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匈牙利炎性肠病患者白细胞介素-1β和白细胞介素-1受体拮抗剂基因多态性存在显著差异。

Significant differences in the interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in a Hungarian population with inflammatory bowel disease.

作者信息

Nemetz A, Köpe A, Molnár T, Kovács A, Fehér J, Tulassay Z, Nagy F, García-González M A, Peña A S

机构信息

Dept. of Gastroenterology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

Scand J Gastroenterol. 1999 Feb;34(2):175-9. doi: 10.1080/00365529950173041.

DOI:10.1080/00365529950173041
PMID:10192196
Abstract

BACKGROUND

There is growing evidence of the importance of genetic predisposition and the activation of the mucosal immune system in the pathogenesis of inflammatory bowel disease. Thus, genes involved in the regulation of inflammation are receiving increased attention. We have studied whether Crohn's disease (CD) or ulcerative colitis (UC) is associated with certain allelic combinations of IL1B/IL1RA gene polymorphisms in a different European population than the ones studied so far.

METHODS

Ninety-six patients with UC, 97 with CD, and 132 healthy individuals (HC) were typed for the polymorphic regions in exon 5 of the IL1B gene and in intron 2 of the IL1RA gene, using polymerase chain reaction-based methods.

RESULTS

In CD homozygotes for allele 1 in IL1B gene polymorphism were more often present (72% versus 28%; P = 0.01) in the subgroup of patients carrying at least one copy of allele 2 in IL1RA gene polymorphism. This association was not found in HC (HC versus CD; P = 0.03) or UC. However, in UC patients with pancolitis a similar trend was observed (75% versus 25%). Several genotype combinations characterized by the presence of allele 2 of the IL1RA gene polymorphism were more common in CD (P = 0.001) and UC (P = 0.049) than in HC.

CONCLUSIONS

Our data support the concept that CD and severe UC have a genetic disequilibrium in the distribution of IL1B and IL1RA gene polymorphisms. These findings together with functional studies will contribute to the understanding of the pathogenesis of the chronicity of inflammation in these diseases.

摘要

背景

越来越多的证据表明,遗传易感性和黏膜免疫系统激活在炎症性肠病发病机制中具有重要作用。因此,参与炎症调节的基因受到了越来越多的关注。我们研究了克罗恩病(CD)或溃疡性结肠炎(UC)是否与白细胞介素1β(IL1B)/白细胞介素1受体拮抗剂(IL1RA)基因多态性的某些等位基因组合相关,研究对象为与迄今所研究的不同的欧洲人群。

方法

采用基于聚合酶链反应的方法,对96例UC患者、97例CD患者和132名健康个体(HC)的IL1B基因第5外显子和IL1RA基因第2内含子的多态性区域进行分型。

结果

在IL1RA基因多态性中携带至少一个2等位基因拷贝的患者亚组中,IL1B基因多态性1等位基因的纯合子在CD患者中更常见(72%对28%;P = 0.01)。在HC(HC与CD比较;P = 0.03)或UC患者中未发现这种关联。然而,在全结肠炎的UC患者中观察到类似趋势(75%对25%)。以IL1RA基因多态性2等位基因存在为特征的几种基因型组合在CD患者(P = 0.001)和UC患者(P = 0.049)中比在HC中更常见。

结论

我们的数据支持这样的概念,即CD和重度UC在IL1B和IL1RA基因多态性分布上存在遗传失衡。这些发现与功能研究一起将有助于理解这些疾病中炎症慢性化的发病机制。

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