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掌跖脓疱病中IL19、IL20和IL24基因的关联分析

Association analysis of IL19, IL20 and IL24 genes in palmoplantar pustulosis.

作者信息

Kingo K, Mössner R, Kõks S, Rätsep R, Krüger U, Vasar E, Reich K, Silm H

机构信息

Department of Dermatology and Venereology, University of Tartu, Tartu, Estonia.

出版信息

Br J Dermatol. 2007 Apr;156(4):646-52. doi: 10.1111/j.1365-2133.2006.07731.x. Epub 2007 Jan 30.

Abstract

BACKGROUND

Interleukin (IL) 19, IL-20 and IL-24 belong to the IL-10 cytokine family and have been identified to play a role in the regulation of epidermal functions and in inflammation. The genes encoding IL-19, IL-20 and IL-24 are located within a gene cluster on chromosome 1q31-32 and carry frequent genetic variations.

OBJECTIVES

This study investigated whether variations in the IL19, IL20 and IL24 genes that have previously been associated with plaque-type psoriasis may also play a role in palmoplantar pustulosis (PPP).

PATIENTS

Fifteen polymorphisms were analysed in 43 patients with PPP and in 149 healthy control subjects.

RESULTS

The rare allele of IL20 1380 A-->G (rs2981573) was less frequent in patients with PPP compared with healthy controls (OR 1 x 95, 95% CI 1 x 00-3 x 79). Haplotype analyses of IL19 and IL20 suggested an increased risk for PPP associated with IL20 haplotype GAA (OR 2 x 39, 95% CI 1 x 17-4 x 86) and a reduced risk for PPP associated both with IL19 haplotype GATGATA (OR 0 x 41, 95% CI 0 x 16-1 x 05) and IL20 haplotype GGG (OR 0 x 48, 95% CI 0 x 23-0 x 98). Extended haplotype analysis revealed an association of IL19/IL20 haplotype GACACCGGAA with a higher risk for PPP (OR 2 x 31, 95% CI 1 x 05-5 x 10) and of IL20/IL24 haplotype CAAAC with a reduced risk for PPP (OR 0 x 12, 95% CI 0 x 02-0 x 82).

CONCLUSIONS

This exploratory study supports the hypothesis that variations of genes of the IL-19 subfamily of cytokines influence susceptibility to PPP. However, due to the limited size of the study samples, this current concept should be considered as preliminary and the results need to be confirmed in future independent studies.

摘要

背景

白细胞介素(IL)-19、IL-20和IL-24属于IL-10细胞因子家族,已被证实参与调节表皮功能和炎症反应。编码IL-19、IL-20和IL-24的基因位于1号染色体1q31 - 32的一个基因簇内,且存在频繁的基因变异。

目的

本研究旨在探讨先前已发现的与斑块状银屑病相关的IL19、IL20和IL24基因变异是否也在掌跖脓疱病(PPP)中起作用。

患者

对43例PPP患者和149名健康对照者分析了15个多态性位点。

结果

与健康对照相比,PPP患者中IL20基因1380 A→G(rs2981573)的罕见等位基因频率较低(比值比[OR]1.95,95%置信区间[CI]1.00 - 3.79)。对IL19和IL20的单倍型分析表明,与IL20单倍型GAA相关的PPP风险增加(OR 2.39,95%CI 1.17 - 4.86),而与IL19单倍型GATGATA(OR 0.41,95%CI 0.16 - 1.05)和IL20单倍型GGG(OR 0.48,95%CI 0.23 - 0.98)相关的PPP风险降低。扩展单倍型分析显示,IL19/IL20单倍型GACACCGGAA与较高的PPP风险相关(OR 2.31,95%CI 1.05 - 5.10),而IL20/IL24单倍型CAAAC与较低的PPP风险相关(OR 0.12,95%CI 0.02 - 0.82)。

结论

这项探索性研究支持细胞因子IL - 19亚家族基因变异影响PPP易感性的假说。然而,由于研究样本量有限,目前这一概念应被视为初步的,结果需要在未来的独立研究中得到证实。

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