» Articles » PMID: 34414909

Current Concepts and Molecular Mechanisms in Pharmacogenetics of Essential Hypertension

Overview
Specialty Pharmacology
Date 2021 Aug 20
PMID 34414909
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Hypertension is a leading age-related disease in our society and if left untreated, leads to fatal cardiovascular complications. The prevalence of hypertension has increased and becomes a significant global health economic burden, particularly in lower-income societies. Many loci associated with blood pressure and hypertension have been reported by genome-wide association studies that provided potential targets for pharmacotherapy. Pharmacogenetic research had shown interindividual variations in drug efficacy, safety, and tolerability. This could be due to genetic polymorphisms in the pharmacokinetics (genes involved in a transporter, plasma protein binding, and metabolism) or pharmacodynamic pathway (receptors, ion channels, enzymes). Pharmacogenetics promises great hope toward targeted therapy, but challenges remain in implementing pharmacogenetic aided antihypertensive therapy in clinical practice. Using various databases, we analyzed the underlying mechanisms between the candidate gene polymorphisms and antihypertensive drug interactions and the challenges of implementing precision medicine. We review the emergence of pharmacogenetics and its relevance to clinical pharmacological practice.

Citing Articles

Therapeutical Approach to Arterial Hypertension - Current State of the Art.

Radosavljevic M, Vucevic D, Samardzic J, Radenkovic M, Radosavljevic T Curr Med Chem. 2024; 31(29):4602-4620.

PMID: 38303535 DOI: 10.2174/0109298673274823231220063652.


Efficacy and safety of olmesartan medoxomil-amlodipine besylate tablet in Chinese patients with essential hypertension: A prospective, single-arm, multi-center, real-world study.

Cui Z, Qiu Z, Cheng W, Hu W, Ma G, Cai X J Clin Hypertens (Greenwich). 2023; 26(1):5-16.

PMID: 37667532 PMC: 10795096. DOI: 10.1111/jch.14700.

References
1.
Beitelshees A, Gong Y, Wang D, Schork N, Cooper-DeHoff R, Langaee T . KCNMB1 genotype influences response to verapamil SR and adverse outcomes in the INternational VErapamil SR/Trandolapril STudy (INVEST). Pharmacogenet Genomics. 2007; 17(9):719-29. PMC: 2713584. DOI: 10.1097/FPC.0b013e32810f2e3c. View

2.
Wang X, Wang G, Shi J, Aa J, Comas R, Liang Y . CES1 genetic variation affects the activation of angiotensin-converting enzyme inhibitors. Pharmacogenomics J. 2015; 16(3):220-30. PMC: 6329299. DOI: 10.1038/tpj.2015.42. View

3.
Nurnberger J, Dammer S, Mitchell A, Siffert W, Wenzel R, Gossl M . Effect of the C825T polymorphism of the G protein beta 3 subunit on the systolic blood pressure-lowering effect of clonidine in young, healthy male subjects. Clin Pharmacol Ther. 2003; 74(1):53-60. DOI: 10.1016/S0009-9236(03)00087-0. View

4.
Vandell A, Lobmeyer M, Gawronski B, Langaee T, Gong Y, Gums J . G protein receptor kinase 4 polymorphisms: β-blocker pharmacogenetics and treatment-related outcomes in hypertension. Hypertension. 2012; 60(4):957-64. PMC: 3462355. DOI: 10.1161/HYPERTENSIONAHA.112.198721. View

5.
Gotoh Y, Imaizumi Y, Watanabe M, Shibata E, Clark R, Giles W . Inhibition of transient outward K+ current by DHP Ca2+ antagonists and agonists in rabbit cardiac myocytes. Am J Physiol. 1991; 260(5 Pt 2):H1737-42. DOI: 10.1152/ajpheart.1991.260.5.H1737. View