Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women

• Published in: American journal of respiratory cell and molecular biology Vol. 56; no. 3; pp. 332 - 341
• Main Authors: 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.
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 01.03.2017
• Subjects: African Americans; Age; Aged; Alleles; Applications; Bioinformatics; Cadherins; Cadherins - genetics; Chronic obstructive pulmonary disease; Computer Science; Demography; Emphysema; Female; Females; Gene expression; Gene Expression Regulation; Genetic Loci; Genetic Predisposition to Disease; Genetics; Genome-Wide Association Study; Genomes; Health risk assessment; Hispanic people; Human genetics; Humans; Life Sciences; Lung; Lung - metabolism; Lung diseases; Male; Males; Mens health; Methodology; Middle Aged; Original Research; Polymorphism, Single Nucleotide; Polymorphism, Single Nucleotide - genetics; Population; Pulmonary Disease, Chronic Obstructive; Pulmonary Disease, Chronic Obstructive - genetics; Risk Factors; Santé publique et épidémiologie; Smoking; Statistics; Studies; Womens health; genetics; growth and development; genome-wide association study; sex; chronic obstructive pulmonary disease
• ISSN: 1044-1549; 1535-4989
• DOI: 10.1165/rcmb.2016-0172OC

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 . 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 ). 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 ) 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.