摘要
Metabolic dysfunction-associated fatty liver disease(MAFLD)is a complex,heterogenous and progressive disease that is characterised by substantial phenotypic variability,which results in disparate clinical presentations and outcomes(1-4).Notably,only a proportion of patients with MAFLD progress to the more advanced stages of the disease.Therefore,the identification of the subgroups that have a high risk of disease progression is of paramount importance for clinical care,as well as drug development and clinical trials(5).
基金
supported by the National Health and Medical Research Council of Australia(NHMRC)Program and Investigator Grants(Nos.2008983,1053206,and 1149976)
Project and Ideas Grants(Nos.1107178,1108422,and 2001692).