ESC Heart Failure (Feb 2025)
Early diagnosis, disease stage and prognosis in wild‐type transthyretin amyloid cardiomyopathy: The DIAMOND study
- Giacomo Tini,
- Beatrice Musumeci,
- Paolo Milani,
- Mattia Zampieri,
- Angelo Giuseppe Caponetti,
- Francesca Fabris,
- Andrea Foli,
- Alessia Argirò,
- Carlotta Mazzoni,
- Christian Gagliardi,
- Simone Longhi,
- Giulia Saturi,
- Giuseppe Vergaro,
- Alberto Aimo,
- Ludovica De Fazio,
- Guerino Giuseppe Varrà,
- Matteo Serenelli,
- Gioele Fabbri,
- Laura De Michieli,
- Giuseppe Palmiero,
- Giuseppe Ciliberti,
- Samuela Carigi,
- Margherita Zanoletti,
- Giulia Elena Mandoli,
- Giulia Ricci Lucchi,
- Valeria Rella,
- Enrico Monti,
- Elisa Gardini,
- Michela Bartolotti,
- Lia Crotti,
- Elisa Merli,
- Roberta Mussinelli,
- Pier Filippo Vianello,
- Matteo Cameli,
- Francesca Marzo,
- Federico Guerra,
- Giuseppe Limongelli,
- Alberto Cipriani,
- Stefano Perlini,
- Laura Obici,
- Federico Perfetto,
- Emanuele Barbato,
- Italo Porto,
- Gianfranco Sinagra,
- Marco Merlo,
- Michele Emdin,
- Elena Biagini,
- Francesco Cappelli,
- Giovanni Palladini,
- Marco Canepa
Affiliations
- Giacomo Tini
- Department of Cardiology, Department of Clinical and Molecular Medicine Sapienza University of Rome Rome Italy
- Beatrice Musumeci
- Department of Cardiology, Department of Clinical and Molecular Medicine Sapienza University of Rome Rome Italy
- Paolo Milani
- Department of Molecular Medicine University of Pavia Pavia Italy
- Mattia Zampieri
- Tuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy
- Angelo Giuseppe Caponetti
- Cardiology Unit, St. Orsola Hospital IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy
- Francesca Fabris
- Department of Molecular Medicine University of Pavia Pavia Italy
- Andrea Foli
- Department of Molecular Medicine University of Pavia Pavia Italy
- Alessia Argirò
- Tuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy
- Carlotta Mazzoni
- Tuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy
- Christian Gagliardi
- Cardiology Unit, St. Orsola Hospital IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy
- Simone Longhi
- Cardiology Unit, St. Orsola Hospital IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy
- Giulia Saturi
- Department of Experimental, Diagnostic and Specialty Medicine University of Bologna Bologna Italy
- Giuseppe Vergaro
- Interdisciplinary Center of Health Sciences Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio Pisa Italy
- Alberto Aimo
- Interdisciplinary Center of Health Sciences Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio Pisa Italy
- Ludovica De Fazio
- Department of Cardiology, Department of Clinical and Molecular Medicine Sapienza University of Rome Rome Italy
- Guerino Giuseppe Varrà
- Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano‐Isontina (ASUGI) University of Trieste Trieste Italy
- Matteo Serenelli
- Cardiologic Center University of Ferrara Ferrara Italy
- Gioele Fabbri
- Cardiologic Center University of Ferrara Ferrara Italy
- Laura De Michieli
- Department of Cardio‐Thoraco‐Vascular Sciences and Public Health University of Padua Padua Italy
- Giuseppe Palmiero
- Inherited and Rare Cardiovascular Disease Unit University of Campania ‘Luigi Vanvitelli’, AORN dei Colli, Monaldi Hospital Naples Italy
- Giuseppe Ciliberti
- Cardiology and Arrhythmology Clinic, University Hospital ‘Lancisi‐Umberto I‐ Salesi’, Department of Biomedical Sciences and Public Health Marche Polytechnic University Ancona Italy
- Samuela Carigi
- Cardiology Unit Infermi Hospital Rimini Italy
- Margherita Zanoletti
- Cardiology Unit Ospedale Policlinico San Martino IRCCS Genoa Italy
- Giulia Elena Mandoli
- Department of Medical Biotechnologies, Division of Cardiology University of Siena Siena Italy
- Giulia Ricci Lucchi
- U.O. Cardiologia Ospedale di Lugo, AUSL della Romagna Lugo Italy
- Valeria Rella
- Department of Cardiology, San Luca Hospital, Cardiomyopathy Unit IRCCS Istituto Auxologico Italiano Milan Italy
- Enrico Monti
- U.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna Forlì Italy
- Elisa Gardini
- U.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna Forlì Italy
- Michela Bartolotti
- U.O. Cardiologia Ospedale di Cesena, AUSL della Romagna Cesena Italy
- Lia Crotti
- Department of Cardiology, San Luca Hospital, Cardiomyopathy Unit IRCCS Istituto Auxologico Italiano Milan Italy
- Elisa Merli
- Cardiology Unit Ospedale per gli Infermi Faenza Italy
- Roberta Mussinelli
- Department of Molecular Medicine University of Pavia Pavia Italy
- Pier Filippo Vianello
- Cardiology Unit Ospedale Policlinico San Martino IRCCS Genoa Italy
- Matteo Cameli
- Department of Medical Biotechnologies, Division of Cardiology University of Siena Siena Italy
- Francesca Marzo
- Cardiology Unit Infermi Hospital Rimini Italy
- Federico Guerra
- Cardiology and Arrhythmology Clinic, University Hospital ‘Lancisi‐Umberto I‐ Salesi’, Department of Biomedical Sciences and Public Health Marche Polytechnic University Ancona Italy
- Giuseppe Limongelli
- Inherited and Rare Cardiovascular Disease Unit University of Campania ‘Luigi Vanvitelli’, AORN dei Colli, Monaldi Hospital Naples Italy
- Alberto Cipriani
- Department of Cardio‐Thoraco‐Vascular Sciences and Public Health University of Padua Padua Italy
- Stefano Perlini
- Department of Molecular Medicine University of Pavia Pavia Italy
- Laura Obici
- Department of Molecular Medicine University of Pavia Pavia Italy
- Federico Perfetto
- Tuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy
- Emanuele Barbato
- Department of Cardiology, Department of Clinical and Molecular Medicine Sapienza University of Rome Rome Italy
- Italo Porto
- Cardiology Unit Ospedale Policlinico San Martino IRCCS Genoa Italy
- Gianfranco Sinagra
- European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart‐ERN GUARD‐Heart London UK
- Marco Merlo
- European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart‐ERN GUARD‐Heart London UK
- Michele Emdin
- Interdisciplinary Center of Health Sciences Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio Pisa Italy
- Elena Biagini
- Cardiology Unit, St. Orsola Hospital IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy
- Francesco Cappelli
- Tuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy
- Giovanni Palladini
- Department of Molecular Medicine University of Pavia Pavia Italy
- Marco Canepa
- Cardiology Unit Ospedale Policlinico San Martino IRCCS Genoa Italy
- DOI
- https://doi.org/10.1002/ehf2.15091
- Journal volume & issue
-
Vol. 12,
no. 1
pp. 379 – 388
Abstract
Abstract Aims 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. Methods 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. Results 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. Conclusions 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.
Keywords
- Cardiac amyloidosis
- Disease stage
- NAC score
- Prognostic scoring
- Wild‐type transthyretin cardiac amyloidosis