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Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos

Authors :
Lindsey A. Roth
Pedro C. Avila
Denise Serebrisky
Emerita Brigino-Buenaventura
Eugene R. Bleecker
Karla Sandoval
William Rodriguez-Cintron
Rocio Chapela
Deborah A. Meyers
Brian J. O'Roak
Fred Lurmann
Catarina D. Campbell
Shannon Thyne
Esteban G. Burchard
Adam Davis
Christopher R. Gignoux
Rajesh Kumar
Rasika A. Mathias
Kelley Meade
Jose R. Rodriguez-Santana
Fernando D. Martinez
Luisa N. Borrell
Steven J. Mack
Albert M. Levin
Evan E. Eichler
Cheryl A. Winkler
Scott T. Weiss
Elizabeth A. Nguyen
Donglei Hu
Celeste Eng
Carole Ober
Andrés Moreno-Estrada
Dara G. Torgerson
L. Keoki Williams
Kathleen C. Barnes
Joshua Galanter
Katherine K. Nishimura
Scott Huntsman
Benjamin A. Raby
Badri Padhukasahasram
Ryan D. Hernandez
Michael A. LeNoir
Pierre-Antoine Gourraud
Jean G. Ford
Dan L. Nicolae
Kiana Mohajeri
Carlos Bustamante
Maria Pino-Yanes
Saunak Sen
Harold J. Farber
Source :
Journal of Allergy and Clinical Immunology. 135:1502-1510
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Background IgE is a key mediator of allergic inflammation, and its levels are frequently increased in patients with allergic disorders. Objective We sought to identify genetic variants associated with IgE levels in Latinos. Methods We performed a genome-wide association study and admixture mapping of total IgE levels in 3334 Latinos from the Genes-environments & Admixture in Latino Americans (GALA II) study. Replication was evaluated in 454 Latinos, 1564 European Americans, and 3187 African Americans from independent studies. Results We confirmed associations of 6 genes identified by means of previous genome-wide association studies and identified a novel genome-wide significant association of a polymorphism in the zinc finger protein 365 gene (ZNF365) with total IgE levels (rs200076616, P = 2.3 × 10 −8 ). We next identified 4 admixture mapping peaks (6p21.32-p22.1, 13p22-31, 14q23.2, and 22q13.1) at which local African, European, and/or Native American ancestry was significantly associated with IgE levels. The most significant peak was 6p21.32-p22.1, where Native American ancestry was associated with lower IgE levels ( P = 4.95 × 10 −8 ). All but 22q13.1 were replicated in an independent sample of Latinos, and 2 of the peaks were replicated in African Americans (6p21.32-p22.1 and 14q23.2). Fine mapping of 6p21.32-p22.1 identified 6 genome-wide significant single nucleotide polymorphisms in Latinos, 2 of which replicated in European Americans. Another single nucleotide polymorphism was peak-wide significant within 14q23.2 in African Americans (rs1741099, P = 3.7 × 10 −6 ) and replicated in non–African American samples ( P = .011). Conclusion We confirmed genetic associations at 6 genes and identified novel associations within ZNF365 , HLA-DQA1 , and 14q23.2. Our results highlight the importance of studying diverse multiethnic populations to uncover novel loci associated with total IgE levels.

Details

ISSN :
00916749
Volume :
135
Database :
OpenAIRE
Journal :
Journal of Allergy and Clinical Immunology
Accession number :
edsair.doi.dedup.....1eb6c8eab2e0d2704ea1fa5231228007
Full Text :
https://doi.org/10.1016/j.jaci.2014.10.033