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A 12-week, randomized, double-blind study to evaluate the efficacy and safety of liver function after using fermented ginseng powder (GBCK25).

Authors :
Su-Jin Jung
Ji-Hyun Hwang
Soo-Hyun Park
Eun-Kyung Choi
Ki-Chan Ha
Hyang-Im Baek
Dong-Gue Shin
Jeong-Hun Seo
Soo-Wan Chae
Source :
Food & Nutrition Research; 2020, Vol. 64, p1-11, 11p
Publication Year :
2020

Abstract

Background: Recently, clinical research has suggested that red ginseng components play a role in liver protection and combating fatigue. However, fermented ginseng has not been analyzed for liver-protective or anti- fatigue effects. Objective: This study evaluates the positive effects of fermented ginseng powder (GBCK25) on liver function. Methods: Ninety participants with elevated alanine aminotransferase levels (35 ≤ ALT ≤1 05 IU/L) were randomized to one of three groups. The participants were treated with GBCK25 tablets at a dose of 500 mg/ day (high dose), 125 mg/day (low dose), or placebo group daily for 12 weeks. The primary outcomes included changes in ALT and gamma-glutamyl transferase (GGT) levels. The secondary outcomes included changes in aspartate amino-transferase (AST), high-sensitivity C-reactive protein (hs-CRP), multidimensional fatigue scale, lipid profile, and antioxidant markers. Results: In male subjects, after 12 weeks of low-dose GBCK25 (125 mg) supplementation, the GGT (P = 0.036) and hs-CRP (P = 0.021) levels decreased significantly more than those in the placebo group. High-dose GBCK25 (500 mg) supplementation significantly decreased the fatigue score compared with the placebo group. There were no clinically significant differences between the groups when studying any safety parameter. Conclusion: Our results suggest that GBCK25 supplementation has beneficial effects on liver function. Trial registration: This study was registered at Clinical Trials.gov (NCT03260543). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16546628
Volume :
64
Database :
Complementary Index
Journal :
Food & Nutrition Research
Publication Type :
Academic Journal
Accession number :
146731690
Full Text :
https://doi.org/10.29219/fnr.v64.3517