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Genome-wide Association Study Identifies Peanut Allergy-Specific Loci and Evidence of Epigenetic Mediation in U.S. Children

Food allergy (FA) affects 2–10% of U.S. 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 U.S. participants (1,315 children; 1,444 parents) from the Ch...

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Detalles Bibliográficos
Autores principales: Hong, Xiumei, Hao, Ke, Ladd-Acosta, Christine, Hansen, Kasper D, Tsai, Hui-Ju, Liu, Xin, Xu, Xin, Thornton, Timothy A., Caruso, Deanna, Keet, Corinne A, Sun, Yifei, Wang, Guoying, Luo, Wei, Kumar, Rajesh, Fuleihan, Ramsay, Singh, Anne Marie, Kim, Jennifer S, Story, Rachel E, Gupta, Ruchi S, Gao, Peisong, Chen, Zhu, Walker, Sheila O., Bartell, Tami R, Beaty, Terri H, Fallin, M Daniele, Schleimer, Robert, Holt, Patrick G, Nadeau, Kari Christine, Wood, Robert A, Pongracic, Jacqueline A, Weeks, Daniel E, Wang, Xiaobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340086/
https://www.ncbi.nlm.nih.gov/pubmed/25710614
http://dx.doi.org/10.1038/ncomms7304
Descripción
Sumario:Food allergy (FA) affects 2–10% of U.S. 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 U.S. participants (1,315 children; 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 likely poses significant genetic risk for PA.