Evidence map›Paper›PMID 39301748›Full record

ArticleESC heart failure2025

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 and 40 more

Abstract readMulticenter Study
In one paragraph

Article in ESC heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

50 authors.

Giacomo TiniDepartment of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Beatrice MusumeciDepartment of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Paolo MilaniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Mattia ZampieriTuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
Angelo Giuseppe CaponettiCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Francesca FabrisDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Andrea FoliDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Alessia ArgiròTuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
Carlotta MazzoniTuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
Christian GagliardiCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Simone LonghiCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Giulia SaturiDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Giuseppe VergaroInterdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Alberto AimoInterdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Ludovica De FazioDepartment of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Guerino Giuseppe VarràCenter for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy.
Matteo SerenelliCardiologic Center, University of Ferrara, Ferrara, Italy.
Gioele FabbriCardiologic Center, University of Ferrara, Ferrara, Italy.
Laura De MichieliDepartment of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Giuseppe PalmieroInherited and Rare Cardiovascular Disease Unit, University of Campania 'Luigi Vanvitelli', AORN dei Colli, Monaldi Hospital, Naples, Italy.
Giuseppe CilibertiCardiology and Arrhythmology Clinic, University Hospital 'Lancisi-Umberto I- Salesi', Department of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.
Samuela CarigiCardiology Unit, Infermi Hospital, Rimini, Italy.
Margherita ZanolettiCardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Giulia Elena MandoliDepartment of Medical Biotechnologies, Division of Cardiology, University of Siena, Siena, Italy.
Giulia Ricci LucchiU.O. Cardiologia, Ospedale di Lugo, AUSL della Romagna, Lugo, Italy.
Valeria RellaDepartment of Cardiology, San Luca Hospital, Cardiomyopathy Unit, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Enrico MontiU.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna, Forlì, Italy.
Elisa GardiniU.O. Cardiologia, Ospedale di Forlì, AUSL della Romagna, Forlì, Italy.
Michela BartolottiU.O. Cardiologia, Ospedale di Cesena, AUSL della Romagna, Cesena, Italy.
Lia CrottiDepartment of Cardiology, San Luca Hospital, Cardiomyopathy Unit, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Elisa MerliCardiology Unit, Ospedale per gli Infermi, Faenza, Italy.
Roberta MussinelliDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Pier Filippo VianelloCardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Matteo CameliDepartment of Medical Biotechnologies, Division of Cardiology, University of Siena, Siena, Italy.
Francesca MarzoCardiology Unit, Infermi Hospital, Rimini, Italy.
Federico GuerraCardiology and Arrhythmology Clinic, University Hospital 'Lancisi-Umberto I- Salesi', Department of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.
Giuseppe LimongelliInherited and Rare Cardiovascular Disease Unit, University of Campania 'Luigi Vanvitelli', AORN dei Colli, Monaldi Hospital, Naples, Italy.
Alberto CiprianiDepartment of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Stefano PerliniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Laura ObiciDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Federico PerfettoTuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
Emanuele BarbatoDepartment of Cardiology, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Italo PortoCardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Gianfranco SinagraEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.
Marco MerloEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart, London, UK.
Michele EmdinInterdisciplinary Center of Health Sciences, Scuola Superiore Sant'Anna, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Elena BiaginiCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Francesco CappelliTuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
Giovanni PalladiniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Marco CanepaCardiology Unit, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.ORCID https://orcid.org/0000-0001-9063-5576

Funding

Pfizer 64890405
6 · The paper itself

Abstract

aimsDisease 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.

methodsWe 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.

resultsOnly 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.

conclusionsIn 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.

Indexed as

Amyloid Neuropathies, FamilialCardiomyopathiesEarly DiagnosisAgedFemaleFollow-Up StudiesHumansItalyMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateCardiac amyloidosisDisease stageNAC scorePrognostic scoringWild‐type transthyretin cardiac amyloidosis

Identifiers

PMID39301748
PMCPMC11769659

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.