›› 2010, Vol. 5 ›› Issue (06): 449-453.

• 论著 • 上一篇    下一篇

基质金属蛋白酶-3基因多态性与颈动脉狭窄的相关性

孙晓明,宋玉强,赵仁亮,张晨   

  1. 山东省青岛市青岛大学医学院附属医院神经内科
  • 收稿日期:2009-07-09 修回日期:2009-06-09 出版日期:2010-06-20 发布日期:2010-06-20
  • 通讯作者: 张晨

Study of Association between Matrix Metalloproteinase-3 Gene Promoter Polymorphisms and Carotid Artery Stenosis

SUN Xiao-Ming, SONG Yu-Qiang, ZHANGChen, et al.   

  • Received:2009-07-09 Revised:2009-06-09 Online:2010-06-20 Published:2010-06-20
  • Contact: ZHANG Chen

摘要: 目的 探讨基质金属蛋白酶-3(Matrix metalloproteinase-3,MMP-3)启动子-1612 5A/6A基因多态性与颈动脉狭窄的关系,同时检测血清MMP-3水平及与颈动脉狭窄的相关机制。方法 采用聚合酶链反应-限制性酶切片段长度多态性(PCR-RFLP)方法分析421例颈动脉狭窄患者和171例对照组MMP-3启动子-1612 5A/6A基因多态性,同时用酶联免疫吸附法(Enzyme Linked ImmunoSorbent Assay,ELISA)测定两组研究对象的血清MMP-3水平。结果 颈动脉狭窄组6A/6A基因型频率与对照组相比差异有统计学意义(OR=2.55,95%CI 1.07~6.07,P=0.026),同时6A等位基因频率在颈动脉狭窄组明显高于对照组(OR=1.58,95%CI 1.08~2.33,P=0.014)。颈动脉狭窄组的MMP-3血浆浓度与对照组相比明显增高(19±9 vs 16±7μg/L,P<0.01)。MMP-3基因6A/6A纯合子和血浆MMP-3浓度明显相关(P<0.01)。结论 MMP-3启动子-1612 5A/6A基因多态性与颈动脉狭窄有关,6A等位基因可能是颈动脉狭窄的遗传易感标志,这可能与MMP-3血浆浓度增加有关。

关键词: 基质金属蛋白酶-3; 基因多态性; 颈动脉狭窄

Abstract: Objective To detect a possible association between Matrix metalloproteinase-3 (MMP-3) promoter-1612 5A/6A polymorphisms and increased risk of carotid stenosis. To investigate the mechanisms by which MMP-3 polymorphisms are involved by examining serum concentrations of MMP-3.Methods A total of 421 carotid-artery stenosis patients who underwent carotid B-mode ultrasonography and control subjects without significant sternosis were selected into the study. The MMP-3 genotype was determined by polymerase chain reaction-restriction fragment length Polymorphism (PCR-RFLP) and the serum MMP-3 concentration was quantified with enzyme-linked immunosorbent assay (ELISA).Results The 6A/6A genotype was associated with carotid sternosis (OR=2.55, 95%CI 1.07-6.07, P=0.026), and the frequency of the 6A allele was significantly higher in patients with carotid sternosis (OR=1.58, 95%CI 1.08-2.33, P=0.014). Carotid sternosis patients had higher serum MMP-3 concentration than controls (19±9 vs 16±7μg/L, P<0.01). There was a strong association between MMP-3-1612 5A/6A genotype and serum concentrations of MMP-3.Conclusion MMP-3 promoter -1612 5A/6A polymorphisms are associated with carotid stenosis, and 6A allele predicts an increased risk of carotid stenosis, in which the increased serum concentration of MMP-3 is involved.

Key words: Matrix metalloproteinase 3; Genetic polymorphism; Carotid stenosis