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MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis

INTRODUCTION: Metabolic associated fatty liver disease (MAFLD) is a novel concept for fatty liver disease. Different from non-alcoholic fatty liver disease (NAFLD), the diagnosis of MAFLD requires the presence of metabolic risks. This study aimed to characterize patients with liver steatosis but wit...

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Autores principales: Huang, Jiaofeng, Xue, Wenjuan, Wang, Mingfang, Wu, Yinlian, Singh, Medha, Zhu, Yueyong, Kumar, Rahul, Lin, Su
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326380/
https://www.ncbi.nlm.nih.gov/pubmed/34349535
http://dx.doi.org/10.2147/DMSO.S316096
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author Huang, Jiaofeng
Xue, Wenjuan
Wang, Mingfang
Wu, Yinlian
Singh, Medha
Zhu, Yueyong
Kumar, Rahul
Lin, Su
author_facet Huang, Jiaofeng
Xue, Wenjuan
Wang, Mingfang
Wu, Yinlian
Singh, Medha
Zhu, Yueyong
Kumar, Rahul
Lin, Su
author_sort Huang, Jiaofeng
collection PubMed
description INTRODUCTION: Metabolic associated fatty liver disease (MAFLD) is a novel concept for fatty liver disease. Different from non-alcoholic fatty liver disease (NAFLD), the diagnosis of MAFLD requires the presence of metabolic risks. This study aimed to characterize patients with liver steatosis but without metabolic risks (non-MR-steatosis) which may not be diagnosed by MAFLD criteria. METHODS: Consecutive patients who underwent biopsy were included in this study. The clinic-pathological characteristics of non-MR-steatosis, NAFLD and MAFLD were compared. RESULTS: A total of 1217 cases were included. There were 426 (35.00%) cases with MAFLD, 585 (48.07%) with NAFLD and 168 (13.80%) with non-MR-steatosis. The majority of the cases were infected with HBV (93.26%). The age and metabolic profiles were highest in MAFLD and lowest in non-MR-steatosis. The body mass index (BMI) level was also lowest in non-MR-steatosis (20.78 ± 1.54 kg/m(2)). The ALT and AST levels of the non-MR-steatosis group were not statistically different from those of MAFLD or NAFLD groups (p > 0.05). Histologically, there was no significant difference in the degrees of inflammation and fibrosis among the three groups. The severity of steatosis in non-MR-steatosis group was lower than MAFLD or NAFLD groups (p < 0.05). These results were consistent in both HBV and non-HBV subgroups. CONCLUSION: MAFLD criteria may overlook some steatotic patients without metabolic risks, who may also have steatohepatitis and significant fibrosis.
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spelling pubmed-83263802021-08-03 MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis Huang, Jiaofeng Xue, Wenjuan Wang, Mingfang Wu, Yinlian Singh, Medha Zhu, Yueyong Kumar, Rahul Lin, Su Diabetes Metab Syndr Obes Original Research INTRODUCTION: Metabolic associated fatty liver disease (MAFLD) is a novel concept for fatty liver disease. Different from non-alcoholic fatty liver disease (NAFLD), the diagnosis of MAFLD requires the presence of metabolic risks. This study aimed to characterize patients with liver steatosis but without metabolic risks (non-MR-steatosis) which may not be diagnosed by MAFLD criteria. METHODS: Consecutive patients who underwent biopsy were included in this study. The clinic-pathological characteristics of non-MR-steatosis, NAFLD and MAFLD were compared. RESULTS: A total of 1217 cases were included. There were 426 (35.00%) cases with MAFLD, 585 (48.07%) with NAFLD and 168 (13.80%) with non-MR-steatosis. The majority of the cases were infected with HBV (93.26%). The age and metabolic profiles were highest in MAFLD and lowest in non-MR-steatosis. The body mass index (BMI) level was also lowest in non-MR-steatosis (20.78 ± 1.54 kg/m(2)). The ALT and AST levels of the non-MR-steatosis group were not statistically different from those of MAFLD or NAFLD groups (p > 0.05). Histologically, there was no significant difference in the degrees of inflammation and fibrosis among the three groups. The severity of steatosis in non-MR-steatosis group was lower than MAFLD or NAFLD groups (p < 0.05). These results were consistent in both HBV and non-HBV subgroups. CONCLUSION: MAFLD criteria may overlook some steatotic patients without metabolic risks, who may also have steatohepatitis and significant fibrosis. Dove 2021-07-27 /pmc/articles/PMC8326380/ /pubmed/34349535 http://dx.doi.org/10.2147/DMSO.S316096 Text en © 2021 Huang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Huang, Jiaofeng
Xue, Wenjuan
Wang, Mingfang
Wu, Yinlian
Singh, Medha
Zhu, Yueyong
Kumar, Rahul
Lin, Su
MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title_full MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title_fullStr MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title_full_unstemmed MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title_short MAFLD Criteria May Overlook a Subtype of Patient with Steatohepatitis and Significant Fibrosis
title_sort mafld criteria may overlook a subtype of patient with steatohepatitis and significant fibrosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326380/
https://www.ncbi.nlm.nih.gov/pubmed/34349535
http://dx.doi.org/10.2147/DMSO.S316096
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