• David B Kantor, Cameron D Palmer, Taylor R Young, Yan Meng, Zofia K Gajdos, Helen Lyon, Alkes L Price, Samuela Pollack, Stephanie J London, Laura R Loehr, Lewis J Smith, Rajesh Kumar, David R Jacobs, Marcy F Petrini, George T O'Connor, Wendy B White, George Papanicolaou, Kristin M Burkart, Susan R Heckbert, R Graham Barr, and Joel N Hirschhorn.
• Division of Critical Care Medicine, Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA, 02115, USA. david.kantor@childrens.harvard.edu
• Hum. Genet. 2013 Sep 1; 132 (9): 1039-47.

AbstractAsthma originates from genetic and environmental factors with about half the risk of disease attributable to heritable causes. Genome-wide association studies, mostly in populations of European ancestry, have identified numerous asthma-associated single nucleotide polymorphisms (SNPs). Studies in populations with diverse ancestries allow both for identification of robust associations that replicate across ethnic groups and for improved resolution of associated loci due to different patterns of linkage disequilibrium between ethnic groups. Here we report on an analysis of 745 African-American subjects with asthma and 3,238 African-American control subjects from the Candidate Gene Association Resource (CARe) Consortium, including analysis of SNPs imputed using 1,000 Genomes reference panels and adjustment for local ancestry. We show strong evidence that variation near RAD50/IL13, implicated in studies of European ancestry individuals, replicates in individuals largely of African ancestry. Fine mapping in African ancestry populations also refined the variants of interest for this association. We also provide strong or nominal evidence of replication at loci near ORMDL3/GSDMB, IL1RL1/IL18R1, and 10p14, all previously associated with asthma in European or Japanese populations, but not at the PYHIN1 locus previously reported in studies of African-American samples. These results improve the understanding of asthma genetics and further demonstrate the utility of genetic studies in populations other than those of largely European ancestry.

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