Wu Qin, Wang Cong, Chen En Qiang, Tang Hong, Li Zhen Zhen, Lei Xue Zhong
Department of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.
Department of Nursing, West China Hospital, Sichuan University, Chengdu, China.
Hepat Mon. 2015 Dec 19;15(12):e32707. doi: 10.5812/hepatmon.32707. eCollection 2015 Dec.
There is growing evidence that interferon lambda 4 (IFNL4) polymorphism is related to sustained virological response (SVR) in hepatitis C virus (HCV) infection. We analyzed the relationship between IFNL4 (rs368234815) polymorphism and SVR in dual- and triple- therapy in HCV genotype 1, 2, 3 and 4 infected Asian, Caucasian and African patients.
We performed a systematic search of PubMed, Medline, Embase, EBSCO and Web of Science databases up to July 2015. Data of qualified studies were analyzed using the meta-analysis method in Stata 12.0 software.
Ten studies involving 4765 patients were included in the analysis. Of overall studies, SVR was more frequent in TT/TT genotype compared to TT /ΔG+ΔG /ΔG (OR = 4.439, 95% CI: 3.410 - 5.778). Genotype stratification analyses revealed rs368234815 TT/ TT was associated with higher SVR in G1, G2/3 and G4 HCV patients (ORG1 = 4.661, 95% CI: 3.937 - 5.518; ORG2/3 = 1.896, 95% CI: 1.265 - 2.841; ORG4 = 6.074; 95% CI: 3.129 - 11.788). Ethnicity stratification analyses of G1 patients showed that SVR was more frequent with TT/ TT genotype in Asians (OR= 8.245, 95% CI: 5.475 - 12.416), Caucasians (OR = 4.166, 95% CI: 3.441 - 5.042) and Africans (SVR: 37.5% vs 17.0%, P = 0.017). Moreover, similar results presented in therapy stratification analyses both in patients with dual-therapy (OR = 3.857; 95% CI: 3.288 - 4.524) or triple-therapy (OR = 8.119; 95% CI: 4.942 - 13.340).
Favorable IFNL4 rs368234815 genotype is a strong predictor of SVR in HCV patients, irrespective of HCV genotypes, ethnicity or treatment regimen. Thus, detection for IFNL4 rs368234815 polymorphism may be beneficial to guide the clinician in the individualization of therapy and design.
越来越多的证据表明,干扰素λ4(IFNL4)基因多态性与丙型肝炎病毒(HCV)感染的持续病毒学应答(SVR)相关。我们分析了IFNL4(rs368234815)基因多态性与HCV 1、2、3和4型感染的亚洲、白种人和非洲患者在双联和三联疗法中的SVR之间的关系。
我们对截至2015年7月的PubMed、Medline、Embase、EBSCO和Web of Science数据库进行了系统检索。使用Stata 12.0软件中的荟萃分析方法对合格研究的数据进行分析。
分析纳入了10项涉及4765例患者的研究。在所有研究中,与TT/ΔG+ΔG/ΔG基因型相比,TT/TT基因型的SVR更为常见(OR = 4.439,95%CI:3.410 - 5.778)。基因型分层分析显示,rs368234815 TT/TT与G1、G2/3和G4 HCV患者更高的SVR相关(ORG1 = 4.661,95%CI:3.937 - 5.518;ORG2/3 = 1.896,95%CI:1.265 - 2.841;ORG4 = 6.074;95%CI:3.129 - 11.788)。对G1患者的种族分层分析表明,亚洲人(OR = 8.245,95%CI:5.475 - 12.416)、白种人(OR = 4.166,95%CI:3.441 - 5.042)和非洲人(SVR:37.5%对17.0%,P = 0.017)中,TT/TT基因型的SVR更为常见。此外,在双联疗法(OR = 3.857;9%CI:3.288 - 4.524)或三联疗法(OR = 8.119;95%CI:4.942 - 13.340)的患者中,治疗分层分析也呈现出类似结果。
有利的IFNL4 rs368234815基因型是HCV患者SVR的有力预测指标,无论HCV基因型、种族或治疗方案如何。因此,检测IFNL4 rs368234815基因多态性可能有助于指导临床医生进行个体化治疗和设计。