Evidence map›Paper›PMID 31392541›Full record

Trial reportBiological trace element research2020

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.

Kazuhiro Katayama, Atsushi Hosui, Yoshiyuki Sakai, Minoru Itou, Yasushi Matsuzaki, Yoriyuki Takamori, Keiko Hosho, Tomomi Tsuru, Yasuhiro Takikawa, Kojiro Michitaka and 8 more

2 registry-linked trialsOpen access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Biological trace element research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02321865 phase3completednot on this map

Dose Adjustment Study of NPC-02 in Patients With Zinc Deficiency

TypeinterventionalSponsorNobelpharmaRan2015 to 2015Enrolled43ConditionsZinc DeficiencyArmsNPC-02
NCT02337569 phase3completednot on this map

A Randomized, Double-Blind, Placebo Controlled Study of NPC-02 in Patients With Zinc Deficiency

TypeinterventionalSponsorNobelpharmaRan2015 to 2015Enrolled57ConditionsZinc DeficiencyArmsNPC-02, Placebos
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
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  6. Article
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  10. Review
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  13. Article
  14. Zinc deficiency in patients with chronic liver disease in Japan.Hepatology research : the official journal of the Japan Society of Hepatology · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 13 institutions in 1 country.

Kazuhiro KatayamaDepartment of Hepato-biliary and Pancreatic Oncology, Osaka International Cancer Institute, 3-1-69, Otemae, Chuo-ku, Osaka, 541-8567, Japan. katayama-ka@mc.pref.osaka.jp.ORCID http://orcid.org/0000-0002-6987-1176
Atsushi HosuiDepartment of Gastroenterology and Hepatology, Osaka Rosai Hospital, Osaka, Japan.
Yoshiyuki SakaiDivision of Hepatobiliary and Pancreatic Diseases, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Minoru ItouDepartment of Internal Medicine, Kurume Clinical Pharmacology Clinic, Fukuoka, Japan.
Yasushi MatsuzakiDepartment of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki, Japan.
Yoriyuki TakamoriDepartment of Internal Medicine, Teikyo University Hospital, Tokyo, Japan.
Keiko Hosho2nd Department of Internal Medicine, Tottori University Hospital, Tottori, Japan.
Tomomi TsuruDepartment of Rheumatology, PS Clinic, Fukuoka, Japan.
Yasuhiro TakikawaDivision of Hepatology, Department of Internal Medicine, Iwate Medical University Hospital, Iwate, Japan.
Kojiro MichitakaDepartment of Gastroenterology, Ehime Prefectural Central Hospital, Matsuyama, Ehime, Japan.
Eishin OgawaDepartment of Pediatrics, Teikyo University Hospital, Tokyo, Japan.
Yoko MiyoshiDepartment of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Toshifumi ItoDepartment of Gastroenterology and Hepatology, Japan Community Healthcare Organization Osaka Hospital, Osaka, Japan.
Shinobu IdaDepartment of Pediatric Gastroenterology and Nutrition, Osaka Women's and Children's Hospital, Osaka, Japan.
Izumi HamadaDepartment of Research and Development, Nobelpharma Co., Ltd., Tokyo, Japan.
Katsunori MiyoshiDepartment of Research and Development, Nobelpharma Co., Ltd., Tokyo, Japan.
Hiroko KodamaDepartment of Health and Dietetics, Faculty of Health and Medical Science, Teikyo Heisei University, Tokyo, Japan.
Tetsuo TakeharaDepartment of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Osaka, Japan.
Teikyo University Hospital · JPThe University of Osaka · JPEhime Prefectural Central Hospital · JPHyogo Medical University · JPIwate Medical University · JPOno Clinic · JPOsaka Hospital · JPOsaka International Cancer Institute · JPOsaka Rosai Hospital · JPOsaka Women's and Children's Hospital · JPTeikyo Heisei University · JPTokyo Medical University Ibaraki Medical Center · JPTottori University Hospital · JP

Funding

Nobelpharma Co., Ltd. None
6 · The paper itself

Abstract

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.

Indexed as

Liver DiseasesZincZinc AcetateAgedChronic DiseaseDietary SupplementsDouble-Blind MethodFemaleHumansMaleMiddle AgedZincZinc AcetateChronic liver diseaseDose adjustmentHypozincemiaNPC-02Serum zinc concentrationZinc deficiency

Identifiers

PMID31392541
PMCPMC7150658
OpenAlexW2966414696

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.