy. Most patients were in early disease stages, probably related to the diagnosis in the context of familial screening. The stepwise algorithm proposal helped apply the staging in clinical practice; however, it must be validated in more extensive and prospective studies.

Indexed as

Classification algorithmFabry diseaseHypertrophic cardiomyopathyStaging

Identifiers

PMID41716719
PMCPMC12914314

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