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中国人群中白细胞介素(IL)-12和IL-27基因多态性与慢性阻塞性肺疾病的关联

Association of interleukin (IL)-12 and IL-27 gene polymorphisms with chronic obstructive pulmonary disease in a Chinese population.

作者信息

Huang Na, Liu Lin, Wang Xiao-Zhen, Liu Dan, Yin Si-Yuan, Yang Xiao-Dong

机构信息

Department of Respiratory Medicine, West China Hospital of Sichuan University, Chengdu, China.

出版信息

DNA Cell Biol. 2008 Sep;27(9):527-31. doi: 10.1089/dna.2007.0715.

Abstract

The pathogenesis of chronic obstructive pulmonary disease (COPD) is not fully understood, and environment and genetic factors have been investigated. Moreover, cytokine genes play an important role in COPD pathogenesis. However, the molecular mechanism of COPD induced by the factors is still unknown. The present study was undertaken to clarify a role of interleukin (IL)-12 16974A/C and IL-27 4730T/C, -964A/G, and 2905T/G polymorphisms in Chinese subjects with COPD. Polymerase chain reaction/restriction fragment length polymorphism (PCR/RFLP) and sequence analyses were used to type IL-12 and IL-27 polymorphisms in 120 patients with COPD and 100 healthy controls. There were significant differences in the genotype and allele distribution of -964A/G and 2905T/G polymorphisms of the IL-27 gene among cases and controls in a Chinese population. When compared with the control group, subjects with AG genotype of the IL-27 -964A/G had a 2.22-fold decreased risk of COPD (odds ratio [OR] = 0.450, 95% confidence interval [CI]: 0.245-0.826; p = 0.009), and subjects with TG genotype of the IL-27 2905T/G had a 2.85-fold decreased risk of COPD (OR = 0.351, 95% CI: 0.137-0.899; p = 0.024). Compared with the TAT haplotype, the TGG haplotype was associated with a significantly decreased risk of COPD (OR = 0.29, 95% CI: 0.108-0.784; p = 0.010). Even after Bonferroni corrections, significant associations with COPD were observed for the AG genotype of the IL-27 -964A/G and the TGG haplotype of the IL-27 gene. Our data suggest that polymorphisms in the IL-27 gene may play a role in the development of COPD in Chinese population.

摘要

慢性阻塞性肺疾病(COPD)的发病机制尚未完全明确,环境和遗传因素已得到研究。此外,细胞因子基因在COPD发病机制中发挥重要作用。然而,这些因素诱发COPD的分子机制仍不清楚。本研究旨在阐明白细胞介素(IL)-12 16974A/C和IL-27 4730T/C、-964A/G以及2905T/G多态性在中国COPD患者中的作用。采用聚合酶链反应/限制性片段长度多态性(PCR/RFLP)和序列分析对120例COPD患者和100例健康对照者的IL-12和IL-27多态性进行分型。在中国人群中,病例组和对照组之间IL-27基因-964A/G和2905T/G多态性的基因型和等位基因分布存在显著差异。与对照组相比,IL-27 -964A/G的AG基因型受试者患COPD的风险降低了2.22倍(比值比[OR]=0.450,95%置信区间[CI]:0.245 - 0.826;p = 0.009),IL-27 2905T/G的TG基因型受试者患COPD的风险降低了2.85倍(OR = 0.351,95%CI:0.137 - 0.899;p = 0.024)。与TAT单倍型相比,TGG单倍型与COPD风险显著降低相关(OR = 0.29,95%CI:0.108 - 0.784;p = 0.010)。即使经过Bonferroni校正,仍观察到IL-27 -964A/G的AG基因型和IL-27基因的TGG单倍型与COPD存在显著关联。我们的数据表明,IL-27基因多态性可能在中国人群COPD的发生发展中起作用。

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