A genome-wide association study of asthma symptoms in Latin American children

Detalhes bibliográficos
Autor(a) principal: Costa, Gustavo N. O.
Data de Publicação: 2015
Outros Autores: Dudbridge, Frank, Fiaccone, Rosemeire Leovigildo, Silva, Thiago M. da, Strina, Agostino, Figueiredo, Camila A., Rodrigues, Laura C., Barreto, Mauricio Lima
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFBA
Texto Completo: http://repositorio.ufba.br/ri/handle/ri/19061
Resumo: Background: Asthma is a chronic disease of the airways and, despite the advances in the knowledge of associated genetic regions in recent years, their mechanisms have yet to be explored. Several genome-wide association studies have been carried out in recent years, but none of these have involved Latin American populations with a high level of miscegenation, as is seen in the Brazilian population. Methods: 1246 children were recruited from a longitudinal cohort study in Salvador, Brazil. Asthma symptoms were identified in accordance with an International Study of Asthma and Allergies in Childhood (ISAAC)questionnaire. Following quality control, 1 877 526 autosomal SNPs were tested for association with childhood asthma symptoms by logistic regression using an additive genetic model. We complemented the analysis with an stimate of the phenotypic variance explained by common genetic variants. Replications were investigated in independent Mexican and US Latino samples. Results: Two chromosomal regions reached genome-wide significance level for childhood asthma symptoms: the 14q11 region flanking the DAD1 and OXA1L genes (rs1999071, MAF 0.32, OR 1.78, 95 % CI 1.45–2.18, p-value 2.83 × 10−8)and 15q22 region flanking the FOXB1 gene (rs10519031, MAF 0.04, OR 3.0, 95 % CI 2.02–4.49,p-value 6.68 × 10−8 and rs8029377, MAF 0.03, OR 2.49, 95 % CI 1.76–3.53, p-value 2.45 × 10− 7). eQTL analysis suggests that rs1999071 regulates the expression of OXA1L gene. However, the original findings were not replicated in the Mexican or US Latino samples. Conclusions: We conclude that the 14q11 and 15q22 regions may be associated with asthma symptoms in childhood.
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spelling Costa, Gustavo N. O.Dudbridge, FrankFiaccone, Rosemeire LeovigildoSilva, Thiago M. daStrina, AgostinoFigueiredo, Camila A.Rodrigues, Laura C.Barreto, Mauricio LimaCosta, Gustavo N. O.Dudbridge, FrankFiaccone, Rosemeire LeovigildoSilva, Thiago M. daStrina, AgostinoFigueiredo, Camila A.Rodrigues, Laura C.Barreto, Mauricio Lima2016-05-04T12:34:23Z2016-05-04T12:34:23Z20151471-2156http://repositorio.ufba.br/ri/handle/ri/19061v.16, p.1-11Background: Asthma is a chronic disease of the airways and, despite the advances in the knowledge of associated genetic regions in recent years, their mechanisms have yet to be explored. Several genome-wide association studies have been carried out in recent years, but none of these have involved Latin American populations with a high level of miscegenation, as is seen in the Brazilian population. Methods: 1246 children were recruited from a longitudinal cohort study in Salvador, Brazil. Asthma symptoms were identified in accordance with an International Study of Asthma and Allergies in Childhood (ISAAC)questionnaire. Following quality control, 1 877 526 autosomal SNPs were tested for association with childhood asthma symptoms by logistic regression using an additive genetic model. We complemented the analysis with an stimate of the phenotypic variance explained by common genetic variants. Replications were investigated in independent Mexican and US Latino samples. Results: Two chromosomal regions reached genome-wide significance level for childhood asthma symptoms: the 14q11 region flanking the DAD1 and OXA1L genes (rs1999071, MAF 0.32, OR 1.78, 95 % CI 1.45–2.18, p-value 2.83 × 10−8)and 15q22 region flanking the FOXB1 gene (rs10519031, MAF 0.04, OR 3.0, 95 % CI 2.02–4.49,p-value 6.68 × 10−8 and rs8029377, MAF 0.03, OR 2.49, 95 % CI 1.76–3.53, p-value 2.45 × 10− 7). eQTL analysis suggests that rs1999071 regulates the expression of OXA1L gene. However, the original findings were not replicated in the Mexican or US Latino samples. Conclusions: We conclude that the 14q11 and 15q22 regions may be associated with asthma symptoms in childhood.Submitted by Maria Creuza Silva (mariakreuza@yahoo.com.br) on 2016-05-04T12:34:23Z No. of bitstreams: 1 Art Per Estrang Mauricio L. Barreto. 2015.pdf: 1967757 bytes, checksum: 8839bb063988fc4af52bf6b679a8fd1d (MD5)Made available in DSpace on 2016-05-04T12:34:23Z (GMT). No. of bitstreams: 1 Art Per Estrang Mauricio L. Barreto. 2015.pdf: 1967757 bytes, checksum: 8839bb063988fc4af52bf6b679a8fd1d (MD5) Previous issue date: 2015-12LondonBioMed CentralBrasilhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669662/pdf/12863_2015_Article_296.pdfreponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAAsthma symptomsGenome-wide associationLatin AmericaChildrenA genome-wide association study of asthma symptoms in Latin American childrenBMC Genetinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessengORIGINALArt Per Estrang Mauricio L. Barreto. 2015.pdfArt Per Estrang Mauricio L. 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dc.title.pt_BR.fl_str_mv A genome-wide association study of asthma symptoms in Latin American children
dc.title.alternative.pt_BR.fl_str_mv BMC Genet
title A genome-wide association study of asthma symptoms in Latin American children
spellingShingle A genome-wide association study of asthma symptoms in Latin American children
Costa, Gustavo N. O.
Asthma symptoms
Genome-wide association
Latin America
Children
title_short A genome-wide association study of asthma symptoms in Latin American children
title_full A genome-wide association study of asthma symptoms in Latin American children
title_fullStr A genome-wide association study of asthma symptoms in Latin American children
title_full_unstemmed A genome-wide association study of asthma symptoms in Latin American children
title_sort A genome-wide association study of asthma symptoms in Latin American children
author Costa, Gustavo N. O.
author_facet Costa, Gustavo N. O.
Dudbridge, Frank
Fiaccone, Rosemeire Leovigildo
Silva, Thiago M. da
Strina, Agostino
Figueiredo, Camila A.
Rodrigues, Laura C.
Barreto, Mauricio Lima
author_role author
author2 Dudbridge, Frank
Fiaccone, Rosemeire Leovigildo
Silva, Thiago M. da
Strina, Agostino
Figueiredo, Camila A.
Rodrigues, Laura C.
Barreto, Mauricio Lima
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Costa, Gustavo N. O.
Dudbridge, Frank
Fiaccone, Rosemeire Leovigildo
Silva, Thiago M. da
Strina, Agostino
Figueiredo, Camila A.
Rodrigues, Laura C.
Barreto, Mauricio Lima
Costa, Gustavo N. O.
Dudbridge, Frank
Fiaccone, Rosemeire Leovigildo
Silva, Thiago M. da
Strina, Agostino
Figueiredo, Camila A.
Rodrigues, Laura C.
Barreto, Mauricio Lima
dc.subject.por.fl_str_mv Asthma symptoms
Genome-wide association
Latin America
Children
topic Asthma symptoms
Genome-wide association
Latin America
Children
description Background: Asthma is a chronic disease of the airways and, despite the advances in the knowledge of associated genetic regions in recent years, their mechanisms have yet to be explored. Several genome-wide association studies have been carried out in recent years, but none of these have involved Latin American populations with a high level of miscegenation, as is seen in the Brazilian population. Methods: 1246 children were recruited from a longitudinal cohort study in Salvador, Brazil. Asthma symptoms were identified in accordance with an International Study of Asthma and Allergies in Childhood (ISAAC)questionnaire. Following quality control, 1 877 526 autosomal SNPs were tested for association with childhood asthma symptoms by logistic regression using an additive genetic model. We complemented the analysis with an stimate of the phenotypic variance explained by common genetic variants. Replications were investigated in independent Mexican and US Latino samples. Results: Two chromosomal regions reached genome-wide significance level for childhood asthma symptoms: the 14q11 region flanking the DAD1 and OXA1L genes (rs1999071, MAF 0.32, OR 1.78, 95 % CI 1.45–2.18, p-value 2.83 × 10−8)and 15q22 region flanking the FOXB1 gene (rs10519031, MAF 0.04, OR 3.0, 95 % CI 2.02–4.49,p-value 6.68 × 10−8 and rs8029377, MAF 0.03, OR 2.49, 95 % CI 1.76–3.53, p-value 2.45 × 10− 7). eQTL analysis suggests that rs1999071 regulates the expression of OXA1L gene. However, the original findings were not replicated in the Mexican or US Latino samples. Conclusions: We conclude that the 14q11 and 15q22 regions may be associated with asthma symptoms in childhood.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2016-05-04T12:34:23Z
dc.date.available.fl_str_mv 2016-05-04T12:34:23Z
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dc.identifier.issn.none.fl_str_mv 1471-2156
dc.identifier.number.pt_BR.fl_str_mv v.16, p.1-11
identifier_str_mv 1471-2156
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url http://repositorio.ufba.br/ri/handle/ri/19061
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dc.publisher.none.fl_str_mv BioMed Central
dc.publisher.country.fl_str_mv Brasil
publisher.none.fl_str_mv BioMed Central
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