Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , , , , , , , , , , , , , , , |
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. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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 |
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1799130414151892992 |