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Hepatic Fibrosis and Steatosis in Metabolic Syndrome
BACKGROUND: Metabolic syndrome (MetS) is a group of factors associated with increased risks of cardiovascular disease and overall mortality. Nonalcoholic fatty liver disease (NAFLD) is a common disorder that has been shown to cause hepatic steatosis and fibrosis. The relationship between NAFLD and M...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for the Study of Obesity
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987451/ https://www.ncbi.nlm.nih.gov/pubmed/35283365 http://dx.doi.org/10.7570/jomes21062 |
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author | Gangireddy, Venu Gopala Reddy Pilkerton, Courtney Xiang, Jun Tinajero, Ruben Ashcraft, Amie M. |
author_facet | Gangireddy, Venu Gopala Reddy Pilkerton, Courtney Xiang, Jun Tinajero, Ruben Ashcraft, Amie M. |
author_sort | Gangireddy, Venu Gopala Reddy |
collection | PubMed |
description | BACKGROUND: Metabolic syndrome (MetS) is a group of factors associated with increased risks of cardiovascular disease and overall mortality. Nonalcoholic fatty liver disease (NAFLD) is a common disorder that has been shown to cause hepatic steatosis and fibrosis. The relationship between NAFLD and MetS appears to be bidirectional, but very few studies have examined the role of MetS in hepatic steatosis and fibrosis. The present study investigated the relationships between MetS and its components and the severity of hepatic fibrosis and steatosis, and fibrosis independent of steatosis. METHODS: The study was a cross-sectional population-based survey of 4,678 National Health and Nutrition Examination Survey participants from 2017 to 2018 in the United States. Hepatic fibrosis and steatosis were measured using liver elastography. The MetS components were assessed using demographic, examination, laboratory, and self-reported data. RESULTS: Using survey-weighted population estimates, 26% of the population had steatosis, 7.5% had fibrosis, and 3.3% had fibrosis without steatosis. The adjusted odds ratio for any level of steatosis was 4.12 times higher (95% confidence interval [CI], 3.16–5.37) and any level of fibrosis was 3.34 times higher (95% CI, 2.26–4.94) among participants with MetS than those without. The adjusted odds ratio for fibrosis without steatosis is 2.67 times higher (95% CI, 1.47–4.87) among participants with MetS than those without. CONCLUSION: The presence of MetS significantly increases the risk of hepatic fibrosis and steatosis, providing evidence for MetS to be considered an additional independent risk factor for hepatic fibrosis together with other known etiologies. |
format | Online Article Text |
id | pubmed-8987451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Society for the Study of Obesity |
record_format | MEDLINE/PubMed |
spelling | pubmed-89874512022-04-13 Hepatic Fibrosis and Steatosis in Metabolic Syndrome Gangireddy, Venu Gopala Reddy Pilkerton, Courtney Xiang, Jun Tinajero, Ruben Ashcraft, Amie M. J Obes Metab Syndr Original Article BACKGROUND: Metabolic syndrome (MetS) is a group of factors associated with increased risks of cardiovascular disease and overall mortality. Nonalcoholic fatty liver disease (NAFLD) is a common disorder that has been shown to cause hepatic steatosis and fibrosis. The relationship between NAFLD and MetS appears to be bidirectional, but very few studies have examined the role of MetS in hepatic steatosis and fibrosis. The present study investigated the relationships between MetS and its components and the severity of hepatic fibrosis and steatosis, and fibrosis independent of steatosis. METHODS: The study was a cross-sectional population-based survey of 4,678 National Health and Nutrition Examination Survey participants from 2017 to 2018 in the United States. Hepatic fibrosis and steatosis were measured using liver elastography. The MetS components were assessed using demographic, examination, laboratory, and self-reported data. RESULTS: Using survey-weighted population estimates, 26% of the population had steatosis, 7.5% had fibrosis, and 3.3% had fibrosis without steatosis. The adjusted odds ratio for any level of steatosis was 4.12 times higher (95% confidence interval [CI], 3.16–5.37) and any level of fibrosis was 3.34 times higher (95% CI, 2.26–4.94) among participants with MetS than those without. The adjusted odds ratio for fibrosis without steatosis is 2.67 times higher (95% CI, 1.47–4.87) among participants with MetS than those without. CONCLUSION: The presence of MetS significantly increases the risk of hepatic fibrosis and steatosis, providing evidence for MetS to be considered an additional independent risk factor for hepatic fibrosis together with other known etiologies. Korean Society for the Study of Obesity 2022-03-30 2022-03-14 /pmc/articles/PMC8987451/ /pubmed/35283365 http://dx.doi.org/10.7570/jomes21062 Text en Copyright © 2022 Korean Society for the Study of Obesity https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Gangireddy, Venu Gopala Reddy Pilkerton, Courtney Xiang, Jun Tinajero, Ruben Ashcraft, Amie M. Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title | Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title_full | Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title_fullStr | Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title_full_unstemmed | Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title_short | Hepatic Fibrosis and Steatosis in Metabolic Syndrome |
title_sort | hepatic fibrosis and steatosis in metabolic syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987451/ https://www.ncbi.nlm.nih.gov/pubmed/35283365 http://dx.doi.org/10.7570/jomes21062 |
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