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基质金属蛋白酶-9基因多态性与急性冠状动脉综合征的关联研究 被引量:13

Study of relations between matrix metalloproteinase-9 poly morphism(C-1562T) and acute coronary syndrome in Han population of China
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摘要 目的研究中国汉族人群基质金属蛋白酶9(maxtrixmetalloproteinase9,MMP9)基因C1562T多态性与急性冠状动脉综合征(acutecoronarysyndrome,ACS)发病的关联性。方法用聚合酶链反应限制性片段长度多态性分析法分析101例经冠状动脉(冠脉)造影确诊的ACS患者MMP9基因的C1562T多态性,以同期冠脉造影阴性、排除冠心病诊断的105例患者为对照组,比较两组间MMP9基因多态性频率分布的差异,并结合造影情况,探讨MMP9基因多态性与ACS发病及冠状动脉狭窄程度的关系。结果ACS患者CT+TT基因型频率(27.7%)明显高于对照组(13.3%),两组差异有统计学意义(χ2=6.567,P=0.01),T等位基因频率在ACS组和对照组分别为14.9%、7.2%(χ2=5.617,P=0.018);MMP9基因C1562T多态性分布与ACS冠脉狭窄程度差异无统计学意义(χ2=0.601,P=0.896)。结论MMP9基因C1562T多态性可能与中国汉族人群ACS有关,MMP9基因1562T等位基因可能是ACS遗传易感性的基因标记之一;MMP9基因C1562T多态性与ACS冠脉狭窄程度无关。 Objective To investigate the association betwee n acute coronary syndrome(ACS) and functional matrix metalloproteinase-9 polymor phism(C-1562-T). Methods This study was conducted with a case -control design including 101 patients with angiographically documented ACS and 105 control subjects who were free from coronary artery disease and had norma l angiograms. Genotype was determined by polymerase chain reaction-restriction fragment lengt h polymorphism for the common C-1562-T functional promoter polymor phism of the MMP-9 gene.The relationship between the polymorphism i n the MMP-9 gene and the severity of coronary arterial stenosis was analyzed. Resu lts The results of individual polymorphisms analysis showed that the fr equency of C/T and T/T genotypes of the C-1562-T polyporphism(27.2%) in patien ts with ACS was significantly higher than that in those with a normal angiogram( 13.34%).The frequencies of -1562T allele were 14.9% and 7.2% in ACS group and c ontrol group respectively (χ~2=5.617,P=0018). The frequencies of C/T and T/T genotypes of the C-1562-T polymorphism were not statistically different am ong ACS patients with normal and one,two,three or more significantly diseased ve ssels(χ~2=0.601,P=0.896). Conclusion The present findi ng s suggest that the genetic polymorphism in MMP-9 promoter (C-1562 - T) is associated with the susceptibility to ACS in the Han population of China. And the C-1562-T polymorphsim may not be useful as a predictor of the severity of coronary atherosclerosis.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2005年第3期313-316,共4页 Chinese Journal of Medical Genetics
关键词 基质金属蛋白酶-9 基因多态性 急性冠状动脉综合征 等位基因 遗传易感性 matrix metalloproteinases genetic polymorphism acute coronary syndrome
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参考文献15

  • 1Fuster V, Badimon L, Badimon JJ, et al. The pathogenesis of coronary artery disease and the acute coronary syndromes. N Engl J Med, 1992,326 : 242-250. 被引量:1
  • 2Zaltsman AB, Newby AC. Increased secretion of gelatinases A and B from the aortas of cholesterol fed rabbits: relationship to lesion severity.Atherosclerosis, 1997, 130 : 61-70. 被引量:1
  • 3Galis ZS, Sukhova GK, Lark MW, et al. Increased expression of matrix metalloproteinases and matrix degrading activity in vulnerable regions of human atherosclerotic plaques. J Clin Invest, 1994, 94:2493-2503. 被引量:1
  • 4Zhang B, Shu Ye, Stefan-Martin H, et al. Functional polymorphism in the regulatory region of gelatinase B gene in relation to severity of coronary atherosclerosis, Circulation, 1999, 99: 1788-1794. 被引量:1
  • 5Morgan AR, Zhang B, Tapper W, et al. H aplotypic analysis of theMMP-9 gene in relation to coronary artery disease. Haplotypic J Mol Med, 2003,81:321-326. 被引量:1
  • 6Wang J, Warzzecha D, Wilcken D, et al. Polymorphism in the gelatinase B gene and the severity of coronary arterial stenosis. Clin Sci(Lond), 2001,101:87-92. 被引量:1
  • 7Cho HJ,Chae IH, Park KW, et al. Functional polymorphism in the promoter region of the gelatinase B gene in relation to coronary artery disease and restenosis'after percutaneous coronary intervention, J Hun Genet,2002, 47:88-91. 被引量:1
  • 8赵永辉,王燕妮,祝家庆,马爱群,崔长琮,赵庆斌.血小板膜糖蛋白Ⅰa基因多态性与心肌梗塞的关系[J].中华医学遗传学杂志,2003,20(5):417-420. 被引量:5
  • 9Burzotta F, Leone AM, Paeiaroni K, et al. G20210A prothrombin gene variant and clinical outcome in patients with a first acute coronary syndrome. Haematologica, 2004, 89:1134-1138. 被引量:1
  • 10Kullo U, Elwards ED, Schwartz RS. Vulnerable plaque: pathobiology, and clinical implications. Ann Intern Med, 1998, 129: 1050-1060. 被引量:1

二级参考文献11

  • 1Fuster V, Badimon L, Badimon JJ, et al. The pathogenesis of coronary artery disease and the acute coronary syndromes. N Engl J Med, 1992, 326 : 242-250. 被引量:1
  • 2Saelman EU, Nieuwenhuis HK, Hese KM, et al. Platelet adhesion to collagen type Ⅰ through Ⅷ under conditions of stasis and flow is mediated by GP Ⅰ a/Ⅱ a (α2β1-integrin). Blood, 1994,83 : 1244-1250. 被引量:1
  • 3Murata K, Motayama T, Kotake C, et al. Collagen types in various layers of the human aorta and their changes with the atherosclerotic process. Atherosclerosis, 1986, 60 : 251-252. 被引量:1
  • 4Kritzik M, Savage B, Nugent DJ, et al. Nucleotide polymorphisms in the a2 gene define mutiple alleles that are associated with differences in platelet α2β1 density. Blood, 1998,92 : 2382-2388. 被引量:1
  • 5Bevers EM, Comfurlus P, van Rijn JL, er al. Generation of Prothrombin-converting activity and the exposure of phosphatldylserine at the outer surface of platelet. Eur J Biochem, 1982, 122 : 429-436. 被引量:1
  • 6Kirchhofer D, Tschopp TB, Stelner B, et al. Role of collagenadherent platelets in mediating fibrin formation in flowing whole blood. Blood, 1995, 86 : 3815-3822. 被引量:1
  • 7Rissanen A, Nikkila EE. Role of family history in coronary heart disease at young age, in Roskamm H(ed),Myocardial Infarction at Young Age. Heidelberg, Germany, Springer, 1981 : 64. 被引量:1
  • 8Kunlcki TJ, Orckekowski R, Annis D, et al. Variability of integrin alpha 2 beta I activity on human platelets. Blood, 1993,82 : 2693-2703. 被引量:1
  • 9Kunicki TJ, Kritzik M, Annis DS, et al. Hereditary variation in platelet integrin alpha 2 beta 1 density is associated with two silent polymorphisms in the alpha 2 gene coding sequence. Blood, 1997,89 : 1939-1943. 被引量:1
  • 10Santoso S, Kunicki TJ, Kroll H, et al. Association of the platelet glycoprotein I a C807T gene polymorphism with nonfatal myocardial infarction in younger patients. Blood, 1999, 93:2449-2453. 被引量:1

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