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中国南方系统性红斑狼疮患者白细胞介素-10启动子多态性

Interleukin-10 promoter polymorphisms in Southern Chinese patients with systemic lupus erythematosus.

作者信息

Mok C C, Lanchbury J S, Chan D W, Lau C S

机构信息

Queen Mary Hospital, Pokfulam, Hong Kong, China.

出版信息

Arthritis Rheum. 1998 Jun;41(6):1090-5. doi: 10.1002/1529-0131(199806)41:6<1090::AID-ART16>3.0.CO;2-6.

Abstract

OBJECTIVE

To study the genetic association of interleukin-10 (IL-10) promoter polymorphisms in Southern Chinese patients with systemic lupus erythematosus (SLE), and to investigate possible associations with clinical manifestations of the disease.

METHODS

DNA was extracted from 88 Chinese patients with SLE and 83 ethnically matched controls. The IL-10 promoter region between positions -533 and -1120 was amplified by polymerase chain reaction, and polymorphisms were detected by restriction-enzyme cleavage.

RESULTS

No significant difference in the allele or haplotype frequencies between SLE patients and controls could be demonstrated. The *A and *C alleles at the -597 position were linked to the *T and C alleles at the -824 position, respectively. However, when clinical features were examined, the A allele at the -597 position and the T allele at the -824 position were significantly associated with lupus nephritis, by chi-square analysis (P < 0.001, odds ratio 4.19, 95% confidence interval 2.02-8.71). Similarly, the haplotype -1087A/-824T/-597A was also associated with renal involvement (P < 0.001, odds ratio 3.62, 95% confidence interval 1.80-7.31).

CONCLUSION

IL-10 promoter polymorphisms are not strong determinants of susceptibility to the development of SLE, per se, in Southern Chinese individuals. However, IL-10 genotypes are strongly associated with certain clinical manifestations of SLE and may have a role in predicting disease prognosis.

摘要

目的

研究中国南方系统性红斑狼疮(SLE)患者白细胞介素-10(IL-10)启动子多态性的遗传关联,并探讨其与疾病临床表现的可能关联。

方法

从88例中国SLE患者和83例种族匹配的对照中提取DNA。通过聚合酶链反应扩增-533至-1120位之间的IL-10启动子区域,并通过限制性内切酶切割检测多态性。

结果

SLE患者与对照之间的等位基因或单倍型频率无显著差异。-597位的A和C等位基因分别与-824位的T和C等位基因连锁。然而,在检查临床特征时,通过卡方分析,-597位的A等位基因和-824位的T等位基因与狼疮性肾炎显著相关(P<0.001,优势比4.19,95%置信区间2.02-8.71)。同样,单倍型-1087A/-824T/-597*A也与肾脏受累相关(P<0.001,优势比3.62,95%置信区间1.80-7.31)。

结论

IL-10启动子多态性本身并非中国南方个体发生SLE易感性的强决定因素。然而,IL-10基因型与SLE的某些临床表现密切相关,可能在预测疾病预后中起作用。

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