CYP2C19 gene variants increase stroke recurrence risk in LAA patients :- Medznat
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Are CYP2C19 polymorphisms a critical predictor of recurrent ischemic stroke risk?

Large-artery atherosclerotic stroke Large-artery atherosclerotic stroke
Large-artery atherosclerotic stroke Large-artery atherosclerotic stroke

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Patients with large-artery atherosclerotic stroke who are poor or intermediate CYP2C19 metabolizers have over twice the long-term recurrence risk of ischemic events compared with extensive metabolizers, especially when treated with clopidogrel.

Genotype-driven antiplatelet response remains a major focus in stroke precision medicine, as CYP2C19 polymorphisms directly influence clopidogrel metabolism and clinical effectiveness. Emerging evidence indicates that variations in this enzyme may shape long-term cerebrovascular outcomes, particularly in patients with large-artery atherosclerosis (LAA) stroke who rely on antiplatelet therapy for secondary prevention.

The investigators aimed to determine whether CYP2C19 polymorphisms were linked with long-term recurrent ischemic events in people presenting with acute LAA stroke. The study analyzed a sub-dataset from the National Cerebral and Cardiovascular Center (NCVC) Genome Registry, which functioned as part of a multicenter, prospective, observational cohort. Eligible participants included individuals who presented with LAA stroke within 7 days of symptom onset and provided consent for CYP2C19 genotyping between 2004 and 2022. Participants were categorized into three metabolizer groups based on CYP2C19 genotypes:

  • Extensive metabolizers (*1/*1)
  • Intermediate metabolizers (*1/*2 or *1/*3)
  • Poor metabolizers (*2/*2, *2/*3, or *3/*3)

The primary endpoint focused on the recurrence of symptomatic ischemic stroke or transient ischemic attack (TIA). Statistical analyses evaluated long-term outcomes and adjusted for key clinical covariates. The analysis included 369 patients with LAA stroke (median age 74 years; 26% female) and followed them for a median duration of 5.1 years. The findings were as follows:

  • Individuals classified as poor or intermediate metabolizers experienced a substantially higher rate of recurrent symptomatic ischemic stroke or TIA compared with extensive metabolizers.
  • The adjusted hazard ratio (HR) reached 2.33 (95% confidence interval [CI]: 1.28–4.24), indicating a more than two-fold increase in long-term risk.
  • When the analysis was limited to patients receiving clopidogrel therapy, the recurrence risk intensified, with poor/intermediate metabolizers showing an adjusted HR of 5.26 (95% CI: 1.87–14.56), underscoring the strong influence of CYP2C19 functionality on antiplatelet effectiveness.

The investigation demonstrated that CYP2C19 loss-of-function variants were associated with markedly higher long-term ischemic recurrence among patients with LAA stroke, particularly in those treated with clopidogrel. These findings reinforced the relevance of genotype-guided antiplatelet selection and highlighted the increasing role of pharmacogenomics in optimizing secondary stroke prevention strategies.

Source:

Journals of the American College of Cardiology

Article:

CYP2C19 Polymorphism and Clopidogrel Efficacy in Long-Term Outcomes of Large-Artery Atherosclerotic Stroke: The NCVC Genome Registry

Authors:

Takeshi Yoshimoto et al.

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