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.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
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.

Références

Nihon Jibiinkoka Gakkai Kaiho. 2013 Jan;116(1):17-26
pubmed: 23484369
J Nutr Biochem. 2020 Mar;77:108240
pubmed: 31841960
Nutrients. 2018 Jan 11;10(1):
pubmed: 29324654
PLoS One. 2015 Nov 11;10(11):e0141262
pubmed: 26559814
Nutrients. 2012 Aug;4(8):841-58
pubmed: 23016120
J Nutr. 2015 Apr 1;146(4):858S-885S
pubmed: 26962190
Br J Nutr. 2008 Jun;99 Suppl 3:S14-23
pubmed: 18598584
Biol Trace Elem Res. 2020 May;195(1):71-81
pubmed: 31392541
J Am Diet Assoc. 2001 Mar;101(3):294-301
pubmed: 11269606
PLoS One. 2012;7(11):e50568
pubmed: 23209782
Nutrients. 2017 Nov 25;9(12):
pubmed: 29186856
Consult Pharm. 2016 May;31(5):267-70
pubmed: 27178656
Nutrients. 2018 Feb 11;10(2):
pubmed: 29439479
Am J Epidemiol. 2018 Nov 1;187(11):2481-2490
pubmed: 30060121
Future Oncol. 2018 Aug;14(19):1977-1988
pubmed: 30074413
J Nutr. 1990 Nov;120 Suppl 11:1474-9
pubmed: 2243291
J Trace Elem Med Biol. 2006;20(1):3-18
pubmed: 16632171
Pediatr Endocrinol Rev. 2008 Jun;5(4):889-96
pubmed: 18552751
BMJ. 2019 Aug 28;366:l4898
pubmed: 31462531
Yakugaku Zasshi. 2012;132(3):271-7
pubmed: 22382829
Acta Otolaryngol. 2009 Oct;129(10):1115-20
pubmed: 19037756
Am J Physiol Endocrinol Metab. 2003 Nov;285(5):E1010-20
pubmed: 12865259
Physiol Rev. 2015 Jul;95(3):749-84
pubmed: 26084690
Int J Mol Sci. 2016 Mar 04;17(3):336
pubmed: 26959009
JAMA. 2015 Apr 28;313(16):1657-65
pubmed: 25919529
Br J Nutr. 2012 Dec 14;108(11):1962-71
pubmed: 23244547
Physiol Rev. 1993 Jan;73(1):79-118
pubmed: 8419966
Am J Epidemiol. 2007 Dec 1;166(11):1337-44
pubmed: 18000021

Auteurs

Kei Furihata (K)

Biostatistics, Data Science, Clinical Administration, Zeria Pharmaceutical Co., Ltd., 10-11, Nihonbashi Kobuna-cho, Chuo-ku, Tokyo 103-8351, Japan.

Masaru Tsuchikawa (M)

Biostatistics, Data Science, Clinical Administration, Zeria Pharmaceutical Co., Ltd., 10-11, Nihonbashi Kobuna-cho, Chuo-ku, Tokyo 103-8351, Japan.

Takaki Miwa (T)

Department of Otorhinolaryngology, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Ishikawa 920-0293, Japan.

Yuji Naito (Y)

Department of Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, 465 Kajii-chi, Kawaramachi-Hirokoji Kamigyo-ku, Kyoto 602-8566, Japan.

Koji Oba (K)

Department of Biostatistics, School of Public Health, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

Masafumi Sakagami (M)

Department of Otolaryngology-Head and Neck Surgery, Hyogo College of Medicine, 1-1 Mukogawa, Nishinomiya, Hyogo 663-8501, Japan.

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Classifications MeSH