| Literature DB >> 30753892 |
Mohamed H Solayman1, Taimour Y Langaee2, Yan Gong2, Mohamed H Shahin2, Stephen T Turner3, Arlene B Chapman4, John G Gums5, Eric Boerwinkle6, Amber L Beitelshees7, Manal El-Hamamsy8, Lamia El-Wakeel8, Rhonda M Cooper-DeHoff2, Osama A Badary8, Julie A Johnson9.
Abstract
β-blockers show variable efficacy as antihypertensives. Herein, we evaluated plasma miRNAs as biomarkers for defining antihypertensive response to β-blockers. Expression of 22 β-blocker pharmacodynamics-related miRNAs was assessed in baseline plasma samples from 30 responders and 30 non-responders to metoprolol from the PEAR-2 study (Discovery). Logistic regression was performed to identify miRNAs significantly associated with metoprolol response. Those miRNAs were profiled in baseline plasma samples from 25 responders and 25 non-responders to atenolol from the PEAR study (validation). In discovery, miR-101, miR-27a, miR-22, miR-19a, and let-7e were significantly associated with metoprolol response (P = 0.01, 0.017, 0.025, 0.025, and 0.04, respectively). In validation, miR-19a was significantly associated with atenolol response (P = 0.038). Meta-analysis between PEAR-2 and PEAR revealed significant association between miR-19a (P = 0.004), miR-101 (P = 0.006), and let-7e (P = 0.012) and β-blocker response. Hence, miR-19a, miR-101, and let-7e, which regulate β1-adrenergic receptor and other β-blocker pharmacodynamics-related genes, may be biomarkers for antihypertensive response to β-blockers.Entities:
Keywords: Antihypertensive response; Beta-blocker; Biomarker; Hypertension; microRNA
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Year: 2019 PMID: 30753892 PMCID: PMC6467266 DOI: 10.1016/j.ejps.2019.02.013
Source DB: PubMed Journal: Eur J Pharm Sci ISSN: 0928-0987 Impact factor: 4.384