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Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial
The essential trace element zinc maintains liver functions. Liver diseases can alter overall zinc concentrations, and hypozincemia is associated with various hepatic pathologies. Modulating systemic zinc through dietary supplementation is potentially useful for liver diseases. We evaluated the usefu...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150658/ https://www.ncbi.nlm.nih.gov/pubmed/31392541 http://dx.doi.org/10.1007/s12011-019-01851-y |
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author | Katayama, Kazuhiro Hosui, Atsushi Sakai, Yoshiyuki Itou, Minoru Matsuzaki, Yasushi Takamori, Yoriyuki Hosho, Keiko Tsuru, Tomomi Takikawa, Yasuhiro Michitaka, Kojiro Ogawa, Eishin Miyoshi, Yoko Ito, Toshifumi Ida, Shinobu Hamada, Izumi Miyoshi, Katsunori Kodama, Hiroko Takehara, Tetsuo |
author_facet | Katayama, Kazuhiro Hosui, Atsushi Sakai, Yoshiyuki Itou, Minoru Matsuzaki, Yasushi Takamori, Yoriyuki Hosho, Keiko Tsuru, Tomomi Takikawa, Yasuhiro Michitaka, Kojiro Ogawa, Eishin Miyoshi, Yoko Ito, Toshifumi Ida, Shinobu Hamada, Izumi Miyoshi, Katsunori Kodama, Hiroko Takehara, Tetsuo |
author_sort | Katayama, Kazuhiro |
collection | PubMed |
description | The essential trace element zinc maintains liver functions. Liver diseases can alter overall zinc concentrations, and hypozincemia is associated with various hepatic pathologies. Modulating systemic zinc through dietary supplementation is potentially useful for liver diseases. We evaluated the usefulness of zinc (NPC-02; acetate formulation) supplementation. We conducted two NPC-02 studies on zinc-deficient patients (serum zinc < 70 μg/dL). Study 1: double-blind, randomized, placebo-controlled trial on 57 subjects with chronic liver diseases comparing serum zinc in patients given NPC-02 (NPC-02 group) versus placebo (Placebo group). Study 2: dose adjustment study on 43 subjects with/without liver diseases to determine proportions maintaining serum zinc target (≥ 80 μg/dL but < 200 μg/dL). In study 1, NPC-02 subjects had higher serum zinc concentrations at week 8 than Placebo subjects (83.2 ± 20.2 and 61.3 ± 12.0, respectively; P < 0.0001), and more NPC-02 than Placebo subjects achieved the serum zinc target (15/27 vs. 1/26). In study 2, the NPC-02-induced serum zinc increase was dose-dependent in subjects both with and without liver diseases (r = 0.5143, P = 0.0022 and r = 0.5753, P = 0.0005, respectively). Interestingly, there was a marginally positive correlation between serum zinc and albumin levels in subjects with but not in those without liver diseases (r = 0.4028, P = 0.0631 and r = 0.1360, P = 0.5567, respectively). NPC-02 dose-dependently increases serum zinc in hypozincemic patients, regardless of liver disease. NPC-02 is a potentially effective therapy for liver cirrhosis, in which zinc deficiency is common. Clinical trial registry number: NCT02337569, NCT02321865. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12011-019-01851-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7150658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-71506582020-04-18 Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial Katayama, Kazuhiro Hosui, Atsushi Sakai, Yoshiyuki Itou, Minoru Matsuzaki, Yasushi Takamori, Yoriyuki Hosho, Keiko Tsuru, Tomomi Takikawa, Yasuhiro Michitaka, Kojiro Ogawa, Eishin Miyoshi, Yoko Ito, Toshifumi Ida, Shinobu Hamada, Izumi Miyoshi, Katsunori Kodama, Hiroko Takehara, Tetsuo Biol Trace Elem Res Article The essential trace element zinc maintains liver functions. Liver diseases can alter overall zinc concentrations, and hypozincemia is associated with various hepatic pathologies. Modulating systemic zinc through dietary supplementation is potentially useful for liver diseases. We evaluated the usefulness of zinc (NPC-02; acetate formulation) supplementation. We conducted two NPC-02 studies on zinc-deficient patients (serum zinc < 70 μg/dL). Study 1: double-blind, randomized, placebo-controlled trial on 57 subjects with chronic liver diseases comparing serum zinc in patients given NPC-02 (NPC-02 group) versus placebo (Placebo group). Study 2: dose adjustment study on 43 subjects with/without liver diseases to determine proportions maintaining serum zinc target (≥ 80 μg/dL but < 200 μg/dL). In study 1, NPC-02 subjects had higher serum zinc concentrations at week 8 than Placebo subjects (83.2 ± 20.2 and 61.3 ± 12.0, respectively; P < 0.0001), and more NPC-02 than Placebo subjects achieved the serum zinc target (15/27 vs. 1/26). In study 2, the NPC-02-induced serum zinc increase was dose-dependent in subjects both with and without liver diseases (r = 0.5143, P = 0.0022 and r = 0.5753, P = 0.0005, respectively). Interestingly, there was a marginally positive correlation between serum zinc and albumin levels in subjects with but not in those without liver diseases (r = 0.4028, P = 0.0631 and r = 0.1360, P = 0.5567, respectively). NPC-02 dose-dependently increases serum zinc in hypozincemic patients, regardless of liver disease. NPC-02 is a potentially effective therapy for liver cirrhosis, in which zinc deficiency is common. Clinical trial registry number: NCT02337569, NCT02321865. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12011-019-01851-y) contains supplementary material, which is available to authorized users. Springer US 2019-08-07 2020 /pmc/articles/PMC7150658/ /pubmed/31392541 http://dx.doi.org/10.1007/s12011-019-01851-y Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Katayama, Kazuhiro Hosui, Atsushi Sakai, Yoshiyuki Itou, Minoru Matsuzaki, Yasushi Takamori, Yoriyuki Hosho, Keiko Tsuru, Tomomi Takikawa, Yasuhiro Michitaka, Kojiro Ogawa, Eishin Miyoshi, Yoko Ito, Toshifumi Ida, Shinobu Hamada, Izumi Miyoshi, Katsunori Kodama, Hiroko Takehara, Tetsuo Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title | Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title_full | Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title_fullStr | Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title_full_unstemmed | Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title_short | Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial |
title_sort | effects of zinc acetate on serum zinc concentrations in chronic liver diseases: a multicenter, double-blind, randomized, placebo-controlled trial and a dose adjustment trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150658/ https://www.ncbi.nlm.nih.gov/pubmed/31392541 http://dx.doi.org/10.1007/s12011-019-01851-y |
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