期刊文献+

对氧磷酯酶-1L/M55位点基因多态性与缺血性脑卒中关系的研究 被引量:1

The relationship between paraoxonase-1 L/M55 gene polymorphism and cerebral arterial thrombosis
下载PDF
导出
摘要 目的探讨对氧磷酯酶(PON1)L/M55基因多态性与缺血性脑卒中(CAT)的相关性。方法用聚合酶链式反应-限制性长度片断多态性(PCR-RFLP)技术,对143例CAT患者和122例相匹配的正常对照组PON1L/M55基因型及等位基因频率进行检测,并做统计学分析。结果CAT组与对照组PON1L/M55基因多态性的基因型分布分别为LL型85.31%(122/143)、88.52%(108/122);LM型10.49%(15/143)、8.20%(10/122);MM型4.20%(6/143)、3.28%(4/122),CAT组与对照组组间比较三种基因型差异无统计学意义(P>0.05)。结论PON1L/M55基因多态性与缺血性脑卒中的发病无关。 Objective To explore the relationship between the PON1 L/M55 gene polymorphism and cerebral arterial thrombosis (CAT). Methods A total of 143 CAT patients and 122 control subjects were enrolled in this study for examination of PON1 L/M55 gene polymorphisms by using poIymerise chain reaction - restriction fragment length polymorphism ( PCR - RFLP). Results The distribution of the PON1 L/M55 polymorphism between CAT patients and control groups was LL genotype: 85.31% ( 122/143), 88.52% (108/122) ; LM genotype : 10.49% ( 15/143 ), 8.20% (10/122) ; MM genotype : 4.20% (6/143), 3.28% (4/122). There were no significant difference for LL, LM, MM genotypes of PON1 L/M55 polymorphism between CAT patients and control groups (P 〉 0. 05). Conclusion There is no significant association between PON1 L/M55 polymorphism and cerebral arterial thrombosis.
出处 《宁夏医学杂志》 CAS 2009年第4期327-328,F0002,共3页 Ningxia Medical Journal
基金 宁夏科技厅科技攻关项目
关键词 对氧磷酯酶1 基因多态性 缺血性脑卒中 Paraoxonase - 1 Polymorphism Cerebral arterial thrombosis
  • 相关文献

参考文献9

二级参考文献19

  • 1各类脑血管疾病诊断要点[J].中华神经科杂志,1996,29(6):379-380. 被引量:33055
  • 2叶苇苇 主编.预防医学[M].北京:人民卫生出版社,2000.330-339. 被引量:1
  • 3Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N,Shaw N, Lane C R, Lim E P, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley G Q, Lander E S. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet, 1999, 22(3):231~238. 被引量:1
  • 4Halushka M K, Fan J B, Bentley K, Hsie L, Shen N, Weder A,Cooper R, Lipshutz R, Chakravarti A. Patterns of single-nuoleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nat Genet, 1999, 22(3):239~247. 被引量:1
  • 5Nickerson D A, Taylor S L, Weiss K M, Clark A G, Hutchinson R G, Stengard J, Salomaa V, Vartiainen E, Boerwinkle E, Sing C F. DNA sequence diversity in a 9. 7-kb region of the human lipoprotein lipase gene. Nat Genet, 1998, 19(3): 233~240. 被引量:1
  • 6Cambien F, Poirier O, Nicaud V, Herrmann S M, Mallet C,Ricard S, Behague I, Hallet V, Blanc H, Loukaci V, Thillet J,Evans A, Ruidavets J B, Arveiler D, Luc G, Tiret L. Sequence diversity in 36 candidate genes for cardiovascular disorders. Am JHumGenet, 1999, 65(1):183~191. 被引量:1
  • 7Primo-Parmo S L, Sorenson R C, Teiber J, La Du B N. The human serum paraoxonse/arylesterase gene is one member of a multigene family. Genomics, 1996, 33: 498~507. 被引量:1
  • 8Leviev I, James R W. Promoter polymorphisms of human paraoxonase PON1 gene and serum paraoxonase activities and concentrations. Arterioscler Thromb Vasc Biol, 2000, 20: 516~521. 被引量:1
  • 9Suehiro T, Nakamura T, Inoue M, Shiinoki T, Ikeda Y, Kumon Y,Shindo M, Tanaka H, Hashimoto K. A polymorphism upstream from the human paraoxonase gene and its association with PON 1 expression. Atherosclerosis, 2000, 150: 295~298. 被引量:1
  • 10Yamada R, Tanaka T, Ohnishi Y, Suematsu K, Minami M, Seki T, Yukioka M, Maeda A, Murata N, Saiki O, Teshima R, Kudo O, Ishikawa K, Ueyosi A, Tateishi H, Inaba M, Goto H, Nishizawa Y, Tohma S, Ochi T, Yamamoto K, Nakamura Y. Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population. Hum Genet, 2000, 106(3):293~297. 被引量:1

共引文献33084

同被引文献9

引证文献1

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