我们的网站为什么显示成这样?

可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:

|本期目录/Table of Contents|

黏附分子E选择素A128C基因多态性与冠心病的关系(PDF)

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2007年第5期
页码:
547-549/555
栏目:
临床研究
出版日期:
2007-10-01

文章信息/Info

Title:
Correlation between Eselectin A128C gene polymorphism and coronary heart disease
作者:
饶丹1姜红2曾秋棠3郭和平3 王敏3李明慧3葛均波2
1.武汉亚洲心脏病医院心内科,湖北 武汉 430022; 2.复旦大学中山医院心内科;3.华中科技大学同济医学院心血管病研究所
Author(s):
RAO Dan1 JIANG Hong2 ZENG Qiutang3 GUO Heping3 WANG Min3 LI Minghui3 GE Junbo2
1.Department of Cardiology, Wuhan Asian Heart Hospital, Wuhan 430022, Hubei, China; 2.Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China; 3.Institute of Cardiovascular Disease, Tongji Medical College, Huazhong University of Sc
关键词:
冠状动脉疾病 E选择素 基因多态性 限制性片段长度
Keywords:
coronary disease Eselectin gene polymorphyism restriction fragment length
分类号:
R541.4
DOI:
-
文献标识码:
A
摘要:
目的 研究中国汉族人群黏附分子E 选择素(E selectin)基因外显子4,128编码处碱基A/C多态性与冠心病(CHD)的相关关系,探讨通过黏附分子Eselectin基因型筛选CHD易患人群和高危人群的可能性。方法 入选145例CHD患者,其中73例为急性冠脉综合征(ACS),72例为稳定型冠心病(SCHD),并入选144例为对照组。所有CHD患者均经冠状动脉造影证实。 采用聚合酶链反应限制性片段长度多态性(PCRRFLP)技术,分析E选择素基因型。 结果 与对照组相比,ACS 患者和SCHD患者的E选择素基因型频率和等位基因频率差异均有显著性。基因型频率的相对风险分析发现,CC+AC基因型患冠心病的风险是AA基因型的5.843倍(OR=5.843,95%CI:3.066-11.133)。结论 E选择素基因A/C多态性与CHD相关,C等位基因可能是CHD发病的遗传易感基因。
Abstract:
AIM To study the correlation between Eselectin gene polymorphism in exon 4 codon 128 and coronary heart disease (CHD) in ChineseHan population and the possibility of using the gene type to screen the susceptible and highrisk CHD population. METHODS The genotypes of Eselectin were detected by polymerase chain reactionrestriction fragment length polymorphism (PCRRFLP) in 145 CHD cases, including 73 with acute coronary syndrome (ACS) patients and 72 cases with stable coronary heart disease (SCHD), and 144 controls. RESULTS There was significant difference in the frequencies of genotype and allete in A/C polymorphism between CHD and control group, and between ACS and SCHD respectively(P<0.01 and P<0.05). The relative CHD risk in those with genotype CC+AC was 5.843 times that in those with genotype AA (OR=5.843, 95%CI: 3.06611.133). CONCLUSION Eselectin gene A/C polymorphyism is significantly associated with the occurrence, development and severity of CHD. C allele of Eselectin may be a genetic fac or that may determine an individual′s susceptibility to CHD.

参考文献/References

[1] Blankenberg S, Barbaux S, Tiret L. Adhesion molecules and atherosclerosis[J]. Atherosclerosis, 2003, 170(2):191-203.

[2] Ye SQ, Usher D, Virgil D, et al. A PstI polymorphism detects the mutation of Serine128 to Arginine in CD 62E genea risk factor for coronary artery disease[J]. J Biomed Sci, 1999, 6(1):18-21.

[3] Ross R. Atherosclerosisan inflammatory disease[J]. New Engl J Med, 1999, 340(2): 115-126.

[4] O′Brien KD, McDonald TO, Chait A, et al. Neovascular expression of Eselectin, intercellular adhesion moleculE1, and vascular cell adhesion moleculE1 in human atherosclerosis and their relation to intimal leukocyte content[J]. Circulation,1996, 93(4):672-682.

[5] Nooteboom A, van der Linden CJ, Hendriks T. Modulation of adhesion molecule expression on endothelial cells after induction by lipopolysaccharidEstimulated whole blood[J]. Scand J Immunol, 2004, 59(5):440-448.

[6] Alonso R, Mata P, De Andres R, et al. Sustained longterm improvement of arterial endothelial function in heterozygous familial hypercholesterolemia patients treated with simvastatin[J]. Atherosclerosis, 2001, 157(2):423-429.

[7] Rauchhaus M, Gross M, Schulz S, et al. The Eselectin SER128ARG gene polymorphism and restenosis after successful coronary angioplasty[J]. Int J Cardiol, 2002, 83(3): 249-257.

[8] Kilickap M, Tutar E, Aydintug O, et al. Increase in soluble Eselectin level after PTCA and stent implantation: a potential marker of restenosis[J] . Int J Cardiol, 2004,93(1):13-18.

备注/Memo

备注/Memo:
收稿日期:2006-05-23 基金项目:教育部留学人员基金项目资助(No.教外司留[2002]247号) 作者简介:饶丹,副主任医师,硕士Email:raodan@126.com
更新日期/Last Update: