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Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients

This study investigated differences in lipidomic profile features in nonalcoholic steatohepatitis (NASH) between mild and significant liver fibrosis cases among patients with morbid obesity. Wedge liver biopsy was performed during sleeve gastrectomy and significant liver fibrosis was defined as a fi...

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Autores principales: Wu, Hua-Chien, Hsieh, Yin-Ru, Wang, Weu, Chang, Ching-Wen, Chang, I-Wei, Chen, Chi-Long, Chang, Chun-Chao, Chang, Chia-Hsuan, Kao, Wei-Yu, Huang, Shih-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253728/
https://www.ncbi.nlm.nih.gov/pubmed/37297926
http://dx.doi.org/10.3390/jcm12113730
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author Wu, Hua-Chien
Hsieh, Yin-Ru
Wang, Weu
Chang, Ching-Wen
Chang, I-Wei
Chen, Chi-Long
Chang, Chun-Chao
Chang, Chia-Hsuan
Kao, Wei-Yu
Huang, Shih-Yi
author_facet Wu, Hua-Chien
Hsieh, Yin-Ru
Wang, Weu
Chang, Ching-Wen
Chang, I-Wei
Chen, Chi-Long
Chang, Chun-Chao
Chang, Chia-Hsuan
Kao, Wei-Yu
Huang, Shih-Yi
author_sort Wu, Hua-Chien
collection PubMed
description This study investigated differences in lipidomic profile features in nonalcoholic steatohepatitis (NASH) between mild and significant liver fibrosis cases among patients with morbid obesity. Wedge liver biopsy was performed during sleeve gastrectomy and significant liver fibrosis was defined as a fibrosis score ≥ 2. We selected patients with NASH with non/mild fibrosis (stage F0–F1; n = 30) and NASH with significant fibrosis (stage F2–F4; n = 30). The results of the liver tissue lipidomic analysis revealed that the fold changes of triglyceride (TG) (52:6); cholesterol ester (CE) (20:1); phosphatidylcholine (PC) (38:0) and (50:8); phosphatidic acid (PA) (40:4); phosphatidylinositol (PI) (49:4); phosphatidylglycerol (PG) (40:2); and sphingomyelin (SM) (35:0) and (37:0) were significantly lower in patients with NASH with F2–F4 than those with NASH with F0–F1 (p < 0.05). However, the fold changes of PC (42:4) were relatively higher in patients with NASH with stage 2–4 fibrosis (p < 0.05). Moreover, predictive models incorporating serum markers levels, ultrasonographic studies, and levels of specific lipid components [PC (42:4) and PG (40:2)] yielded the highest area under receiver operating curve (0.941), suggesting a potential correlation between NASH fibrosis stages and liver lipid accumulation among specific lipid species subclasses. This study demonstrated that the concentrations of particular lipid species in the liver correlate with NASH fibrosis stages and may indicate hepatic steatosis regression or progression in patients with morbid obesity.
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spelling pubmed-102537282023-06-10 Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients Wu, Hua-Chien Hsieh, Yin-Ru Wang, Weu Chang, Ching-Wen Chang, I-Wei Chen, Chi-Long Chang, Chun-Chao Chang, Chia-Hsuan Kao, Wei-Yu Huang, Shih-Yi J Clin Med Article This study investigated differences in lipidomic profile features in nonalcoholic steatohepatitis (NASH) between mild and significant liver fibrosis cases among patients with morbid obesity. Wedge liver biopsy was performed during sleeve gastrectomy and significant liver fibrosis was defined as a fibrosis score ≥ 2. We selected patients with NASH with non/mild fibrosis (stage F0–F1; n = 30) and NASH with significant fibrosis (stage F2–F4; n = 30). The results of the liver tissue lipidomic analysis revealed that the fold changes of triglyceride (TG) (52:6); cholesterol ester (CE) (20:1); phosphatidylcholine (PC) (38:0) and (50:8); phosphatidic acid (PA) (40:4); phosphatidylinositol (PI) (49:4); phosphatidylglycerol (PG) (40:2); and sphingomyelin (SM) (35:0) and (37:0) were significantly lower in patients with NASH with F2–F4 than those with NASH with F0–F1 (p < 0.05). However, the fold changes of PC (42:4) were relatively higher in patients with NASH with stage 2–4 fibrosis (p < 0.05). Moreover, predictive models incorporating serum markers levels, ultrasonographic studies, and levels of specific lipid components [PC (42:4) and PG (40:2)] yielded the highest area under receiver operating curve (0.941), suggesting a potential correlation between NASH fibrosis stages and liver lipid accumulation among specific lipid species subclasses. This study demonstrated that the concentrations of particular lipid species in the liver correlate with NASH fibrosis stages and may indicate hepatic steatosis regression or progression in patients with morbid obesity. MDPI 2023-05-29 /pmc/articles/PMC10253728/ /pubmed/37297926 http://dx.doi.org/10.3390/jcm12113730 Text en © 2023 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
Wu, Hua-Chien
Hsieh, Yin-Ru
Wang, Weu
Chang, Ching-Wen
Chang, I-Wei
Chen, Chi-Long
Chang, Chun-Chao
Chang, Chia-Hsuan
Kao, Wei-Yu
Huang, Shih-Yi
Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title_full Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title_fullStr Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title_full_unstemmed Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title_short Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients
title_sort potential hepatic lipid markers associated with nonalcoholic steatohepatitis and fibrosis in morbid obesity patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253728/
https://www.ncbi.nlm.nih.gov/pubmed/37297926
http://dx.doi.org/10.3390/jcm12113730
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