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Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women.
Hardin, Megan; Cho, Michael H; Sharma, Sunita; Glass, Kimberly; Castaldi, Peter J; McDonald, Merry-Lynn; Aschard, Hugues; Senter-Sylvia, Jody; Tantisira, Kelan; Weiss, Scott T; Hersh, Craig P; Morrow, Jarrett D; Lomas, David; Agusti, Alvar; Bakke, Per; Gulsvik, Amund; O'Connor, George T; Dupuis, Josée; Hokanson, John; Crapo, James D; Beaty, Terri H; Laird, Nan; Silverman, Edwin K; DeMeo, Dawn L.
Afiliação
  • Hardin M; 1 Channing Division of Network Medicine and.
  • Cho MH; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Sharma S; 1 Channing Division of Network Medicine and.
  • Glass K; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Castaldi PJ; 3 Division of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado.
  • McDonald ML; 1 Channing Division of Network Medicine and.
  • Aschard H; 1 Channing Division of Network Medicine and.
  • Senter-Sylvia J; 1 Channing Division of Network Medicine and.
  • Tantisira K; 4 Harvard School of Public Health, Boston, Massachusetts.
  • Weiss ST; 1 Channing Division of Network Medicine and.
  • Hersh CP; 1 Channing Division of Network Medicine and.
  • Morrow JD; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Lomas D; 1 Channing Division of Network Medicine and.
  • Agusti A; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Bakke P; 1 Channing Division of Network Medicine and.
  • Gulsvik A; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • O'Connor GT; 1 Channing Division of Network Medicine and.
  • Dupuis J; 2 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Hokanson J; 5 Department of Medicine, University College London, London, United Kingdom.
  • Crapo JD; 6 Thoracic Institute, Hospital Clinic, Barcelona, Spain.
  • Beaty TH; 7 Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Laird N; 8 Department of Geriatric Medicine Ullevaal, Institute of Clinical Medicine, Oslo University Hospital University of Oslo, Oslo, Norway.
  • Silverman EK; 9 Boston University School of Medicine, Boston, Massachusetts.
  • DeMeo DL; 10 Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Am J Respir Cell Mol Biol ; 56(3): 332-341, 2017 03.
Article em En | MEDLINE | ID: mdl-27854507
ABSTRACT
Chronic obstructive pulmonary disease (COPD) is a complex disease with strong environmental and genetic influences and sexually dimorphic features. Although genetic risk factors for COPD have been identified, much of the heritability remains unexplained. Sex-based genetic association studies may uncover additional COPD genetic risk factors. We studied current and former smokers from COPD case-control cohorts (COPDGene non-Hispanic whites and African Americans, Evaluation of COPD Longitudinally to Identify Predictive Surrogate End-Points, and Genetics of Chronic Obstructive Lung Disease). COPD was defined as post-bronchodilator forced expiratory volume in 1 second/forced vital capacity less than 0.70 and forced expiratory volume in 1 second percent predicted less than 80. Testing was performed across all cohorts and combined in a meta-analysis adjusted for age, pack-years, and genetic ancestry. We first performed genome-wide single-nucleotide polymorphism (SNP)-by-sex interaction testing on the outcome of COPD affection status. We performed sex-stratified association testing for SNPs with interaction P less than 10-6. We examined over 8 million SNPs in four populations, including 6,260 subjects with COPD (40.6% female) and 5,269 smoking control subjects (47.3% female). The SNP rs9615358 in the cadherin gene CELSR1 approached genome-wide significance for an interaction with sex (P = 1.24 × 10-7). In the sex-stratified meta-analysis, this SNP was associated with COPD among females (odds ratio, 1.37 [95% confidence interval, 1.25-1.49]; P = 3.32 × 10-7) but not males (odds ratio, 0.90 [95% confidence interval, 0.79-1.01]; P = 0.06). CELSR1 is involved in fetal lung development. In a human fetal lung tissue dataset, we observed greater CELSR1 expression in female compared with male samples. This SNP-by-sex genome-wide association analysis identified the fetal lung development gene, CELSR1, as a potential sex-specific risk factor for COPD. Identifying sex-specific genetic risk factors may reveal new insights into sexually dimorphic features of COPD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Predisposição Genética para Doença / Doença Pulmonar Obstrutiva Crônica / Estudo de Associação Genômica Ampla / Loci Gênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Predisposição Genética para Doença / Doença Pulmonar Obstrutiva Crônica / Estudo de Associação Genômica Ampla / Loci Gênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article