Luan Bo, Han Yaling, Zhang Xiaolin, Kang Jian, Yan Chenghui
Department of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Mol Biol Rep. 2010 Jan;37(1):399-403. doi: 10.1007/s11033-009-9845-3.
SDF-1 has been demonstrated to be involved in the pathophysiology of atherosclerosis. This study was aimed to investigate whether the SDF1-3'A polymorphism (rs1801157) is associated to myocardial infarction (MI) in a sample of Chinese Han population. A total of 560 patients with MI and 532 controls were enrolled in the study. The SDF1-3'A polymorphism was determined by polymerase chain reaction -restriction fragment length polymorphism (PCR-RFLP) analysis. A significant difference in genotype distribution and allele frequency was observed between patients and controls (P = 0.003 and P = 0.001, respectively). The A allele carriers had a significantly reduced MI risk compared with the GG homozygotes (OR, 0.69; 95% CI, 0.52-0.92; adjusted P = 0.007) in a logistic regression model after controlling conventional risk factors. The present study showed a significant association between the SDF1-3'A polymorphism and MI in Chinese Han population.
基质细胞衍生因子-1(SDF-1)已被证明参与动脉粥样硬化的病理生理学过程。本研究旨在探讨在中国汉族人群样本中,SDF1基因3'端A等位基因多态性(rs1801157)是否与心肌梗死(MI)相关。本研究共纳入560例心肌梗死患者和532例对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析确定SDF1基因3'端A等位基因多态性。患者与对照之间在基因型分布和等位基因频率上存在显著差异(分别为P = 0.003和P = 0.001)。在控制传统危险因素后的逻辑回归模型中,与GG纯合子相比,A等位基因携带者的心肌梗死风险显著降低(比值比,0.69;95%可信区间,0.52 - 0.92;校正P = 0.007)。本研究表明,在中国汉族人群中,SDF1基因3'端A等位基因多态性与心肌梗死之间存在显著关联。