Abstract:In recent years, with the increasing incidence of obesity and other metabolic diseases, the prevalence of non-alcoholic fatty liver disease (NAFLD) has increased and it has become a major health problem affecting more than one quarter of the world's population. Recently, experts reached a consensus that NAFLD does not reflect the current knowledge, and metabolic dysfunction-associated fatty liver disease (MAFLD) was suggested as a more appropriate term. MAFLD is not just a simple renaming of NAFLD. The definit… Show more
“…Hepatotoxins (drugs, alcohol consumption, viral or bacterial infection, and lipid deposition) or autoimmune response can induce acute liver injury and chronic liver diseases such as viral hepatitis, drug-induced liver injury, autoimmune hepatitis, alcoholic liver disease, and non-alcoholic fatty liver disease (NAFLD). 1 Hepatic fibrosis is a common complication of almost all types of hepatopathies, and if left untreated, liver fibrosis may eventually progress to cirrhosis, liver failure, and hepatocellular carcinoma (HCC). 2 , 3 , 4 Fibrosis is a dynamic process that can be prevented or reverted by eliminating pathogenic factors or carrying out appropriate therapeutic interventions, such as with antiviral drugs that delay the progression of virus-associated hepatic fibrosis.…”
“…Hepatotoxins (drugs, alcohol consumption, viral or bacterial infection, and lipid deposition) or autoimmune response can induce acute liver injury and chronic liver diseases such as viral hepatitis, drug-induced liver injury, autoimmune hepatitis, alcoholic liver disease, and non-alcoholic fatty liver disease (NAFLD). 1 Hepatic fibrosis is a common complication of almost all types of hepatopathies, and if left untreated, liver fibrosis may eventually progress to cirrhosis, liver failure, and hepatocellular carcinoma (HCC). 2 , 3 , 4 Fibrosis is a dynamic process that can be prevented or reverted by eliminating pathogenic factors or carrying out appropriate therapeutic interventions, such as with antiviral drugs that delay the progression of virus-associated hepatic fibrosis.…”
“…MAFLD includes a spectrum of liver histological progressions ranging from simple steatosis to varying degrees of fibrosis with infiltration of inflammatory cells. Compared with NAFLD patients, MAFLD patients are more at risk of having broad metabolic traits and higher fibrosis levels [ 3 , 4 ]. Like other chronic liver diseases, it can develop into cirrhosis if fibrosis progresses [ 5 ].…”
Background: Diabetes mellitus (DM) is a comorbidity commonly presenting with metabolic-dysfunction-associated fatty liver disease (MAFLD); however, few tests for interaction have been reported. Our target was to evaluate the prognostic implications of DM in patients with different forms of MAFLD. Methods: Using data from the Third National Health and Nutrition Examination Survey (NHANES III) in the United States, we screened 14,797 participants aged 20–74 who received ultrasound examinations from 1988–1994. Among them, 4599 patients met the diagnosis of MAFLD, and we defined mortality as the outcome event. Survival analysis of competitive risk events was performed using Cox regression and sub-distributed risk ratio (SHR). Results: During 21.1 years of follow-up, cardiovascular diseases seemed to be the most common cause of death among MAFLD patients. Of them, DM was present in 25.48% and was independently associated with increased risk of all-cause mortality (HRs: 1.427, 95% CIs: 1.256–1.621, p < 0.001) and cause-specific mortality (cardiovascular-related mortality (HRs: 1.458, 95% CIs: 1.117–1.902, p = 0.005), non-cardiovascular-related mortality (HRs: 1.423, 95% CIs: 1.229–1.647, p < 0.001), and non-cancer-related mortality (HRs: 1.584, 95% CIs: 1.368–1.835, p < 0.001), respectively). Surprisingly, this association was more significant for young patients (p-value for interaction <0.001). Moreover, DM had a greater risk of all-cause and cause-specific mortality among overweight and obese MAFLD patients (p-value for interaction <0.001). Conclusions: DM increased the risk of all-cause and cause-specific mortality (cardiovascular-related, non-cardiovascular-related, and non-cancer-related) in MAFLD patients, especially in younger patients with excess obesity.
“…In 2020, the consensus of an international expert group recommended changing the name of NAFLD to MAFLD. 10 The new diagnostic criteria are based on histological (liver biopsy), radiographic, and blood biomarker evidence of hepatic fat accumulation (hepatocellular steatosis) in combination with one of the following conditions; overweight, obesity, type 2 diabetes, or metabolic dysfunction. 11 Diagnosis is based on the presence of metabolic dysfunction, which is a positive diagnostic criterion, not an exclusion-based diagnosis, and absence of excessive alcohol consumption is no longer a diagnostic criterion.…”
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confidence: 99%
“…However, this definition lacks consideration of disease heterogeneity and hinders the study of precision therapy. In 2020, the consensus of an international expert group recommended changing the name of NAFLD to MAFLD 10 . The new diagnostic criteria are based on histological (liver biopsy), radiographic, and blood biomarker evidence of hepatic fat accumulation (hepatocellular steatosis) in combination with one of the following conditions; overweight, obesity, type 2 diabetes, or metabolic dysfunction 11 .…”
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