Advances in hypertrophic cardiomyopathy
Main Author: | |
---|---|
Publication Date: | 2022 |
Format: | Other |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10362/143971 |
Summary: | Copyright © 2022 Sociedade Portuguesa de Cardiologia. Publicado por Elsevier España, S.L.U. All rights reserved. |
id |
RCAP_76636c06cd5cb6e14a80b4be9caf9896 |
---|---|
oai_identifier_str |
oai:run.unl.pt:10362/143971 |
network_acronym_str |
RCAP |
network_name_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository_id_str |
https://opendoar.ac.uk/repository/7160 |
spelling |
Advances in hypertrophic cardiomyopathyWhat the cardiologist needs to knowAtrial fibrillationHeart failureHypertrophic cardiomyopathyNonfamilialPrognosisSarcomere positiveSudden cardiac deathTreatmentCopyright © 2022 Sociedade Portuguesa de Cardiologia. Publicado por Elsevier España, S.L.U. All rights reserved.Hypertrophic cardiomyopathy (HCM) is known as the most common genetic heart disease, characterized by otherwise unexplained left ventricular (LV) hypertrophy. In spite of major advances in whole genome sequence techniques, it is still not possible to identify the causal mutation in approximately half of HCM patients. Consequently, a new HCM concept, "beyond the sarcomere" is being developed, supported by data from recent HCM registries which reveal two distinct HCM subgroups: sarcomere positive HCM subgroup and nonfamilial HCM subgroup. Sarcomere positive HCM patients tend to be younger age at diagnosis, have fewer co-morbidities, present more often with reverse septal morphology, more myocardial fibrosis, less LV outflow tract obstruction, and a worse prognosis when compared to nonfamilial HCM patients. These subgroups, with different molecular basis, phenotypes and clinical profiles, will likely require specific management strategies. Important research advances have also been made concerning diagnosis, sudden cardiac death stratification and therapy. In this article, we seek to review recent relevant knowledge, summarizing the advances in this complex and heterogeneous disease.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)RUNToste, Alexandra2022-09-22T22:37:27Z2022-062022-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/other11application/pdfhttp://hdl.handle.net/10362/143971eng0304-4750PURE: 46536743https://doi.org/10.1016/j.repc.2021.05.015info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T18:05:18Zoai:run.unl.pt:10362/143971Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:35:52.045697Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Advances in hypertrophic cardiomyopathy What the cardiologist needs to know |
title |
Advances in hypertrophic cardiomyopathy |
spellingShingle |
Advances in hypertrophic cardiomyopathy Toste, Alexandra Atrial fibrillation Heart failure Hypertrophic cardiomyopathy Nonfamilial Prognosis Sarcomere positive Sudden cardiac death Treatment |
title_short |
Advances in hypertrophic cardiomyopathy |
title_full |
Advances in hypertrophic cardiomyopathy |
title_fullStr |
Advances in hypertrophic cardiomyopathy |
title_full_unstemmed |
Advances in hypertrophic cardiomyopathy |
title_sort |
Advances in hypertrophic cardiomyopathy |
author |
Toste, Alexandra |
author_facet |
Toste, Alexandra |
author_role |
author |
dc.contributor.none.fl_str_mv |
NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM) RUN |
dc.contributor.author.fl_str_mv |
Toste, Alexandra |
dc.subject.por.fl_str_mv |
Atrial fibrillation Heart failure Hypertrophic cardiomyopathy Nonfamilial Prognosis Sarcomere positive Sudden cardiac death Treatment |
topic |
Atrial fibrillation Heart failure Hypertrophic cardiomyopathy Nonfamilial Prognosis Sarcomere positive Sudden cardiac death Treatment |
description |
Copyright © 2022 Sociedade Portuguesa de Cardiologia. Publicado por Elsevier España, S.L.U. All rights reserved. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-22T22:37:27Z 2022-06 2022-06-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/other |
format |
other |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10362/143971 |
url |
http://hdl.handle.net/10362/143971 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
0304-4750 PURE: 46536743 https://doi.org/10.1016/j.repc.2021.05.015 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
11 application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
_version_ |
1833596822365405184 |