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强直性脊柱炎中白细胞介素-1β和白细胞介素-1受体拮抗剂基因多态性

Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in ankylosing spondylitis.

作者信息

van der Paardt M, Crusius J B A, García-González M A, Baudoin P, Kostense P J, Alizadeh B Z, Dijkmans B A C, Peña A S, van der Horst-Bruinsma I E

机构信息

The Jan van Breemen Institute, Amsterdam, The Netherlands.

出版信息

Rheumatology (Oxford). 2002 Dec;41(12):1419-23. doi: 10.1093/rheumatology/41.12.1419.

Abstract

OBJECTIVE

Since ulcerative colitis and Crohn's disease, which are associated with ankylosing spondylitis (AS), have been found to be variably associated with the IL-1B and the IL-1RN genes encoding interleukin-1beta (IL-1beta) and the interleukin-1 receptor antagonist (IL-1ra), we have investigated whether these polymorphisms in IL-1B and IL-1RN are also involved in AS.

METHODS

DNA was isolated from peripheral blood of 106 patients with AS and 104 healthy controls. All patients and controls were Dutch Caucasians. Bi-allelic polymorphisms at positions +3,953 and -511 in the IL-1B gene, and a penta-allelic polymorphism in intron 2 of the IL-1RN gene were studied by polymerase chain reaction-based methods.

RESULTS

Allele IL-1RN*2 was significantly increased in AS (odds ratio=1.60; 95% confidence interval=1.20-2.80; P=0.031) compared with healthy controls, and independent from the polymorphism in loci IL-1B-511 and IL-1B+3,953. No significant associations were found between AS and the IL-1B-511 or IL-1B+3,953 polymorphisms.

CONCLUSION

Similar to other chronic inflammatory diseases, AS is associated with the IL-1RN*2 allele. Further studies are necessary to determine the biological significance of these findings in relation to susceptibility or severity of the disease.

摘要

目的

鉴于已发现与强直性脊柱炎(AS)相关的溃疡性结肠炎和克罗恩病与编码白细胞介素 - 1β(IL - 1β)的IL - 1B基因及白细胞介素 - 1受体拮抗剂(IL - 1ra)的IL - 1RN基因存在不同程度的关联,我们研究了IL - 1B和IL - 1RN中的这些多态性是否也与AS有关。

方法

从106例AS患者和104名健康对照者的外周血中提取DNA。所有患者和对照均为荷兰白种人。采用基于聚合酶链反应的方法研究IL - 1B基因第+3953位和 - 511位的双等位基因多态性以及IL - 1RN基因内含子2中的五等位基因多态性。

结果

与健康对照相比,AS患者中IL - 1RN*2等位基因显著增加(优势比 = 1.60;95%置信区间 = 1.20 - 2.80;P = 0.031),且独立于IL - 1B - 511和IL - 1B + 3953位点的多态性。未发现AS与IL - 1B - 511或IL - 1B + 3953多态性之间存在显著关联。

结论

与其他慢性炎症性疾病相似,AS与IL - 1RN*2等位基因相关。有必要进一步研究以确定这些发现与疾病易感性或严重程度相关的生物学意义。

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