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Racial and ethnic differences in pharmacotherapy to prevent coronary artery disease and thrombotic events.

Tamargo, J; Kaski, JC; Kimura, T; Barton, JC; Yamamoto, K; Komiyama, M; Drexel, H; Lewis, BS; Agewall, S; Hasegawa, K (2022) Racial and ethnic differences in pharmacotherapy to prevent coronary artery disease and thrombotic events. Eur Heart J Cardiovasc Pharmacother, 8 (7). pp. 738-751. ISSN 2055-6845 https://doi.org/10.1093/ehjcvp/pvac040
SGUL Authors: Kaski, Juan Carlos

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Abstract

Awareness of racial/ethnic disparities represents a key challenge for healthcare systems that attempt to provide effective healthcare and to reduce existing inequalities in the use of and adherence to guideline-recommended cardiovascular drugs to improve clinical outcomes for cardiovascular disease (CVD). In this review, we describe important racial/ethnic differences between and within ethnic groups in the prevalence, risk factors, haemostatic factors, anti-inflammatory and endothelial markers, recurrence, and outcomes of CVD. We discuss important differences in the selection, doses, and response [efficacy and adverse drug reactions (ADRs)] in ethnically diverse patients treated with antithrombotics or lipid-lowering drugs. Differences in drug response are mainly related to racial/ethnic differences in the frequency of polymorphisms in genes encoding drug-metabolizing enzymes (DMEs) and drug transporters. These polymorphisms markedly influence the pharmacokinetics, dose requirements, and safety of warfarin, clopidogrel, and statins. This review aims to support a better understanding of the genetic differences between and among populations to identify patients who may experience an ADR or a lack of drug response, thus optimizing therapy and improving outcomes. The greater the understanding of the differences in the genetic variants of DMEs and transporters that determine the differences in the exposure, efficacy, and safety of cardiovascular drugs between races/ethnicities, the greater the probability that personalized medicine will become a reality.

Item Type: Article
Additional Information: © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
Keywords: Adverse drug reaction, Cardiovascular disease, Drug-metabolizing enzymes, Dual antiplatelet therapy, Racial/ethnic disparities, Cardiovascular Agents, Cardiovascular Diseases, Clopidogrel, Coronary Artery Disease, Fibrinolytic Agents, Hemostatics, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Imidazoles, Lipids, Organosilicon Compounds, Warfarin, Humans, Cardiovascular Diseases, Organosilicon Compounds, Imidazoles, Warfarin, Lipids, Cardiovascular Agents, Fibrinolytic Agents, Hemostatics, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Coronary Artery Disease, Clopidogrel, Cardiovascular disease, Dual antiplatelet therapy, Racial, ethnic disparities, Adverse drug reaction, Drug-metabolizing enzymes, 1102 Cardiorespiratory Medicine and Haematology, 1115 Pharmacology and Pharmaceutical Sciences
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Eur Heart J Cardiovasc Pharmacother
ISSN: 2055-6845
Language: eng
Dates:
DateEvent
November 2022Published
29 September 2022Published Online
13 July 2022Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
B2017/BMD-3738Comunidad de MadridUNSPECIFIED
UNSPECIFIEDNational Hospital OrganizationUNSPECIFIED
PubMed ID: 35848895
Web of Science ID: WOS:000837522600001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115026
Publisher's version: https://doi.org/10.1093/ehjcvp/pvac040

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