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Published in: Virology Journal 1/2017

Open Access 01-12-2017 | Research

SVR Rates of HCV-infected population under PEG-IFN-α/R treatment in Northwest China

Authors: Yanhua Li, Jiuping Wang, Juan Wang, Yunfeng Xiao, Bin Xu, Hongwei Li, Liu Yang, Xiaoke Hao, Yueyun Ma

Published in: Virology Journal | Issue 1/2017

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Abstract

Background

Chronic HCV Patients taking PEG-IFN-α/R from different ethnic groups have different probabilities of reaching a sustained viral response (SVR). There are many influence factors, such as HCV genotype, IL-28B single-nucleotide polymorphisms (SNP), Fibrosis 4 index (FIB-4), and aspartate aminotransferase-to-platelet ratio index (APRI) score. But the baseline factors in relation to treatment outcome was still not much clear.

Methods

We evaluated data from 231 chronic HCV patients with or without liver fibrosis and their antiviral efficacy after treatment with pegylated interferon plus ribavirin (PEG-IFN-α/R) for 24–48 weeks. IL-28B SNP and HCV genotypes were analyzed with genome sequencing using pyrosequencing.

Results

Sustained viral response (SVR) rates of patients with HCV 1b and 2a genotypes were 52.25% (58/111) and 75.28% (67/89) (P < 0.01). SVR rates of patients with IL-28B rs8099917 TT, rs12979860 CC and rs12980275 AA were 92.41% (25/27), 92.86% (26/28) and 88.89% (24/27) separately. We found that SVR rates in HCV 1b and 2a patients were only 31.0 and 39.4% if their FIB-4 > 3.25. In addition, when their APRI > 2, only 30.3% of HCV 1b patients and 50.2% of HCV 2a patients could obtain SVR.

Conclusions

There were high proportion of HCV genotype 1b and 2a in Northwest China. In both HCV 1b and 2a genotypes, patients with protective-genotype of IL-28B were more likely to obtain SVR. However, those with significant fibrosis or cirrhosis were less likely, no matter their genotype. Combined factors of HCV genotype, IL-28B genotype, FIB-4 and ARPI may indicate high prediction and clinical value regarding treatment with PEG-IFN-α/R and prognostic evaluation of chronic hepatitis C patients.
Literature
1.
go back to reference Antonelli A, Pistello M. New Therapies, Markers and Therapeutic Targets in HCV Chronic Infection, and HCV Extrahepatic Manifestations. Curr Drug Targets. 2015. Antonelli A, Pistello M. New Therapies, Markers and Therapeutic Targets in HCV Chronic Infection, and HCV Extrahepatic Manifestations. Curr Drug Targets. 2015.
2.
go back to reference Gower E, Estes C, Blach S, Razavi-Shearer K, Razavi H. Global epidemiology and genotype distribution of the hepatitis C virus infection. J Hepatol. 2014;61:S45–57.CrossRefPubMed Gower E, Estes C, Blach S, Razavi-Shearer K, Razavi H. Global epidemiology and genotype distribution of the hepatitis C virus infection. J Hepatol. 2014;61:S45–57.CrossRefPubMed
3.
go back to reference Pellicelli AM, Romano M, Stroffolini T, Mazzoni E, Mecenate F, Monarca R, Picardi A, Bonaventura ME, Mastropietro C, Vignally P, et al. HCV genotype 1a shows a better virological response to antiviral therapy than HCV genotype 1b. BMC Gastroenterol. 2012;12:162.CrossRefPubMedPubMedCentral Pellicelli AM, Romano M, Stroffolini T, Mazzoni E, Mecenate F, Monarca R, Picardi A, Bonaventura ME, Mastropietro C, Vignally P, et al. HCV genotype 1a shows a better virological response to antiviral therapy than HCV genotype 1b. BMC Gastroenterol. 2012;12:162.CrossRefPubMedPubMedCentral
4.
go back to reference Gane EJ, Stedman CA, Hyland RH, Ding X, Svarovskaia E, Symonds WT, Hindes RG, Berrey MM. Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C. N Engl J Med. 2013;368:34–44.CrossRefPubMed Gane EJ, Stedman CA, Hyland RH, Ding X, Svarovskaia E, Symonds WT, Hindes RG, Berrey MM. Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C. N Engl J Med. 2013;368:34–44.CrossRefPubMed
5.
go back to reference Lawitz E, Poordad FF, Pang PS, Hyland RH, Ding X, Mo H, Symonds WT, McHutchison JG, Membreno FE. Sofosbuvir and ledipasvir fixed-dose combination with and without ribavirin in treatment-naive and previously treated patients with genotype 1 hepatitis C virus infection (LONESTAR): an open-label, randomised, phase 2 trial. Lancet. 2014;383:515–23.CrossRefPubMed Lawitz E, Poordad FF, Pang PS, Hyland RH, Ding X, Mo H, Symonds WT, McHutchison JG, Membreno FE. Sofosbuvir and ledipasvir fixed-dose combination with and without ribavirin in treatment-naive and previously treated patients with genotype 1 hepatitis C virus infection (LONESTAR): an open-label, randomised, phase 2 trial. Lancet. 2014;383:515–23.CrossRefPubMed
6.
go back to reference Chhatwal J, Kanwal F, Roberts MS, Dunn MA. Cost-effectiveness and budget impact of hepatitis C virus treatment with sofosbuvir and ledipasvir in the United States. Ann Intern Med. 2015;162:397–406.CrossRefPubMedPubMedCentral Chhatwal J, Kanwal F, Roberts MS, Dunn MA. Cost-effectiveness and budget impact of hepatitis C virus treatment with sofosbuvir and ledipasvir in the United States. Ann Intern Med. 2015;162:397–406.CrossRefPubMedPubMedCentral
7.
go back to reference Trinks J, Hulaniuk ML, Caputo M, Pratx LB, Re V, Fortuny L, Pontoriero A, Frias A, Torres O, Nunez F, et al. Distribution of genetic polymorphisms associated with hepatitis C virus (HCV) antiviral response in a multiethnic and admixed population. Pharmacogenomics J. 2014;14:549–54.CrossRefPubMed Trinks J, Hulaniuk ML, Caputo M, Pratx LB, Re V, Fortuny L, Pontoriero A, Frias A, Torres O, Nunez F, et al. Distribution of genetic polymorphisms associated with hepatitis C virus (HCV) antiviral response in a multiethnic and admixed population. Pharmacogenomics J. 2014;14:549–54.CrossRefPubMed
8.
go back to reference Wu CK, Chang KC, Tseng PL, Lu SN, Chen CH, Wang JH, Lee CM, Lin MT, Yen YH, Hung CH, Hu TH. Comparison of therapeutic response and clinical outcome between HCV patients with normal and abnormal alanine transaminase levels. PLoS One. 2016;11:e0142378.CrossRefPubMedPubMedCentral Wu CK, Chang KC, Tseng PL, Lu SN, Chen CH, Wang JH, Lee CM, Lin MT, Yen YH, Hung CH, Hu TH. Comparison of therapeutic response and clinical outcome between HCV patients with normal and abnormal alanine transaminase levels. PLoS One. 2016;11:e0142378.CrossRefPubMedPubMedCentral
9.
go back to reference Wang M, Zhang Y, Li Z, Zhang H, Zhang Z, Yue D, Zhou R, Li X, Wu S, Li J. Hepatitis C virus (HCV) genotype 2a has a better virologic response to antiviral therapy than HCV genotype 1b. Int J Clin Exp Med. 2015;8:7446–56.PubMedPubMedCentral Wang M, Zhang Y, Li Z, Zhang H, Zhang Z, Yue D, Zhou R, Li X, Wu S, Li J. Hepatitis C virus (HCV) genotype 2a has a better virologic response to antiviral therapy than HCV genotype 1b. Int J Clin Exp Med. 2015;8:7446–56.PubMedPubMedCentral
10.
go back to reference Liu T, Sha K, Yang L, Wang Y, Zhang L, Liu X, Yang F. IL-28B polymorphisms correlated with treatment response in HCV-4 mono-infected patients: a meta-analysis. PLoS One. 2014;9:e91316.CrossRefPubMedPubMedCentral Liu T, Sha K, Yang L, Wang Y, Zhang L, Liu X, Yang F. IL-28B polymorphisms correlated with treatment response in HCV-4 mono-infected patients: a meta-analysis. PLoS One. 2014;9:e91316.CrossRefPubMedPubMedCentral
11.
go back to reference Mechie NC, Rover C, Cameron S, Amanzada A. Predictability of IL-28B-polymorphism on protease-inhibitor-based triple-therapy in chronic HCV-genotype-1 patients: A meta-analysis. World J Hepatol. 2014;6:759–65.CrossRefPubMedPubMedCentral Mechie NC, Rover C, Cameron S, Amanzada A. Predictability of IL-28B-polymorphism on protease-inhibitor-based triple-therapy in chronic HCV-genotype-1 patients: A meta-analysis. World J Hepatol. 2014;6:759–65.CrossRefPubMedPubMedCentral
13.
go back to reference Shindo H, Maekawa S, Komase K, Miura M, Kadokura M, Sueki R, Komatsu N, Shindo K, Amemiya F, Nakayama Y, et al. IL-28B (IFN-lambda3) and IFN-alpha synergistically inhibit HCV replication. J Viral Hepat. 2013;20:281–9.CrossRefPubMed Shindo H, Maekawa S, Komase K, Miura M, Kadokura M, Sueki R, Komatsu N, Shindo K, Amemiya F, Nakayama Y, et al. IL-28B (IFN-lambda3) and IFN-alpha synergistically inhibit HCV replication. J Viral Hepat. 2013;20:281–9.CrossRefPubMed
14.
go back to reference Yoshida H, Shiratori Y, Moriyama M, Arakawa Y, Ide T, Sata M, Inoue O, Yano M, Tanaka M, Fujiyama S, et al. Interferon therapy reduces the risk for hepatocellular carcinoma: national surveillance program of cirrhotic and noncirrhotic patients with chronic hepatitis C in Japan. IHIT Study Group. Inhibition of Hepatocarcinogenesis by Interferon Therapy. Ann Intern Med. 1999;131:174–81.CrossRefPubMed Yoshida H, Shiratori Y, Moriyama M, Arakawa Y, Ide T, Sata M, Inoue O, Yano M, Tanaka M, Fujiyama S, et al. Interferon therapy reduces the risk for hepatocellular carcinoma: national surveillance program of cirrhotic and noncirrhotic patients with chronic hepatitis C in Japan. IHIT Study Group. Inhibition of Hepatocarcinogenesis by Interferon Therapy. Ann Intern Med. 1999;131:174–81.CrossRefPubMed
15.
go back to reference Singal AG, Volk ML, Jensen D, Di Bisceglie AM, Schoenfeld PS. A sustained viral response is associated with reduced liver-related morbidity and mortality in patients with hepatitis C virus. Clin Gastroenterol Hepatol. 2010;8:280–8. 288 e281.CrossRefPubMed Singal AG, Volk ML, Jensen D, Di Bisceglie AM, Schoenfeld PS. A sustained viral response is associated with reduced liver-related morbidity and mortality in patients with hepatitis C virus. Clin Gastroenterol Hepatol. 2010;8:280–8. 288 e281.CrossRefPubMed
16.
go back to reference Chinese Society of Hepatology CMA, Wei L, Chinese Society of Infectious Diseases CMA, Hou JL. The guideline of prevention and treatment for hepatitis C: a 2015 update. Zhonghua Gan Zang Bing Za Zhi. 2015;23:906–23. Chinese Society of Hepatology CMA, Wei L, Chinese Society of Infectious Diseases CMA, Hou JL. The guideline of prevention and treatment for hepatitis C: a 2015 update. Zhonghua Gan Zang Bing Za Zhi. 2015;23:906–23.
17.
go back to reference Chinese Society of Infectious Diseases CMA, Hou JL. The guideline of prevention and treatment for chronic hepatitis B: a 2015 update. Zhonghua Gan Zang Bing Za Zhi. 2015;23:888–905. Chinese Society of Infectious Diseases CMA, Hou JL. The guideline of prevention and treatment for chronic hepatitis B: a 2015 update. Zhonghua Gan Zang Bing Za Zhi. 2015;23:888–905.
18.
go back to reference Lens S, Torres F, Puigvehi M, Marino Z, Londono MC, Martinez SM, Garcia-Juarez I, Garcia-Criado A, Gilabert R, Bru C, et al. Predicting the development of liver cirrhosis by simple modelling in patients with chronic hepatitis C. Aliment Pharmacol Ther. 2016;43:364–74.CrossRefPubMed Lens S, Torres F, Puigvehi M, Marino Z, Londono MC, Martinez SM, Garcia-Juarez I, Garcia-Criado A, Gilabert R, Bru C, et al. Predicting the development of liver cirrhosis by simple modelling in patients with chronic hepatitis C. Aliment Pharmacol Ther. 2016;43:364–74.CrossRefPubMed
19.
go back to reference Andres-Otero MJ, De-Blas-Giral I, Puente-Lanzarote JJ, Serrano-Aullo T, Morandeira MJ, Lorente S, Lou-Bonafonte JM. Multiple approaches to assess fourteen non-invasive serum indexes for the diagnosis of liver fibrosis in chronic hepatitis C patients. Clin Biochem. 2016;49:560–5.CrossRefPubMed Andres-Otero MJ, De-Blas-Giral I, Puente-Lanzarote JJ, Serrano-Aullo T, Morandeira MJ, Lorente S, Lou-Bonafonte JM. Multiple approaches to assess fourteen non-invasive serum indexes for the diagnosis of liver fibrosis in chronic hepatitis C patients. Clin Biochem. 2016;49:560–5.CrossRefPubMed
20.
go back to reference Gu L, Tong W, Yuan M, Lu T, Li C, Lu L. An increased diversity of HCV isolates were characterized among 393 patients with liver disease in China representing six genotypes, 12 subtypes, and two novel genotype 6 variants. J Clin Virol. 2013;57:311–7.CrossRefPubMedPubMedCentral Gu L, Tong W, Yuan M, Lu T, Li C, Lu L. An increased diversity of HCV isolates were characterized among 393 patients with liver disease in China representing six genotypes, 12 subtypes, and two novel genotype 6 variants. J Clin Virol. 2013;57:311–7.CrossRefPubMedPubMedCentral
21.
go back to reference Waldenstrom J, Farkkila M, Rembeck K, Norkrans G, Langeland N, Morch K, Pedersen C, Rauning Buhl M, Nieminen U, Nuutinen H, et al. Short interferon and ribavirin treatment for HCV genotype 2 or 3 infection: NORDynamIC trial and real-life experience. Scand J Gastroenterol. 2016;51:337–43.CrossRefPubMed Waldenstrom J, Farkkila M, Rembeck K, Norkrans G, Langeland N, Morch K, Pedersen C, Rauning Buhl M, Nieminen U, Nuutinen H, et al. Short interferon and ribavirin treatment for HCV genotype 2 or 3 infection: NORDynamIC trial and real-life experience. Scand J Gastroenterol. 2016;51:337–43.CrossRefPubMed
22.
go back to reference Tamori A, Yoshida K, Kurai O, Kioka K, Hai H, Kozuka R, Motoyama H, Kawamura E, Hagihara A, Uchida-Kobayashi S, et al. Randomized trial of combined triple therapy comprising two types of peginterferon with simeprevir in patients with HCV genotype 1b. Hepatol Res. 2016;46:1311–20.CrossRefPubMed Tamori A, Yoshida K, Kurai O, Kioka K, Hai H, Kozuka R, Motoyama H, Kawamura E, Hagihara A, Uchida-Kobayashi S, et al. Randomized trial of combined triple therapy comprising two types of peginterferon with simeprevir in patients with HCV genotype 1b. Hepatol Res. 2016;46:1311–20.CrossRefPubMed
23.
go back to reference Deming P, Martin MT, Chan J, Dilworth TJ, El-Lababidi R, Love BL, Mohammad RA, Nguyen A, Spooner LM, Wortman SB. Therapeutic advances in HCV genotype 1 infection: insights from the society of infectious diseases pharmacists. Pharmacotherapy. 2016;36:203–17.CrossRefPubMed Deming P, Martin MT, Chan J, Dilworth TJ, El-Lababidi R, Love BL, Mohammad RA, Nguyen A, Spooner LM, Wortman SB. Therapeutic advances in HCV genotype 1 infection: insights from the society of infectious diseases pharmacists. Pharmacotherapy. 2016;36:203–17.CrossRefPubMed
24.
go back to reference Ban JY, Yoo KH. Promoter polymorphism (rs12770170, −184C/T) of microseminoprotein, beta as a risk factor for benign prostatic hyperplasia in Korean population. Int Neurourol J. 2014;18:63–7.CrossRefPubMedPubMedCentral Ban JY, Yoo KH. Promoter polymorphism (rs12770170, −184C/T) of microseminoprotein, beta as a risk factor for benign prostatic hyperplasia in Korean population. Int Neurourol J. 2014;18:63–7.CrossRefPubMedPubMedCentral
26.
go back to reference Shaker O, Rashad A, Abd El Aziz G, El Raziky M. Is rs8099917 polymorphism of IL-28B gene a good predictor of response to therapy of HCV than rs12979860? An Egyptian study. Cell Biochem Biophys. 2015;71:307–14.CrossRefPubMed Shaker O, Rashad A, Abd El Aziz G, El Raziky M. Is rs8099917 polymorphism of IL-28B gene a good predictor of response to therapy of HCV than rs12979860? An Egyptian study. Cell Biochem Biophys. 2015;71:307–14.CrossRefPubMed
27.
go back to reference Khubaib B, Saleem S, Idrees M, Afzal S, Wasim M. The genotype CC of IL-28B SNP rs12979860 is significantly associated with a sustained virological response in chronic HCV-infected Pakistani patients. J Dig Dis. 2015;16:293–8.CrossRefPubMed Khubaib B, Saleem S, Idrees M, Afzal S, Wasim M. The genotype CC of IL-28B SNP rs12979860 is significantly associated with a sustained virological response in chronic HCV-infected Pakistani patients. J Dig Dis. 2015;16:293–8.CrossRefPubMed
28.
go back to reference Al-Qahtani A, Al-Anazi M, Abdo AA, Sanai FM, Al-Hamoudi W, Alswat KA, Al-Ashgar HI, Khan MQ, Albenmousa A, Khalaf N, et al. Correlation between genetic variations and serum level of interleukin 28B with virus genotypes and disease progression in chronic hepatitis C virus infection. J Immunol Res. 2015;2015:768470.CrossRefPubMedPubMedCentral Al-Qahtani A, Al-Anazi M, Abdo AA, Sanai FM, Al-Hamoudi W, Alswat KA, Al-Ashgar HI, Khan MQ, Albenmousa A, Khalaf N, et al. Correlation between genetic variations and serum level of interleukin 28B with virus genotypes and disease progression in chronic hepatitis C virus infection. J Immunol Res. 2015;2015:768470.CrossRefPubMedPubMedCentral
29.
go back to reference Tanaka Y, Nishida N, Sugiyama M, Kurosaki M, Matsuura K, Sakamoto N, Nakagawa M, Korenaga M, Hino K, Hige S, et al. Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Nat Genet. 2009;41:1105–9.CrossRefPubMed Tanaka Y, Nishida N, Sugiyama M, Kurosaki M, Matsuura K, Sakamoto N, Nakagawa M, Korenaga M, Hino K, Hige S, et al. Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Nat Genet. 2009;41:1105–9.CrossRefPubMed
30.
31.
go back to reference Kogiso T, Tokushige K, Hashimoto E, Ikarashi Y, Kodama K, Taniai M, Torii N, Shiratori K. Safety and efficacy of long-term tolvaptan therapy for decompensated liver cirrhosis. Hepatol Res. 2016;46:E194–200.CrossRefPubMed Kogiso T, Tokushige K, Hashimoto E, Ikarashi Y, Kodama K, Taniai M, Torii N, Shiratori K. Safety and efficacy of long-term tolvaptan therapy for decompensated liver cirrhosis. Hepatol Res. 2016;46:E194–200.CrossRefPubMed
Metadata
Title
SVR Rates of HCV-infected population under PEG-IFN-α/R treatment in Northwest China
Authors
Yanhua Li
Jiuping Wang
Juan Wang
Yunfeng Xiao
Bin Xu
Hongwei Li
Liu Yang
Xiaoke Hao
Yueyun Ma
Publication date
01-12-2017
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2017
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/s12985-017-0708-6

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