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

TitleWhole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics.
Publication TypeJournal Article
Year of Publication2017
AuthorsSá, ACaroline C, Webb, A, Gong, Y, McDonough, CW, Datta, S, Langaee, TY, Turner, ST, Beitelshees, AL, Chapman, AB, Boerwinkle, E, Gums, JG, Scherer, SE, Cooper-Dehoff, RM, Sadee, W, Johnson, JA
JournalSci Rep
Volume7
Issue1
Pagination16068
Date Published2017 Nov 22
ISSN2045-2322
KeywordsAlleles, Biomarkers, Blood Pressure, CCAAT-Enhancer-Binding Protein-delta, Chlorthalidone, Diuretics, Female, Gene Expression Profiling, Gene Expression Regulation, Humans, Hydrochlorothiazide, Logistic Models, Male, Middle Aged, Potassium, Reproducibility of Results, RNA, Messenger, ROC Curve, Transcription Factors, Uric Acid
Abstract

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) and TSC22D3 (p = 1.9 × 10) 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.

DOI10.1038/s41598-017-16343-z
Alternate JournalSci Rep
PubMed ID29167564
PubMed Central IDPMC5700078
Grant ListU19 GM061388 / GM / NIGMS NIH HHS / United States
UL1 TR000064 / TR / NCATS NIH HHS / United States
U01 GM074492 / GM / NIGMS NIH HHS / United States
UL1 TR001427 / TR / NCATS NIH HHS / United States
UL1 TR000135 / TR / NCATS NIH HHS / United States
UL1 TR000454 / TR / NCATS NIH HHS / United States
U19 GM061390 / GM / NIGMS NIH HHS / United States

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