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2
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Relationship between ITPA polymorphisms and hemolytic anemia in HCV-infected patients after ribavirin-based therapy: a meta-analysis.利巴韦林治疗的丙型肝炎病毒感染患者中ITPA基因多态性与溶血性贫血的关系:一项荟萃分析
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本文引用的文献

1
The role of viral and host genetics in natural history and treatment of chronic HCV infection.病毒和宿主遗传学在慢性 HCV 感染的自然史和治疗中的作用。
Best Pract Res Clin Gastroenterol. 2012 Aug;26(4):413-27. doi: 10.1016/j.bpg.2012.09.004.
2
ITPA gene polymorphisms significantly affect hemoglobin decline and treatment outcomes in patients coinfected with HIV and HCV.ITPA 基因多态性显著影响 HIV 和 HCV 共感染患者的血红蛋白下降和治疗结局。
J Med Virol. 2012 Jul;84(7):1106-14. doi: 10.1002/jmv.23302.
3
Determinants of response to triple therapy of telaprevir, peginterferon, and ribavirin in previous non-responders infected with HCV genotype 1.既往对 HCV 基因型 1 感染者的 telaprevir、聚乙二醇干扰素和利巴韦林三联治疗无应答者对三联治疗应答的决定因素。
J Med Virol. 2012 Jul;84(7):1097-105. doi: 10.1002/jmv.23262.
4
Genetic variants at the ITPA locus protect against ribavirin-induced hemolytic anemia and dose reduction in an HCV G2/G3 cohort.ITPA 基因座的遗传变异可预防 HCV G2/G3 队列患者发生利巴韦林诱导的溶血性贫血和剂量减少。
Eur J Gastroenterol Hepatol. 2012 Aug;24(8):890-6. doi: 10.1097/MEG.0b013e3283546efd.
5
Association of two polymorphisms of the IL28B gene with viral factors and treatment response in 1,518 patients infected with hepatitis C virus.在 1518 例丙型肝炎病毒感染患者中,IL28B 基因的两个多态性与病毒因素和治疗反应相关联。
J Gastroenterol. 2012 May;47(5):596-605. doi: 10.1007/s00535-012-0531-1. Epub 2012 Mar 23.
6
Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C.全基因组关联研究鉴定出反映聚乙二醇干扰素和利巴韦林治疗慢性丙型肝炎时血小板减少的 ITPA/DDRGK1 变体。
Hum Mol Genet. 2011 Sep 1;20(17):3507-16. doi: 10.1093/hmg/ddr249. Epub 2011 Jun 9.
7
Common genetic polymorphism of ITPA gene affects ribavirin-induced anemia and effect of peg-interferon plus ribavirin therapy.ITPA 基因常见遗传多态性影响利巴韦林诱导的贫血和聚乙二醇干扰素联合利巴韦林治疗的效果。
J Med Virol. 2011 Jun;83(6):1048-57. doi: 10.1002/jmv.22069.
8
Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR.肌苷三磷酸酶基因突变可预防 HCV2/3 抗病毒治疗期间的贫血,但不会减少 RBV 的剂量减少或增加 SVR。
Hepatology. 2011 Feb;53(2):389-95. doi: 10.1002/hep.24068. Epub 2011 Jan 10.
9
Influence of ITPA polymorphisms on decreases of hemoglobin during treatment with pegylated interferon, ribavirin, and telaprevir.ITPA 多态性对聚乙二醇干扰素、利巴韦林和替拉瑞韦治疗期间血红蛋白降低的影响。
Hepatology. 2011 Feb;53(2):415-21. doi: 10.1002/hep.24058. Epub 2011 Jan 18.
10
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase function.肌苷三磷酸通过腺嘌呤核苷琥珀酸合成酶功能防止利巴韦林诱导的三磷酸腺苷丢失。
Gastroenterology. 2011 Apr;140(4):1314-21. doi: 10.1053/j.gastro.2010.12.038. Epub 2011 Jan 1.

ITPA基因多态性与聚乙二醇干扰素-α联合利巴韦林治疗结局的关联

Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy.

作者信息

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

机构信息

Tatsuya Fujino, Laboratory for Clinical Investigation, National Hospital Organization Nagasaki Medical Center, Ohmura, Nagasaki 856-8562, Japan.

出版信息

World J Gastrointest Pharmacol Ther. 2013 Aug 6;4(3):54-60. doi: 10.4292/wjgpt.v4.i3.54.

DOI:10.4292/wjgpt.v4.i3.54
PMID:23919217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3729868/
Abstract

AIM

To analyzed the association between inosine triphosphatase (ITPA) (rs1127354) genotypes and sustained virological response (SVR) rates in peginterferon (Peg-IFN)α + ribavirin (RBV) treatment.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。