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Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms
BACKGROUND: Transthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreov...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700255/ https://www.ncbi.nlm.nih.gov/pubmed/36444226 http://dx.doi.org/10.1016/j.jaccao.2022.07.007 |
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author | Gonzalez-Lopez, Esther Escobar-Lopez, Luis Obici, Laura Saturi, Giulia Bezard, Mélanie Saith, Sunil E. AbouEzzeddine, Omar F. Mussinelli, Roberta Gagliardi, Christian Kharoubi, Mounira Griffin, Jan M. Dispenzieri, Angela Vilches, Silvia Perlini, Stefano Longhi, Simone Oghina, Silvia Rivas, Adrian Grogan, Martha Maurer, Mathew S. Damy, Thibaud Palladini, Giovanni Rapezzi, Claudio Garcia-Pavia, Pablo |
author_facet | Gonzalez-Lopez, Esther Escobar-Lopez, Luis Obici, Laura Saturi, Giulia Bezard, Mélanie Saith, Sunil E. AbouEzzeddine, Omar F. Mussinelli, Roberta Gagliardi, Christian Kharoubi, Mounira Griffin, Jan M. Dispenzieri, Angela Vilches, Silvia Perlini, Stefano Longhi, Simone Oghina, Silvia Rivas, Adrian Grogan, Martha Maurer, Mathew S. Damy, Thibaud Palladini, Giovanni Rapezzi, Claudio Garcia-Pavia, Pablo |
author_sort | Gonzalez-Lopez, Esther |
collection | PubMed |
description | BACKGROUND: Transthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. OBJECTIVES: The aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. METHODS: Clinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. RESULTS: A total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). CONCLUSIONS: After a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis. |
format | Online Article Text |
id | pubmed-9700255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97002552022-11-27 Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms Gonzalez-Lopez, Esther Escobar-Lopez, Luis Obici, Laura Saturi, Giulia Bezard, Mélanie Saith, Sunil E. AbouEzzeddine, Omar F. Mussinelli, Roberta Gagliardi, Christian Kharoubi, Mounira Griffin, Jan M. Dispenzieri, Angela Vilches, Silvia Perlini, Stefano Longhi, Simone Oghina, Silvia Rivas, Adrian Grogan, Martha Maurer, Mathew S. Damy, Thibaud Palladini, Giovanni Rapezzi, Claudio Garcia-Pavia, Pablo JACC CardioOncol Mini-Focus Issue: Amyloidosis BACKGROUND: Transthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. OBJECTIVES: The aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. METHODS: Clinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. RESULTS: A total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). CONCLUSIONS: After a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis. Elsevier 2022-11-15 /pmc/articles/PMC9700255/ /pubmed/36444226 http://dx.doi.org/10.1016/j.jaccao.2022.07.007 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mini-Focus Issue: Amyloidosis Gonzalez-Lopez, Esther Escobar-Lopez, Luis Obici, Laura Saturi, Giulia Bezard, Mélanie Saith, Sunil E. AbouEzzeddine, Omar F. Mussinelli, Roberta Gagliardi, Christian Kharoubi, Mounira Griffin, Jan M. Dispenzieri, Angela Vilches, Silvia Perlini, Stefano Longhi, Simone Oghina, Silvia Rivas, Adrian Grogan, Martha Maurer, Mathew S. Damy, Thibaud Palladini, Giovanni Rapezzi, Claudio Garcia-Pavia, Pablo Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title | Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title_full | Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title_fullStr | Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title_full_unstemmed | Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title_short | Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms |
title_sort | prognosis of transthyretin cardiac amyloidosis without heart failure symptoms |
topic | Mini-Focus Issue: Amyloidosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700255/ https://www.ncbi.nlm.nih.gov/pubmed/36444226 http://dx.doi.org/10.1016/j.jaccao.2022.07.007 |
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