Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient

Detalhes bibliográficos
Autor(a) principal: Rosa, A
Data de Publicação: 2010
Outros Autores: Fonseca, BV, Krug, T, Manso, H, Gouveia, L, Albergaria, I, Gaspar, G, Correia, M, Viana-Baptista, M, Simões, RM, Pinto, AN, Taipa, R, Ferreira, C, Fontes, JR, Gabriel, JP, Matos, I, Lopes, G, Ferro, JM, Vicente, AM, Oliveira, SA
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.23/300
Resumo: BACKGROUND: The genetic contribution to stroke is well established but it has proven difficult to identify the genes and the disease-associated alleles mediating this effect, possibly because only nuclear genes have been intensely investigated so far. Mitochondrial DNA (mtDNA) has been implicated in several disorders having stroke as one of its clinical manifestations. The aim of this case-control study was to assess the contribution of mtDNA polymorphisms and haplogroups to ischemic stroke risk. METHODS: We genotyped 19 mtDNA single nucleotide polymorphisms (SNPs) defining the major European haplogroups in 534 ischemic stroke patients and 499 controls collected in Portugal, and tested their allelic and haplogroup association with ischemic stroke risk. RESULTS: Haplogroup H1 was found to be significantly less frequent in stroke patients than in controls (OR = 0.61, 95% CI = 0.45-0.83, p = 0.001), when comparing each clade against all other haplogroups pooled together. Conversely, the pre-HV/HV and U mtDNA lineages emerge as potential genetic factors conferring risk for stroke (OR = 3.14, 95% CI = 1.41-7.01, p = 0.003, and OR = 2.87, 95% CI = 1.13-7.28, p = 0.021, respectively). SNPs m.3010G>A, m.7028C>T and m.11719G>A strongly influence ischemic stroke risk, their allelic state in haplogroup H1 corroborating its protective effect. CONCLUSION: Our data suggests that mitochondrial haplogroup H1 has an impact on ischemic stroke risk in a Portuguese sample.
id RCAP_38d69536f2b9a55cb3a45d221d771155
oai_identifier_str oai:repositorio.hospitaldebraga.pt:10400.23/300
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patientIsquemia CerebralDNA MitocondrialPredisposição Genética para DoençaHaplótiposAcidente Vascular CerebralBACKGROUND: The genetic contribution to stroke is well established but it has proven difficult to identify the genes and the disease-associated alleles mediating this effect, possibly because only nuclear genes have been intensely investigated so far. Mitochondrial DNA (mtDNA) has been implicated in several disorders having stroke as one of its clinical manifestations. The aim of this case-control study was to assess the contribution of mtDNA polymorphisms and haplogroups to ischemic stroke risk. METHODS: We genotyped 19 mtDNA single nucleotide polymorphisms (SNPs) defining the major European haplogroups in 534 ischemic stroke patients and 499 controls collected in Portugal, and tested their allelic and haplogroup association with ischemic stroke risk. RESULTS: Haplogroup H1 was found to be significantly less frequent in stroke patients than in controls (OR = 0.61, 95% CI = 0.45-0.83, p = 0.001), when comparing each clade against all other haplogroups pooled together. Conversely, the pre-HV/HV and U mtDNA lineages emerge as potential genetic factors conferring risk for stroke (OR = 3.14, 95% CI = 1.41-7.01, p = 0.003, and OR = 2.87, 95% CI = 1.13-7.28, p = 0.021, respectively). SNPs m.3010G>A, m.7028C>T and m.11719G>A strongly influence ischemic stroke risk, their allelic state in haplogroup H1 corroborating its protective effect. CONCLUSION: Our data suggests that mitochondrial haplogroup H1 has an impact on ischemic stroke risk in a Portuguese sample.BioMedCentralRepositório Científico do Hospital de BragaRosa, AFonseca, BVKrug, TManso, HGouveia, LAlbergaria, IGaspar, GCorreia, MViana-Baptista, MSimões, RMPinto, ANTaipa, RFerreira, CFontes, JRGabriel, JPMatos, ILopes, GFerro, JMVicente, AMOliveira, SA2012-07-13T08:10:42Z2010-01-01T00:00:00Z2010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.23/300engBMC Med Genet. 2008 Jul 1;9:57.info: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:RCAAP2022-09-21T09:01:53Zoai:repositorio.hospitaldebraga.pt:10400.23/300Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:54:42.696004Repositório 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 Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
title Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
spellingShingle Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
Rosa, A
Isquemia Cerebral
DNA Mitocondrial
Predisposição Genética para Doença
Haplótipos
Acidente Vascular Cerebral
title_short Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
title_full Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
title_fullStr Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
title_full_unstemmed Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
title_sort Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
author Rosa, A
author_facet Rosa, A
Fonseca, BV
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, RM
Pinto, AN
Taipa, R
Ferreira, C
Fontes, JR
Gabriel, JP
Matos, I
Lopes, G
Ferro, JM
Vicente, AM
Oliveira, SA
author_role author
author2 Fonseca, BV
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, RM
Pinto, AN
Taipa, R
Ferreira, C
Fontes, JR
Gabriel, JP
Matos, I
Lopes, G
Ferro, JM
Vicente, AM
Oliveira, SA
author2_role 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 Científico do Hospital de Braga
dc.contributor.author.fl_str_mv Rosa, A
Fonseca, BV
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, RM
Pinto, AN
Taipa, R
Ferreira, C
Fontes, JR
Gabriel, JP
Matos, I
Lopes, G
Ferro, JM
Vicente, AM
Oliveira, SA
dc.subject.por.fl_str_mv Isquemia Cerebral
DNA Mitocondrial
Predisposição Genética para Doença
Haplótipos
Acidente Vascular Cerebral
topic Isquemia Cerebral
DNA Mitocondrial
Predisposição Genética para Doença
Haplótipos
Acidente Vascular Cerebral
description BACKGROUND: The genetic contribution to stroke is well established but it has proven difficult to identify the genes and the disease-associated alleles mediating this effect, possibly because only nuclear genes have been intensely investigated so far. Mitochondrial DNA (mtDNA) has been implicated in several disorders having stroke as one of its clinical manifestations. The aim of this case-control study was to assess the contribution of mtDNA polymorphisms and haplogroups to ischemic stroke risk. METHODS: We genotyped 19 mtDNA single nucleotide polymorphisms (SNPs) defining the major European haplogroups in 534 ischemic stroke patients and 499 controls collected in Portugal, and tested their allelic and haplogroup association with ischemic stroke risk. RESULTS: Haplogroup H1 was found to be significantly less frequent in stroke patients than in controls (OR = 0.61, 95% CI = 0.45-0.83, p = 0.001), when comparing each clade against all other haplogroups pooled together. Conversely, the pre-HV/HV and U mtDNA lineages emerge as potential genetic factors conferring risk for stroke (OR = 3.14, 95% CI = 1.41-7.01, p = 0.003, and OR = 2.87, 95% CI = 1.13-7.28, p = 0.021, respectively). SNPs m.3010G>A, m.7028C>T and m.11719G>A strongly influence ischemic stroke risk, their allelic state in haplogroup H1 corroborating its protective effect. CONCLUSION: Our data suggests that mitochondrial haplogroup H1 has an impact on ischemic stroke risk in a Portuguese sample.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01T00:00:00Z
2010-01-01T00:00:00Z
2012-07-13T08:10:42Z
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/10400.23/300
url http://hdl.handle.net/10400.23/300
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Med Genet. 2008 Jul 1;9:57.
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 BioMedCentral
publisher.none.fl_str_mv BioMedCentral
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
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
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
repository.mail.fl_str_mv
_version_ 1799130414151892992