Metabolic dysfunction associated fatty liver disease and coronavirus disease 2019: clinical relationship and current management

被引:0
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作者
Yanlan Xu
Xinyu Yang
Hua Bian
Mingfeng Xia
机构
[1] Zhongshan Hospital,Department of Endocrinology
[2] Fudan University,Department of Geriatrics, Qingpu Branch of Zhongshan Hospital
[3] Fudan University,undefined
[4] Fudan Institute for Metabolic Diseases,undefined
关键词
SARS-CoV-2; COVID-19; Fatty liver; MAFLD; Liver injury;
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学科分类号
摘要
The coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). At present, the COVID-19 has been prevalent worldwide for more than a year and caused more than four million deaths. Liver injury was frequently observed in patients with COVID-19. Recently, a new definition of metabolic dysfunction associated fatty liver disease (MAFLD) was proposed by a panel of international experts, and the relationship between MAFLD and COVID-19 has been actively investigated. Several previous studies indicated that the patients with MAFLD had a higher prevalence of COVID-19 and a tendency to develop severe type of respiratory infection, and others indicated that liver injury would be exacerbated in the patients with MAFLD once infected with COVID-19. The mechanism underlying the relationship between MAFLD and COVID-19 infection has not been thoroughly investigated, and recent studies indicated that multifactorial mechanisms, such as altered host angiotensin converting enzyme 2 (ACE2) receptor expression, direct viral attack, disruption of cholangiocyte function, systemic inflammatory reaction, drug-induced liver injury, hepatic ischemic and hypoxic injury, and MAFLD-related glucose and lipid metabolic disorders, might jointly contribute to both of the adverse hepatic and respiratory outcomes. In this review, we discussed the relationship between MAFLD and COVID-19 based on current available literature, and summarized the recommendations for clinical management of MAFLD patients during the pandemic of COVID-19.
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