Department of Emergency, Rui Jin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China.
Department of Neurology & Institute of Neurology, Rui Jin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China.
Thromb Res. 2017 Aug;156:29-35. doi: 10.1016/j.thromres.2017.05.027. Epub 2017 May 26.
Given the important role of CD147 in the development of atherosclerosis, we speculated that CD147 genetic polymorphisms might influence the formation of carotid atherosclerotic plaques. The study was to investigate the association between CD147 gene polymorphisms and susceptibility to carotid atherosclerotic plaques in individuals with cerebral infarction (CI).
Eight SNPs in the regulatory and coding regions of the CD147 gene were examined using polymerase chain reaction-ligase detection reaction (PCR-LDR) in DNA samples from 732 Chinese patients with CI, divided into a carotid plaque group (n=475) and a non-carotid plaque group (n=257).
Significant differences were found in the genotypes and allele frequencies of the rs4919862 SNP between the carotid plaque and non-carotid plaque groups of CI patients (P<0.05), while the frequencies of the C allele and the CC genotype in the non-carotid plaque group were significantly lower than those in the carotid plaque group, and the frequencies of the T allele in the non-carotid plaque group were significantly higher than those in the carotid plaque group (P<0.05). In addition, there was strong linkage disequilibrium among the rs4919862, rs8637 and rs8259 sites. In a haplotype analysis, the occurrence rate of the haplotype GATGCAGC was 2.095 times higher in the carotid plaque group than in the non-carotid plaque group (P<0.05).
These results showed that the rs4919862 SNP of CD147 was closely associated with carotid atherosclerotic plaques formation. Thus, polymorphisms of the CD147 gene may be related to the tendency for carotid atherosclerotic plaques.
鉴于 CD147 在动脉粥样硬化发展中的重要作用,我们推测 CD147 基因多态性可能影响颈动脉粥样硬化斑块的形成。本研究旨在探讨 CD147 基因多态性与脑梗死(CI)患者颈动脉粥样硬化斑块易感性的关系。
采用聚合酶链反应-连接酶检测反应(PCR-LDR)法,对 732 例 CI 患者的 DNA 样本中 CD147 基因调控区和编码区的 8 个 SNP 进行检测,将患者分为颈动脉斑块组(n=475)和非颈动脉斑块组(n=257)。
CI 患者颈动脉斑块组和非颈动脉斑块组 rs4919862 位点的基因型和等位基因频率存在显著差异(P<0.05),非颈动脉斑块组的 C 等位基因和 CC 基因型频率明显低于颈动脉斑块组,T 等位基因频率明显高于颈动脉斑块组(P<0.05)。此外,rs4919862、rs8637 和 rs8259 位点之间存在强连锁不平衡。在单体型分析中,颈动脉斑块组 GATGCAGC 单体型的发生率明显高于非颈动脉斑块组(P<0.05)。
这些结果表明,CD147 的 rs4919862 位点与颈动脉粥样硬化斑块的形成密切相关。因此,CD147 基因多态性可能与颈动脉粥样硬化斑块的发生趋势有关。