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Lack of association between an interleukin-1 receptor antagonist gene polymorphism and ulcerative colitis.

机译:白介素1受体拮抗剂基因多态性与溃疡性结肠炎之间缺乏关联。

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摘要

BACKGROUND: Recently, the association of a polymorphism in the gene coding for the anti-inflammatory cytokine interleukin-1 receptor antagonist with ulcerative colitis has been reported. This was interpreted as a possible genetic predisposition for severity of the inflammatory response. AIMS: To examine this polymorphism in a southern German population. SUBJECTS: The study included 234 healthy controls, 57 patients with ulcerative colitis, including 31 patients with pancolitis, 44 first degree healthy relatives of patients with ulcerative colitis, and 65 patients with Crohn's disease. METHODS: Genotypes were determined by a polymerase chain reaction amplification of the intron 2 fragment harbouring a variable number of tandem repeat nucleotide sequences. Amplification products were separated on a 2% agarose gel. RESULTS: The allele frequency for allele 2 was 27% in healthy controls, 28% in Crohn's disease, and 21% in patients with ulcerative colitis. The same allele frequency (21%) was found in a subgroup of patients with ulcerative colitis affecting the whole colon. Thus for allele 2 as well as for all other alleles, genotypes, or carriage rates no significant differences were found compared with controls. All allele frequencies in the control population were similar to those in earlier studies. CONCLUSIONS: No association of a polymorphism in the interleukin-1 receptor antagonist gene with ulcerative colitis could be identified in this southern German population. The findings of an earlier study reporting an increased frequency of allele 2, particularly in patients with pancolitis, could not be confirmed.
机译:背景:最近,已经报道了抗炎细胞因子白介素1受体拮抗剂编码基因多态性与溃疡性结肠炎的关联。这被认为是炎症反应严重程度的可能的遗传易感性。目的:研究德国南部人群的这种多态性。研究对象:该研究包括234名健康对照者,57名溃疡性结肠炎患者,其中包括31名胰腺炎患者,44名溃疡性结肠炎患者的一级健康亲属和65名克罗恩病患者。方法:通过内含子2片段的聚合酶链反应扩增确定基因型,该片段具有可变数目的串联重复核苷酸序列。在2%琼脂糖凝胶上分离扩增产物。结果:健康对照组中等位基因2的等位基因频率为27%,克罗恩氏病为28%,溃疡性结肠炎患者为21%。在影响整个结肠的溃疡性结肠炎患者亚组中发现了相同的等位基因频率(21%)。因此,对于等位基因2以及所有其他等位基因,基因型或运输率,与对照相比没有发现显着差异。对照人群中所有等位基因频率均与早期研究相似。结论:在这个德国南部人群中,没有发现白介素1受体拮抗剂基因的多态性与溃疡性结肠炎的相关性。早期研究发现等位基因2的频率增加,特别是在胰腺炎患者中,这一发现尚未得到证实。

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