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白细胞介素28B基因多态性作为慢性丙型肝炎持续病毒学应答的预测指标:系统评价与荟萃分析

Interleukin 28B polymorphisms as predictors of sustained virological response in chronic hepatitis C: systematic review and meta-analysis.

作者信息

Cariani E, Roli L, Missale G, Villa E, Ferrari C, Trenti T

机构信息

Department of Laboratory Medicine, Clinical Pathology-Toxicology, Ospedale S Agostino-Estense, Modena, Italy.

UO Infectious Diseases and Hepatology, Azienda Ospedaliero-Universitaria, Parma, Italy.

出版信息

Pharmacogenomics J. 2016 Feb;16(1):18-29. doi: 10.1038/tpj.2015.28. Epub 2015 Apr 28.

DOI:10.1038/tpj.2015.28
PMID:25918016
Abstract

Polymorphism of interleukin 28B gene represents a powerful outcome predictor for interferon-based regimens in hepatitis C virus infection. However, some studies report conflicting results. The predictive value of interleukin 28B genotype over the outcome interferon-α/ribavirin treatment was thoroughly evaluated and compared with virological predictors of response. Literature revision was performed on PubMed. Pooled odds ratios (ORs) were calculated by fixed- or random-effects models. Heterogeneity and publication bias were also assessed. Sixty-two eligible papers including 20 290 patients were retrieved. Both polymorphisms (rs12979860 and rs8099917) were strongly associated with response (OR=4.09 and 4.00, respectively), however, the association was weaker for subjects infected with viral genotypes 2 and 3 (OR=1.52 and 1.49, respectively). Compared with interleukin 28B genotype, the association with response was lower for baseline viremia (OR=2.15) and higher for rapid virological response (OR=13.86). These results provide a critical evaluation of interleukin 28B genotype as a pharmacogenetic predictor in hepatitis C patients.

摘要

白细胞介素28B基因多态性是丙型肝炎病毒感染中基于干扰素治疗方案疗效的有力预测指标。然而,一些研究报告了相互矛盾的结果。对白细胞介素28B基因型在α干扰素/利巴韦林治疗疗效方面的预测价值进行了全面评估,并与反应的病毒学预测指标进行了比较。在PubMed上进行了文献综述。采用固定效应或随机效应模型计算合并比值比(OR)。还评估了异质性和发表偏倚。检索到62篇符合条件的论文,共纳入20290例患者。两种多态性(rs12979860和rs8099917)均与治疗反应密切相关(OR分别为4.09和4.00),然而,对于感染病毒基因型2和3的患者,这种相关性较弱(OR分别为1.52和1.49)。与白细胞介素28B基因型相比,基线病毒血症与治疗反应的相关性较低(OR=2.15),而快速病毒学反应与治疗反应的相关性较高(OR=13.86)。这些结果为白细胞介素28B基因型作为丙型肝炎患者药物遗传学预测指标提供了重要评估。

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An in vitro diagnostic certified point of care single nucleotide test for IL28B polymorphisms.一种用于检测IL28B基因多态性的体外诊断认证即时检测单核苷酸检测方法。
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EGFR rs11506105 and IFNL3 SNPs but not rs8099917 are strongly associated with treatment responses in Iranian patients with chronic hepatitis C.

本文引用的文献

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Therapy of hepatitis C--back to the future.丙型肝炎的治疗——回归未来。
N Engl J Med. 2014 May 22;370(21):2043-7. doi: 10.1056/NEJMe1403619. Epub 2014 May 4.
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Treating hepatitis C in lower-income countries.在低收入国家治疗丙型肝炎。
N Engl J Med. 2014 May 15;370(20):1869-71. doi: 10.1056/NEJMp1400160. Epub 2014 Apr 10.
3
Cost-effectiveness of sofosbuvir-based triple therapy for untreated patients with genotype 1 chronic hepatitis C.索磷布韦为基础的三联疗法治疗初治基因 1 型慢性丙型肝炎的成本效益。
表皮生长因子受体(EGFR)基因单核苷酸多态性(SNP)rs11506105和干扰素λ3(IFNL3)基因SNP与伊朗慢性丙型肝炎患者的治疗反应密切相关,但rs8099917并非如此。
Genes Immun. 2017 Sep;18(3):144-151. doi: 10.1038/gene.2017.12. Epub 2017 Jul 13.
4
The Prevalence of Hepatitis C Virus Core Amino Acid 70 Substitution and Genotypes of Polymorphisms Near the IFNL3 Gene in Iranian Patients With Chronic Hepatitis C.伊朗慢性丙型肝炎患者中丙型肝炎病毒核心氨基酸70位点替代及IFNL3基因附近多态性基因型的流行情况
Hepat Mon. 2016 May 3;16(6):e37011. doi: 10.5812/hepatmon.37011. eCollection 2016 Jun.
5
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World J Gastroenterol. 2015 Nov 14;21(42):12101-13. doi: 10.3748/wjg.v21.i42.12101.
Hepatology. 2014 May;59(5):1692-705. doi: 10.1002/hep.27010. Epub 2014 Apr 1.
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J Gen Virol. 2013 Jun;94(Pt 6):1259-1265. doi: 10.1099/vir.0.051052-0. Epub 2013 Mar 13.
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