Relationship between CYP2C19*2, *3 gene polymorphism and the recurrence in ischemic stroke patients treated with

Yu Yan1, Ruixiao Hao1, Xiuyuan Zhao1

  • 1Department of Neurology, Tianjin Medical University Second Hospital, Tianjin, China.

Insights

CYP2C19*2 gene variants and poor CYP2C19 metabolism increase stroke recurrence risk in patients treated with clopidogrel. Carriers of CYP2C19*2 and *3 are more prone to recurrent strokes than CYP2C19*1 carriers.

Area of Science:

  • Pharmacogenomics
  • Cardiovascular Medicine
  • Clinical Genetics

Background:

  • The association between CYP2C19 gene variants (*2, *3) and clopidogrel efficacy in ischemic stroke patients remains debated.
  • This study aimed to clarify the correlation between CYP2C19 *2,*3 genotypes, metabolic status, and stroke recurrence.

Approach:

  • A comprehensive meta-analysis was conducted, including 9 articles with 10 trials and 1333 ischemic stroke patients.
  • Literature search spanned major databases (CNKI, Wanfang, VIP, CBM, PubMed, Cochrane) up to December 2020.
  • Meta-analysis was performed using RevMan 5.3 software.

Key Points:

  • CYP2C19*2 GA/AA genotypes significantly elevated recurrent stroke risk compared to GG (OR=2.50, 95% CI: 1.66–3.75).
  • Poor metabolizers (PM) and intermediate metabolizers (IM) of CYP2C19 showed a higher risk of recurrent stroke than extensive metabolizers (EM).
  • No significant difference in recurrence risk was observed for CYP2C19*3 GA vs. GG genotype.

Conclusions:

  • CYP2C19*2 gene mutations and altered CYP2C19 metabolism are linked to increased stroke recurrence in patients on clopidogrel.
  • Individuals carrying CYP2C19*2 and *3 variants face a higher likelihood of recurrent stroke compared to CYP2C19*1 carriers.
Abstract

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