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Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene 被引量:3

Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene
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摘要 AIM: To investigate the frequency and distribution of /V-acetyltransferase 2 (NAT2) and uridine 5'-diphosphate (UDP)-glucuronosyltransferase 1A7 (UGT1A7) genes in patients with ulcerative colitis (UC) and Crohn's disease (CD). METHODS: Frequencies and distributions of IVAT2 and UGT1A7SNPs as well as their haplotypes were investigated in 95 patients with UC, 60 patients with CD, and 200 gender-matched, unrelated, healthy, control volunteers by PCR-restriction fragment length polymorphism (RFLP), PCR-denaturing high-performance liquid chromatography (DHPLC), and direct DNA sequencing. RESULTS: Multiple logistic regression analysis revealed that the frequency of haplotype, NAT2*7B, significantly increased in CD patients, compared to that in controls (P= 0.0130, OR = 2.802, 95%CI = 1.243-6.316). However, there was no association between NAT2 haplotypes and UC, or between any UGT1A7haplotypes and inflammatory bowel disease (IBD). CONCLUSION: It is likely that the NAT2 gene is one ofthe determinants for CD in Japanese. Alternatively, a new CD determinant may exist in the 8p22 region, where NAT2 is located. AIM: To investigate the frequency and distribution of N-acetyltransferase 2 (NAT2) and uridine 5′-diphosphate (UDP)-glucuronosyltransferase 1A7 (UGT1A7) genes in patients with ulcerative colitis (UC) and Crohn's disease (CD).METHODS: Frequencies and distributions of NAT2 and UGT1A7SNPs as well as their haplotypes were investigated in 95 patients with UC, 60 patients with CD, and 200gender-matched, unrelated, healthy, control volunteers by PCR-restriction fragment length polymorphism (RFLP),PCR-denaturing high-performance liquid chromatography (DHPLC), and direct DNA sequencing.RESULTS: Multiple logistic regression analysis revealed that the frequency of haplotype, NAT2*7B, significantly increased in CD patients, compared to that in controls (P= 0.0130, OR = 2.802, 95%CI = 1.243-6.316). However,there was no association between NAT2 haplotypes and UC, or between any UGT1A7haplotypes and inflammatory bowel disease (IBD).CONCLUSION: It is likely that the NAT2 gene is one of the determinants for CD in Japanese. Alternatively, a new CD determinant may exist in the 8p22 region, whereNAT2is located.
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第31期4833-4837,共5页 世界胃肠病学杂志(英文版)
关键词 Crohn's disease N-acetyltransferase 2 gene POLYMORPHISM Disease-susceptible gene Association study Japanese population 克隆氏病 肠疾病 日本 单模标本 N-乙酰基转移酶2 基因表达
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  • 1Fiocchi C. Inflammatory bowel disease: etiology and pathogenesis.Gastroenterology 1998; 115:182-205.
  • 2Farrell RJ, Peppercorn MA. Ulcerative colitis. Lancet 2002;359:331-340.
  • 3Yang H, Taylor KD, Rotter JI. Inflammatory bowel disease. I.Genetic epidemiology. Mol Genet Metab 2001; 74:1-21.
  • 4Watts DA, Satsangi J. The genetic jigsaw of inflammatory bowel disease. Gut 2002; 50(Suppl 3): s31-36.
  • 5Taylor KD, Yang H, Rotter JI. Inflammatory bowel disease.Ⅱ. Gene mapping. Mol Genet Metab 2001; 74- 22-44.
  • 6Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP,Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, GowerRousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G.Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001; 411:599-603.
  • 7Ogura Y, Bonen DK, Inohara M, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP,Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nunez G,Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001; 411:603-606.
  • 8Inoue N, Tamura K, Kinouchi Y, Fukuda Y, Takahashi S,Ogura Y, Inohara N, Nunez G, Kishi Y, Koike Y, Shimosegawa T, Shimoyama T, Hibi T. Lack of common NOD2 variants in Japanese patients with Crohn's disease. Gastroenterology 2002;123:86-91.
  • 9Yamazaki K, Takazoe M, Tanaka T, Kazumori T, Nakamura U. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease. J Hum Genet 2002;47:469-472.
  • 10Hein DW, Doll MA, Rustan TD, Gray K, Feng Y, Ferguson RJ,Grant DM. Metabolic activation and deactivation of arylamine carcinogens by recombinant human NAT1 and polymorphic NAT2 acetyltransferases. Carcinogenesis 1993; 14:1633-1638.

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