期刊文献+

ABCA1基因多态性与冠心病的相关研究 被引量:3

The Association between ABCA1 Gene R219K Polymorphism and Coronary Heart Disease
下载PDF
导出
摘要 目的探讨三磷酸腺苷结合盒转运子A1(ATP binding cassette transporter1,ABCA1)基因R219K多态性与冠心病(coronary heart disease,CHD)易感性的关系。方法采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测了162例冠心病患者和186名对照的ABCA1基因R219K基因型和等位基因的分布。结果两组基因型频率均符合Hardy-Weinberg平衡。对照组的RK和KK基因型的频率显著高于CHD组(73.66%比56.17%,P<0.05),同样,对照组K等位基因的频率显著高于CHD组(48.66%比36.11%,P<0.01)。调整年龄、性别、体重指数、吸烟和高血压等因素后,携带至少1个219K等位基因的个体显著减少患冠心病的危险(OR=0.38;95%CI=0.22-0.65)。结论ABCA1基因R219K多态性与中国温州汉族人群冠心病的遗传易感性相关,其中K等位基因可能是冠心病的保护因子。 Objective To explore the association between ATP binding cassette transporter I(ABCA1) gene R219K polymorphism and coronary heart disease(CHD) in Chinese Han Population. Methods Using polymerase chain reaction-restrictive fragment length polymorphism (PCR-RFLP), 162 CHD patients and 186 controls were analyzed for the polymorphism, genotype and allele distribution of ABCA1 gene R219K. Results The distribution of ABCA1 genotype in beth groups was in Hardy-Weinberg equilibrium. The frequency of RK and KK genotype in control group was significantly higher than that in CHD group(73.66% vs 56.17%, P 〈 0.05) ; similarly, the frequency of K allele in control group was signifieandy higher that in CHD group (48.66 % vs 36.11%, P 〈 0.01 ). After adjusted for the influence of age, gender and other CHD risk factors by multiple Logistic regression analysis, those people who have at least one allele markedly decrease CHD risk (OR= 0.38, 95%CI = 0.22 - 0.65). Conclusions ABCA1 gene R219K polymorphism is associated with CHD risk in Chinese Han population, K allele may serve as a genetic protective factor for coronary heart disease.
出处 《心脑血管病防治》 2008年第5期304-307,共4页 CARDIO-CEREBROVASCULAR DISEASE PREVENTION AND TREATMENT
关键词 冠心病 三磷酸腺苷结合盒转运子A1 多态性 Coronary heart disease ATP binding cassette transporter 1 Polymorphism
  • 相关文献

参考文献10

  • 1Oram JF. Tangier disease and ABCA1 [J ]. Biochim Biophys Acta, 2000,1529(1 - 3):321 - 330.
  • 2Singaraja RR,Brunham LR, Visscher H, et al. Efflux and Atherosclerosis.The Clinical and Biochemical Impact of Variations in the ABCA1 gene[J]. A rterioscler Thromb Vasc Biol, 2003, 23(8) : 1322 - 1332.
  • 3Clee SM, Zwinderman AH, Engcrt JC, et al. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease[J]. Circulation, 2001, 103(9):1198- 1205.
  • 4Tregonet DA, Ricard S, Nieaud V,et al. In-Depth Haplotype Analysis ABCA1 Gene Polymorphisms in Relation to Plasma ApoA1 Levels and Myocardial Infarction[J]. Arterioscler Thromb Vasc Biol, 2004,24(4):775 - 781.
  • 5高润霖.急性心肌梗死诊断和治疗指南[J].中华心血管病杂志,2001,29(12):710-725. 被引量:4901
  • 6Cenarro A, ArtiedaM, Castillo S, et al. A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia[J]. J Med Genet, 2003, 40(3): 163- 168.
  • 7Attie AD, Kastelein JP, Hayden MR. Pivotal role of ABCA1 in reverse cholesterol transport influencing HDL levels and susceptibility to atheresclerosis[J] J. Lipid Res, 2001,42(11):1717-1726.
  • 8Soro-Paavonen A, Naukkarinen J, Lee-Rueckert M,et al. Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL[J]. J Lipid Res, 2007,48(6) : 1409 - 1416.
  • 9Bisoendial RJ, Hovingh GK, Levels JH, et al. Restoration of endothelial function by increasing high-density lipolarotein in subjects with isolated low high-density lipoprotein[J]. Circulation, 2003,107(23) :2944 - 2948.
  • 10Frikke-Schmidt R, Non:lestgaard BG, Jensen GB, et al. Genetic variation in ABCA1 predicts isehemic heart disease in the general population[J]. Arterioscler Thromb Vase Biol, 2008,28(1):180- 186.

共引文献4900

同被引文献33

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部