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Can zinc enhance response interferon therapy for patients with HCV-related liver disease?

Can zinc enhance response interferon therapy for patients with HCV-related liver disease?
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摘要 Patients with liver disease may be at risk of zinc depletion.Zinc supplementation has been shown to contribute to inhibition of liver fibrosis and improvement in hepatic encephalopathy.However,little is known about the anti-inflammatory effect of zinc on hepatitis C virus(HCV)-related chronic liver disease.The standard of care for chronic HCV has improved markedly since the approval of interferon(IFN) therapy more than a decade ago.Over the past 20 years,IFN therapy has improved to more effectively eliminate the virus,progressing from single IFN therapy to combination therapy with ribavirin(RBV) and finally to pegylated IFN(PEG-IFN) therapy.However,even combined therapy with PEG-IFN and RBV for 48 wk is unable to eliminate the virus in some 40% of hepatitis C cases,particularly those with genotype 1b and high viral load.Treatment options for patients who have relapsed or are refractory to treatment with PEG-IFN and RBV therefore need to be critically assessed.This paper overviews the relationship between chronic liver disease and zinc metabolism. Patients with liver disease may be at risk of zinc deple- tion. Zinc supplementation has been shown to contrib- ute to inhibition of liver fibrosis and improvement in hepatic encephalopathy. However, little is known about the anti-inflammatory effect of zinc on hepatitis C vi- rus (HCV)-related chronic liver disease. The standard of care for chronic HCV has improved markedly since the approval of interferon (IFN) therapy more than a decade ago. Over the past 20 years, IFN therapy has improved to more effectively eliminate the virus, pro- gressing from single IFN therapy to c(~mbination ther- apy with ribavirin (RBV) and finally to pegylated IFN (PEG-IFN) therapy. However, even combined therapy with PEG-IFN and RBV for 48 wk is unable to eliminate the virus in some 40% of hepatitis C cases, particularly those with genotype lb and high viral load. Treatment options for patients who have relapsed or are refrac- tory to treatment with PEG-IFN and RBV therefore need to be critically assessed. This paper overviews the relationship between chronic liver disease and zinc metabolism.
作者 Toru Ishikawa
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第25期3196-3200,共5页 世界胃肠病学杂志(英文版)
关键词 联合治疗 肝脏疾病 干扰素 HCV 补锌 患者 丙型肝炎病毒 利巴韦林 Chronic hepatitis C, Zinc Interferon therapy
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