The Effectiveness of Silymarin in the Prevention of Anti‑Tuberculosis Drug‑Induced Hepatotoxicity: A Randomized Controlled Clinical Trial Publisher

Summary: Could silymarin protect patients taking TB medicines? A small trial found lower liver enzyme levels after two weeks, but larger studies are needed. #Tuberculosis #LiverHealth

Talebi A ; Soltani R ; Khorvash F ; Jouabadi S M
Source: International Journal of Preventive Medicine Published:2023

Abstract

Background: Several animal studies have shown the protective effect of silymarin (the extract of Silybum marianum seeds) against anti‑tuberculosis drug‑induced hepatotoxicity (ATDH). However, the knowledge of ATDH of silymarin in humans is scarce. In this study, we aimed to clinically evaluate it. Methods: During this randomized controlled clinical trial, 36 new cases of tuberculosis (TB) were enrolled to receive either silymarin 150 mg twice daily for two weeks along with a standard anti‑TB therapeutic regimen (experimental group; n = 16) or standard anti‑TB therapeutic regimen alone (control group; n = 21). Liver function tests (serum AST, ALT, ALP, and total bilirubin) at the end of weeks 1 and 2 as well as the rate of ATDH during the study were determined and compared between the groups. Results: No significant differences between the experimental and control groups were observed at the end of the first week regarding liver function tests; However, at the end of the second week, the mean serum levels of AST (P = 0.03) and ALP (P = 0.04) were significantly lower in the experimental group. ALT (P = 0.016) and ALP (P = 0.027) levels in the experimental group significantly decreased during the study, while the changes in the control group were not significant. Two patients in the control group (9.5%) developed ATDH, while no one in the experimental group manifested this adverse effect. Conclusions: Our study suggests that silymarin use has the potential for the reduction of anti‑TB drug‑induced hepatotoxicity. © 2023 International Journal of Preventive Medicine.