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作 者:李新霞[1] 代华平[1] 朱敏[1] 庞宝森[1] 马力[1] 吕月平[1] 王辰[1]
机构地区:[1]首都医科大学附属北京朝阳医院北京呼吸疾病研究所
出 处:《中国实用内科杂志》2007年第13期1014-1016,共3页Chinese Journal of Practical Internal Medicine
基 金:首都医学发展研究基金(2002-1005)
摘 要:目的 研究转化生长因子-β1(TGF-β1)T869C、G915C基因多态性与特发性肺纤维化(IPF)的相关性。方法 应用聚合酶链反应-限制性内切酶片段长度多态性技术(PCR-RFLP)检测2002年1月至2006年1月在首都医科大学附属北京朝阳医院住院确诊的47例IPF患者和47例年龄、性别、民族、吸烟情况匹配的对照者的TGF—β1 T869C、G915C基因多态性。结果 IPF组和对照组TGF—β1 T869C基因型频率分布趋势不同,差异有显著性意义(P〈0.05);2组中等位基因频率分布趋势相似,差异无显著性意义(P〉0.05)。IPF组与对照组比较,TC基因型的OR值为0.421,95%CI为0、184~0.964,与IPF的发生呈显著负相关;而CC基因型的OR值为2.374,95%CI为1、038~5.433,与IPF的发生呈显著正相关。IPF组和对照组TGF-β1 G915C基因的CC突变基因型与C等位基因频率均为0。结论 TGF-β1+915位点基因多态性与IPF的发生可能无相关性,而TGF-β1+869位点的TC基因型和CC基因型可能与IPF的发生有关,提示有必要进一步扩大样本量进行TGF-β1+869位点基因多态性与IPF关联的相关研究。Objective To observe the relationship between the gene polymorphisms of Transforming Growth Factor-beta 1 (TGF-β1)T869C,G915C and Idiopathic Pulmonary Fibrosis(IPF). Methods Polymerase chain reaction(PCR)and restriction fragment length polymorphism(RFLP) were performed to analyze the TGF-β1 T869C ,G915 C gene polymorphisms in 47 IPF patients and 47 heahhy controls matched in age,sex, race and smoke state. Results ( 1 ) There was a significant difference in T869C genotype distribution of TGF-β1 between IPF cases and controls( P 〈 0. 05 ) ;however, there was no significant difference in T869C allele gene frequencies of TGF-β1 ( P 〉 0. 05 ). The OR of TC genotype for IPF was 0. 421 (95% CI:0. 184 -0. 964), showing a significant negative association between TC genotype and the development of IPF. The OR of CC genotype for 'IPF was 2. 374(95% CI:1. 038 -5. 433 ), showing a positive association between CC genotype and the development of IPF. (2)The frequencies of the CC mutational genotype of TGF-β1 G915C were 0% in both IPF cases and controls. The frequencies of C allele gene in both IPF cases and controls were 0%. Conclusion It is concluded that the TGF-β1 G915C gene polymorphism may have no effect on the predisposition to IPF;however,the TC genotype and CC genotype of TGF-β1 T869C may have significant influence on the susceptibility to IPF.
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