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Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population
INTRODUCTION: The prevalence of non-alcoholic fatty liver disease (NAFLD) in non-lean patients is significantly increased, and obesity significantly increases the risk of cirrhosis and HCC in NAFLD patients. However, whether there is a difference in clinical manifestations of NAFLD between overweigh...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601616/ https://www.ncbi.nlm.nih.gov/pubmed/37231905 http://dx.doi.org/10.1159/000530845 |
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author | Li, Min-ran Li, Jin-zhong Li, Jie-ying Wang, Cun-chuan Yuan, Rui-kun Ye, Li-hong Liu, Yun-yan Liang, Xu-jing Zhang, Hai-cong Liu, Zhi-quan Zeng, Dong-yu Zhang, Xue-dong Wang, De-hua Li, Jun-qing Li, Tao-yuan Yang, Liu Cao, Yang Pan, Yun Lin, Xun-ge Pan, Calvin Q. Dai, Er-hei Dong, Zhi-yong |
author_facet | Li, Min-ran Li, Jin-zhong Li, Jie-ying Wang, Cun-chuan Yuan, Rui-kun Ye, Li-hong Liu, Yun-yan Liang, Xu-jing Zhang, Hai-cong Liu, Zhi-quan Zeng, Dong-yu Zhang, Xue-dong Wang, De-hua Li, Jun-qing Li, Tao-yuan Yang, Liu Cao, Yang Pan, Yun Lin, Xun-ge Pan, Calvin Q. Dai, Er-hei Dong, Zhi-yong |
author_sort | Li, Min-ran |
collection | PubMed |
description | INTRODUCTION: The prevalence of non-alcoholic fatty liver disease (NAFLD) in non-lean patients is significantly increased, and obesity significantly increases the risk of cirrhosis and HCC in NAFLD patients. However, whether there is a difference in clinical manifestations of NAFLD between overweight and obesity remains unclear. The objective of this study was to assess the clinical and histological features of NAFLD among a non-lean population. METHODS: Current study enrolled consecutive non-lean (body mass index [BMI] >23 kg/m(2)) patients with NAFLD and available liver biopsy results. Patients were stratified by BMI into two groups for the comparison of their clinical and histological variables, which included the overweight (BMI 23∼<28 kg/m(2)) and the obese (BMI ≥28 kg/m(2)). Risk factors for moderate to severe fibrosis (stage >1) were also analyzed through the logistic regression model. RESULTS: Among 184 non-lean patients with metabolic-associated fatty liver disease enrolled, 65 and 119 were overweight and obese, respectively. Patients in the obesity group had a significantly lower level of gamma-glutamyl transpeptidase, higher levels of platelet, glucose, prothrombin time, and more common of moderate to severe inflammatory activity when compared to those in the overweight group. However, a significant low frequency of moderate to severe fibrosis was found in the obesity group versus the overweight group (19.33% vs. 40.00%, p = 0.002). Binary logistics regression analysis of fibrosis found that aspartate transaminase (AST), BMI, alanine transaminase (ALT), and cholesterol (CHOL) were independent predictors for moderate to severe fibrosis in non-lean patients with NAFLD. Compared with the traditional fibrosis-4 (AUC = 0.77) and aminotransferase to platelet ratio index (AUC = 0.79) indexes, the combined index based on AST, BMI, ALT, and CHOL was more accurate in predicting moderate to severe fibrosis in non-lean patients with NAFLD (AUC = 0.87). CONCLUSIONS: Clinical and histological features differed between obesity and overweight patients with NAFLD. When compared to the traditional serum markers, the combination index including AST, BMI, ALT, and CHOL provided a better model to predict moderate to severe fibrosis in non-lean patients with NAFLD. |
format | Online Article Text |
id | pubmed-10601616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106016162023-10-27 Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population Li, Min-ran Li, Jin-zhong Li, Jie-ying Wang, Cun-chuan Yuan, Rui-kun Ye, Li-hong Liu, Yun-yan Liang, Xu-jing Zhang, Hai-cong Liu, Zhi-quan Zeng, Dong-yu Zhang, Xue-dong Wang, De-hua Li, Jun-qing Li, Tao-yuan Yang, Liu Cao, Yang Pan, Yun Lin, Xun-ge Pan, Calvin Q. Dai, Er-hei Dong, Zhi-yong Obes Facts Research Article INTRODUCTION: The prevalence of non-alcoholic fatty liver disease (NAFLD) in non-lean patients is significantly increased, and obesity significantly increases the risk of cirrhosis and HCC in NAFLD patients. However, whether there is a difference in clinical manifestations of NAFLD between overweight and obesity remains unclear. The objective of this study was to assess the clinical and histological features of NAFLD among a non-lean population. METHODS: Current study enrolled consecutive non-lean (body mass index [BMI] >23 kg/m(2)) patients with NAFLD and available liver biopsy results. Patients were stratified by BMI into two groups for the comparison of their clinical and histological variables, which included the overweight (BMI 23∼<28 kg/m(2)) and the obese (BMI ≥28 kg/m(2)). Risk factors for moderate to severe fibrosis (stage >1) were also analyzed through the logistic regression model. RESULTS: Among 184 non-lean patients with metabolic-associated fatty liver disease enrolled, 65 and 119 were overweight and obese, respectively. Patients in the obesity group had a significantly lower level of gamma-glutamyl transpeptidase, higher levels of platelet, glucose, prothrombin time, and more common of moderate to severe inflammatory activity when compared to those in the overweight group. However, a significant low frequency of moderate to severe fibrosis was found in the obesity group versus the overweight group (19.33% vs. 40.00%, p = 0.002). Binary logistics regression analysis of fibrosis found that aspartate transaminase (AST), BMI, alanine transaminase (ALT), and cholesterol (CHOL) were independent predictors for moderate to severe fibrosis in non-lean patients with NAFLD. Compared with the traditional fibrosis-4 (AUC = 0.77) and aminotransferase to platelet ratio index (AUC = 0.79) indexes, the combined index based on AST, BMI, ALT, and CHOL was more accurate in predicting moderate to severe fibrosis in non-lean patients with NAFLD (AUC = 0.87). CONCLUSIONS: Clinical and histological features differed between obesity and overweight patients with NAFLD. When compared to the traditional serum markers, the combination index including AST, BMI, ALT, and CHOL provided a better model to predict moderate to severe fibrosis in non-lean patients with NAFLD. S. Karger AG 2023-05-22 /pmc/articles/PMC10601616/ /pubmed/37231905 http://dx.doi.org/10.1159/000530845 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Research Article Li, Min-ran Li, Jin-zhong Li, Jie-ying Wang, Cun-chuan Yuan, Rui-kun Ye, Li-hong Liu, Yun-yan Liang, Xu-jing Zhang, Hai-cong Liu, Zhi-quan Zeng, Dong-yu Zhang, Xue-dong Wang, De-hua Li, Jun-qing Li, Tao-yuan Yang, Liu Cao, Yang Pan, Yun Lin, Xun-ge Pan, Calvin Q. Dai, Er-hei Dong, Zhi-yong Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title | Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title_full | Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title_fullStr | Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title_full_unstemmed | Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title_short | Clinical Features of Non-Alcoholic Fatty Liver Disease in the Non-Lean Population |
title_sort | clinical features of non-alcoholic fatty liver disease in the non-lean population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601616/ https://www.ncbi.nlm.nih.gov/pubmed/37231905 http://dx.doi.org/10.1159/000530845 |
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