ORIGINAL RESEARCH article

Front. Neurol.

Sec. Stroke

Volume 16 - 2025 | doi: 10.3389/fneur.2025.1552073

The Role of ADAMTS-1 rs402007 Polymorphism in the Vulnerability of Carotid Atherosclerotic Plaques from Cerebral Infarction Autopsies

Provisionally accepted
Yongjian  LiuYongjian LiuYongmin  DengYongmin DengZhixing  DuZhixing DuShuowen  ZhangShuowen ZhangLitao  ChenLitao ChenXiaojing  YanXiaojing Yan*Yongbin  PeiYongbin Pei*
  • The First hospital of Hebei Medical University, Shijiazhuang, China

The final, formatted version of the article will be published soon.

Objective: To investigate the association between ADAMTS7 rs402007 polymorphism and carotid plaque vulnerability as well as atorvastatin’s lipid-lowering efficacy in cerebral infarction patients.Methods: We enrolled 684 cerebral infarction patients, categorized into stable (n=338) and vulnerable plaque (n=346) groups by carotid ultrasound. Clinical data, biochemical markers (LDL-C, TC, HCY, FIB), and rs402007 (G/C) genotypes (dominant model: GG vs. GC+CC) were compared. Genotyping used TaqMan assays (ABI 7500 Fast). Logistic regression assessed plaque vulnerability risk factors and rs402007–LDL-C interaction. Atorvastatin efficacy was compared across genotypes.Results: Diabetes, LDL-C, TC, HCY, and FIB differed between groups (P<0.05). GC+CC genotypes were more frequent in the vulnerable plaque group (χ²=5.618, P=0.018). Independent risk factors for vulnerability included diabetes, LDL-C, HCY, and FIB (P<0.05); rs402007 interacted with LDL-C (P<0.05). Atorvastatin efficacy rates were 82.29% (GG), 84.27% (GC), and 89.27% (CC). Lipid levels improved post-treatment in all genotypes (P<0.05). The CC genotype showed superior efficacy vs. GG (P<0.05).Conclusion: ADAMTS7 rs402007 polymorphism is linked to carotid plaque vulnerability and modulates atorvastatin’s lipid-lowering efficacy.

Keywords: ADAMTS-1 gene, atorvastatin, Cerebral Infarction, carotid atherosclerosis, efficacy

Received: 27 Dec 2024; Accepted: 10 Apr 2025.

Copyright: © 2025 Liu, Deng, Du, Zhang, Chen, Yan and Pei. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Xiaojing Yan, The First hospital of Hebei Medical University, Shijiazhuang, China
Yongbin Pei, The First hospital of Hebei Medical University, Shijiazhuang, China

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