Lycium chinense Miller fruit extract lowers liver enzyme levels in subjects with mild hepatic dysfunction: a randomized, double-blind, placebo-controlled clinical trial.

Purpose: In our previous study, we showed that Lycium chinense Miller fruit extract (LFE) exerted hepatoprotective effects in mice. In the current study, we examined the effect of LFE on liver enzyme levels in subjects with mild hepatic dysfunction. Methods: A total of 90 subjects, aged 19 to 70 yea...

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Detalles Bibliográficos
Publicado en:European Journal of Nutrition Vol. 62; no. 3; pp. 1415 - 1426
Autores principales: Oh, Mi-Ra, Jung, Su-Jin, Chae, Soo-Wan, Park, Byung-Hyun, Lee, Seung-Ok
Formato: research tables/charts randomized controlled trial Journal Article
Publicado: Springer Nature Apr2023
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Purpose: In our previous study, we showed that Lycium chinense Miller fruit extract (LFE) exerted hepatoprotective effects in mice. In the current study, we examined the effect of LFE on liver enzyme levels in subjects with mild hepatic dysfunction. Methods: A total of 90 subjects, aged 19 to 70 years old, with abnormal alanine aminotransferase (ALT) levels, were randomly placed into either an LFE (n = 45) treatment group or a placebo group (n = 45). During the 12-week clinical trial, subjects in each group received either LFE or placebo capsules, and were instructed to take four tablets per day (1760 mg/day). The primary outcome of the study was the changes of ALT and γ-glutamyltransferase (GGT) levels in each subject. The safety of LFE supplementation was assessed and adverse events were recorded. Results: LFE supplementation for 12 weeks resulted in a significant reduction of ALT (P = 0.0498) and GGT (P = 0.0368) levels in comparison to the placebo. No clinically significant changes were observed in any safety parameters. Conclusion: These results suggest that LFE can be applied to subjects with mild hepatic dysfunction with no possible side effects. Trial registration: This study was registered at the Clinical Research Information Service (CRIS) as no. KCT0003985.