TY - JOUR
T1 - Identification of four novel loci in Asthma in European American and African American Populations
AU - Almoguera, Berta
AU - Vazquez, Lyam
AU - Mentch, Frank
AU - Connolly, John
AU - Pacheco, Jennifer A.
AU - Sundaresan, Agnes S.
AU - Peissig, Peggy L.
AU - Linneman, James G.
AU - McCarty, Catherine A.
AU - Crosslin, David
AU - Carrell, David S.
AU - Lingren, Todd
AU - Namjou-Khales, Bahram
AU - Harley, John B.
AU - Larson, Eric
AU - Jarvik, Gail P.
AU - Brilliant, Murray
AU - Williams, Marc S.
AU - Kullo, Iftikhar J.
AU - Hysinger, Erik B.
AU - Sleiman, Patrick M.A.
AU - Hakonarson, Hakon
N1 - Funding Information:
The authors thank all patients and control subjects for their participation in the study. They also thank the U.S. Department of Veterans Affairs and the Electronic Medical Records and Genomics network and co-directors, Teri Manolio and Rongling Li, for their support.
Publisher Copyright:
© Copyright 2017 by the American Thoracic Society.
PY - 2017/2/15
Y1 - 2017/2/15
N2 - Rationale: Despite significant advances in knowledge of the genetic architecture of asthma, specific contributors to the variability in the burden between populations remain uncovered. Objectives: To identify additional genetic susceptibility factors of asthma in European American and African American populations. Methods: A phenotyping algorithm mining electronic medical records was developed and validated to recruit cases with asthma and control subjects from the Electronic Medical Records and Genomics network. Genome-wide association analyses were performed in pediatric and adult asthma cases and control subjects with European American and African American ancestry followed by metaanalysis. Nominally significant results were reanalyzed conditioning on allergy status. Measurements and Main Results: The validation of the algorithm yielded an average of 95.8% positive predictive values for both cases and control subjects. The algorithm accrued 21,644 subjects (65.83% European American and 34.17% African American). We identified four novel population-specific associations with asthma after metaanalyses: loci 6p21.31, 9p21.2, and 10q21.3 in the European American population, and the PTGES gene in African Americans. TEK at 9p21.2, which encodes TIE2, has been shown to be involved in remodeling the airway wall in asthma, and the association remained significant after conditioning by allergy. PTGES, which encodes the prostaglandin E synthase, has also been linked to asthma, where deficient prostaglandin E2 synthesis has been associated with airway remodeling. Conclusions: This study adds to understanding of the genetic architecture of asthma in European Americans and African Americans and reinforces the need to study populations of diverse ethnic backgrounds to identify shared and unique genetic predictors of asthma.
AB - Rationale: Despite significant advances in knowledge of the genetic architecture of asthma, specific contributors to the variability in the burden between populations remain uncovered. Objectives: To identify additional genetic susceptibility factors of asthma in European American and African American populations. Methods: A phenotyping algorithm mining electronic medical records was developed and validated to recruit cases with asthma and control subjects from the Electronic Medical Records and Genomics network. Genome-wide association analyses were performed in pediatric and adult asthma cases and control subjects with European American and African American ancestry followed by metaanalysis. Nominally significant results were reanalyzed conditioning on allergy status. Measurements and Main Results: The validation of the algorithm yielded an average of 95.8% positive predictive values for both cases and control subjects. The algorithm accrued 21,644 subjects (65.83% European American and 34.17% African American). We identified four novel population-specific associations with asthma after metaanalyses: loci 6p21.31, 9p21.2, and 10q21.3 in the European American population, and the PTGES gene in African Americans. TEK at 9p21.2, which encodes TIE2, has been shown to be involved in remodeling the airway wall in asthma, and the association remained significant after conditioning by allergy. PTGES, which encodes the prostaglandin E synthase, has also been linked to asthma, where deficient prostaglandin E2 synthesis has been associated with airway remodeling. Conclusions: This study adds to understanding of the genetic architecture of asthma in European Americans and African Americans and reinforces the need to study populations of diverse ethnic backgrounds to identify shared and unique genetic predictors of asthma.
KW - Asthma
KW - Genetics
KW - Genome-wide association study
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U2 - 10.1164/rccm.201604-0861OC
DO - 10.1164/rccm.201604-0861OC
M3 - Article
C2 - 27611488
AN - SCOPUS:85014939628
SN - 1073-449X
VL - 195
SP - 456
EP - 463
JO - American journal of respiratory and critical care medicine
JF - American journal of respiratory and critical care medicine
IS - 4
ER -