Early diagnosis, disease stage and prognosis in wild-type transthyretin amyloid cardiomyopathy: The DIAMOND study.

Cardiac amyloidosis Disease stage NAC score Prognostic scoring Wild‐type transthyretin cardiac amyloidosis

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
20 Sep 2024
Historique:
revised: 27 08 2024
received: 04 08 2024
accepted: 06 09 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 20 9 2024
Statut: aheadofprint

Résumé

Disease staging and prognostic scoring in wild-type transthyretin-related cardiac amyloidosis (ATTRwt-CA) can be captured by two systems (NAC and Columbia scores). However, uncertainty remains as epidemiology of the disease is evolving rapidly. We evaluated features associated with staging systems across ATTRwt-CA patients from different diagnostic pathways, and their association with prognosis. We performed an analysis on DIAMOND patients with available data to evaluate NAC and Columbia score. DIAMOND was a retrospective study from 17 Italian referral centres for CA, enrolling 1281 patients diagnosed between 2016 and 2021, and aimed at describing characteristics of pathways leading to ATTRwt-CA diagnosis. Of the original cohort, 811 patients were included in this analysis. Each patient had NAC and Columbia score calculated. Patients were grouped according to NAC and Columbia scoring classes. We described characteristics of patients according to staging classes and diagnostic pathways at diagnosis. Prevalence of early diagnoses, defined as NAC Ia, NYHA class I, no use of diuretics, no history of heart failure (HF) hospitalizations nor of atrial fibrillation prior to diagnosis, was investigated. Finally, prognostic variables were tested alone and grouped as NAC or Columbia scores in Cox univariate and multivariate regression analyses. Prognosis was investigated as all-cause mortality, in the whole population and dividing patients in HF versus other diagnostic pathways. Only 1% of the study population had an early ATTRwt-CA diagnosis. Distribution of prognostic variables and of NAC and Columbia classes was heterogeneous across diagnostic pathways. The prevalence of NAC III and Columbia III was higher in the HF diagnostic pathway, but all NAC and Columbia classes were present in all pathways. Both NAC and Columbia scores were associated with all-cause mortality at univariate Cox regression analysis in the whole population, in patients from the HF diagnostic pathway and in those from other pathways. At multivariate analysis, Columbia score remained significantly associated with the outcome, together with age at diagnosis, left ventricular ejection fraction and maximal wall thickness. In this contemporary nationwide cohort, an ATTRwt-CA early diagnosis was very rare. Disease staging with NAC and Columbia scoring systems determined classes of patients with heterogeneous features. Both scores were significantly associated with mortality, but other variables also had prognostic significance.

Identifiants

pubmed: 39301748
doi: 10.1002/ehf2.15091
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Pfizer
ID : 64890405

Informations de copyright

© 2024 The Author(s). ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Giacomo Tini (G)

Department of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Beatrice Musumeci (B)

Department of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Paolo Milani (P)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Mattia Zampieri (M)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Angelo Giuseppe Caponetti (AG)

Cardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.

Francesca Fabris (F)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Andrea Foli (A)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Alessia Argirò (A)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Carlotta Mazzoni (C)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Christian Gagliardi (C)

Cardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.

Simone Longhi (S)

Cardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.

Giulia Saturi (G)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.

Giuseppe Vergaro (G)

Interdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Alberto Aimo (A)

Interdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Ludovica De Fazio (L)

Department of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Guerino Giuseppe Varrà (GG)

Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy.

Matteo Serenelli (M)

Cardiologic Center, University of Ferrara, Ferrara, Italy.

Gioele Fabbri (G)

Cardiologic Center, University of Ferrara, Ferrara, Italy.

Laura De Michieli (L)

Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Cardiology Unit, University Hospital of Padova, Padua, Italy.

Giuseppe Palmiero (G)

Inherited and Rare Cardiovascular Disease Unit, University of Campania 'Luigi Vanvitelli', AORN dei Colli, Monaldi Hospital, Naples, Italy.

Giuseppe Ciliberti (G)

Cardiology and Arrhythmology Clinic, University Hospital 'Lancisi-Umberto I- Salesi', Department of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.

Samuela Carigi (S)

Cardiology Unit, Infermi Hospital, Rimini, Italy.

Margherita Zanoletti (M)

Cardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.

Giulia Elena Mandoli (GE)

Department of Medical Biotechnologies, Division of Cardiology, University of Siena, Siena, Italy.

Giulia Ricci Lucchi (GR)

U.O. Cardiologia, Ospedale di Lugo, AUSL della Romagna, Lugo, Italy.

Valeria Rella (V)

Department of Cardiology, San Luca Hospital, Cardiomyopathy Unit, IRCCS Istituto Auxologico Italiano, Milan, Italy.

Enrico Monti (E)

U.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna, Forlì, Italy.

Elisa Gardini (E)

U.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna, Forlì, Italy.

Michela Bartolotti (M)

U.O. Cardiologia, Ospedale di Cesena, AUSL della Romagna, Cesena, Italy.

Lia Crotti (L)

U.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna, Forlì, Italy.
Department of Medicine and Surgery, University Milano Bicocca, Milan, Italy.

Elisa Merli (E)

Cardiology Unit, Ospedale per gli Infermi, Faenza, Italy.

Roberta Mussinelli (R)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Pier Filippo Vianello (PF)

Cardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.

Matteo Cameli (M)

Department of Medical Biotechnologies, Division of Cardiology, University of Siena, Siena, Italy.

Francesca Marzo (F)

Cardiology Unit, Infermi Hospital, Rimini, Italy.

Federico Guerra (F)

Cardiology and Arrhythmology Clinic, University Hospital 'Lancisi-Umberto I- Salesi', Department of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.

Giuseppe Limongelli (G)

Inherited and Rare Cardiovascular Disease Unit, University of Campania 'Luigi Vanvitelli', AORN dei Colli, Monaldi Hospital, Naples, Italy.

Alberto Cipriani (A)

Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Cardiology Unit, University Hospital of Padova, Padua, Italy.

Stefano Perlini (S)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Laura Obici (L)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Federico Perfetto (F)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Emanuele Barbato (E)

Department of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Italo Porto (I)

Cardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Department of Internal Medicine, University of Genova, Genoa, Italy.

Gianfranco Sinagra (G)

European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.
Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy.

Marco Merlo (M)

European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.
Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy.

Michele Emdin (M)

Interdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Elena Biagini (E)

Cardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.

Francesco Cappelli (F)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Giovanni Palladini (G)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

Marco Canepa (M)

Cardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Department of Internal Medicine, University of Genova, Genoa, Italy.

Classifications MeSH