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Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)

BACKGROUND: There exists a wide interindividual variability in blood pressure (BP) response to β(1)‐blockers. To identify the genetic determinants of this variability, we performed a pharmacogenomic genome‐wide meta‐analysis of genetic variants influencing β(1)‐blocker BP response. METHODS AND RESUL...

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Autores principales: Singh, Sonal, Warren, Helen R., Hiltunen, Timo P., McDonough, Caitrin W., El Rouby, Nihal, Salvi, Erika, Wang, Zhiying, Garofalidou, Tatiana, Fyhrquist, Frej, Kontula, Kimmo K., Glorioso, Valeria, Zaninello, Roberta, Glorioso, Nicola, Pepine, Carl J., Munroe, Patricia B., Turner, Stephan T., Chapman, Arlene B., Boerwinkle, Eric, Johnson, Julie A., Gong, Yan, Cooper‐DeHoff, Rhonda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759913/
https://www.ncbi.nlm.nih.gov/pubmed/31423876
http://dx.doi.org/10.1161/JAHA.119.013115
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author Singh, Sonal
Warren, Helen R.
Hiltunen, Timo P.
McDonough, Caitrin W.
El Rouby, Nihal
Salvi, Erika
Wang, Zhiying
Garofalidou, Tatiana
Fyhrquist, Frej
Kontula, Kimmo K.
Glorioso, Valeria
Zaninello, Roberta
Glorioso, Nicola
Pepine, Carl J.
Munroe, Patricia B.
Turner, Stephan T.
Chapman, Arlene B.
Boerwinkle, Eric
Johnson, Julie A.
Gong, Yan
Cooper‐DeHoff, Rhonda M.
author_facet Singh, Sonal
Warren, Helen R.
Hiltunen, Timo P.
McDonough, Caitrin W.
El Rouby, Nihal
Salvi, Erika
Wang, Zhiying
Garofalidou, Tatiana
Fyhrquist, Frej
Kontula, Kimmo K.
Glorioso, Valeria
Zaninello, Roberta
Glorioso, Nicola
Pepine, Carl J.
Munroe, Patricia B.
Turner, Stephan T.
Chapman, Arlene B.
Boerwinkle, Eric
Johnson, Julie A.
Gong, Yan
Cooper‐DeHoff, Rhonda M.
author_sort Singh, Sonal
collection PubMed
description BACKGROUND: There exists a wide interindividual variability in blood pressure (BP) response to β(1)‐blockers. To identify the genetic determinants of this variability, we performed a pharmacogenomic genome‐wide meta‐analysis of genetic variants influencing β(1)‐blocker BP response. METHODS AND RESULTS: Genome‐wide association analysis for systolic BP and diastolic BP response to β(1)‐blockers from 5 randomized clinical trials consisting of 1254 patients with hypertension of European ancestry were combined in meta‐analysis and single nucleotide polymorphisms (SNPs) with P<10(−4) were tested for replication in 2 independent randomized clinical trials of β(1)‐blocker–treated patients of European ancestry (n=1552). Regions harboring the replicated SNPs were validated in a β(1)‐blocker–treated black cohort from 2 randomized clinical trials (n=315). A missense SNP rs28404156 in BST1 was associated with systolic BP response to β(1)‐blockers in the discovery meta‐analysis (P=9.33×10(−5), β=−3.21 mm Hg) and replicated at Bonferroni significance (P=1.85×10(−4), β=−4.86 mm Hg) in the replication meta‐analysis with combined meta‐analysis approaching genome‐wide significance (P=2.18×10(−7)). This SNP in BST1 is in linkage disequilibrium with several SNPs with putative regulatory functions in nearby genes, including CD38,FBXL5, and FGFBP1, all of which have been implicated in BP regulation. SNPs in this genetic region were also associated with BP response in the black cohort. CONCLUSIONS: Data from randomized clinical trials of 8 European ancestry and 2 black cohorts support the assumption that BST1 containing locus on chromosome 4 is associated with β(1)‐blocker BP response. Given the previous associations of this region with BP, this is a strong candidate region for future functional studies and potential use in precision medicine approaches for BP management and risk prediction.
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spelling pubmed-67599132019-09-30 Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies) Singh, Sonal Warren, Helen R. Hiltunen, Timo P. McDonough, Caitrin W. El Rouby, Nihal Salvi, Erika Wang, Zhiying Garofalidou, Tatiana Fyhrquist, Frej Kontula, Kimmo K. Glorioso, Valeria Zaninello, Roberta Glorioso, Nicola Pepine, Carl J. Munroe, Patricia B. Turner, Stephan T. Chapman, Arlene B. Boerwinkle, Eric Johnson, Julie A. Gong, Yan Cooper‐DeHoff, Rhonda M. J Am Heart Assoc Systematic Review and Meta‐analysis BACKGROUND: There exists a wide interindividual variability in blood pressure (BP) response to β(1)‐blockers. To identify the genetic determinants of this variability, we performed a pharmacogenomic genome‐wide meta‐analysis of genetic variants influencing β(1)‐blocker BP response. METHODS AND RESULTS: Genome‐wide association analysis for systolic BP and diastolic BP response to β(1)‐blockers from 5 randomized clinical trials consisting of 1254 patients with hypertension of European ancestry were combined in meta‐analysis and single nucleotide polymorphisms (SNPs) with P<10(−4) were tested for replication in 2 independent randomized clinical trials of β(1)‐blocker–treated patients of European ancestry (n=1552). Regions harboring the replicated SNPs were validated in a β(1)‐blocker–treated black cohort from 2 randomized clinical trials (n=315). A missense SNP rs28404156 in BST1 was associated with systolic BP response to β(1)‐blockers in the discovery meta‐analysis (P=9.33×10(−5), β=−3.21 mm Hg) and replicated at Bonferroni significance (P=1.85×10(−4), β=−4.86 mm Hg) in the replication meta‐analysis with combined meta‐analysis approaching genome‐wide significance (P=2.18×10(−7)). This SNP in BST1 is in linkage disequilibrium with several SNPs with putative regulatory functions in nearby genes, including CD38,FBXL5, and FGFBP1, all of which have been implicated in BP regulation. SNPs in this genetic region were also associated with BP response in the black cohort. CONCLUSIONS: Data from randomized clinical trials of 8 European ancestry and 2 black cohorts support the assumption that BST1 containing locus on chromosome 4 is associated with β(1)‐blocker BP response. Given the previous associations of this region with BP, this is a strong candidate region for future functional studies and potential use in precision medicine approaches for BP management and risk prediction. John Wiley and Sons Inc. 2019-08-19 /pmc/articles/PMC6759913/ /pubmed/31423876 http://dx.doi.org/10.1161/JAHA.119.013115 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Systematic Review and Meta‐analysis
Singh, Sonal
Warren, Helen R.
Hiltunen, Timo P.
McDonough, Caitrin W.
El Rouby, Nihal
Salvi, Erika
Wang, Zhiying
Garofalidou, Tatiana
Fyhrquist, Frej
Kontula, Kimmo K.
Glorioso, Valeria
Zaninello, Roberta
Glorioso, Nicola
Pepine, Carl J.
Munroe, Patricia B.
Turner, Stephan T.
Chapman, Arlene B.
Boerwinkle, Eric
Johnson, Julie A.
Gong, Yan
Cooper‐DeHoff, Rhonda M.
Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title_full Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title_fullStr Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title_full_unstemmed Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title_short Genome‐Wide Meta‐Analysis of Blood Pressure Response to β(1)‐Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)
title_sort genome‐wide meta‐analysis of blood pressure response to β(1)‐blockers: results from icaps (international consortium of antihypertensive pharmacogenomics studies)
topic Systematic Review and Meta‐analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759913/
https://www.ncbi.nlm.nih.gov/pubmed/31423876
http://dx.doi.org/10.1161/JAHA.119.013115
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