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Metabolic Syndrome, Nonalcoholic Fatty Liver Disease, and Chronic Hepatitis B: A Narrative Review

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INFECTIOUS DISEASES AND THERAPY
卷 12, 期 1, 页码 53-66

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SPRINGER LONDON LTD
DOI: 10.1007/s40121-022-00725-6

关键词

Alanine aminotransferase; Chronic hepatitis B; Hepatic steatosis; Hepatitis B virus; Metabolic syndrome; Nonalcoholic fatty liver disease

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Chronic hepatitis B often coexists with metabolic syndrome and nonalcoholic fatty liver disease. Both metabolic syndrome and nonalcoholic fatty liver disease are associated with obesity and insulin resistance, which can lead to adverse effects on the liver and other organs. The relationship among chronic hepatitis B, metabolic syndrome, and nonalcoholic fatty liver disease is complex and requires further investigation.
Chronic hepatitis B (CHB) remains a relatively major public health problem. Simultaneously, an unhealthy lifestyle causes a series of metabolic abnormalities, the most critical of which are metabolic syndrome (MS) and nonalcoholic fatty liver disease (NAFLD). Therefore, it is increasingly common for MS and NAFLD to coexist with CHB. MS is a cluster of metabolic disorders, while NAFLD is always considered as the manifestation of MS in the liver. The aim of this article is to review recent advances to explain the complex relationship among MS, NAFLD, and hepatitis B virus (HBV) infection. MS and NAFLD both have obesity and insulin resistance as central factors and both can lead to adverse hepatic and extrahepatic outcomes. However, there is insufficient evidence to associate NAFLD with all components of MS, and genetically related NAFLD has little association with MS. Incidences of MS and NAFLD are inversely associated with HBV infection. However, the effect of HBV infection on the risk of insulin resistance and dyslipidemia is not well understood. Evidence from both clinical studies and animal experiments suggested that hepatic steatosis inhibits HBV replication. MS and NAFLD may have adverse effects on CHB disease progression and prognosis. Furthermore, in related studies of CHB with normal alanine aminotransferase (ALT), the roles of MS and NAFLD should also be emphasized. In conclusion, there are complicated interactions that are not yet fully defined among MS, NAFLD, and CHB. To control chronic liver disease effectively, the relationship among the three must be clarified.

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