Comparison of MAFLD and NAFLD diagnostic criteria in real world

Background and aims Metabolic associated fatty liver disease (MAFLD) is a novel concept proposed in 2020, the utility of which has not been tested and validated in real world. We aimed to compare the characteristics of MAFLD and non‐alcoholic fatty liver disease (NAFLD). Methods The data was retriev...

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Published inLiver international Vol. 40; no. 9; pp. 2082 - 2089
Main Authors Lin, Su, Huang, Jiaofeng, Wang, Mingfang, Kumar, Rahul, Liu, Yuxiu, Liu, Shiying, Wu, Yinlian, Wang, Xiaozhong, Zhu, Yueyong
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.09.2020
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Summary:Background and aims Metabolic associated fatty liver disease (MAFLD) is a novel concept proposed in 2020, the utility of which has not been tested and validated in real world. We aimed to compare the characteristics of MAFLD and non‐alcoholic fatty liver disease (NAFLD). Methods The data was retrieved from the third National Health and Nutrition Examination Surveys of the United States, which is an unbiased survey dataset and frequently used for the study of fatty liver disease. Results A total of 13 083 cases with completed ultrasonography and laboratory data were identified from the NHANES III database. MAFLD was diagnosed in 4087/13 083 (31.24%) participants, while NAFLD in 4347/13 083 (33.23%) amongst the overall population and 4347/12 045 (36.09%) in patients without alcohol intake and other liver diseases. Compared with NAFLD, MAFLD patients were significantly older, had higher BMI level, higher proportions of metabolic comorbidities (diabetes, hypertension) and higher HOMA‐IR, lipid and liver enzymes. MAFLD patients with alcohol consumption were younger than those without, and more likely to be male. They had less metabolic disorder but higher liver enzymes. There were more cases with advance fibrosis in MAFLD patients with alcohol consumption. Conclusion MAFLD definition is more practical for identifying patients with fatty liver disease with high risk of disease progression.
Bibliography:Funding information
This research is supported by Chinese National 13th Five‐Year Plan's Science and Technology Projects (2017ZX10202201), Fujian Province Health Youth Research Project (2019‐1‐37) and Fujian Medical University Sailing Fund Project (2018QH1047).
Su Lin and Jiaofeng Huang contributed equally to this manuscript, and share first authorship.
Handling Editor: Luca Valenti
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ISSN:1478-3223
1478-3231
1478-3231
DOI:10.1111/liv.14548