Eunice Y Lee1,2, Angel C Y Mak2, Donglei Hu2, Satria Sajuthi3, Marquitta J White2, Kevin L Keys2, Walter Eckalbar1, Luke Bonser2, Scott Huntsman2, Cydney Urbanek3, Celeste Eng2, Deepti Jain4, Gonçalo Abecasis5,6, Hyun M Kang5, Soren Germer7, Michael C Zody7, Deborah A Nickerson8,9,10, David Erle2, Elad Ziv2, Jose Rodriguez-Santana11, Max A Seibold3,12,13, Esteban G Burchard1,2. 1. Department of Bioengineering and Therapeutic Sciences and. 2. Department of Medicine, University of California, San Francisco, San Francisco, California. 3. Department of Pediatrics, Center for Genes, Environment, and Health, and. 4. Department of Biostatistics and. 5. Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan. 6. Regeneron Pharmaceuticals, Tarrytown, New York. 7. New York Genome Center, New York, New York. 8. Department of Genome Sciences, University of Washington, Seattle, Washington. 9. Northwest Genomics Center, Seattle, Washington. 10. Brotman Baty Institute, Seattle, Washington. 11. Centro de Neumología Pediátrica, San Juan, Puerto Rico; and. 12. Department of Pediatrics, National Jewish Health, Denver, Colorado. 13. Division of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado-Anschutz Medical Campus, Aurora, Colorado.
Abstract
Rationale: Puerto Ricans have the highest childhood asthma prevalence in the United States (23.6%); however, the etiology is uncertain. Objectives: In this study, we sought to uncover the genetic architecture of lung function in Puerto Rican youth with and without asthma who were recruited from the island (n = 836). Methods: We used admixture-mapping and whole-genome sequencing data to discover genomic regions associated with lung function. Functional roles of the prioritized candidate SNPs were examined with chromatin immunoprecipitation sequencing, RNA sequencing, and expression quantitative trait loci data.Measurements and Main Results: We discovered a genomic region at 1q32 that was significantly associated with a 0.12-L decrease in the lung volume of exhaled air (95% confidence interval, -0.17 to -0.07; P = 6.62 × 10-8) with each allele of African ancestry. Within this region, two SNPs were expression quantitative trait loci of TMEM9 in nasal airway epithelial cells and MROH3P in esophagus mucosa. The minor alleles of these SNPs were associated with significantly decreased lung function and decreased TMEM9 gene expression. Another admixture-mapping peak was observed on chromosome 5q35.1, indicating that each Native American ancestry allele was associated with a 0.15-L increase in lung function (95% confidence interval, 0.08-0.21; P = 5.03 × 10-6). The region-based association tests identified four suggestive windows that harbored candidate rare variants associated with lung function.Conclusions: We identified common and rare genetic variants that may play a critical role in lung function among Puerto Rican youth. We independently validated an inflammatory pathway that could potentially be used to develop more targeted treatments and interventions for patients with asthma.
Rationale: Puerto Ricans have the highest childhood asthma prevalence in the United States (23.6%); however, the etiology is uncertain. Objectives: In this study, we sought to uncover the genetic architecture of lung function in Puerto Rican youth with and without asthma who were recruited from the island (n = 836). Methods: We used admixture-mapping and whole-genome sequencing data to discover genomic regions associated with lung function. Functional roles of the prioritized candidate SNPs were examined with chromatin immunoprecipitation sequencing, RNA sequencing, and expression quantitative trait loci data.Measurements and Main Results: We discovered a genomic region at 1q32 that was significantly associated with a 0.12-L decrease in the lung volume of exhaled air (95% confidence interval, -0.17 to -0.07; P = 6.62 × 10-8) with each allele of African ancestry. Within this region, two SNPs were expression quantitative trait loci of TMEM9 in nasal airway epithelial cells and MROH3P in esophagus mucosa. The minor alleles of these SNPs were associated with significantly decreased lung function and decreased TMEM9 gene expression. Another admixture-mapping peak was observed on chromosome 5q35.1, indicating that each Native American ancestry allele was associated with a 0.15-L increase in lung function (95% confidence interval, 0.08-0.21; P = 5.03 × 10-6). The region-based association tests identified four suggestive windows that harbored candidate rare variants associated with lung function.Conclusions: We identified common and rare genetic variants that may play a critical role in lung function among Puerto Rican youth. We independently validated an inflammatory pathway that could potentially be used to develop more targeted treatments and interventions for patients with asthma.
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