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학술저널
저자정보
Lei Miao (Department of Gastroenterology The Second Affiliated Hospital of Wenzhou Medical University) Jing Xu (Department of Endocrinology The Second Affiliated Hospital of Wenzhou Medical University) Giovanni Targher (Department of Medicine University and Azienda Ospedaliera Universitaria Integrata of Verona) Christopher D Byrne (Southampton National Institute for Health Research Biomedical Research Centre University Hospital S) Ming-Hua Zheng (Department of Hepatology the First Affiliated Hospital of Wenzhou Medical University)
저널정보
대한간학회 Clinical and Molecular Hepatology Clinical and Molecular Hepatology 제28권 제4호
발행연도
2022.10
수록면
725 - 738 (14page)

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Non-alcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease with a global prevalence of about 55% in people with type 2 diabetes mellitus (T2DM). T2DM, obesity and NAFLD are three closely inter-related pathological conditions. In addition, T2DM is one of the strongest clinical risk factors for the faster progression of NAFLD to non-alcoholic steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma. Increasing evidence suggests that newer classes of glucose-lowering drugs, such as peroxisome proliferator-activated receptor agonists, glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors or sodium-glucose cotransporter-2 inhibitors, could reduce the rates of NAFLD progression. This narrative review aims to briefly summarize the recent results from randomized controlled trials testing the efficacy and safety of old and new glucose-lowering drugs for the treatment of NAFLD or NASH in adults both with and without coexisting T2DM.

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