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Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver
Adipose tissue and skeletal muscle is associated with non-alcoholic fatty liver disease (NAFLD). This study evaluates the association between body composition and histologic severity in patients with NAFLD. Using the cross-sectional CT images at the level of L3 vertebra and the histologic findings o...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227703/ https://www.ncbi.nlm.nih.gov/pubmed/34207587 http://dx.doi.org/10.3390/diagnostics11061061 |
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author | Kang, Min-Kyu Baek, Jung-Hun Kweon, Young-Oh Tak, Won-Young Jang, Se-Young Lee, Yu-Rim Hur, Keun Kim, Gyeonghwa Lee, Hye-Won Han, Man-Hoon Choi, Joon-Hyuk Park, Soo-Young Park, Jung-Gil |
author_facet | Kang, Min-Kyu Baek, Jung-Hun Kweon, Young-Oh Tak, Won-Young Jang, Se-Young Lee, Yu-Rim Hur, Keun Kim, Gyeonghwa Lee, Hye-Won Han, Man-Hoon Choi, Joon-Hyuk Park, Soo-Young Park, Jung-Gil |
author_sort | Kang, Min-Kyu |
collection | PubMed |
description | Adipose tissue and skeletal muscle is associated with non-alcoholic fatty liver disease (NAFLD). This study evaluates the association between body composition and histologic severity in patients with NAFLD. Using the cross-sectional CT images at the level of L3 vertebra and the histologic findings of 178 patients with biopsy-proven NAFLD, we analyzed the correlation of the histologic findings to the skeletal muscle index (SMI), subcutaneous adipose tissue index (SATI), and visceral adipose tissue index (VATI), which is defined as the body composition area (cm(2)) by height squared (m(2)). The clinical and laboratory features with body composition were analyzed to determine the risk factors for advanced fibrosis. The VATI significantly increased in severe non-alcoholic steatohepatitis (NASH) or advanced fibrosis. In addition, the VATI was correlated with the NAFLD activity score (NAS) and the fibrosis stage. In multivariate analyses, age (odds ratio (OR), 1.09; 95% confidence interval (CI), 1.02–1.19; p = 0.025), severe NASH (OR, 8.66; 95% CI, 2.13–46.40; p = 0.005), and visceral adiposity (OR, 6.77; 95% CI, 1.81–29.90; p = 0.007) were independently associated with advanced fibrosis in patients with NAFLD. Visceral adiposity is correlated with the histologic severity of NAFLD, which is independently associated with advanced fibrosis. |
format | Online Article Text |
id | pubmed-8227703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82277032021-06-26 Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver Kang, Min-Kyu Baek, Jung-Hun Kweon, Young-Oh Tak, Won-Young Jang, Se-Young Lee, Yu-Rim Hur, Keun Kim, Gyeonghwa Lee, Hye-Won Han, Man-Hoon Choi, Joon-Hyuk Park, Soo-Young Park, Jung-Gil Diagnostics (Basel) Article Adipose tissue and skeletal muscle is associated with non-alcoholic fatty liver disease (NAFLD). This study evaluates the association between body composition and histologic severity in patients with NAFLD. Using the cross-sectional CT images at the level of L3 vertebra and the histologic findings of 178 patients with biopsy-proven NAFLD, we analyzed the correlation of the histologic findings to the skeletal muscle index (SMI), subcutaneous adipose tissue index (SATI), and visceral adipose tissue index (VATI), which is defined as the body composition area (cm(2)) by height squared (m(2)). The clinical and laboratory features with body composition were analyzed to determine the risk factors for advanced fibrosis. The VATI significantly increased in severe non-alcoholic steatohepatitis (NASH) or advanced fibrosis. In addition, the VATI was correlated with the NAFLD activity score (NAS) and the fibrosis stage. In multivariate analyses, age (odds ratio (OR), 1.09; 95% confidence interval (CI), 1.02–1.19; p = 0.025), severe NASH (OR, 8.66; 95% CI, 2.13–46.40; p = 0.005), and visceral adiposity (OR, 6.77; 95% CI, 1.81–29.90; p = 0.007) were independently associated with advanced fibrosis in patients with NAFLD. Visceral adiposity is correlated with the histologic severity of NAFLD, which is independently associated with advanced fibrosis. MDPI 2021-06-09 /pmc/articles/PMC8227703/ /pubmed/34207587 http://dx.doi.org/10.3390/diagnostics11061061 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kang, Min-Kyu Baek, Jung-Hun Kweon, Young-Oh Tak, Won-Young Jang, Se-Young Lee, Yu-Rim Hur, Keun Kim, Gyeonghwa Lee, Hye-Won Han, Man-Hoon Choi, Joon-Hyuk Park, Soo-Young Park, Jung-Gil Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title | Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title_full | Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title_fullStr | Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title_full_unstemmed | Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title_short | Association of Skeletal Muscle and Adipose Tissue Distribution with Histologic Severity of Non-Alcoholic Fatty Liver |
title_sort | association of skeletal muscle and adipose tissue distribution with histologic severity of non-alcoholic fatty liver |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227703/ https://www.ncbi.nlm.nih.gov/pubmed/34207587 http://dx.doi.org/10.3390/diagnostics11061061 |
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