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白细胞介素-18启动子多态性与1型糖尿病易感性的关联。

Association of IL-18 promoter polymorphisms with predisposition to Type 1 diabetes.

作者信息

Mojtahedi Z, Naeimi S, Farjadian S, Omrani G R, Ghaderi A

机构信息

Department of Immunology, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Diabet Med. 2006 Mar;23(3):235-9. doi: 10.1111/j.1464-5491.2006.01786.x.

Abstract

AIMS

IL-18, a potent IFN-gamma-inducing cytokine, is capable of polarizing the immune response to a Th1 phenotype. Recent studies have demonstrated an association between single-nucleotide polymorphisms located at positions -607 (A/C) and -137 (C/G) in the promoter region of IL-18 gene and Type 1 diabetes. The aim of the present study was to determine whether the same polymorphisms of the gene were associated with Type 1 diabetes in Iranians.

METHODS

In 112 patients with Type 1 diabetes and 194 non-diabetic control subjects, these two single-nucleotide polymorphisms were analysed by sequence-specific PCR.

RESULTS

Allele and genotype frequencies of the IL-18 gene polymorphisms were similar in the whole group of Type 1 diabetic patients and controls. However, categorizing patients according to age at onset of diabetes revealed a significant difference in distribution of the genotypes at position -137 between patients with older age at onset (> 15 years) (GG 49%, GC 34%, CC 17%) and control subjects (GG 57.7%, GC 36.6%, CC 5.7%) (P = 0.027). Frequency of the C allele at position -137 was significantly higher in these patients than in controls (P = 0.038). Moreover, there was an association between -607AA/-137CC genotype combination and susceptibility to Type 1 diabetes in this subgroup of patients (pc = 0.027).

CONCLUSIONS

The results of this study show that polymorphisms of IL-18 promoter confer susceptibility to Type 1 diabetes in Iranian individuals with onset at older ages. Further investigations are necessary to clarify the effect of IL-18 variants on immune regulation.

摘要

目的

白细胞介素-18(IL-18)是一种强效的干扰素-γ诱导细胞因子,能够使免疫反应向Th1表型极化。最近的研究表明,IL-18基因启动子区域位于-607(A/C)和-137(C/G)位置的单核苷酸多态性与1型糖尿病之间存在关联。本研究的目的是确定该基因的相同多态性是否与伊朗人的1型糖尿病相关。

方法

对112例1型糖尿病患者和194例非糖尿病对照者,采用序列特异性PCR分析这两个单核苷酸多态性。

结果

在整个1型糖尿病患者组和对照组中,IL-18基因多态性的等位基因和基因型频率相似。然而,根据糖尿病发病年龄对患者进行分类后发现,发病年龄较大(>15岁)的患者(GG 49%,GC 34%,CC 17%)与对照者(GG 57.7%,GC 36.6%,CC 5.7%)在-137位置的基因型分布存在显著差异(P = 0.027)。这些患者中-137位置C等位基因的频率显著高于对照者(P = 0.038)。此外,在该亚组患者中,-607AA/-137CC基因型组合与1型糖尿病易感性之间存在关联(pc = 0.027)。

结论

本研究结果表明,IL-18启动子多态性使发病年龄较大的伊朗个体易患1型糖尿病。需要进一步研究以阐明IL-18变体对免疫调节的影响。

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