AP-HP, Hôpital Trousseau, Pediatric Pulmonary Department, Inserm U938, Paris, France.
PLoS One. 2012;7(7):e41913. doi: 10.1371/journal.pone.0041913. Epub 2012 Jul 30.
The clinical course of cystic fibrosis (CF) varies between patients bearing identical CFTR mutations, suggesting the involvement of modifier genes. We assessed the association of lung disease severity with the variant AGER -429 T/C, coding for RAGE, a pro-inflammatory protein, in CF patients from the French CF Gene Modifier Study. We analyzed the lung function of 967 CF patients p.Phe508del homozygous. FEV(1) was analyzed as CF-specific percentile adjusted on age, height and mortality. AGER -429T/C polymorphism was genotyped and its function was evaluated in vitro by measurement of the luciferase activity. AGER -429 minor allele (C) was associated with poorer lung function (p = 0.03). In vitro, the promoter activity was higher in cells transfected with AGER -429C compared to cells transfected with the AGER -429T allele (p = 0.016 in BEAS-2B cells). AGER seems to be a modifier gene of lung disease severity in CF, and could be an interesting biomarker of CF airway inflammation. The functional promoter AGER -429C variant is associated with an increased RAGE expression that can lead to an increased lung inflammation and a more severe lung disease.
囊性纤维化(CF)患者携带相同 CFTR 突变,但临床病程存在差异,提示存在修饰基因的参与。我们评估了法国 CF 基因修饰研究中,与编码促炎蛋白 RAGE 的AGER-429T/C 变异与 CF 患者肺部疾病严重程度的相关性。我们分析了 967 名 p.Phe508del 纯合子 CF 患者的肺功能。FEV1 采用根据年龄、身高和死亡率调整的 CF 特异性百分位数进行分析。AGER-429T/C 多态性进行了基因分型,并通过测量荧光素酶活性评估其体外功能。AGER-429 次要等位基因(C)与较差的肺功能相关(p = 0.03)。体外研究中,与转染 AGER-429T 等位基因的细胞相比,转染 AGER-429C 等位基因的细胞中启动子活性更高(在 BEAS-2B 细胞中,p = 0.016)。AGER 似乎是 CF 肺部疾病严重程度的修饰基因,可能是 CF 气道炎症的一个有意义的生物标志物。功能性启动子 AGER-429C 变异与 RAGE 表达增加相关,这可能导致肺部炎症增加和更严重的肺部疾病。