Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.

Bibliographic Details
Main Author: Rosa, A
Publication Date: 2008
Other Authors: Fonseca, B, Krug, T, Manso, H, Gouveia, L, Albergaria, I, Gaspar, G, Correia, M, Viana-Baptista, M, Simões, R, Pinto, A, Taipa, R, Ferreira, C, Fontes, J, Silva, M, Gabriel, J, Matos, I, Lopes, G, Ferro, J, Vicente, A, Oliveira, S
Format: Article
Language: eng
Source: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Download full: http://hdl.handle.net/10400.10/49
Summary: 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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spelling Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.Acidente isquémico transitórioFactores de riscoEnfarte do miocárdioEstudos de caso-controloBACKGROUND: 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.BioMed CentralRepositório do Hospital Prof. Doutor Fernando FonsecaRosa, AFonseca, BKrug, TManso, HGouveia, LAlbergaria, IGaspar, GCorreia, MViana-Baptista, MSimões, RPinto, ATaipa, RFerreira, CFontes, JSilva, MGabriel, JMatos, ILopes, GFerro, JVicente, AOliveira, S2010-03-04T16:54:30Z2008-01-01T00:00:00Z2008-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.10/49engBMC Med Genet. 2008; 9:571471-2350info: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:RCAAP2022-09-20T15:51:06Zoai:repositorio.hff.min-saude.pt:10400.10/49Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:51:26.620182Repositório 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 patients.
title Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
spellingShingle Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
Rosa, A
Acidente isquémico transitório
Factores de risco
Enfarte do miocárdio
Estudos de caso-controlo
title_short Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
title_full Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
title_fullStr Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
title_full_unstemmed Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
title_sort Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
author Rosa, A
author_facet Rosa, A
Fonseca, B
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, R
Pinto, A
Taipa, R
Ferreira, C
Fontes, J
Silva, M
Gabriel, J
Matos, I
Lopes, G
Ferro, J
Vicente, A
Oliveira, S
author_role author
author2 Fonseca, B
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, R
Pinto, A
Taipa, R
Ferreira, C
Fontes, J
Silva, M
Gabriel, J
Matos, I
Lopes, G
Ferro, J
Vicente, A
Oliveira, S
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 do Hospital Prof. Doutor Fernando Fonseca
dc.contributor.author.fl_str_mv Rosa, A
Fonseca, B
Krug, T
Manso, H
Gouveia, L
Albergaria, I
Gaspar, G
Correia, M
Viana-Baptista, M
Simões, R
Pinto, A
Taipa, R
Ferreira, C
Fontes, J
Silva, M
Gabriel, J
Matos, I
Lopes, G
Ferro, J
Vicente, A
Oliveira, S
dc.subject.por.fl_str_mv Acidente isquémico transitório
Factores de risco
Enfarte do miocárdio
Estudos de caso-controlo
topic Acidente isquémico transitório
Factores de risco
Enfarte do miocárdio
Estudos de caso-controlo
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 2008
dc.date.none.fl_str_mv 2008-01-01T00:00:00Z
2008-01-01T00:00:00Z
2010-03-04T16:54:30Z
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/10400.10/49
url http://hdl.handle.net/10400.10/49
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Med Genet. 2008; 9:57
1471-2350
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 BioMed Central
publisher.none.fl_str_mv BioMed Central
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
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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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