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Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression

A recent genome-wide analysis discovered an association between a haplotype (from rs317689/rs315135/rs7297610) on Chromosome 12q15 and blood pressure response to hydrochlorothiazide in African-Americans. Our aim was to replicate this association and investigate possible functional mechanisms. We obs...

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Autores principales: Duarte, Julio D., Turner, Stephen T., Tran, BaoAnh, Chapman, Arlene B., Bailey, Kent R., Gong, Yan, Gums, John G., Langaee, Taimour Y., Beitelshees, Amber L., Cooper-Dehoff, Rhonda M., Boerwinkle, Eric, Johnson, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360116/
https://www.ncbi.nlm.nih.gov/pubmed/22350108
http://dx.doi.org/10.1038/tpj.2012.4
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author Duarte, Julio D.
Turner, Stephen T.
Tran, BaoAnh
Chapman, Arlene B.
Bailey, Kent R.
Gong, Yan
Gums, John G.
Langaee, Taimour Y.
Beitelshees, Amber L.
Cooper-Dehoff, Rhonda M.
Boerwinkle, Eric
Johnson, Julie A.
author_facet Duarte, Julio D.
Turner, Stephen T.
Tran, BaoAnh
Chapman, Arlene B.
Bailey, Kent R.
Gong, Yan
Gums, John G.
Langaee, Taimour Y.
Beitelshees, Amber L.
Cooper-Dehoff, Rhonda M.
Boerwinkle, Eric
Johnson, Julie A.
author_sort Duarte, Julio D.
collection PubMed
description A recent genome-wide analysis discovered an association between a haplotype (from rs317689/rs315135/rs7297610) on Chromosome 12q15 and blood pressure response to hydrochlorothiazide in African-Americans. Our aim was to replicate this association and investigate possible functional mechanisms. We observed similar associations between this haplotype and hydrochlorothiazide response in an independent sample of 746 Caucasians and African-Americans randomized to hydrochlorothiazide or atenolol treatment. The haplotype association was driven by variation at rs7297610, where C/C genotypes were associated with greater mean (systolic: 3.4mmHg, P=0.0275; diastolic: 2.5mmHg, P=0.0196) responses to hydrochlorothiazide vs. T-allele carriers. Such an association was absent in atenolol-treated participants, supporting this as hydrochlorothiazide-specific. Expression analyses in hydrochlorothiazide-treated African-Americans showed differential leukocyte YEATS4 expression between rs7297610 genotype groups at baseline (P=0.024), and reduced expression in C/C genotypes (P=0.009), but not in T-carriers. Our data confirm previous genome-wide findings at 12q15 and suggest differential YEATS4 expression could underpin rs7297610-associated HCTZ response variability, which may have future implications for guiding thiazide treatment.
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spelling pubmed-33601162013-12-01 Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression Duarte, Julio D. Turner, Stephen T. Tran, BaoAnh Chapman, Arlene B. Bailey, Kent R. Gong, Yan Gums, John G. Langaee, Taimour Y. Beitelshees, Amber L. Cooper-Dehoff, Rhonda M. Boerwinkle, Eric Johnson, Julie A. Pharmacogenomics J Article A recent genome-wide analysis discovered an association between a haplotype (from rs317689/rs315135/rs7297610) on Chromosome 12q15 and blood pressure response to hydrochlorothiazide in African-Americans. Our aim was to replicate this association and investigate possible functional mechanisms. We observed similar associations between this haplotype and hydrochlorothiazide response in an independent sample of 746 Caucasians and African-Americans randomized to hydrochlorothiazide or atenolol treatment. The haplotype association was driven by variation at rs7297610, where C/C genotypes were associated with greater mean (systolic: 3.4mmHg, P=0.0275; diastolic: 2.5mmHg, P=0.0196) responses to hydrochlorothiazide vs. T-allele carriers. Such an association was absent in atenolol-treated participants, supporting this as hydrochlorothiazide-specific. Expression analyses in hydrochlorothiazide-treated African-Americans showed differential leukocyte YEATS4 expression between rs7297610 genotype groups at baseline (P=0.024), and reduced expression in C/C genotypes (P=0.009), but not in T-carriers. Our data confirm previous genome-wide findings at 12q15 and suggest differential YEATS4 expression could underpin rs7297610-associated HCTZ response variability, which may have future implications for guiding thiazide treatment. 2012-02-21 2013-06 /pmc/articles/PMC3360116/ /pubmed/22350108 http://dx.doi.org/10.1038/tpj.2012.4 Text en Users may view, print, copy, download and 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
Duarte, Julio D.
Turner, Stephen T.
Tran, BaoAnh
Chapman, Arlene B.
Bailey, Kent R.
Gong, Yan
Gums, John G.
Langaee, Taimour Y.
Beitelshees, Amber L.
Cooper-Dehoff, Rhonda M.
Boerwinkle, Eric
Johnson, Julie A.
Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title_full Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title_fullStr Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title_full_unstemmed Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title_short Association of Chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
title_sort association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential yeats4 expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360116/
https://www.ncbi.nlm.nih.gov/pubmed/22350108
http://dx.doi.org/10.1038/tpj.2012.4
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