Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children

Xiumei Hong(Johns Hopkins University), Ke Hao(Icahn School of Medicine at Mount Sinai), Christine Ladd‐Acosta(Johns Hopkins University), Kasper D. Hansen(Johns Hopkins University), Hui‐Ju Tsai(Northwestern University), Xin Liu(Lurie Children's Hospital), Xin Xu(Southern Medical University), Timothy A. Thornton(University of Washington), Deanna Caruso(Johns Hopkins University), Corinne Keet(Johns Hopkins University), Yifei Sun(Johns Hopkins University), Guoying Wang(Johns Hopkins University), Wei Luo(Icahn School of Medicine at Mount Sinai), Rajesh Kumar(Lurie Children's Hospital), Ramsay Fuleihan(Lurie Children's Hospital), Anne Marie Singh(Lurie Children's Hospital), Jennifer S. Kim(Lurie Children's Hospital), Rachel E. Story(Lurie Children's Hospital), Ruchi S. Gupta(Lurie Children's Hospital), Peisong Gao(Johns Hopkins Medicine), Zhu Chen(Johns Hopkins University), Sheila O. Walker(Johns Hopkins University), Tami R. Bartell(Lurie Children's Hospital), Terri H. Beaty(Johns Hopkins University), M. Daniele Fallin(Johns Hopkins University), Robert P. Schleimer(Northwestern University), Patrick G. Holt(University of Western Australia), Kari C. Nadeau(Stanford University), Robert A. Wood(Johns Hopkins University), Jacqueline A. Pongracic(Lurie Children's Hospital), Daniel E. Weeks(University of Pittsburgh), Xiaobin Wang(Johns Hopkins Medicine)
Nature Communications
February 24, 2015
Cited by 246Open Access
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Abstract

Food allergy (FA) affects 2%-10% of US children and is a growing clinical and public health problem. Here we conduct the first genome-wide association study of well-defined FA, including specific subtypes (peanut, milk and egg) in 2,759 US participants (1,315 children and 1,444 parents) from the Chicago Food Allergy Study, and identify peanut allergy (PA)-specific loci in the HLA-DR and -DQ gene region at 6p21.32, tagged by rs7192 (P=5.5 × 10(-8)) and rs9275596 (P=6.8 × 10(-10)), in 2,197 participants of European ancestry. We replicate these associations in an independent sample of European ancestry. These associations are further supported by meta-analyses across the discovery and replication samples. Both single-nucleotide polymorphisms (SNPs) are associated with differential DNA methylation levels at multiple CpG sites (P<5 × 10(-8)), and differential DNA methylation of the HLA-DQB1 and HLA-DRB1 genes partially mediate the identified SNP-PA associations. This study suggests that the HLA-DR and -DQ gene region probably poses significant genetic risk for PA.


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