Prognostic value of CMR-derived extracellular volume in AL amyloidosis: a multicenter study.

AL amyloidosis cardiac MRI cardiac amyloidosis myocardial extracellular volume prognosis

Journal

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
ISSN: 1744-2818
Titre abrégé: Amyloid
Pays: England
ID NLM: 9433802

Informations de publication

Date de publication:
25 Sep 2024
Historique:
medline: 25 9 2024
pubmed: 25 9 2024
entrez: 25 9 2024
Statut: aheadofprint

Résumé

This study aimed to assess the prognostic value of cardiac magnetic resonance (CMR) variables and compare them with biological and echocardiographic markers in patients with AL cardiac amyloidosis (CA). We conducted a prospective study across three tertiary centres, where patients underwent clinical examination, blood tests, echocardiography, and CMR. The primary endpoint was all-cause mortality. A total of 176 patients with AL CA were included, with a median age of 68 years (IQR 58-75). According to the 2004 Mayo Clinic staging, 121 patients (69%) were in stage 3. During a median follow-up of 22 months (IQR 8-48), 45 patients died, and 55 were hospitalized for heart failure. Patients who died had higher NT-proBNP and troponin levels, and lower LVEF, cardiac output, and longitudinal strain. Among CMR variables, extracellular volume (ECV) was most strongly associated with all-cause mortality. In multivariate Cox models, including Mayo Clinic staging, ECV ≥ 0.45 was independently associated with mortality (HR 2.36, CI 95% 1.47-5.60) and also with heart failure hospitalizations (HR 4.10, 95%CI 2.15-8.8). ECV is a powerful predictor of outcomes in AL CA, providing additional prognostic value on top of Mayo Clinic staging.

Sections du résumé

BACKGROUND UNASSIGNED
This study aimed to assess the prognostic value of cardiac magnetic resonance (CMR) variables and compare them with biological and echocardiographic markers in patients with AL cardiac amyloidosis (CA).
METHODS UNASSIGNED
We conducted a prospective study across three tertiary centres, where patients underwent clinical examination, blood tests, echocardiography, and CMR. The primary endpoint was all-cause mortality.
RESULTS UNASSIGNED
A total of 176 patients with AL CA were included, with a median age of 68 years (IQR 58-75). According to the 2004 Mayo Clinic staging, 121 patients (69%) were in stage 3. During a median follow-up of 22 months (IQR 8-48), 45 patients died, and 55 were hospitalized for heart failure. Patients who died had higher NT-proBNP and troponin levels, and lower LVEF, cardiac output, and longitudinal strain. Among CMR variables, extracellular volume (ECV) was most strongly associated with all-cause mortality. In multivariate Cox models, including Mayo Clinic staging, ECV ≥ 0.45 was independently associated with mortality (HR 2.36, CI 95% 1.47-5.60) and also with heart failure hospitalizations (HR 4.10, 95%CI 2.15-8.8).
CONCLUSION UNASSIGNED
ECV is a powerful predictor of outcomes in AL CA, providing additional prognostic value on top of Mayo Clinic staging.

Identifiants

pubmed: 39319571
doi: 10.1080/13506129.2024.2406842
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-8

Auteurs

Martin Nicol (M)

Cardiology Department Lariboisière Saint Louis Hospital, University of Paris, France.
Groupe Hospitalier privé Ambroise Paré-Hartmann, Département d'Imagerie Cardiaque, Neuilly sur Seine, France.

Cassiel Kitzinger (C)

Radiology Department Lariboisière, University of Paris, France.

Mathilde Baudet (M)

Cardiology Department Lariboisière Saint Louis Hospital, University of Paris, France.

Alyssa Faradji (A)

Radiology Department Lariboisière, University of Paris, France.

Théo Pezel (T)

Cardiology Department Lariboisière Saint Louis Hospital, University of Paris, France.

David Lavergne (D)

Hematology Department, Dupuytren University Hospital, Limoges, France.

Arnaud Jaccard (A)

Hematology Department, Dupuytren University Hospital, Limoges, France.

Giuseppe Vergaro (G)

Cardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Alberto Aimo (A)

Cardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Michele Emdin (M)

Cardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Stephanie Harel (S)

Immuno-Hematology Department, Saint Louis Hospital, University of Paris, France.

Bruno Royer (B)

Immuno-Hematology Department, Saint Louis Hospital, University of Paris, France.

Alexis Talbot (A)

Immuno-Hematology Department, Saint Louis Hospital, University of Paris, France.

Valérie Bousson (V)

Radiology Department Lariboisière, University of Paris, France.

Laurent Macron (L)

Groupe Hospitalier privé Ambroise Paré-Hartmann, Département d'Imagerie Cardiaque, Neuilly sur Seine, France.

Bertrand Arnulf (B)

Immuno-Hematology Department, Saint Louis Hospital, University of Paris, France.

Damien Logeart (D)

Cardiology Department Lariboisière Saint Louis Hospital, University of Paris, France.

Classifications MeSH