Fujino Tatsuya, Aoyagi Yoko, Takahashi Mariko, Yada Ryoko, Yamamoto Naoko, Ohishi Yuki, Nishiura Akihiko, Kohjima Motoyuki, Yoshimoto Tsuyoshi, Fukuizumi Kunitaka, Nakashima Manabu, Kato Masaki, Kotoh Kazuhiro, Nakamuta Makoto, Enjoji Munechika
Tatsuya Fujino, Laboratory for Clinical Investigation, National Hospital Organization Nagasaki Medical Center, Ohmura, Nagasaki 856-8562, Japan.
World J Gastrointest Pharmacol Ther. 2013 Aug 6;4(3):54-60. doi: 10.4292/wjgpt.v4.i3.54.
To analyzed the association between inosine triphosphatase (ITPA) (rs1127354) genotypes and sustained virological response (SVR) rates in peginterferon (Peg-IFN)α + ribavirin (RBV) treatment.
Patients who underwent Peg-IFNα + RBV combination therapy were enrolled (n = 120) and they had no history of other IFN-based treatments. Variation in hemoglobin levels during therapy, cumulative reduction of RBV dose, frequency of treatment withdrawal, and SVR rates were investigated in each ITPA genotype.
In patients with ITPA CC genotype, hemoglobin decline was significantly greater and the percentage of patients in whom total RBV dose was < 60% of standard and/or treatment was withdrawn was significantly higher compared with CA/AA genotype. However, SVR rates were equivalent between CC and CA/AA genotypes, and within a subset of patients with Interleukin 28B (IL28B) (rs8099917) TT genotype, SVR rates tended to be higher in patients with ITPA CC genotype, although the difference was not significant.
ITPA CC genotype was a disadvantageous factor for Peg-IFNα + RBV treatment in relation to completion rates and RBV dose. However, CC genotype was not inferior to CA/AA genotype for SVR rates. When full-length treatment is accomplished, it is plausible that more SVR is achieved in patients with ITPA CC variant, especially in a background of IL28B TT genotype.
分析肌苷三磷酸酶(ITPA)(rs1127354)基因型与聚乙二醇干扰素(Peg-IFN)α联合利巴韦林(RBV)治疗中持续病毒学应答(SVR)率之间的关联。
纳入接受Peg-IFNα联合RBV治疗的患者(n = 120),这些患者无其他基于干扰素治疗的病史。研究每种ITPA基因型在治疗期间血红蛋白水平的变化、RBV剂量的累积减少、治疗中断频率和SVR率。
与CA/AA基因型相比,ITPA CC基因型患者的血红蛋白下降明显更大,且总RBV剂量<标准剂量60%和/或中断治疗的患者百分比显著更高。然而,CC基因型与CA/AA基因型的SVR率相当,在白细胞介素28B(IL28B)(rs8099917)TT基因型的患者亚组中,ITPA CC基因型患者的SVR率虽有升高趋势,但差异不显著。
就完成率和RBV剂量而言,ITPA CC基因型是Peg-IFNα联合RBV治疗的不利因素。然而,CC基因型在SVR率方面并不逊于CA/AA基因型。当完成全程治疗时,ITPA CC变异型患者,尤其是在IL28B TT基因型背景下,更有可能实现更高的SVR。