Evidence map›Paper›PMID 39841451›Full record

ArticleJAMA cardiology2025

Clinical Phenotype and Prognosis of Asymptomatic Patients With Transthyretin Cardiac Amyloid Infiltration.

Aldostefano Porcari, Yousuf Razvi, Francesco Cappelli, Christian Nitsche, Matteo Serenelli, Simone Longhi, Giulio Sinigiani, Alberto Cipriani, Alberto Aimo, Daniela Tomasoni and 22 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  9. Review
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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

32 authors.

Aldostefano PorcariNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Yousuf RazviNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Francesco CappelliCardiomyopathy Unit, Careggi University Hospital, University of Florence, Florence, Italy.
Christian NitscheDivision of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Matteo SerenelliCardiologic Centre, University of Ferrara, Cona, Italy.
Simone LonghiEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart, ERN GUARD-Heart, Trieste, Italy.
Giulio SinigianiDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Alberto CiprianiDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Alberto AimoInstitute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Daniela TomasoniCardiology, Azienda Socio Sanitaria Territoiale Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Mattia ZampieriCardiomyopathy Unit, Careggi University Hospital, University of Florence, Florence, Italy.
Anna CantoneCardiologic Centre, University of Ferrara, Cona, Italy.
Valentina AllegroCenter for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste, Trieste, Italy.
Giuseppe VergaroInstitute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Ahmad MasriKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Marcus UreyDivision of Cardiovascular Diseases, Department of Medicine, University of California, San Diego, La Jolla.
Adam IoannouNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Aviva PetrieNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Navid NooryDepartment of Cardiology and Clinical Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Finn GustafssonDepartment of Cardiology and Clinical Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Michael PoledniczekDivision of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Michele EmdinInstitute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Marco MetraCardiology, Azienda Socio Sanitaria Territoiale Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Gianfranco SinagraCenter for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste, Trieste, Italy.
Ana Martinez-NaharroNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Ashutosh D WechalekarNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Helen LachmanNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Carol WhelanNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Philip N HawkinsNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Scott D SolomonCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Julian D GillmoreNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.
Marianna FontanaNational Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Patients with transthyretin (ATTR) cardiac amyloid infiltration are increasingly diagnosed at earlier disease stages with no heart failure (HF) symptoms and a wide range of cardiac amyloid infiltration. Objective: To characterize the clinical phenotype and natural history of asymptomatic patients with ATTR cardiac amyloid infiltration. Design, Setting, and Participants: This cohort study analyzed data of all patients at 12 international centers for amyloidosis from January 1, 2008, through December 31, 2023. Inclusion criteria were asymptomatic ATTR cardiac amyloid infiltration, defined as an absence of HF history, HF signs and symptoms, diuretic therapy, and plasma cell dyscrasia with evidence of myocardial uptake on bone scintigraphy. If plasma cell dyscrasia was present, histologic confirmation of ATTR amyloid was required. Exposure: Asymptomatic ATTR cardiac amyloid infiltration. Main Outcomes and Measures: The primary outcomes were all-cause and cardiovascular (CV) mortality. The secondary outcomes were unplanned HF hospitalization, unplanned CV-related hospitalization, and a composite outcome of CV mortality and HF hospitalization. Results: The study comprised 485 patients with asymptomatic ATTR cardiac amyloid infiltration (mean [SD] age, 74.9 [9.9] years, 85.8% male, 112 [23.1%] with hereditary ATTR amyloidosis), with 369 (76.1%) having grade 2 or 3 and 116 (23.9%) having grade 1 cardiac uptake at baseline. Patients with grade 2 or 3 uptake exhibited significantly more cardiac functional and structural abnormalities vs patients with grade 1 uptake. At 3 years, compared with grade 1 uptake, patients with grade 2 or 3 uptake had greater development of HF (54.3% [95% CI, 47.7%-61.3%] vs 23.1% [95% CI, 14.8%-35.1%]), greater outpatient diuretic initiation and N-terminal pro-B-type natriuretic peptide progression (35.0% [95% CI, 28.0%-43.2%] vs 12.4% [95% CI, 6.3%-23.7%]), and greater HF hospitalization (8.7% [95% CI, 5.9%-12.9%] vs 0%) and unplanned CV hospitalization (20.0% [95% CI, 15.7%-25.3%] vs 4.3% [95% CI, 1.6%-11.3%]). Over a median follow-up of 37 months (IQR, 20-64 months), the all-cause death rate was similar between patients with grade 1 vs 2 and 3 uptake; however, those with grade 2 or 3 compared with grade 1 uptake had a significantly higher risk of CV mortality (unadjusted hazard ratio, 5.30; 95% CI, 1.92-14.65). Conclusions and Relevance: This study shows that asymptomatic ATTR cardiac amyloid infiltration encompasses a wide spectrum of disease severity, with patients with grade 2 or 3 cardiac uptake experiencing an increased rate of CV events and CV mortality and patients with grade 1 uptake experiencing a lower CV event rate and predominantly non-CV mortality. These findings support the use of disease-modifying treatments in asymptomatic patients with grade 2 or 3 uptake and highlight the need of large-scale studies to assess their role in grade 1 uptake.

Indexed as

Amyloid Neuropathies, FamilialCardiomyopathiesMyocardiumAgedAged, 80 and overAsymptomatic DiseasesCohort StudiesFemaleHeart FailureHospitalizationHumansMaleMiddle AgedPhenotypePrognosisRetrospective Studies

Identifiers

PMID39841451
PMCPMC12079285

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Registered trials

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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.