Oral Zinc Supplementation Decreases the Risk of HCC Development in Patients With HCV Eradicated by DAA.


Journal

Hepatology communications
ISSN: 2471-254X
Titre abrégé: Hepatol Commun
Pays: United States
ID NLM: 101695860

Informations de publication

Date de publication:
12 2021
Historique:
revised: 14 06 2021
received: 08 03 2021
accepted: 21 06 2021
pubmed: 10 11 2021
medline: 22 1 2022
entrez: 9 11 2021
Statut: ppublish

Résumé

We have reported that the plasma zinc concentration gradually decreases with the progression of fibrosis and is related to hepatocellular carcinoma (HCC) development. The aim of this study was to examine the impact of the zinc concentration on HCC development (study 1) and the relationship between zinc intake and HCC development (study 2) in patients with hepatitis C virus (HCV) eradicated by direct-acting antivirals (DAAs). A total of 599 sustained virological response (SVR) patients treated with DAAs without a history of HCC were retrospectively analyzed in this study. Eighty patients received supplemental zinc (Zn treatment group), and 519 patients did not receive zinc (no Zn treatment group). In study 1, the cumulative incidence rate of HCC was compared between the Zn treatment group and the no Zn treatment group. In study 2, the risk factors for HCC development were examined in the no Zn treatment group. In study 1, in the Zn treatment group, HCC did not develop during follow-up, and the cumulative risk of HCC was significantly lower in the Zn treatment group than in the no Zn treatment group (P = 0.048). In study 2, the 1-year and 3-year cumulative incidence rates of HCC were 1.8% and 5.6%, respectively. The risk factors for HCC identified by multivariate analysis were male sex, cirrhosis, low platelet count before treatment, and low serum zinc concentration 12 weeks after the end of DAA therapy. Conclusion: The Zn concentration is related to HCC development in patients with HCV eradicated by DAA therapy. Oral zinc supplementation is recommended as a means of suppressing HCC development in patients who have achieved SVR.

Identifiants

pubmed: 34752016
doi: 10.1002/hep4.1782
pmc: PMC8631098
doi:

Substances chimiques

Antiviral Agents 0
Zinc J41CSQ7QDS

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2001-2008

Informations de copyright

© 2021 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.

Références

Free Radic Biol Med. 2003 Apr 1;34(7):908-10
pubmed: 12654479
Am J Clin Nutr. 1970 Feb;23(2):170-7
pubmed: 5415563
J Hepatol. 2014 Nov;61(1 Suppl):S79-90
pubmed: 25443348
Hepatol Res. 2007 Jun;37(6):405-9
pubmed: 17539814
Am J Clin Pathol. 1965 Oct;44(4):426-35
pubmed: 5839914
Hepatology. 2020 Jan;71(1):44-55
pubmed: 31222774
Hepatol Res. 2019 May;49(5):570-578
pubmed: 30623521
Free Radic Res. 2004 Jun;38(6):573-80
pubmed: 15346648
N Engl J Med. 1956 Aug 30;255(9):403-8
pubmed: 13358854
Lancet. 1984 Sep 1;2(8401):493-5
pubmed: 6147551
Nutr J. 2013 Jun 06;12:74
pubmed: 23742732
Ann Intern Med. 2017 May 2;166(9):637-648
pubmed: 28319996
J Nutr. 2001 Dec;131(12):3208-11
pubmed: 11739867
Cancer Biol Ther. 2014 Apr;15(4):353-60
pubmed: 24448510
Nutrition. 2014 Nov-Dec;30(11-12):1409-14
pubmed: 25280421
Nutrients. 2018 Dec 10;10(12):
pubmed: 30544767
Cancers (Basel). 2020 May 26;12(6):
pubmed: 32466400
Gastroenterology. 2017 Oct;153(4):996-1005.e1
pubmed: 28642197
Gastroenterology. 2014 May;146(5):1176-92
pubmed: 24631495
Commun Biol. 2018 Aug 22;1:113
pubmed: 30271993

Auteurs

Atsushi Hosui (A)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Takashi Tanimoto (T)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Toru Okahara (T)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Munehiro Ashida (M)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Kohsaku Ohnishi (K)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Yuhei Wakahara (Y)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Yukihiro Kusumoto (Y)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Toshio Yamaguchi (T)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Yuka Sueyoshi (Y)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Motohiro Hirao (M)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Takuya Yamada (T)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Naoki Hiramatsu (N)

Department of Gastroenterology and Hepatology, Osaka-Rosai Hospital, Sakai, Osaka, Japan.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH