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单核细胞趋化蛋白-1基因A-2518G多态性与急性冠脉综合征相关性研究 被引量:4

Correlation between polymorphism of monocyte chemoatt-ractant protein-1 gene A-2518G single nucleotide and acute coronary syndrome
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摘要 目的探讨中国苏南地区汉族人群单核细胞趋化蛋白-1(MCP-1)基因启动子区A-2518G单核苷酸多态性与ACS发病的相关性。方法采用病例-对照研究方法,选择临床确诊的ACS484例(ACS组),其中急性心肌梗死(AMI)290例,不稳定性心绞痛(UAP)194例。经冠脉造影排除冠心病者346例为对照组,包括冠脉硬化症(CAS组)166例和冠脉无狭窄(冠脉正常组)180例。利用聚合酶链式反应-限制性酶切片段长度多态性技术(PCR-RFLP)检测MCP.1基因A-2518G多态性。结果MCP.1基因A-2518G单核苷酸多态性在ACS组和对照组中均存在AA、AG和GG三种基因型。二组基因型分布符合Hardy-Weinberg平衡(P〉0.05),具有群体代表性。与对照组相比,ACS组中AA(15.32%vs.16.12%)、AG(53.47%vs.51.86%)和GG(31.21%vs.32.02%)基因型和G(57.95%VS.57.95%)等位基因频率差异均无统计学意义(P值分别为0.083、0.673、0.821和1.000)。对性别、年龄、吸烟、糖尿病、TC和LDL等6个相关因素行Logistic回归分析显示,MCP.1基因A-2518G单核苷酸多态性与ACS的发病无相关性(P〉0.05)。对男性ACS、女性ACS、AMI、UAP和早发ACS等5个亚组进行MCP-1基因A-2518G多态性分析,结果显示,男性和女性ACS分别与对照组相比、AMI和UAP分别与冠脉正常组相比以及早发ACS与年龄相匹配的对照组相比,AA、AG和GG基因型和G等位基因频率差异均无统计学意义(均P〉0.05)。结论在中国苏南地区汉族人群中,MCP-1基因存在A-2518G单核苷酸多态性,该多态性与ACS发病无显著相关性。 Objective To investigate the possible correlation between the monocyte chemoattractant protein-1 (MCP-1) gene A-2518G single nucleotide polymorphism (SNPs) in the promoter region and acute coronary syndrome (ACS) in Chinese Han ethnic population of Sunan region. Methods This study was conducted with a case-control design in 484 ACS patients including 290 acute myocardial infarction (AMI) patients and 194 patients with unstable angina pectoris (UAP) and 346 control subjects ruled out coronary disease by coronary angiography (control group), including 166 patients with coronary atherosclerosis and 180 subjects without coronary stenosis. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used for the detection of the A-2518G polymorphism in MCP-1 gene, and then thefrequency of genetype was statistically analyzed. Results There were AA, AG and GG genotypes of MCP-1 gene A-2518G polymorphism in the ACS group and control group. The two groups could be considered as a genetic equilibrium representative by Hardy-Weinberg equilibrium (P 〉 0. 05 ). Compared with the control group, the frequencies of AA genotype ( 15. 32% vs. 16. 12% ), AG genotype (53.47% vs. 51.86% ), GG genotype (31.21% vs. 32. 02% ) and G allele genotype (57.95% vs. 57.95% ) in ACS group were not significantly different ( P was 0. 083, 0. 673, 0. 821 and 1.00, respectively). Multivariate logistic regression analysis indicated that there was no significant correlation between MCP-1 gene A-2518G polymorphism and ACS regardless of differences in gender, age, smoking, diabetes, TG and LDL-C (P 〉 0. 05 ). There was no significant difference in gender and age of ACS onset between two groups (P 〉 0. 05). There were no significant differences in the frequencies of AA, AG and GG genotypes and G allele genotype among AMI group, UAP group and normal coronary group (P 〉 0. 05). Conclusions The data shows that MCP-1 gene A-25-18G polymorphism is not associated with the risk of ACS in the Chinese Han ethnic population living in Sunan region.
出处 《中华急诊医学杂志》 CAS CSCD 北大核心 2012年第7期687-693,共7页 Chinese Journal of Emergency Medicine
基金 江苏大学临床医学科技发展基金(JCY20080065)
关键词 单核细胞趋化蛋白-1 单核苷酸多态性 急性冠脉综合征 Monocyte chemoattractant protein-1 Single nucleotide polymorphism Acute coronarysyndrome
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参考文献19

  • 1Chen MS,Bhatt DL. Highlights of the 2002 update to the 2000 American College of Cardiology/American Heart Association acute coronary syndrome guidelines[J].Cardiology in Review,2003,(03):113-121.
  • 2Ross R. Atherosclerosis:an inflammatory disease[J].New England Journal of Medicine,1999,(02):115-126.
  • 3Dong VM,McDermott DH,Abdi R. Chemokines and diseases[J].European Journal of Dermatology,2003,(03):224-230.
  • 4Jiang Y,Beller DI,Frendl G. Monocyte chemoattractant protein-1 regulates adhesion molecule expression and cytokine production in human monocytes[J].Immunology,1992,(08):2423-2428.
  • 5Yamamoto T,Eckes B,Mauch C. Monocyte chemoattractant protein-1 enhances gene expression and synthesis of matrix metalloproteinase-1 in human fibroblasts by an autocrine IL-1 alpha loop[J].Journal of Immunology,2000,(12):6174-6179.
  • 6Nelken NA,Conghlin SR,Gordon D. Monocyte chemoattractant protein-1 in human atheromatous plaques[J].Journal of Clinical Investigation,1991,(04):1121-1127.
  • 7de Lemos JA,Morrow DA,Sabatine MS. Association between plasma levels of monocyte chemoat-tractant protein-1 and long-term clinical outcomes in patients with acute coronary syndromes[J].Circulation,2003,(05):690-695.
  • 8哈华兰,张钲,王恒大.急性冠脉综合征患者外周血MCP-1和IL-18水平变化的临床意义[J].中国心血管病研究,2005,3(6):427-429. 被引量:17
  • 9Kitamoto S,Nakano K,Hirouchi Y. Cholesterol-bwering independent regression and stabilization of atherosclerotic lesions by pravastatin and by antimonocyte chemoattractant protein-1 therapy in nonhuman primates[J].Arteriosclera Thromb Vasc Biol,2004,(08):1522-1528.
  • 10Kanno K,Tazuma S,Nishioka T. Angiotensin Ⅱ participates in hepatic inflammation and fibrosis through MCP-1 expression[J].Digestive Diseases and Sciences,2005,(05):942-948.

二级参考文献30

  • 1Rovin BH, Lu L, Saxena R. A novel polymorphism in the MCP-1 gene regulatory region that influences MCP-1 expression. Biochem Biophys Res Commun, 1999, 259(2):344.
  • 2Yasuharu T, Katsuhiko K, Yoshikuni y, et al. Polymorphism of the monoeyte ehemoattractant protein (MCP-1) gene is associated with the plasma level of MCP-1 bul nol with carotid intima-media thickness. Hyperlens Res, 2003, 26(9): 677.
  • 3Szalai C, Duha J, Prohaszka Z, et al. Involvement of polymorphisms in the chemukine system in the susceptibility for coronary artery disease (CAD). Coincidence of elevated Lp(a) anti MCP-1-2518 G/G genotype in CAD patients. Atherosclerosis, 2001, 158(1): 233.
  • 4Kitamoto S, Egashira K. Gene therapy targeting monocyte chemoattractant protein-1 for vascular disease. J Atheroscler Thromb, 2002,9(6): 261.
  • 5Cipollone F, Marini M, Fazia M, et al. Elevated circulating levels of monocyte chemoattractant protein-1 in patients with restenosis after coronary angioplasty. Arterioseler Thromb Vasc Biol, 2001, 21 (3):327.
  • 6Reape TJ, Groot PH. Chemokine and atherosclerosis. Atherosclerosis, 1999, 147(2): 213.
  • 7[1]Kuziel WA, Morgan SJ, Sawson TC, et al. Severe reduction in interleukocyte adhesion and monocyte extravasation in mice deficient in CC chemokine receptor. Proc Natl Acad Sci USA,1997, 94:12053-12058
  • 8[2]Moreno PR, Falk E , Palacios IF, et al. Macrophage infiltration in acute coronary syndromes :implications for plaque rupture .Circulation, 1994, 90:775-778
  • 9[3]Liuzzo G, Goronzy JJ, Yang H, et al. monoclonal T-cell proliferation and plaque instability in acute coronary syndromes .Circulation, 2000,101:2883-2888
  • 10[4]Aukrust P,Berge RK,Ueland T,et al. interaction between chemokines and oxidative stress :possible pathogenic role in acute coronary syndrome. J Am Coll Cardiol,2001,37 (2):485-491

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