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Silymarin for Treating Toxic Liver Disease: International Consensus Recommendations.
Gillessen, Anton; Angelico, Francesco; Chen, Jun; Lu, Lungen; Lucena, Maria Isabel; Fu, Qingchun; Xie, Qing; Andrade, Raul J; Xie, Wen; Xu, Xiaoyuan; Yu, Yanyan; Mao, Yi-Min; Nan, Yuemin.
Afiliação
  • Gillessen A; Department of Internal Medicine, Herz-Jesu-Hospital, Muenster, Germany.
  • Angelico F; Department of Public Health and Infectious Diseases, Sapienza University School of Medicine, Rome, Italy.
  • Chen J; Department of Liver Disease Medical Center/Head of the Fourth Department of Liver Disease, Shenzhen Third People's Hospital, Shenzhen, China.
  • Lu L; Department of Gastroenterology, Shanghai General Hospital, Shanghai, China.
  • Lucena MI; Department of Pharmacology, School of Medicine, University of Málaga, Málaga, Spain.
  • Fu Q; Department of Liver Disease, Centre of Shanghai Public Health Clinical Centre, Shanghai, China.
  • Xie Q; Department of Infectious Diseases, Ruijin Hospital, Shanghai, China.
  • Andrade RJ; Services of Gastroenterology & Clinical Pharmacology, Málaga Biomedical Research Institute, IBIMA, University Hospital, University of Málaga, Málaga, Spain.
  • Xie W; Liver Disease Centre, Beijing Ditan Hospital Capital Medical University, Beijing, China.
  • Xu X; Department of Infectious Diseases, Peking University Health Science Centre, Beijing, China.
  • Yu Y; Department of Infectious Disease, Peking University First Hospital, Beijing, China.
  • Mao YM; Department of Gastroenterology, Renji Hospital, Shanghai, China.
  • Nan Y; Department of Liver Diseases, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
Gastro Hep Adv ; 1(5): 882-893, 2022.
Article em En | MEDLINE | ID: mdl-39131840
ABSTRACT
Chronic liver disease (CLD) is a leading health problem impacting the quality of life globally. China shares a major global burden of CLD-including alcoholic liver disease, nonalcoholic fatty liver disease/metabolic dysfunction-associated fatty liver disease, and drug-induced liver injury, except for chronic viral hepatitis. Several exogenous toxins or endogenous metabolic insults trigger hepatic pathology toward steatosis, inflammation, and fibrosis, which, if left untreated, may culminate in liver cirrhosis. Oxidative stress is a common pathomechanism underlying all phenotypes of toxic liver injury; thus, these may be brought under a unified entity, viz. toxic liver disease (TLD). Therefore, a common strategy to treat TLD is to use antioxidants as hepatoprotective agents. The cornerstone for treating fatty liver disease is lifestyle modification, diet, exercise, and behavioral therapy, along with the limited use of pharmacological agents. Available preclinical and clinical evidence indicates that silymarin is a hepatoprotective agent with established antioxidant, anti-inflammatory, antifibrotic effects. An international expert panel of clinicians was convened to discuss combining alcoholic liver disease, nonalcoholic fatty liver disease/metabolic dysfunction-associated fatty liver disease, drug-induced liver injury, and liver cirrhosis under the single definition of TLD, based on the shared pathologic mechanism of oxidative stress. The panel highlighted the significance of silymarin as an antioxidant treatment for TLD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article