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Association between polymorphisms in the Toll-like receptor 4 CD14 and CARD15/NOD2 and inflammatory bowel disease in the Greek population

机译:Toll样受体4CD14和CARD15 / NOD2多态性与希腊人群的炎症性肠病之间的关系

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摘要

AIM: Crohn’s disease (CD) and ulcerative colitis (UC) are multifactorial diseases with a significant genetic background. Apart from CARD15/NOD2 gene, evidence is accumulating that molecules related to the innate immune response such as CD14 or Toll-like receptor 4 (TLR4), are involved in their pathogenesis. In further exploring the genetic background of these diseases, we investigated the variations in the CARD15/NOD2 gene (Arg702Trp, Gly908Arg and Leu1007fsinsC), and polymorphisms in the TLR4 gene (Asp299Gly and Thr399Ile) as well as in the promoter of the CD14 gene (T/C at position -159) in Greek patients with CD and UC.METHODS: DNA was obtained from 120 patients with CD, 85 with UC and 100 healthy individuals. Genotyping was performed by allele specific PCR or by PCR-RFLP analysis.RESULTS: The 299Gly allele frequency of the TLR4 gene and the T allele and TT genotype frequencies of the CD14 promoter were significantly higher in CD patients only compared to healthy individuals (P = 0.026<0.05; P = 0.0048<0.01 and P = 0.047<0.05 respectively). Concerning the NOD2/CARD15 mutations the overall presence in CD patients was significantly higher than that in UC patients or in controls. Additionally, 51.67% of the CD patients were carriers of a TLR4 and/or CD14 polymorphic allele and at least one variant of the NOD2/CARD15, compared to 27% of the UC patients. It should be pointed out that both frequencies significantly increased as compared with the 10% frequency of multiple carriers found in healthy controls. A possible interaction of the NOD2/CARD15 with TLR4 and especially CD14, increased the risk of developing inflammatory bowel disease (IBD).CONCLUSION: Our results indicate that co-existence of a mutation in either the TLR4 or CD14 gene, and in NOD2/CARD15 is associated with an increased susceptibility to developing CD compared to UC, and to developing either CD or UC compared to healthy individuals.
机译:目的:克罗恩病(CD)和溃疡性结肠炎(UC)是具有重要遗传背景的多因素疾病。除了CARD15 / NOD2基因外,越来越多的证据表明,与先天免疫应答相关的分子(例如CD14或Toll样受体4(TLR4))也参与了其发病机理。在进一步探索这些疾病的遗传背景时,我们研究了CARD15 / NOD2基因(Arg702Trp,Gly908Arg和Leu1007fsinsC)的变异以及TLR4基因(Asp299Gly和Thr399Ile)的多态性以及CD14基因的启动子(在希腊CD和UC患者中-159位的T / C方法:DNA从120位CD患者,85位UC患者和100位健康个体中获得。结果:仅CD患者的TLR4基因299Gly等位基因频率和CD14启动子的T等位基因和TT基因型频率显着高于健康个体(P = 0.026 <0.05; P = 0.0048 <0.01和P = 0.047 <0.05)。关于NOD2 / CARD15突变,CD患者的总体存在显着高于UC患者或对照组。另外,相比于UC患者的27%,有51.67%的CD患者是TLR4和/或CD14多态性等位基因以及NOD2 / CARD15的至少一种变体的携带者。应当指出,与健康对照中发现的多种载体的10%频率相比,两种频率均显着增加。 NOD2 / CARD15与TLR4尤其是CD14可能的相互作用增加了发生炎症性肠病(IBD)的风险。结论:我们的结果表明,TLR4或CD14基因以及NOD2 /中存在突变与UC相比,CARD15与CD的易感性增加,与健康个体相比,与CD或UC的易感性增加有关。

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