Frequencies of CYP2C19 Polymorphisms in Mexican Mestizo Patients with Coronary or Cerebral Atherosclerosis and Their Association with Residual Platelet Activity on Clopidogrel Treatment

Background/Objectives: There is wide variability in the individual response to clopidogrel, which depends on CYP2C19 polymorphisms as well as on intrinsic and extrinsic platelet factors. Clopidogrel resistance has been related to an adverse evolution in patients with coronary artery disease. The aim of this study is to analyze the prevalence of CYP2C19 polymorphisms in Mexican mestizo patients and their relationship with clopidogrel platelet response by means of platelet aggregation. Methods: Patients who experienced coronary artery disease (CAD) (N = 160) or stroke (N = 11) and received treatment with clopidogrel were analyzed for CYP2C19 alleles *1, *2, *3, and *17. In total, 81 patients were tested for clopidogrel resistance by ADP-induced aggregation in platelet-rich plasma. CYP2C19 polymorphism was expressed as ultrarapid-, normal-, rapid-, normal/intermediate, intermediate, and poor metabolizers, and the clopidogrel response was assessed by platelet aggregation. Results: The allelic frequencies were 9.6%, 0%, and 11.7% for CYP2C19*2, *3, and *17, respectively. The frequencies of CYP2C19 genotypes were as follows: CYP2C19*1/*1 (62.6%); CYP2C19*1/*17 (19.9%); CYP2C19*1/*2 (12.3%); CYP2C19*2/*17 (2.3%); CYP2C19*2/*2 (2.3%); and CYP2C19*17/*17 (0.6%). Of 81 patients with platelet aggregation, 55.6% were responsive, and 44.4% were resistant to clopidogrel. Clopidogrel resistance had a non-significant trend of association with unfavorable genotypes for metabolism (CYP2C19 *1/*2, *2/*17, and *2/*2) vs. favorable genotypes (CYP2C19 *1/*1, *1/*17, and *17/*17), 64.7% vs. 39.1%, respectively (p = 0.059). Conclusions: The prevalence of CYP2C19 polymorphisms in Mexican mestizo patients is similar to that of the general population. Clopidogrel resistance is a complex in vitro phenomenon that is not explained by CYP2C19 polymorphisms alone.

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Journal
Biomedicines
Published
2026-09-01
DOI
https://doi.org/10.3390/biomedicines14091970
Primary Topic
Antiplatelet Therapy and Cardiovascular Diseases
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article
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article

Frequencies of CYP2C19 Polymorphisms in Mexican Mestizo Patients with Coronary or Cerebral Atherosclerosis and Their Association with Residual Platelet Activity on Clopidogrel Treatment

Claudia Lerma, Raúl Izaguirre-Ávila, Juan Carlos Fernández-López, Evelyn Cortina-de-la-Rosa et al.
Biomedicines
Antiplatelet Therapy and Cardiovascular Diseases
article

Frequencies of CYP2C19 Polymorphisms in Mexican Mestizo Patients with Coronary or Cerebral Atherosclerosis and Their Association with Residual Platelet Activity on Clopidogrel Treatment

Claudia Lerma, Raúl Izaguirre-Ávila, Juan Carlos Fernández-López, Evelyn Cortina-de-la-Rosa, Jesús Manuel Ayala-Guerrero, Elias Vinicio Merlín-González, Beatriz Villegas-Torres
article en

Abstract

Background/Objectives: There is wide variability in the individual response to clopidogrel, which depends on CYP2C19 polymorphisms as well as on intrinsic and extrinsic platelet factors. Clopidogrel resistance has been related to an adverse evolution in patients with coronary artery disease. The aim of this study is to analyze the prevalence of CYP2C19 polymorphisms in Mexican mestizo patients and their relationship with clopidogrel platelet response by means of platelet aggregation. Methods: Patients who experienced coronary artery disease (CAD) (N = 160) or stroke (N = 11) and received treatment with clopidogrel were analyzed for CYP2C19 alleles *1, *2, *3, and *17. In total, 81 patients were tested for clopidogrel resistance by ADP-induced aggregation in platelet-rich plasma. CYP2C19 polymorphism was expressed as ultrarapid-, normal-, rapid-, normal/intermediate, intermediate, and poor metabolizers, and the clopidogrel response was assessed by platelet aggregation. Results: The allelic frequencies were 9.6%, 0%, and 11.7% for CYP2C19*2, *3, and *17, respectively. The frequencies of CYP2C19 genotypes were as follows: CYP2C19*1/*1 (62.6%); CYP2C19*1/*17 (19.9%); CYP2C19*1/*2 (12.3%); CYP2C19*2/*17 (2.3%); CYP2C19*2/*2 (2.3%); and CYP2C19*17/*17 (0.6%). Of 81 patients with platelet aggregation, 55.6% were responsive, and 44.4% were resistant to clopidogrel. Clopidogrel resistance had a non-significant trend of association with unfavorable genotypes for metabolism (CYP2C19 *1/*2, *2/*17, and *2/*2) vs. favorable genotypes (CYP2C19 *1/*1, *1/*17, and *17/*17), 64.7% vs. 39.1%, respectively (p = 0.059). Conclusions: The prevalence of CYP2C19 polymorphisms in Mexican mestizo patients is similar to that of the general population. Clopidogrel resistance is a complex in vitro phenomenon that is not explained by CYP2C19 polymorphisms alone.

BiomedicinesVol. 14(9)
National Institute of Genomic Medicine (MX), Instituto de Medicina Genómica (ES), Instituto Nacional de Cardiología (MX)
No poverty
Openalex Percentile: Top 10%
Antiplatelet Therapy and Cardiovascular Diseases
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