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A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma

Short-acting β(2)-adrenergic receptor agonists (SABAs) are the most commonly prescribed asthma medications worldwide. Response to SABAs is measured as bronchodilator drug response (BDR), which varies among racial/ethnic groups in the U.S(1, 2). However, the genetic variation that contributes to BDR...

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Autores principales: Spear, Melissa L., Hu, Donglei, Pino-Yanes, Maria, Huntsman, Scott, Eng, Celeste, Levin, Albert M., Ortega, Victor E., White, Marquitta J., McGarry, Meghan E., Thakur, Neeta, Galanter, Joshua, Mak, Angel C.Y., Oh, Sam S., Ampleford, Elizabeth, Peters, Stephen P., Davis, Adam, Kumar, Rajesh, Farber, Harold J., Meade, Kelley, Avila, Pedro C., Serebrisky, Denise, Lenoir, Michael A., Brigino-Buenaventura, Emerita, Cintron, William Rodriguez, Thyne, Shannon M., Rodriguez-Santana, Jose R., Ford, Jean G., Chapela, Rocio, Estrada, Andrés Moreno, Sandoval, Karla, Seibold, Max A., Winkler, Cheryl A., Bleecker, Eugene R., Myers, Deborah A., Keoki Williams, L., Hernandez, Ryan D., Torgerson, Dara G., Burchard, Esteban G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414286/
https://www.ncbi.nlm.nih.gov/pubmed/30206298
http://dx.doi.org/10.1038/s41397-018-0042-4
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author Spear, Melissa L.
Hu, Donglei
Pino-Yanes, Maria
Huntsman, Scott
Eng, Celeste
Levin, Albert M.
Ortega, Victor E.
White, Marquitta J.
McGarry, Meghan E.
Thakur, Neeta
Galanter, Joshua
Mak, Angel C.Y.
Oh, Sam S.
Ampleford, Elizabeth
Peters, Stephen P.
Davis, Adam
Kumar, Rajesh
Farber, Harold J.
Meade, Kelley
Avila, Pedro C.
Serebrisky, Denise
Lenoir, Michael A.
Brigino-Buenaventura, Emerita
Cintron, William Rodriguez
Thyne, Shannon M.
Rodriguez-Santana, Jose R.
Ford, Jean G.
Chapela, Rocio
Estrada, Andrés Moreno
Sandoval, Karla
Seibold, Max A.
Winkler, Cheryl A.
Bleecker, Eugene R.
Myers, Deborah A.
Keoki Williams, L.
Hernandez, Ryan D.
Torgerson, Dara G.
Burchard, Esteban G.
author_facet Spear, Melissa L.
Hu, Donglei
Pino-Yanes, Maria
Huntsman, Scott
Eng, Celeste
Levin, Albert M.
Ortega, Victor E.
White, Marquitta J.
McGarry, Meghan E.
Thakur, Neeta
Galanter, Joshua
Mak, Angel C.Y.
Oh, Sam S.
Ampleford, Elizabeth
Peters, Stephen P.
Davis, Adam
Kumar, Rajesh
Farber, Harold J.
Meade, Kelley
Avila, Pedro C.
Serebrisky, Denise
Lenoir, Michael A.
Brigino-Buenaventura, Emerita
Cintron, William Rodriguez
Thyne, Shannon M.
Rodriguez-Santana, Jose R.
Ford, Jean G.
Chapela, Rocio
Estrada, Andrés Moreno
Sandoval, Karla
Seibold, Max A.
Winkler, Cheryl A.
Bleecker, Eugene R.
Myers, Deborah A.
Keoki Williams, L.
Hernandez, Ryan D.
Torgerson, Dara G.
Burchard, Esteban G.
author_sort Spear, Melissa L.
collection PubMed
description Short-acting β(2)-adrenergic receptor agonists (SABAs) are the most commonly prescribed asthma medications worldwide. Response to SABAs is measured as bronchodilator drug response (BDR), which varies among racial/ethnic groups in the U.S(1, 2). However, the genetic variation that contributes to BDR is largely undefined in African Americans with asthma(3). To identify genetic variants that may contribute to differences in BDR in African Americans with asthma, we performed a genome-wide association study (GWAS) of BDR in 949 African American children with asthma, genotyped with the Axiom World Array 4 (Affymetrix, Santa Clara, CA) followed by imputation using 1000 Genomes phase III genotypes. We used linear regression models adjusting for age, sex, body mass index (BMI) and genetic ancestry to test for an association between BDR and genotype at single nucleotide polymorphisms (SNPs). To increase power and distinguish between shared vs. population-specific associations with BDR in children with asthma, we performed a meta-analysis across 949 African Americans and 1,830 Latinos (Total=2,779). Lastly, we performed genome-wide admixture mapping to identify regions whereby local African or European ancestry is associated with BDR in African Americans. We identified a population-specific association with an intergenic SNP on chromosome 9q21 that was significantly associated with BDR (rs73650726, p=7.69×10(−9)). A trans-ethnic meta-analysis across African Americans and Latinos identified three additional SNPs within the intron of PRKG1 that were significantly associated with BDR (rs7903366, rs7070958, and rs7081864, p≤5×10(−8)). Our results failed to replicate in three additional populations of 416 Latinos and 1,615 African Americans. Our findings indicate that both population specific and shared genetic variation contributes to differences in BDR in minority children with asthma, and that the genetic underpinnings of BDR may differ between racial/ethnic groups.
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spelling pubmed-64142862019-03-13 A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma Spear, Melissa L. Hu, Donglei Pino-Yanes, Maria Huntsman, Scott Eng, Celeste Levin, Albert M. Ortega, Victor E. White, Marquitta J. McGarry, Meghan E. Thakur, Neeta Galanter, Joshua Mak, Angel C.Y. Oh, Sam S. Ampleford, Elizabeth Peters, Stephen P. Davis, Adam Kumar, Rajesh Farber, Harold J. Meade, Kelley Avila, Pedro C. Serebrisky, Denise Lenoir, Michael A. Brigino-Buenaventura, Emerita Cintron, William Rodriguez Thyne, Shannon M. Rodriguez-Santana, Jose R. Ford, Jean G. Chapela, Rocio Estrada, Andrés Moreno Sandoval, Karla Seibold, Max A. Winkler, Cheryl A. Bleecker, Eugene R. Myers, Deborah A. Keoki Williams, L. Hernandez, Ryan D. Torgerson, Dara G. Burchard, Esteban G. Pharmacogenomics J Article Short-acting β(2)-adrenergic receptor agonists (SABAs) are the most commonly prescribed asthma medications worldwide. Response to SABAs is measured as bronchodilator drug response (BDR), which varies among racial/ethnic groups in the U.S(1, 2). However, the genetic variation that contributes to BDR is largely undefined in African Americans with asthma(3). To identify genetic variants that may contribute to differences in BDR in African Americans with asthma, we performed a genome-wide association study (GWAS) of BDR in 949 African American children with asthma, genotyped with the Axiom World Array 4 (Affymetrix, Santa Clara, CA) followed by imputation using 1000 Genomes phase III genotypes. We used linear regression models adjusting for age, sex, body mass index (BMI) and genetic ancestry to test for an association between BDR and genotype at single nucleotide polymorphisms (SNPs). To increase power and distinguish between shared vs. population-specific associations with BDR in children with asthma, we performed a meta-analysis across 949 African Americans and 1,830 Latinos (Total=2,779). Lastly, we performed genome-wide admixture mapping to identify regions whereby local African or European ancestry is associated with BDR in African Americans. We identified a population-specific association with an intergenic SNP on chromosome 9q21 that was significantly associated with BDR (rs73650726, p=7.69×10(−9)). A trans-ethnic meta-analysis across African Americans and Latinos identified three additional SNPs within the intron of PRKG1 that were significantly associated with BDR (rs7903366, rs7070958, and rs7081864, p≤5×10(−8)). Our results failed to replicate in three additional populations of 416 Latinos and 1,615 African Americans. Our findings indicate that both population specific and shared genetic variation contributes to differences in BDR in minority children with asthma, and that the genetic underpinnings of BDR may differ between racial/ethnic groups. 2018-09-12 2019-06 /pmc/articles/PMC6414286/ /pubmed/30206298 http://dx.doi.org/10.1038/s41397-018-0042-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Spear, Melissa L.
Hu, Donglei
Pino-Yanes, Maria
Huntsman, Scott
Eng, Celeste
Levin, Albert M.
Ortega, Victor E.
White, Marquitta J.
McGarry, Meghan E.
Thakur, Neeta
Galanter, Joshua
Mak, Angel C.Y.
Oh, Sam S.
Ampleford, Elizabeth
Peters, Stephen P.
Davis, Adam
Kumar, Rajesh
Farber, Harold J.
Meade, Kelley
Avila, Pedro C.
Serebrisky, Denise
Lenoir, Michael A.
Brigino-Buenaventura, Emerita
Cintron, William Rodriguez
Thyne, Shannon M.
Rodriguez-Santana, Jose R.
Ford, Jean G.
Chapela, Rocio
Estrada, Andrés Moreno
Sandoval, Karla
Seibold, Max A.
Winkler, Cheryl A.
Bleecker, Eugene R.
Myers, Deborah A.
Keoki Williams, L.
Hernandez, Ryan D.
Torgerson, Dara G.
Burchard, Esteban G.
A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title_full A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title_fullStr A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title_full_unstemmed A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title_short A Genome-wide Association and Admixture Mapping Study of Bronchodilator Drug Response in African Americans with Asthma
title_sort genome-wide association and admixture mapping study of bronchodilator drug response in african americans with asthma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414286/
https://www.ncbi.nlm.nih.gov/pubmed/30206298
http://dx.doi.org/10.1038/s41397-018-0042-4
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