Coutinho Cyntia Aac, Marson Fernando Al, Marcelino Aline Rb, Bonadia Luciana C, Carlin Marcelo P, Ribeiro Antonio F, Ribeiro Jose D, Bertuzzo Carmen S
Department of Medical Genetics, Faculty of Medical Sciences, University of Campinas 13081-970, P.O. Box: 6111, Campinas, SP, Brazil.
Department of Medical Genetics, Faculty of Medical Sciences, University of Campinas 13081-970, P.O. Box: 6111, Campinas, SP, Brazil ; Department of Pediatrics, School of Medical Sciences, University of Campinas 13081-970, P.O. Box: 6111, Campinas, SP, Brazil.
Int J Mol Epidemiol Genet. 2014 May 29;5(2):87-99. eCollection 2014.
Modifier genes, as the TNF-α gene, can modulate the cystic fibrosis (CF) severity. Thus, -238G>A and -308G>A polymorphisms of TNF-α gene were analyzed as modifiers of CF. In this context, the present study enrolled 49 CF patients (diagnosis performed by sweat test and complete CFTR screening). The -238G>A polymorphism analysis was performed by ARMS-PCR, and -308G>A, by PCR-RFLP. In our data, the -238G>A polymorphism was not associated with clinical variability. The AA genotype for -308G>A polymorphism was a risk factor for early gastrointestinal symptoms (OR=5.98, 95%CI=1.06-49.68) and protection for the first Pseudomonas aeruginosa (OR=0.05, 95%CI=0.0003-0.007). For the first P. aeruginosa, GA genotype was a risk factor (OR=10.2, 95%CI=1.86-84.09); for the same genotype, the diagnosis was made in minor time than the AA genotype (p=0.031). Considering the -308G>A polymorphism alleles, the G allele was a risk factor for early pulmonary symptoms (OR=3.81, 95%CI=1.13-12.97) and P. aeruginosa (OR=66.77, 95%CI=15.18-482.7); however, the same allele showed better transcutaneous oxygen saturation (OR=9.24, 95%CI=1.53-206.1). The A allele was a protective factor for early pulmonary symptoms (OR=12.26, 95%CI=0.08-0.89) and P. aeruginosa (OR=12.15, 95%CI=0002-0007), however, the same allele was a risk factor for worst transcutaneous oxygen saturation (OR=7.01, 95%CI=1.14-157.4). As conclusion, the -308G>A polymorphism of the TNF-α gene was associated with the CF severity.
修饰基因,如肿瘤坏死因子-α(TNF-α)基因,可调节囊性纤维化(CF)的严重程度。因此,对TNF-α基因的-238G>A和-308G>A多态性作为CF的修饰因子进行了分析。在此背景下,本研究纳入了49例CF患者(通过汗液试验和完整的囊性纤维化跨膜传导调节因子(CFTR)筛查进行诊断)。-238G>A多态性分析采用扩增阻滞突变系统聚合酶链反应(ARMS-PCR)进行,-308G>A多态性分析采用聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)进行。在我们的数据中,-238G>A多态性与临床变异性无关。-308G>A多态性的AA基因型是早期胃肠道症状的危险因素(比值比(OR)=5.98,95%置信区间(CI)=1.06-49.68),对首次感染铜绿假单胞菌有保护作用(OR=0.05,95%CI=0.0003-0.007)。对于首次感染铜绿假单胞菌,GA基因型是危险因素(OR=10.2,95%CI=1.86-84.09);对于相同基因型,诊断时间比AA基因型短(p=0.031)。考虑-308G>A多态性等位基因,G等位基因是早期肺部症状的危险因素(OR=3.81,95%CI=1.13-12.97)和铜绿假单胞菌感染的危险因素(OR=66.77,95%CI=15.18-482.7);然而,相同等位基因显示经皮血氧饱和度较好(OR=9.24,95%CI=1.53-206.1)。A等位基因是早期肺部症状的保护因子(OR=12.26,95%CI=0.08-0.89)和铜绿假单胞菌感染的保护因子(OR=12.15,95%CI=0.002-0.007),然而,相同等位基因是经皮血氧饱和度最差的危险因素(OR=7.01,95%CI=1.14-157.4)。结论是,TNF-α基因的-308G>A多态性与CF的严重程度相关。