首页> 外文期刊>Journal of Molecular Neuroscience: MN >The Single Nucleotide Polymorphisms of Chromosome 9p21 and CD147 Were Relevant with the Carotid Plaque Risk in Acute Cerebral Infarction Patients Among Chinese Han Population
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The Single Nucleotide Polymorphisms of Chromosome 9p21 and CD147 Were Relevant with the Carotid Plaque Risk in Acute Cerebral Infarction Patients Among Chinese Han Population

机译:染色体9p21和CD147的单核苷酸多态性与中国汉族人群中急性脑梗死患者的颈动脉斑块风险有关

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摘要

This study focused on the relevance between the carotid plaque formation and the single nucleotide polymorphisms of chromosome 9p21 and CD147 in acute non-cardiogenic cerebral infarction. A total of 937 eligible patients were enrolled and categorized into carotid plaque group or non-carotid plaque group. The baseline data was analyzed, and the SNPs of chromosome 9p21 and CD147 were detected. After analyzing the results of clinic data and SNPs, we found that age, total cholesterol, low density lipoprotein, systolic blood pressure, fasting serum glucose, and NIHSS score are associated with plaque formation. Meanwhile, rs10757274, rs4977574, and rs4919862 existed statistical differences between two groups. We also analyzed linkage disequilibrium, haplotype, and inheritance models of these three SNPs, and drew the ROC curve to assess diagnostic efficiency. The results showed that mutations of SNP rs10757274 and rs4977574 in chromosome 9p21 together with SNP rs4919862 located in gene CD147 were highly relevant with the carotid plague formation in acute cerebral ischemia patients. Compared with single SNP genotype mutation, combined allele mutations on rs10757274 or rs4977574 in chromosome 9p21 with rs4919862 in CD147 resulted in much higher risks of patients, which might be associated with acute cerebral infarction happening.
机译:本研究重点关注颈动脉斑块形成与染色体9p21和CD147的单核苷酸多态性在急性非型脑发生梗死中的相关性。共有937名符合条件的患者,分为颈动脉斑块组或非颈动脉斑块组。分析基线数据,检测到染色体9p21和CD147的SNP。在分析临床数据和SNP的结果后,我们发现年龄,总胆固醇,低密度脂蛋白,收缩压,禁食血清葡萄糖和NIHSS评分与斑块形成相关。同时,RS10757274,RS497574和RS4919862存在两组之间的统计差异。我们还分析了这三个SNP的联动不平衡,单倍型和遗传模型,并制定了ROC曲线来评估诊断效率。结果表明,SNP RS10757274和RS497574在染色体9P21中的突变与位于基因CD147中的SNP RS4919862一起与急性脑缺血患者中的颈动脉瘟疫形成高。与单一SNP基因型突变相比,CD147中的RS10757274或RS4977574中的RS10757274或RS4977574的组合等位基因突变导致CD147的RS4919862导致患者风险更高,这可能与急性脑梗死发生相关。

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