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The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease
Nonalcoholic fatty liver disease (NAFLD), once considered a benign condition, has been associated with several cardiometabolic complications over the past two decades. The worldwide prevalence of NAFLD is as high as 30%. NAFLD requires the absence of a “significant alcohol intake.” Conflicting repor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265351/ https://www.ncbi.nlm.nih.gov/pubmed/37323163 http://dx.doi.org/10.1177/20420188231178370 |
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author | Kulkarni, Anand V. Sarin, Shiv Kumar |
author_facet | Kulkarni, Anand V. Sarin, Shiv Kumar |
author_sort | Kulkarni, Anand V. |
collection | PubMed |
description | Nonalcoholic fatty liver disease (NAFLD), once considered a benign condition, has been associated with several cardiometabolic complications over the past two decades. The worldwide prevalence of NAFLD is as high as 30%. NAFLD requires the absence of a “significant alcohol intake.” Conflicting reports have suggested that moderate alcohol consumption may be protective; therefore, the diagnosis of NAFLD previously relied on negative criteria. However, there has been a significant increase in alcohol consumption globally. Apart from the rise in alcohol-related liver disease (ARLD), alcohol, a major toxin, is associated with an increased risk of several cancers, including hepatocellular carcinoma. Alcohol misuse is a significant contributor to disability-adjusted life years. Recently, the term metabolic dysfunction-associated fatty liver disease (MAFLD) was proposed instead of NAFLD to include the metabolic dysfunction responsible for the major adverse outcomes in patients with fatty liver disease. MAFLD, dependent on the “positive diagnostic criteria” rather than previous exclusion criteria, may identify individuals with poor metabolic health and aid in managing patients at increased risk of all-cause and cardiovascular mortality. Although MAFLD is less stigmatizing than NAFLD, excluding alcohol intake may increase the risk of already existing underreported alcohol consumption in this subgroup of patients. Therefore, alcohol consumption may increase the prevalence of fatty liver disease and its associated complications in patients with MAFLD. This review discusses the effects of alcohol intake and MAFLD on fatty liver disease. |
format | Online Article Text |
id | pubmed-10265351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-102653512023-06-15 The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease Kulkarni, Anand V. Sarin, Shiv Kumar Ther Adv Endocrinol Metab New Insights in MAFLD Nonalcoholic fatty liver disease (NAFLD), once considered a benign condition, has been associated with several cardiometabolic complications over the past two decades. The worldwide prevalence of NAFLD is as high as 30%. NAFLD requires the absence of a “significant alcohol intake.” Conflicting reports have suggested that moderate alcohol consumption may be protective; therefore, the diagnosis of NAFLD previously relied on negative criteria. However, there has been a significant increase in alcohol consumption globally. Apart from the rise in alcohol-related liver disease (ARLD), alcohol, a major toxin, is associated with an increased risk of several cancers, including hepatocellular carcinoma. Alcohol misuse is a significant contributor to disability-adjusted life years. Recently, the term metabolic dysfunction-associated fatty liver disease (MAFLD) was proposed instead of NAFLD to include the metabolic dysfunction responsible for the major adverse outcomes in patients with fatty liver disease. MAFLD, dependent on the “positive diagnostic criteria” rather than previous exclusion criteria, may identify individuals with poor metabolic health and aid in managing patients at increased risk of all-cause and cardiovascular mortality. Although MAFLD is less stigmatizing than NAFLD, excluding alcohol intake may increase the risk of already existing underreported alcohol consumption in this subgroup of patients. Therefore, alcohol consumption may increase the prevalence of fatty liver disease and its associated complications in patients with MAFLD. This review discusses the effects of alcohol intake and MAFLD on fatty liver disease. SAGE Publications 2023-06-05 /pmc/articles/PMC10265351/ /pubmed/37323163 http://dx.doi.org/10.1177/20420188231178370 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | New Insights in MAFLD Kulkarni, Anand V. Sarin, Shiv Kumar The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title | The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title_full | The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title_fullStr | The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title_full_unstemmed | The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title_short | The bidirectional impacts of alcohol consumption and MAFLD for progressive fatty liver disease |
title_sort | bidirectional impacts of alcohol consumption and mafld for progressive fatty liver disease |
topic | New Insights in MAFLD |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265351/ https://www.ncbi.nlm.nih.gov/pubmed/37323163 http://dx.doi.org/10.1177/20420188231178370 |
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