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      Oral Zinc Supplementation Decreases the Risk of HCC Development in Patients With HCV Eradicated by DAA

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          Abstract

          We have reported that the plasma zinc concentration gradually decreases with the progression of fibrosis and is related to hepatocellular carcinoma (HCC) development. The aim of this study was to examine the impact of the zinc concentration on HCC development (study 1) and the relationship between zinc intake and HCC development (study 2) in patients with hepatitis C virus (HCV) eradicated by direct‐acting antivirals (DAAs). A total of 599 sustained virological response (SVR) patients treated with DAAs without a history of HCC were retrospectively analyzed in this study. Eighty patients received supplemental zinc (Zn treatment group), and 519 patients did not receive zinc (no Zn treatment group). In study 1, the cumulative incidence rate of HCC was compared between the Zn treatment group and the no Zn treatment group. In study 2, the risk factors for HCC development were examined in the no Zn treatment group. In study 1, in the Zn treatment group, HCC did not develop during follow‐up, and the cumulative risk of HCC was significantly lower in the Zn treatment group than in the no Zn treatment group ( P = 0.048). In study 2, the 1‐year and 3‐year cumulative incidence rates of HCC were 1.8% and 5.6%, respectively. The risk factors for HCC identified by multivariate analysis were male sex, cirrhosis, low platelet count before treatment, and low serum zinc concentration 12 weeks after the end of DAA therapy. Conclusion: The Zn concentration is related to HCC development in patients with HCV eradicated by DAA therapy. Oral zinc supplementation is recommended as a means of suppressing HCC development in patients who have achieved SVR.

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          Most cited references20

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          Risk of Hepatocellular Cancer in HCV Patients Treated With Direct-Acting Antiviral Agents.

          The risk of hepatocellular cancer (HCC) after sustained virological response (SVR) with direct-acting antivirals (DAA) is unclear. Our aim was to examine the risk and determinants of HCC in patients cured with DAA.
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            New hepatitis C therapies: the toolbox, strategies, and challenges.

            Therapy for hepatitis C is undergoing a revolution. Several new drugs against the hepatitis C virus (HCV) have reached the market and many others, including direct-acting antivirals and host-targeted agents, are in phase II or III clinical development. All-oral, interferon-free combinations of drugs are expected to cure more than 90% of infections. A vast amount of data from clinical trials are presented regularly at international conferences or released to the press before peer-review, creating confusion in the viral hepatitis field. The goal of this review is to clarify the current stage of HCV therapy and drug development. This review describes the different classes of drugs and their mechanisms and properties, as well as treatment strategies in development, including those that are interferon-based and interferon-free. HCV treatment options that will be available in 2014-2015 are presented for each genotype. A number of unanswered questions and challenges remain, such as how to treat special populations, the role of ribavirin in interferon-free regimens, the role of HCV resistance in treatment failures, and how to best re-treat patients who failed on treatment. Strategic choices, cost issues, HCV screening, and improving access to care in resource-constrained areas also are discussed. Copyright © 2014 AGA Institute. Published by Elsevier Inc. All rights reserved.
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              Oral Direct-Acting Agent Therapy for Hepatitis C Virus Infection: A Systematic Review.

              Rapid improvements in hepatitis C virus (HCV) therapy have led to the approval of multiple oral direct-acting antiviral (DAA) regimens by the U.S. Food and Drug Administration (FDA) for treatment of chronic HCV infection.
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                Author and article information

                Contributors
                hosui@osakah.johas.go.jp
                Journal
                Hepatol Commun
                Hepatol Commun
                10.1002/(ISSN)2471-254X
                HEP4
                Hepatology Communications
                John Wiley and Sons Inc. (Hoboken )
                2471-254X
                03 August 2021
                December 2021
                : 5
                : 12 ( doiID: 10.1002/hep4.v5.12 )
                : 2001-2008
                Affiliations
                [ 1 ] Department of Gastroenterology and Hepatology Osaka‐Rosai Hospital Sakai, Osaka Japan
                Author notes
                [*] [* ] ADDRESS CORRESPONDENCE AND REPRINT REQUESTS TO:

                Atsushi Hosui, M.D., Ph.D.

                Department of Gastroenterology and Hepatology, Osaka‐Rosai Hospital

                1179‐3 Nagasone

                Kitaku, Sakai, Osaka, Japan

                E‐mail: hosui@ 123456osakah.johas.go.jp

                Tel.: +81‐722‐52‐3561

                Author information
                https://orcid.org/0000-0003-0777-8045
                Article
                HEP41782
                10.1002/hep4.1782
                8631098
                34752016
                5a57951a-74e8-4490-a04a-66a62d0a4241
                © 2021 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 14 June 2021
                : 08 March 2021
                : 21 June 2021
                Page count
                Figures: 3, Tables: 3, Pages: 8, Words: 5084
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                December 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.9 mode:remove_FC converted:30.11.2021

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