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白细胞介素-1 多态性与强直性脊柱炎易感性的关联:荟萃分析。

The associations between interleukin-1 polymorphisms and susceptibility to ankylosing spondylitis: a meta-analysis.

机构信息

Korea University College of Medicine, 26-1, Anam-dong 5-ga, Seongbuk-gu, Seoul 136-705, Korea.

出版信息

Joint Bone Spine. 2012 Jul;79(4):370-4. doi: 10.1016/j.jbspin.2011.06.010. Epub 2011 Oct 1.

Abstract

OBJECTIVE

The aim of this study was to determine whether polymorphisms of interleukin-1 (IL-1) confer susceptibility to ankylosing spondylitis (AS).

METHODS

The authors conducted meta-analyses on associations between IL-1 polymorphisms and AS susceptibility, using fixed or random effects models. In order to avoid duplications and data previously subjected to meta-analysis, we performed meta-analysis on studies if new data on IL-1 polymorphisms in AS were reported.

RESULTS

A total of nine studies consisting of 20 separate comparisons of association between IL-1 polymorphisms and AS susceptibility were included in this meta-analysis. These were performed on European, Asian, and Latin American population samples. Meta-analysis revealed a significant association between the 2 allele of the IL-1F10.3 polymorphism (rs3811581) and the risk of developing AS in Europeans (OR=0.775, 95% CI=0.605-0.992, P=0.043). Furthermore, the OR of the 2 allele of IL-1A+889 (rs1800587) was found to be significantly increased in Europeans with AS (OR=1.357, 95% CI=1.085-1.697, P=0.007). However, meta-analyses of the IL-1B-511, IL-1B+3953, and ILF7.1 polymorphisms and of the variable numbers of tandem repeats of the IL-1 receptor antagonist gene (IL-1RN VNTR) revealed no association between AS and these polymorphisms.

CONCLUSIONS

In addition to the three known IL-1 polymorphisms, rs2856836, rs17561, and rs1894399, found in previous meta-analysis, this meta-analysis shows that the IL-1F10.3 and IL-1A+889 polymorphisms are associated with the development of AS in Europeans but not in Asians.

摘要

目的

本研究旨在确定白细胞介素-1(IL-1)多态性是否与强直性脊柱炎(AS)易感性相关。

方法

作者采用固定或随机效应模型对 IL-1 多态性与 AS 易感性之间的关联进行荟萃分析。为了避免重复和已进行荟萃分析的数据,我们仅对报告了新的 IL-1 多态性与 AS 相关数据的研究进行荟萃分析。

结果

本荟萃分析共纳入 9 项研究,包括 20 项关于 IL-1 多态性与 AS 易感性之间关联的独立比较,这些研究涉及欧洲、亚洲和拉丁美洲人群样本。荟萃分析显示,IL-1F10.3 多态性(rs3811581)2 等位基因与欧洲人发生 AS 的风险之间存在显著关联(OR=0.775,95%CI=0.605-0.992,P=0.043)。此外,还发现 IL-1A+889(rs1800587)2 等位基因的 OR 在欧洲 AS 患者中显著增加(OR=1.357,95%CI=1.085-1.697,P=0.007)。然而,IL-1B-511、IL-1B+3953 和 ILF7.1 多态性以及 IL-1 受体拮抗剂基因(IL-1RN VNTR)的可变串联重复数的荟萃分析并未显示这些多态性与 AS 之间存在关联。

结论

除了之前荟萃分析中发现的三个已知的 IL-1 多态性(rs2856836、rs17561 和 rs1894399)外,本荟萃分析还显示,IL-1F10.3 和 IL-1A+889 多态性与欧洲人 AS 的发生有关,但与亚洲人无关。

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