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Inosine triphosphatase allele frequency and association withribavirin-induced anaemia in Brazilian patients receiving antiviral therapy forchronic hepatitis C

机译:肌苷三磷酸酶等位基因频率及与利巴韦林引起的接受抗病毒治疗的巴西患者的贫血慢性丙型肝炎

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摘要

Inosine triphosphatase (ITPA) single nucleotide polymorphisms (SNPs) are strongly associated with protection against ribavirin (RBV)-induced anaemia in European, American and Asian patients; however, there is a paucity of data for Brazilian patients. The aim of this study was to evaluate the ITPA SNP (rs7270101/rs1127354) frequency in healthy and hepatitis C virus (HCV)-infected patients from Brazil and the association with the development of severe anaemia during antiviral therapy. ITPA SNPs were determined in 200 HCV infected patients and 100 healthy individuals by sequencing. Biochemical parameters and haemoglobin (Hb) levels were analysed in 97 patients who underwent antiviral therapy. A combination of AArs7270101+CCrs1127354 (100% ITPase activity) was observed in 236/300 individuals. Anaemia was observed in 87.5% and 86.2% of treated patients with AA (rs7270101) and CC genotypes (rs1127354), respectively. Men with AA (rs7270101) showed a considerable reduction in Hb at week 12 compared to those with AC/CC (p = 0.1475). In women, there was no influence of genotype (p = 0.5295). For rs1127354, men with the CC genotype also showed a sudden reduction in Hb compared to those with AC. Allelic distribution of rs7270101 and rs1127354 shows high rates of the genotypes AA and CC, respectively, suggesting that the study population had a great propensity for developing RBV-induced anaemia. Aprogressive Hb reduction during treatment was observed; however, this reduction wasgreater in men at week 12 than in women.
机译:肌苷三磷酸酶(ITPA)单核苷酸多态性(SNP)与欧洲,美洲和亚洲患者抗病毒唑(RBV)引起的贫血的保护作用密切相关;但是,巴西患者的数据很少。这项研究的目的是评估来自巴西健康和丙型肝炎病毒(HCV)感染患者的ITPA SNP(rs7270101 / rs1127354)频率,以及抗病毒治疗期间严重贫血的发生。通过测序确定了200例HCV感染患者和100例健康个体的ITPA SNP。分析了97名接受抗病毒治疗的患者的生化参数和血红蛋白(Hb)水平。在236/300个人中观察到AArs7270101 + CCrs1127354的组合(100%ITPase活性)。分别在接受治疗的AA(rs7270101)和CC基因型(rs1127354)的患者中观察到贫血的比例分别为87.5%和86.2%。与AC / CC的男性相比,AA的男性(rs7270101)在第12周的Hb明显降低(p = 0.1475)。在女性中,没有基因型的影响(p = 0.5295)。对于rs1127354,与患有AC基因型的男性相比,具有CC基因型的男性的Hb也会突然下降。 rs7270101和rs1127354的等位基因分布分别显示AA和CC基因型的发生率较高,这表明该研究人群极易发生RBV引起的贫血。一个观察到治疗期间血红蛋白逐渐降低;但是,这种减少是第12周的男性比女性更大。

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