Journal of Capital Medical University

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Association of ITGA2 dual site variants with recurrent ischemic events in patients undergoing stenting for symptomatic intracranial atherosclerotic stenosis

Dong Yiwen1, Ye Jiadan2, Cheng Sheng1, Yang Hongge1, Li Ze1, Di Xuan1,  Lou Xin3*#, Li Xingang1*#, Ma Ning4,5*#   

  1. 1.Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China; 2.Department of Pharmacy, Fuwai Hospital, Chinese Academy of Medical Sciences, Beijing 100037, China; 3.Department of Radiology, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China; 4.Department of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China; 5.China National Clinical Research Center for Neurologic Diseases, Beijing 100070, China
  • Received:2026-02-13 Revised:2026-03-11 Online:2026-06-21
  • Supported by:
    This study was supported by National Natural Science Foundation of China (82203039), Beijing Science and Technology Planning Project (Z221100007422032), R&D Program of Beijing Municipal Education Commission (KM202210025016).

Abstract: Objective  To investigate the correlation between gene polymorphisms and the occurrence of adverse clinical events following dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic stenosis. Methods  A total of 195 patients were enrolled and categorized into 32 cases (those with clinical adverse events) and 163 controls (without events). Genotyping of 20 single nucleotide polymorphism (SNP) from 17 genes was executed. To address the imbalance in sample size between cases (n=32) and controls (n=163), weighted Logistic regression analysis was performed using frequency weights based on the reciprocal of group proportions. Weights were calculated to account for the unequal case-control ratio and improve the stability and reliability of regression estimates. Results  The ITGA2 rs1126643 (C807T) and rs1062535 (G873A) polymorphisms were significantly correlated with adverse clinical events. Specifically, the mutant frequency of allele C (ITGA2 rs1126643) and allele G (ITGA2 rs1062535) was significantly higher in cases compared to controls (OR=2.97, 95%CI: 1.702-5.172, P=0.000 1; OR=3.27, 95%CI:1.762-6.066, P=0.000 2, respectively). Other genotypes showed no significant differences between the groups. Conclusion  The ITGA2 C807T and G873A polymorphisms are associated with an increased risk of recurrent ischemic events in Chinese patients with symptomatic intracranial atherosclerotic stenosis after stenting. Detection of these variants may help identify individuals at high risk of recurrent ischemic events in this specific population.

Key words: intracranial atherosclerotic stenosis, ischemic events, dual antiplatelet therapy, single nucleotide polymorphism, genetic markers, ITGA2

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