Wang Zhengting, Wang Lei, Fan Rong, Zhou Jie, Zhong Jie
Department of Gastroenterology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine Shanghai 200025, China.
Int J Clin Exp Pathol. 2014 Dec 1;7(12):8952-7. eCollection 2014.
To investigate the association of three polymorphisms in the Interleukin-27 (IL-27) gene with CD risk in Chinese population.
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.
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).
In conclusion, genetic defects in IL-27 gene showed remarkable associations with CD in Chinese.
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。
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。
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)。
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。