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Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis
We treated patients with C-viral chronic hepatitis (CH) and liver cirrhosis (LC) with polaprezinc and determined prospectively the effect on long-term outcome. 62 patients were enrolled. Of these, 32 were administered 1.0 g polaprezinc and the remainder were not administered polaprezinc. We measured...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771250/ https://www.ncbi.nlm.nih.gov/pubmed/19902019 http://dx.doi.org/10.3164/jcbn.08-246 |
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author | Matsuoka, Shunichi Matsumura, Hiroshi Nakamura, Hitomi Oshiro, Shu Arakawa, Yasuo Hayashi, Junpei Sekine, Naoki Nirei, Kazushige Yamagami, Hiroaki Ogawa, Masahiro Nakajima, Noriko Amaki, Shuichi Tanaka, Naohide Moriyama, Mitsuhiko |
author_facet | Matsuoka, Shunichi Matsumura, Hiroshi Nakamura, Hitomi Oshiro, Shu Arakawa, Yasuo Hayashi, Junpei Sekine, Naoki Nirei, Kazushige Yamagami, Hiroaki Ogawa, Masahiro Nakajima, Noriko Amaki, Shuichi Tanaka, Naohide Moriyama, Mitsuhiko |
author_sort | Matsuoka, Shunichi |
collection | PubMed |
description | We treated patients with C-viral chronic hepatitis (CH) and liver cirrhosis (LC) with polaprezinc and determined prospectively the effect on long-term outcome. 62 patients were enrolled. Of these, 32 were administered 1.0 g polaprezinc and the remainder were not administered polaprezinc. We measured the serum zinc concentrations using conventional atomic absorption spectrometry and conducted a prospective study to determine the long-term outcome of the polaprezinc therapy. Changes of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels in the polaprezinc administration group were significantly lower than those of the untreated group. The decrease in platelet count was clearly less than that of the untreated group. The factors that inhibited increases in serum zinc concentrations following administration of polaprezinc included low serum zinc concentration states. Furthermore, the reductions of AST and ALT levels in the low zinc group were significantly greater than those of the high zinc group. When the patients who were administered polaprezinc were divided into two groups whose zinc concentrations increased (zinc responders) or remained stable or decreased (zinc non-responders), the zinc responders had a clearly lower cumulative incidence of HCC than the zinc non-responders. We conclude zinc supplementation improved the long-term outcome in C-viral CH and LC patients. |
format | Text |
id | pubmed-2771250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-27712502009-11-09 Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis Matsuoka, Shunichi Matsumura, Hiroshi Nakamura, Hitomi Oshiro, Shu Arakawa, Yasuo Hayashi, Junpei Sekine, Naoki Nirei, Kazushige Yamagami, Hiroaki Ogawa, Masahiro Nakajima, Noriko Amaki, Shuichi Tanaka, Naohide Moriyama, Mitsuhiko J Clin Biochem Nutr Original Article We treated patients with C-viral chronic hepatitis (CH) and liver cirrhosis (LC) with polaprezinc and determined prospectively the effect on long-term outcome. 62 patients were enrolled. Of these, 32 were administered 1.0 g polaprezinc and the remainder were not administered polaprezinc. We measured the serum zinc concentrations using conventional atomic absorption spectrometry and conducted a prospective study to determine the long-term outcome of the polaprezinc therapy. Changes of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels in the polaprezinc administration group were significantly lower than those of the untreated group. The decrease in platelet count was clearly less than that of the untreated group. The factors that inhibited increases in serum zinc concentrations following administration of polaprezinc included low serum zinc concentration states. Furthermore, the reductions of AST and ALT levels in the low zinc group were significantly greater than those of the high zinc group. When the patients who were administered polaprezinc were divided into two groups whose zinc concentrations increased (zinc responders) or remained stable or decreased (zinc non-responders), the zinc responders had a clearly lower cumulative incidence of HCC than the zinc non-responders. We conclude zinc supplementation improved the long-term outcome in C-viral CH and LC patients. the Society for Free Radical Research Japan 2009-11 2009-10-28 /pmc/articles/PMC2771250/ /pubmed/19902019 http://dx.doi.org/10.3164/jcbn.08-246 Text en Copyright © 2009 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Matsuoka, Shunichi Matsumura, Hiroshi Nakamura, Hitomi Oshiro, Shu Arakawa, Yasuo Hayashi, Junpei Sekine, Naoki Nirei, Kazushige Yamagami, Hiroaki Ogawa, Masahiro Nakajima, Noriko Amaki, Shuichi Tanaka, Naohide Moriyama, Mitsuhiko Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title | Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title_full | Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title_fullStr | Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title_full_unstemmed | Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title_short | Zinc Supplementation Improves the Outcome of Chronic Hepatitis C and Liver Cirrhosis |
title_sort | zinc supplementation improves the outcome of chronic hepatitis c and liver cirrhosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771250/ https://www.ncbi.nlm.nih.gov/pubmed/19902019 http://dx.doi.org/10.3164/jcbn.08-246 |
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