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Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications
About one in seven elderly patients with severe calcific aortic stenosis (AS) also have ATTR amyloid cardiomyopathy (AC-TTR). The reasons for this close association are not fully known, but the two entities are not only related by common epidemiology. For example, it is possible to hypothesize that...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503413/ https://www.ncbi.nlm.nih.gov/pubmed/34650371 http://dx.doi.org/10.1093/eurheartj/suab107 |
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author | Fabbri, Gioele Serenelli, Matteo Cantone, Anna Sanguettoli, Federico Rapezzi, Claudio |
author_facet | Fabbri, Gioele Serenelli, Matteo Cantone, Anna Sanguettoli, Federico Rapezzi, Claudio |
author_sort | Fabbri, Gioele |
collection | PubMed |
description | About one in seven elderly patients with severe calcific aortic stenosis (AS) also have ATTR amyloid cardiomyopathy (AC-TTR). The reasons for this close association are not fully known, but the two entities are not only related by common epidemiology. For example, it is possible to hypothesize that an amyloidotic infiltration of the aortic valve, even partial, can act as a trigger for the development of endothelial damage and subsequent calcification. Another hypothesis is the increased myocardial strain induced by AS may locally favour the process of amyloidogenesis and tissue infiltration. In a patient with AS, the coexistence of AC-TTR can be suspected by careful analysis of the echocardiogram and the ECG, especially if a clinical history of carpal tunnel syndrome coexists. Bone tracer scintigraphy allows a diagnosis of certainty. Recently, several studies have evaluated the prognostic implications of the coexistence of the two entities in candidates for percutaneous aortic valve replacement, showing how amyloidosis would not significantly impact the results of the procedure, but would only be associated with a greater risk of distant heart failure. In patients with AS associated with AC-TTR, valve replacement should not be ruled out in the presence of the usual clinical-haemodynamic indications. |
format | Online Article Text |
id | pubmed-8503413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85034132021-10-13 Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications Fabbri, Gioele Serenelli, Matteo Cantone, Anna Sanguettoli, Federico Rapezzi, Claudio Eur Heart J Suppl Articles About one in seven elderly patients with severe calcific aortic stenosis (AS) also have ATTR amyloid cardiomyopathy (AC-TTR). The reasons for this close association are not fully known, but the two entities are not only related by common epidemiology. For example, it is possible to hypothesize that an amyloidotic infiltration of the aortic valve, even partial, can act as a trigger for the development of endothelial damage and subsequent calcification. Another hypothesis is the increased myocardial strain induced by AS may locally favour the process of amyloidogenesis and tissue infiltration. In a patient with AS, the coexistence of AC-TTR can be suspected by careful analysis of the echocardiogram and the ECG, especially if a clinical history of carpal tunnel syndrome coexists. Bone tracer scintigraphy allows a diagnosis of certainty. Recently, several studies have evaluated the prognostic implications of the coexistence of the two entities in candidates for percutaneous aortic valve replacement, showing how amyloidosis would not significantly impact the results of the procedure, but would only be associated with a greater risk of distant heart failure. In patients with AS associated with AC-TTR, valve replacement should not be ruled out in the presence of the usual clinical-haemodynamic indications. Oxford University Press 2021-10-08 /pmc/articles/PMC8503413/ /pubmed/34650371 http://dx.doi.org/10.1093/eurheartj/suab107 Text en Published on behalf of the European Society of Cardiology. © The Author(s) 2021. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Fabbri, Gioele Serenelli, Matteo Cantone, Anna Sanguettoli, Federico Rapezzi, Claudio Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title | Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title_full | Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title_fullStr | Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title_full_unstemmed | Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title_short | Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
title_sort | transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503413/ https://www.ncbi.nlm.nih.gov/pubmed/34650371 http://dx.doi.org/10.1093/eurheartj/suab107 |
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