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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
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.
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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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