TNF-alpha polymorphisms as a potential modifier gene in the cystic fibrosis.

International journal of molecular epidemiology and genetics Pub Date : 2014-05-29 eCollection Date: 2014-01-01
Cyntia Aac Coutinho, Fernando Al Marson, Aline Rb Marcelino, Luciana C Bonadia, Marcelo P Carlin, Antonio F Ribeiro, Jose D Ribeiro, Carmen S Bertuzzo
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Abstract

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.

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tnf - α多态性在囊性纤维化中的潜在修饰基因。
修饰基因如TNF-α基因可调节囊性纤维化(CF)的严重程度。因此,TNF-α基因的-238G>A和-308G>A多态性被分析为CF的修饰因子。在此背景下,本研究招募了49例CF患者(通过汗液试验和完全CFTR筛查进行诊断)。ARMS-PCR分析-238G>A多态性,PCR-RFLP分析-308G>A多态性。在我们的数据中,-238G>A多态性与临床变异性无关。AA基因型-308G>A多态性是早期胃肠道症状的危险因素(OR=5.98, 95%CI=1.06 ~ 49.68)和对第一铜绿假单胞菌的保护作用(OR=0.05, 95%CI=0.0003 ~ 0.007)。对于第一株铜绿假单胞菌,GA基因型是危险因素(OR=10.2, 95%CI=1.86 ~ 84.09);同一基因型的诊断时间短于AA基因型(p=0.031)。考虑到-308G>A多态性等位基因,G等位基因是早期肺部症状(OR=3.81, 95%CI=1.13-12.97)和铜绿假单胞菌(OR=66.77, 95%CI=15.18-482.7)的危险因素;然而,同一等位基因表现出更好的经皮氧饱和度(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素(OR=12.26, 95%CI=0.08-0.89)和铜绿假单胞菌(OR=12.15, 95%CI=0002-0007),然而,同一等位基因是最差经皮氧饱和度的危险因素(OR=7.01, 95%CI=1.14-157.4)。由此可见,TNF-α基因-308G>A多态性与CF严重程度相关。
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