摘要
目的探讨基质金属蛋白酶-12(MMP-12)血清水平及启动子基因-82A/G多态性与动脉粥样硬化性脑梗死的关系。方法对608例动脉粥样硬化脑梗死和374名健康体检者进行研究,采用ELISA法测定血清MMP-12蛋白水平,同时采用聚合酶链反应-限制性片段长度多态性(PCR—RFLP)方法分析MMP-12基因启动子区-82A/G多态性。结果脑梗死组患者48h内血清MMP-12为(17.36±9.12)ng/ml,对照组为(17.42±7.70)ng/ml,两组比较差异无统计学意义(t=0.047,P=0.962)。脑梗死组AG+GG基因型频率为7.6%,与对照组的5.9%基因型频率比较差异无统计学意义(χ^2=0.281,P=0.584),G等位基因频率在两组间分别为3.8%和2.9%,两组比较差异同样无统计学意义(χ^2=0.746,P=0.374)。结论MMP-12血清水平及基因启动子-82位点的多态与MMP-12基因表达和脑梗死没有相关性。
Objective To investigate the association of serum levels of matrix metalloproteinase-12 (MMP-12) and a functional polymorphism in the promoter -82A/G of the MMP-12 gene with acute atherosclerotic cerebral infarction (ACI) . Methods All 608 cases of acute ACI and 374 healthy controls were included in the study. Serum levels of MMP-12 were measured using the enzyme-linked immunosorbent assay (ELISA). At the same time, polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed on the - 82A/G polymorphism in the MMP-12 gene. Results The serum levels of MMP-12 in ACI group (( 17.36±9. 12) ng/ml) were not significantly higher than those in the healthy control group ( ( 17.42±7. 70) ng/ml, t = 0. 047, P = 0. 962). The frequency of the AG + GG genotypes was not significantly different between the two groups (7.6% vs 5.9 % , χ^2 = 0. 281, P = 0. 584 ) , and the frequencies of the G allele were 3.8% and 2. 9% in the ACI group and the control group respectively which were also not significantly different between the two groups ( χ^2 = 0. 746, P = 0. 374 ). Conclusion There is no correlation between serum level with genetic polymorphism in MMP-12 promoter ( - 82A/G) and cerebral infarction.
出处
《中华神经科杂志》
CAS
CSCD
北大核心
2012年第9期641-645,共5页
Chinese Journal of Neurology
基金
浙江省自然科学基金资助项目(Y2080618)
浙江省中医药科学研究基金计划资助项目(2011ZA111)