期刊文献+

OCTN1、OCTN2基因多态性与广西壮族炎症性肠病患者的相关性研究 被引量:4

Correlation of OCTN1 and OCTN2 Gene Polymorphisms with Inflammatory Bowel Disease in Zhuang Population in Guangxi
下载PDF
导出
摘要 目的研究OCTN1、OCTN2基因单核苷酸多态性(SNP)位点C1672T、G-207C与中国广西壮族炎症性肠病(IBD)易感性的关系。方法分别收集广西无亲缘关系的壮族70例和汉族76例IBD患者及壮族80例和汉族87例健康对照者的肠黏膜组织,苯酚/氯仿法提取各组肠黏膜组织的DNA,采用聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)方法检测OCTN1基因C1672T和OCTN2基因G-207C的基因型,计算基因频率,根据结果分析该突变与IBD的关系。结果本组IBD患者和健康对照者中均未检测出OCTN1基因C1672T和OCTN2基因G-207C突变型。结论 OCTN1基因C1672T和OCTN2基因G-207C与中国广西壮族人炎症性肠病的发病可能无相关性。 Objective To study the correlation between single nucleotide polymorphism(SNP) sites C1672T, G-207C of OCTN1 and OCTN2 gene, and the susceptibility inflammatory bowel disease in Chinese Zhuang population in Guangxi. Methods One hundred and forty-six unrelated IBD patients(Zhuangs 70 eases, Hans 76 cases)and one hundred sixty-four healthy controls (Zhuangs 80 cases, Hans 87 cases)were recruited. Genomic DNA samples were obtained from intestinal tissues by phenol chloroform extraction method. Polymorphisms of OCTN1 gene C1672T and OCTN2 gene G-207C were detected by polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP). Results The mutant genotypes of OCTN1 gene C1672T and OCTN2 gene G-207C were not found in both IBD patients and healthy controls. Conclusion The gene polymorphisms of OCTN1 gene C1672T and OCTN2 gene G-207C are not associated with IBD in the Chinese Zhuang population in Guangxi.
出处 《广西医学》 CAS 2011年第9期1099-1102,共4页 Guangxi Medical Journal
基金 广西自然科学基金资助项目(0832009) 广西研究生教育创新项目(2009105981002M207)
关键词 炎症性肠病 OCTN1基因 OCTN2基因 单核苷酸多态性 广西 Inflammatory bowel disease OCTN1 gene OCTN2 gene Single nucleotide polymorphism Guangxi
  • 相关文献

参考文献4

二级参考文献51

  • 1高敏,曹倩,罗灵和,吴敏良,胡伟玲,姒健敏.NOD2/CARD15基因多态性与克罗恩病患者相关性研究[J].中华内科杂志,2005,44(3):210-212. 被引量:22
  • 2Maria Gazouli,Gerassimos Mantzaris,Athanassios J Archimandritis,George Nasioulas,Nicholas P Anagnou.Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease[J].World Journal of Gastroenterology,2005,11(47):7525-7530. 被引量:12
  • 3[1]Bonen DK,Cho JH.The genetics of inflammatory bowel disease.Gastroenterology 2003;124:521-536
  • 4[2]Ahmad T,Tamboli CP,Jewell D,Colombel JF.Clinical relevance of advances in genetics and pharmacogenetics of IBD.Gastroenterology 2004;126:1533-1549
  • 5[3]Hugot JP,Laurent-Puig P,Gower-Rousseau C,Olson JM,Lee JC,Beaugerie L,Naom L Dupas JL,Van Gossum A,Orholm M,Bonaiti-Pellie C,Weissenbach J,Mathew CG,Lennard-Jones JE,Cortot A,Colombel JF,Thomas G.Mapping of a susceptibility locus for Crohn's disease on chromosome 16.Nature 1996;379:821-823
  • 6[4]Cavanaugh J.International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set:Crohn disease and chromosome 16.Am J Hum Genet 2001;68:1165-1171
  • 7[5]Zouali H,Chamaillard M,Lesage S,Cezard JP,Colombel JF,Belaiche J,Almer S,Tysk C,Montague S,Gassull M,Christensen S,Finkel Y,Gower-Rousseau C,Modigliani R,Macry J,Selinger-Leneman H,Thomas G,Hugot JP.Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease.Eur J Hum Genet 2001;9:731-742
  • 8[6]Brant SR,Panhuysen CI,Bailey-Wilson JE,Rohal PM,Lee S,Mann J,Ravenhill G,Kirschner BS,Hanauer SB,Cho JH,Bayless TM.Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity.Gastroenterology 2000;119:1483-1490
  • 9[7]Gazouli M,Zacharatos P,Mantzaris GJ,Barbatis C,Ikonomo poulos I,Archimandritis AJ,Lukas JC,Papalambros E,Gorgoulis V.Association of NOD2/CARD15 variants with Crohn's disease in a Greek population.Eur J Gastroenterol Hepatol 2004;16:1177-1182
  • 10[8]Gazouli M,Mantzaris G,Kotsinas A,Zacharatos P,Papalambros E,Archimandritis A,Ikonomopoulos J,Gorgoulis VG.Association between polymorphisms in the Toll-like receptor 4,CD14,and CARD15/NOD2 and inflammatory bowel diseasein the Greek population.World J Gastroenterol2005;11:681-685

共引文献777

同被引文献41

引证文献4

二级引证文献33

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