Transforming growth factor-β1 gene polymorphisms associated with chronic obstructive pulmonary disease in Chinese population

被引:0
|
作者
Zhi-guang SU~2
Key Laboratory of Biotherapy of Human Disease
机构
基金
中国国家自然科学基金;
关键词
chronic obstructive pulmonary disease; transforming growth factor-β1; single nucleotide polymorphisms; haplotypes;
D O I
暂无
中图分类号
R563.9 [其他]; R96 [药理学];
学科分类号
1002 ; 100201 ; 100602 ; 100706 ;
摘要
Aim: To determine the frequencies of polymorphism and haplotype in the transforming growth factor-beta 1 (TGF-1) gene promoter in the Chinese population and to investigate the susceptibility of this population to chronic obstructive pulmonary disease (COPD). Methods: The target fragments of the TGF-1 gene promoter were amplified and analyzed by polymerase chain reaction-restriction fragment length polymorphism technique in 84 COPD patients and 97 age- and sex-matched healthy controls. The test for Hardy-Weinberg equilibrium was performed using HWE program of the LINKUTIL package and statistical analysis was carried out with the SPSS statistical package. An expectation maximization algorithm was used for the pairwise linkage disequilibrium test and haplotype analysis. Results: More carriers of the -800A allele, or fewer carriers of the -509T allele, were detected in the COPD patients compared with the non-symptomatic control subjects [for the -800A allele, 29.8% vs 14.4%, respectively, x~2=6.257, degrees of freedom (df)=l, P=0.012; for the -509T allele, 27.3% vs 44.3%, respectively,x~2=5.582, df=l, P=0.018]. The prevalence of the -800A allele was significantly higher in the COPD patients than in control subjects OP=0.009), whereas the frequency of the -509T allele was significantly higher in control subjects than in the COPD patients (P=0.008). In addition, this distribution tendency for the -800A or -509T allele was similar in heavy smokers (smoking history 鈮?0 pack years); (number of packs of cigarettes per day multiplied by the number of years of smoking) X~2=7.235, P=0.007, and X~2=5.636, P=0.018, respectively). The linkage disequilibrium was found between -800 G鈫扐 and -509 C鈫扵 (D>0.60,P<0.0001), and the frequency of the AC haplotype, consisting of the least common base at -800 and the most common base at -509, was significantly higher in patients with COPD than in controls (0.056 vs 0.021, P<0.05). Conclusions: The single nucleotide polymorphism (SNP) in the TGF-1 gene promoter might be associated with COPD, and the -800A/-509C haplotype is possibly one of the susceptibility factors for COPD.
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页码:714 / 720
页数:7
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