摘要
目的:探讨脂联素(APN)水平及其单核苷酸基因多态性(SNP)+45T/G和+276G/T 2个位点与冠心病(CHD)的关系。方法:将195例研究对象分为正常对照组和CHD组,采用实验-对照研究方法,应用酶联免疫吸附法(ELISA)及聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,对血浆APN浓度及APN 2个位点基因多态性进行检测。结果:2组比较,CHD组APN降低(P<0.05);CHD组SNP+45TG+GG基因型和G等位基因的分布频率明显低于正常对照组,差异具有统计学意义(P<0.05);基因SNP+276多态性位点各基因型频率与等位基因频率在2组之间差异均无统计学意义(P>0.05)。结论:CHD患者APN水平下降,SNP+45G等位基因可能为CHD的保护因素;SNP+276位点基因多态性可能与CHD的发生无明显相关性。
Objective:To pursue the relationship between Adiponectin blood level and its single nucleotide polymorphism(SNP) +45 T/G and +276 G/T with Coronary Heart Disease(CHD).Method:Firstly,195 patients were divided into normal control(CO) group and coronary heart disease(CHD) group,and then according to experimental-control study method,Enzyme Linked Immunosorbent Assay(ELISA) and Polymerase Chain Reaction Restriction Fragment Length Polymorphism(PCR-RELP) were used to detect the level of plasma adiponection and polymorphisms of its two polymorphism sites +45 T/G and +276 G/T.Result:In the two groups,APN of CHD group was reduced(P0.05),and Distribution Frequency of SNP +45 TG +GG genotype and G allele of CHD group was also significantly lower than control group,further,the difference was statistically significant(P0.05);On the other hand,the difference of gene SNP +276 polymorphism and allele frequence of the genotype frequencies between two groups were showed no significant difference(P0.05).Conclusion:APN level of patients was lower in CHD group,and SNP +45 G allele might be the protective factor for CHD,and more,SNP +276 polymorphism might not be associated with occurrence of CHD.
出处
《临床心血管病杂志》
CAS
CSCD
北大核心
2011年第4期284-287,共4页
Journal of Clinical Cardiology
基金
宁夏自然科学基金项目(No:NZ09109)
关键词
冠心病
脂联素
基因多态性
adiponectin
coronary artery disease
gene polymorphisms