Efficacy and Safety of Polaprezinc (Zinc Compound) on Zinc Deficiency: A Systematic Review and Dose-Response Meta-Analysis of Randomized Clinical Trials Using Individual Patient Data.
IPD meta-analysis
polaprezinc
serum zinc concentration
systematic review
zinc L-carnosine
zinc deficiency
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
17 Apr 2020
17 Apr 2020
Historique:
received:
13
03
2020
revised:
15
04
2020
accepted:
15
04
2020
entrez:
23
4
2020
pubmed:
23
4
2020
medline:
14
1
2021
Statut:
epublish
Résumé
Zinc intake is recommended for zinc deficiency. In clinical practice, polaprezinc has been used as a zinc replacement therapy for zinc deficiency. However, the efficacy of polaprezinc has not been established. To confirm the efficacy on zinc deficiency of polaprezinc and provide additional information on an appropriate regimen, we conducted a systematic review using individual patient data (IPD). We searched PubMed, the Japanese database Ichushi, and the database owned by the marketing authorization holder of polaprezinc. Randomized placebo-controlled trials that reported the serum zinc concentration were eligible. The mean difference of the change from baseline in serum zinc concentration was estimated using a fixed-effects model. The linear dose-response relationship and the subgroup effects were also assessed. Out of 54 unique randomized clinical trials (RCTs), four studies met the eligibility criteria, and we could access IPD for all of them. All three doses of polaprezinc (75 mg, 150 mg, and 300 mg) and the placebo group were examined. The dose-combined overall polaprezinc increased the change from baseline by a mean of 9.08 µg/dL (95% confidence interval: 5.46, 12.70; heterogeneity: I2 = 0.61%) compared to the placebo. A significant dose-response relationship was confirmed (p < 0.001). Baseline serum zinc concentration was considered an effect modifier in polaprezinc 300 mg. All doses of polaprezinc were tolerable, but a dose-response relationship with adverse events (AEs) was observed in gastrointestinal disorders. The dose of 300 mg may be useful among patients with baseline serum zinc concentration of less than 70 µg/dL, and 150 mg for 70 µg/dL or more.
Identifiants
pubmed: 32316581
pii: nu12041128
doi: 10.3390/nu12041128
pmc: PMC7230469
pii:
doi:
Substances chimiques
Organometallic Compounds
0
Zinc Compounds
0
polaprezinc
0WA1B15A1Z
Carnosine
8HO6PVN24W
Zinc
J41CSQ7QDS
Types de publication
Journal Article
Meta-Analysis
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Zeria Pharmaceutical Co., Ltd.
ID : NA
Déclaration de conflit d'intérêts
K.F. and M.T. are employees of Zeria Pharmaceutical Co., Ltd., T.M., Y.N. and M.S. received consultant fee and travel expenses on this review from Zeria Pharmaceutical Co., Ltd. K.O. received travel expenses on this review from Zeria Pharmaceutical Co., Ltd.
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