Update of the Portuguese Familial Hypercholesterolaemia Study

Detalhes bibliográficos
Autor(a) principal: Medeiros, A.M.
Data de Publicação: 2010
Outros Autores: Alves, A.C., Francisco, V., Bourbon, M., Investigators of the Portuguese FH Study
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.18/234
Resumo: The main aim of the Portuguese Familial Hypercholesterolaemia Study is to identify the genetic cause of hypercholesterolaemia in individuals with a clinical diagnosis of Familial Hypercholesterolaemia (FH). A total of 1340 blood samples were collected from 482 index patients and 858 relatives with the collaboration of clinicians from several hospitals all over the country. The genetic diagnosis of FH in this study is based on the analyses of three genes: LDLR, APOB and PCSK9. In the last 10 years, the Portuguese FH Study identified a genetic defect in a total of 171 index patients, corresponding to an overall of 48% of the total received cases with clinical diagnosis of FH. Although the Simon Broome FH register criteria have been adapted to our study, 59 patients that did not fulfil all criteria were included in the study and a mutation causing disease was identified in 8 of these patients. In the LDLR gene were found 80 different mutations in 165 unrelated index patients: 159 heterozygous, 3 compounds heterozygous and 3 true homozygous. The APOB p.Arg3527Gln and the PCSK9 p.Asp374His mutation were not found in any of our patients since our last report, but a novel mutation in the APOB gene, predicted to cause a single amino acid substitution p.Tyr3560Cys, was found in one patient. The cascade screening in relatives of these 171 index patients allowed the identification and genetic characterization of a total of 404 FH patients in Portugal.
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spelling Update of the Portuguese Familial Hypercholesterolaemia StudyFamilial HypercholesterolaemiaLow density lipoprotein receptorCholesterolCoronary heart diseaseMutationCascade screeningDoenças Cardio e Cérebro-vascularesThe main aim of the Portuguese Familial Hypercholesterolaemia Study is to identify the genetic cause of hypercholesterolaemia in individuals with a clinical diagnosis of Familial Hypercholesterolaemia (FH). A total of 1340 blood samples were collected from 482 index patients and 858 relatives with the collaboration of clinicians from several hospitals all over the country. The genetic diagnosis of FH in this study is based on the analyses of three genes: LDLR, APOB and PCSK9. In the last 10 years, the Portuguese FH Study identified a genetic defect in a total of 171 index patients, corresponding to an overall of 48% of the total received cases with clinical diagnosis of FH. Although the Simon Broome FH register criteria have been adapted to our study, 59 patients that did not fulfil all criteria were included in the study and a mutation causing disease was identified in 8 of these patients. In the LDLR gene were found 80 different mutations in 165 unrelated index patients: 159 heterozygous, 3 compounds heterozygous and 3 true homozygous. The APOB p.Arg3527Gln and the PCSK9 p.Asp374His mutation were not found in any of our patients since our last report, but a novel mutation in the APOB gene, predicted to cause a single amino acid substitution p.Tyr3560Cys, was found in one patient. The cascade screening in relatives of these 171 index patients allowed the identification and genetic characterization of a total of 404 FH patients in Portugal.ElsevierRepositório Científico do Instituto Nacional de SaúdeMedeiros, A.M.Alves, A.C.Francisco, V.Bourbon, M.Investigators of the Portuguese FH Study2011-09-26T12:11:28Z2010-102010-10-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/234engAtherosclerosis. 2010 Oct;212(2):553-8. Epub 2010 Aug 8.0021-9150doi:10.1016/j.atherosclerosis.2010.07.012info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:38:05Zoai:repositorio.insa.pt:10400.18/234Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:35:28.537682Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Update of the Portuguese Familial Hypercholesterolaemia Study
title Update of the Portuguese Familial Hypercholesterolaemia Study
spellingShingle Update of the Portuguese Familial Hypercholesterolaemia Study
Medeiros, A.M.
Familial Hypercholesterolaemia
Low density lipoprotein receptor
Cholesterol
Coronary heart disease
Mutation
Cascade screening
Doenças Cardio e Cérebro-vasculares
title_short Update of the Portuguese Familial Hypercholesterolaemia Study
title_full Update of the Portuguese Familial Hypercholesterolaemia Study
title_fullStr Update of the Portuguese Familial Hypercholesterolaemia Study
title_full_unstemmed Update of the Portuguese Familial Hypercholesterolaemia Study
title_sort Update of the Portuguese Familial Hypercholesterolaemia Study
author Medeiros, A.M.
author_facet Medeiros, A.M.
Alves, A.C.
Francisco, V.
Bourbon, M.
Investigators of the Portuguese FH Study
author_role author
author2 Alves, A.C.
Francisco, V.
Bourbon, M.
Investigators of the Portuguese FH Study
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Medeiros, A.M.
Alves, A.C.
Francisco, V.
Bourbon, M.
Investigators of the Portuguese FH Study
dc.subject.por.fl_str_mv Familial Hypercholesterolaemia
Low density lipoprotein receptor
Cholesterol
Coronary heart disease
Mutation
Cascade screening
Doenças Cardio e Cérebro-vasculares
topic Familial Hypercholesterolaemia
Low density lipoprotein receptor
Cholesterol
Coronary heart disease
Mutation
Cascade screening
Doenças Cardio e Cérebro-vasculares
description The main aim of the Portuguese Familial Hypercholesterolaemia Study is to identify the genetic cause of hypercholesterolaemia in individuals with a clinical diagnosis of Familial Hypercholesterolaemia (FH). A total of 1340 blood samples were collected from 482 index patients and 858 relatives with the collaboration of clinicians from several hospitals all over the country. The genetic diagnosis of FH in this study is based on the analyses of three genes: LDLR, APOB and PCSK9. In the last 10 years, the Portuguese FH Study identified a genetic defect in a total of 171 index patients, corresponding to an overall of 48% of the total received cases with clinical diagnosis of FH. Although the Simon Broome FH register criteria have been adapted to our study, 59 patients that did not fulfil all criteria were included in the study and a mutation causing disease was identified in 8 of these patients. In the LDLR gene were found 80 different mutations in 165 unrelated index patients: 159 heterozygous, 3 compounds heterozygous and 3 true homozygous. The APOB p.Arg3527Gln and the PCSK9 p.Asp374His mutation were not found in any of our patients since our last report, but a novel mutation in the APOB gene, predicted to cause a single amino acid substitution p.Tyr3560Cys, was found in one patient. The cascade screening in relatives of these 171 index patients allowed the identification and genetic characterization of a total of 404 FH patients in Portugal.
publishDate 2010
dc.date.none.fl_str_mv 2010-10
2010-10-01T00:00:00Z
2011-09-26T12:11:28Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.18/234
url http://hdl.handle.net/10400.18/234
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Atherosclerosis. 2010 Oct;212(2):553-8. Epub 2010 Aug 8.
0021-9150
doi:10.1016/j.atherosclerosis.2010.07.012
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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