Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study

Detalhes bibliográficos
Autor(a) principal: Domingues-Montanarie, Sophie
Data de Publicação: 2010
Outros Autores: Fernández-Cadenas, Israel, Rio-Espinola, Alberto del, Corbeto, Natalia, Krug, Tiago, Manso, Helena, Gouveia, Liliana, Sobral, João, Mendioroz, Maite, Fernández-Morales, Jessica, Alvarez-Sabin, José, Ribó, Marc, Rubiera, Marta, Obach, Victor, Martí-Fàbregas, Joan, Freijo, Marimar, Serena, Joaquin, Ferro, José M., Vicente, Astrid M., Oliveira, Sofia A., Montaner, Joan
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10451/6750
Resumo: Copyright © 2010 S. Karger AG
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spelling Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional studyALOX5APSingle nucleotide polymorphismMeta-analysisStrokeGeneticsPDE4DCopyright © 2010 S. Karger AGBackground: Variants in the 5-lipoxygenase-activating protein (ALOX5AP) and phosphodiesterase 4D (PDE4D) genes have first been associated with ischemic stroke (IS) through whole-genome linkage screens. However, association studies obtained conflicting results. We aimed to investigate the contribution of selected single nucleotide polymorphisms (SNPs) in these genes for the first time in a large Iberian population. Methods: A case-control design was used to analyze one SNP in ALOX5AP and five SNPs in PDE4D in a total of 1,092 IS patients and 781 healthy controls of two different subsets from Spain and Portugal. The analysis was adjusted for confounding variables and the results were integrated in a meta-analysis of all case-control studies. In addition, ALOX5AP gene expression levels were determined in controls and IS cases. Results: A first meta-analysis of both subsets showed that the T allele of the SG13S114 SNP in ALOX5AP was a risk factor for IS after Bonferroni correction [OR = 1.22 (1.06–1.40); p = 0.006]. A second meta-analysis of white populations confirmed these results [OR = 1.18 (1.07–1.31); p = 0.001]. ALOX5AP gene expression analysis in a subset of controls and cases revealed that the SG13S114 genotypes modulate mRNA levels of ALOX5AP (p = 0.001) and mRNA levels were higher in IS cases (2.8 ± 2.4%) than in controls (1.4 ± 1.3%; p = 0.003). No association of the variants in PDE4D with IS was observed in our study. Conclusions: The ALOX5AP SG13S114 variant is an independent risk factor for IS in the Iberian population and is associated with ALOX5AP expression levels. The role of this gene in stroke merits further investigation.This study was funded by a grant from the Spanish government (Geno-tPA project FIS PJ060586), the stroke research network (RENEVAS) and the Ramón Areces Foundation. S.D.-M. is the recipient of a grant from the Ramón Areces Foundation, I.F.-C. a postdoctoral grant from the Vall d’Hebron Research Institute (IRVH), A.d.R.-E. received a grant from the Vall d’Hebron Research Institute (IRVH), M.M. received a grant for Formation in Investigation (FI05/00081), and J.F.-M. was a recipient of a grant from La Marató (Chromig Exp. 072310). This work was also supported in part by the Portuguese Fundação para a Ciência e a Tecnologia (FCT) grant PTDC/SAU-GMG/ 64426/2006, FCT fellowships (TK, HM), and the Fundação AstraZeneca/Faculdade de Medicina de Lisboa research fellowship (LG). The Neurovascular Research Laboratory takes part in the International Stroke Genetics Consortium ISGC and in the RENEVAS network.KargerRepositório da Universidade de LisboaDomingues-Montanarie, SophieFernández-Cadenas, IsraelRio-Espinola, Alberto delCorbeto, NataliaKrug, TiagoManso, HelenaGouveia, LilianaSobral, JoãoMendioroz, MaiteFernández-Morales, JessicaAlvarez-Sabin, JoséRibó, MarcRubiera, MartaObach, VictorMartí-Fàbregas, JoanFreijo, MarimarSerena, JoaquinFerro, José M.Vicente, Astrid M.Oliveira, Sofia A.Montaner, Joan2012-07-23T13:32:08Z20102010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/6750engCerebrovasc Dis 2010;29:528–5371015-9770http://dx.doi.org/10.1159/000302738info: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:RCAAP2023-11-08T15:49:11Zoai:repositorio.ul.pt:10451/6750Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:31:40.206093Repositório 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 Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
title Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
spellingShingle Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
Domingues-Montanarie, Sophie
ALOX5AP
Single nucleotide polymorphism
Meta-analysis
Stroke
Genetics
PDE4D
title_short Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
title_full Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
title_fullStr Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
title_full_unstemmed Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
title_sort Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke : a case-control, meta-analysis and functional study
author Domingues-Montanarie, Sophie
author_facet Domingues-Montanarie, Sophie
Fernández-Cadenas, Israel
Rio-Espinola, Alberto del
Corbeto, Natalia
Krug, Tiago
Manso, Helena
Gouveia, Liliana
Sobral, João
Mendioroz, Maite
Fernández-Morales, Jessica
Alvarez-Sabin, José
Ribó, Marc
Rubiera, Marta
Obach, Victor
Martí-Fàbregas, Joan
Freijo, Marimar
Serena, Joaquin
Ferro, José M.
Vicente, Astrid M.
Oliveira, Sofia A.
Montaner, Joan
author_role author
author2 Fernández-Cadenas, Israel
Rio-Espinola, Alberto del
Corbeto, Natalia
Krug, Tiago
Manso, Helena
Gouveia, Liliana
Sobral, João
Mendioroz, Maite
Fernández-Morales, Jessica
Alvarez-Sabin, José
Ribó, Marc
Rubiera, Marta
Obach, Victor
Martí-Fàbregas, Joan
Freijo, Marimar
Serena, Joaquin
Ferro, José M.
Vicente, Astrid M.
Oliveira, Sofia A.
Montaner, Joan
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Domingues-Montanarie, Sophie
Fernández-Cadenas, Israel
Rio-Espinola, Alberto del
Corbeto, Natalia
Krug, Tiago
Manso, Helena
Gouveia, Liliana
Sobral, João
Mendioroz, Maite
Fernández-Morales, Jessica
Alvarez-Sabin, José
Ribó, Marc
Rubiera, Marta
Obach, Victor
Martí-Fàbregas, Joan
Freijo, Marimar
Serena, Joaquin
Ferro, José M.
Vicente, Astrid M.
Oliveira, Sofia A.
Montaner, Joan
dc.subject.por.fl_str_mv ALOX5AP
Single nucleotide polymorphism
Meta-analysis
Stroke
Genetics
PDE4D
topic ALOX5AP
Single nucleotide polymorphism
Meta-analysis
Stroke
Genetics
PDE4D
description Copyright © 2010 S. Karger AG
publishDate 2010
dc.date.none.fl_str_mv 2010
2010-01-01T00:00:00Z
2012-07-23T13:32:08Z
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/10451/6750
url http://hdl.handle.net/10451/6750
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Cerebrovasc Dis 2010;29:528–537
1015-9770
http://dx.doi.org/10.1159/000302738
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 Karger
publisher.none.fl_str_mv Karger
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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