Whole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics

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作者
Ana Caroline C. Sá
Amy Webb
Yan Gong
Caitrin W. McDonough
Somnath Datta
Taimour Y. Langaee
Stephen T. Turner
Amber L. Beitelshees
Arlene B. Chapman
Eric Boerwinkle
John G. Gums
Steven E. Scherer
Rhonda M. Cooper-DeHoff
Wolfgang Sadee
Julie A. Johnson
机构
[1] Center for Pharmacogenomics and Department of Pharmacotherapy and Translational Research,Department of Biomedical Informatics
[2] University of Florida,Department of Biostatistics
[3] Graduate Program in Genetics and Genomics,Department of Medicine
[4] University of Florida,Department of Community Health and Family Medicine
[5] College of Medicine,undefined
[6] The Ohio State University,undefined
[7] University of Florida,undefined
[8] Division of Nephrology and Hypertension,undefined
[9] Mayo Clinic,undefined
[10] Division of Endocrinology,undefined
[11] Diabetes and Nutrition,undefined
[12] University of Maryland,undefined
[13] University of Chicago,undefined
[14] Division of Epidemiology,undefined
[15] University of Texas at Houston,undefined
[16] University of Florida College of Medicine,undefined
[17] Human Genome Sequencing Center,undefined
[18] Baylor College of Medicine,undefined
[19] Division of Cardiovascular Medicine,undefined
[20] Department of Medicine,undefined
[21] University of Florida College of Medicine,undefined
[22] Center for Pharmacogenomics,undefined
[23] Department of Cancer Biology and Genetic,undefined
[24] College of Medicine,undefined
[25] Ohio State University,undefined
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Thiazide diuretics (TD) are commonly prescribed anti-hypertensives worldwide. However, <40% of patients treated with thiazide monotherapy achieve BP control. This study uses whole transcriptome sequencing to identify novel molecular markers associated with BP response to TD. We assessed global RNA expression levels in whole blood samples from 150 participants, representing patients in the upper and lower quartile of BP response to TD from the Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) (50 whites) and from PEAR-2 (50 whites and 50 blacks). In each study cohort, we performed poly-A RNA-sequencing in baseline samples from 25 responders and 25 non-responders to hydrochlorothiazide (HCTZ) or chlorthalidone. At FDR adjusted p-value < 0.05, 29 genes were differentially expressed in relation to HCTZ or chlorthalidone BP response in whites. For each differentially expressed gene, replication was attempted in the alternate white group and PEAR-2 blacks. CEBPD (meta-analysis p = 1.8 × 10−11) and TSC22D3 (p = 1.9 × 10−9) were differentially expressed in all 3 cohorts, and explain, in aggregate, 21.9% of response variability to TD. This is the first report of the use of transcriptome-wide sequencing data to identify molecular markers of antihypertensive drug response. These findings support CEBPD and TSC22D3 as potential biomarkers of BP response to TD.
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