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      Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β‐Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil‐SR Trandolapril Study) Trials

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          Abstract

          Background

          The majority of hypertensive individuals require combination antihypertensive therapy to achieve adequate blood pressure ( BP) control. This study aimed to identify genetic variants associated with uncontrolled BP on combination therapy with a thiazide diuretic and a β‐blocker.

          Methods and Results

          A genome‐wide association study of uncontrolled BP on combination therapy was conducted among 314 white participants of the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) trial. Multivariable logistic regression analysis was used. Genetic variants meeting a suggestive level of significance ( P<1.0E‐05) were tested for replication in an external cohort, INVEST (International Verapamil‐ SR Trandolapril study). We also examined genome‐wide variant associations with systolic and diastolic BP response on combination therapy and tested for replication. We discovered a single nucleotide polymorphism, the rs261316 major allele, at chromosome 15 in the gene ALDH1A2 associated with an increased odds of having uncontrolled BP on combination therapy (odds ratio: 2.56, 95% confidence interval, 1.69–3.88, P=8.64E‐06). This single nucleotide polymorphism replicated (odds ratio: 1.86, 95% confidence interval, 1.35–2.57, P=0.001) and approached genome‐wide significance in the meta‐analysis between discovery and replication cohorts (odds ratio: 2.16, 95% confidence interval, 1.63–2.86, P=8.60E‐08). Other genes in the region surrounding rs261316 ( ALDH1A2) include AQP9 and LIPC.

          Conclusions

          A single nucleotide polymorphism in the gene ALDH1A2 may be associated with uncontrolled BP following treatment with a thiazide diuretic/β‐blocker combination.

          Clinical Trial Registration

          URL: https://www.clinicaltrials.gov. Unique identifier: NCT00246519.

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          Most cited references42

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          Adverse epigenetic signatures by histone methyltransferase Set7 contribute to vascular dysfunction in patients with type 2 diabetes mellitus.

          Cellular studies showed that histone methyltransferase Set7 mediates high glucose-induced inflammation via epigenetic regulation of the transcription factor NF-kB. However, the link between Set7 and vascular dysfunction in patients with diabetes mellitus remains unknown. This study was designed to investigate whether Set7 contributes to vascular dysfunction in patients with type 2 diabetes mellitus (T2DM).
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            Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci

            Blood pressure (BP) is a heritable risk factor for cardiovascular disease. To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP), and pulse pressure (PP), we genotyped ~50,000 SNPs in up to 87,736 individuals of European ancestry and combined these in a meta-analysis. We replicated findings in an independent set of 68,368 individuals of European ancestry. Our analyses identified 11 previously undescribed associations in independent loci containing 31 genes including PDE1A, HLA-DQB1, CDK6, PRKAG2, VCL, H19, NUCB2, RELA, HOXC@ complex, FBN1, and NFAT5 at the Bonferroni-corrected array-wide significance threshold (p < 6 × 10(-7)) and confirmed 27 previously reported associations. Bioinformatic analysis of the 11 loci provided support for a putative role in hypertension of several genes, such as CDK6 and NUCB2. Analysis of potential pharmacological targets in databases of small molecules showed that ten of the genes are predicted to be a target for small molecules. In summary, we identified previously unknown loci associated with BP. Our findings extend our understanding of genes involved in BP regulation, which may provide new targets for therapeutic intervention or drug response stratification.
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              The role of short-chain fatty acid on blood pressure regulation.

              The gut microbiota and its metabolites have been implicated in the regulation of host physiological functions such as inflammatory and metabolic responses. The short-chain fatty acid (SCFA) receptor is expressed in the kidney and blood vessels as well, and has been reported to function as a regulator of blood pressure (BP). This review highlights the role of SCFAs derived from gut microbial fermentation in the regulation of BP.
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                Author and article information

                Contributors
                julie.johnson@ufl.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                02 November 2017
                November 2017
                : 6
                : 11 ( doiID: 10.1002/jah3.2017.6.issue-11 )
                : e006522
                Affiliations
                [ 1 ] Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics University of Florida College of Pharmacy Gainesville FL
                [ 2 ] College of Medicine University of Florida Gainesville FL
                [ 3 ] Section of Nephrology Department of Medicine University of Chicago Chicago IL
                [ 4 ] Division of Nephrology and Hypertension Department of Medicine Mayo Clinic Rochester MN
                [ 5 ] Division of Biomedical Statistics and Informatics Department of Health Sciences Research Mayo Clinic Rochester MN
                [ 6 ] Human Genetics Center and Institute of Molecular Medicine University of Texas Health Science Center Houston TX
                [ 7 ] Division of Endocrinology, Diabetes and Nutrition University of Maryland School of Medicine Baltimore MD
                [ 8 ] RIKEN Center for Integrative Medical Sciences Yokohama Japan
                [ 9 ] Division of Cardiovascular Medicine Department of Medicine University of Florida College of Medicine Gainesville FL
                Author notes
                [*] [* ] Correspondence to: Julie A. Johnson, PharmD, Department of Pharmacotherapy and Translational Research, University of Florida, PO Box 100484, Gainesville, FL 32610‐0484. E‐mail: julie.johnson@ 123456ufl.edu
                Article
                JAH32676
                10.1161/JAHA.117.006522
                5721751
                29097388
                4d002ee7-844d-4698-bc39-1f4979c63908
                © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 12 May 2017
                : 11 September 2017
                Page count
                Figures: 2, Tables: 1, Pages: 18, Words: 8335
                Funding
                Funded by: National Institutes of Health (NIH) Pharmacogenetics Research Network
                Award ID: U01 GM074492
                Funded by: National Center for Advancing Translational Sciences
                Funded by: University of Florida
                Award ID: UL1 TR000064
                Funded by: Emory University
                Award ID: UL1 TR000454
                Funded by: Mayo Clinic
                Award ID: UL1 TR000135
                Funded by: Mayo Foundation
                Funded by: National Heart Lung and Blood Institute
                Award ID: R01 HL74730
                Funded by: BASF Pharma
                Funded by: Abbott Laboratories
                Funded by: NIH
                Award ID: T32 DK104721
                Award ID: KL2 TR001429
                Categories
                Original Research
                Original Research
                Hypertension
                Custom metadata
                2.0
                jah32676
                November 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.6 mode:remove_FC converted:21.11.2017

                Cardiovascular Medicine
                combination therapy,genomics,pharmacogenomics,high blood pressure,hypertension,β‐blockers,thiazide diuretics

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