Comprehensive Testing of Positionally Cloned Asthma Genes in Two Populations

• Published in: American journal of respiratory and critical care medicine 2007-11, Vol.176 (9), p.849-857
• Main Authors: Hersh, Craig P, Raby, Benjamin A, Soto-Quiros, Manuel E, Murphy, Amy J, Avila, Lydiana, Lasky-Su, Jessica, Sylvia, Jody S, Klanderman, Barbara J, Lange, Christoph, Weiss, Scott T, Celedon, Juan C
• Format: Article
• Language: English
• Subjects: A. Asthma and Allergy; ADAM Proteins - genetics; Adolescent; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Asthma; Asthma - ethnology; Asthma - genetics; Biological and medical sciences; Blood and lymphatic vessels; Cardiology. Vascular system; Child; Childrens health; Chromosomes; Chronic obstructive pulmonary disease, asthma; Cloning; Cloning, Molecular; Costa Rica; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - genetics; Disease; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous; DNA-Binding Proteins - genetics; Families & family life; Female; Gene Order; Genes; Hispanic people; Histocompatibility Antigens Class I - genetics; HLA Antigens - genetics; HLA-G Antigens; Humans; Immunoglobulins; Indians, Central American - genetics; Intensive care medicine; Linkage Disequilibrium - genetics; Male; Medical sciences; North America; Pneumology; Polymorphism; Polymorphism, Single Nucleotide - genetics; Proteins; Receptors, G-Protein-Coupled - genetics; Transcription Factors - genetics; White People - genetics; Womens health
• ISSN: 1073-449X; 1535-4970
• DOI: 10.1164/rccm.200704-592OC

Replication of gene-disease associations has become a requirement in complex trait genetics. In studies of childhood asthma from two different ethnic groups, we attempted to replicate associations with five potential asthma susceptibility genes previously identified by positional cloning. We analyzed two family-based samples ascertained through an asthmatic proband: 497 European-American children from the Childhood Asthma Management Program and 439 Hispanic children from the Central Valley of Costa Rica. We genotyped 98 linkage disequilibrium-tagging single-nucleotide polymorphisms (SNPs) in five genes: ADAM33, DPP10, GPR154 (HUGO name: NPSR1), HLA-G, and the PHF11 locus (includes genes SETDB2 and RCBTB1). SNPs were tested for association with asthma and two intermediate phenotypes: airway hyperresponsiveness and total serum immunoglobulin E levels. Despite differing ancestries, linkage disequilibrium patterns were similar in both cohorts. Of the five evaluated genes, SNP-level replication was found only for GPR154 (NPSR1). In this gene, three SNPs were associated with asthma in both cohorts, although the opposite alleles were associated in either study. Weak evidence for locus-level replication with asthma was found in the PHF11 locus, although there was no overlap in the associated SNP across the two cohorts. No consistent associations were observed for the three other genes. These results provide some further support for the role of genetic variation in GPR154 (NPSR1) and PHF11 in asthma susceptibility and also highlight the challenges of replicating genetic associations in complex traits such as asthma, even for genes identified by linkage analysis.