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白细胞介素-27基因三个多态性与中国汉族人群克罗恩病易感性的关联

Association of IL-27 gene three polymorphisms with Crohn's disease susceptibility in a Chinese Han population.

作者信息

Wang Zhengting, Wang Lei, Fan Rong, Zhou Jie, Zhong Jie

机构信息

Department of Gastroenterology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine Shanghai 200025, China.

出版信息

Int J Clin Exp Pathol. 2014 Dec 1;7(12):8952-7. eCollection 2014.

Abstract

OBJECTIVE

To investigate the association of three polymorphisms in the Interleukin-27 (IL-27) gene with CD risk in Chinese population.

METHODS

This case-control study involved 312 CD patients and 479 age- and sex-matched healthy controls. Genotyping was performed using PCR-LDR method. Data were analyzed using Haplo. Stats program.

RESULTS

There were significant differences between patients and controls in allele distributions of rs153109 (Pallele = 0.036). The risk for CD associated with the rs153109-G mutant allele was increased by 26% (95% CI [confidence interval]: 1.02-1.56; P = 0.03) under the additive model and by 45% (95% CI: 1.07-1.97; P = 0.02) under the dominant model. In haplotype analysis, haplotype T-T-G (in order of rs17855750, rs181206 and rs153109) increased the odds of CD by 37% (95% CI: 1.04-1.81; P = 0.028).

CONCLUSIONS

In conclusion, genetic defects in IL-27 gene showed remarkable associations with CD in Chinese.

摘要

目的

探讨白细胞介素-27(IL-27)基因中的三种多态性与中国人群克罗恩病(CD)风险的关联。

方法

本病例对照研究纳入了312例CD患者和479例年龄及性别匹配的健康对照。采用聚合酶链反应-连接酶检测反应(PCR-LDR)方法进行基因分型。使用Haplo. Stats程序分析数据。

结果

rs153109的等位基因分布在患者和对照之间存在显著差异(P等位基因 = 0.036)。在加性模型下,与rs153109 - G突变等位基因相关的CD风险增加了26%(95%置信区间[CI]:1.02 - 1.56;P = 0.03),在显性模型下增加了45%(95% CI:1.07 - 1.97;P = 0.02)。在单倍型分析中,单倍型T - T - G(按rs17855750、rs181206和rs153109的顺序)使CD的几率增加了37%(95% CI:1.04 - 1.81;P = 0.028)。

结论

总之,IL-27基因的遗传缺陷在中国人群中与CD存在显著关联。

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