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LC/MS-Based Untargeted Metabolomics Study in Women with Nonalcoholic Steatohepatitis Associated with Morbid Obesity

Authors :
Universitat Rovira i Virgili
Bertran, L; Capellades, J; Abelló, S; Durán-Bertran, J; Aguilar, C; Martinez, S; Sabench, F; Correig, X; Yanes, O; Auguet, T; Richart, C
Universitat Rovira i Virgili
Bertran, L; Capellades, J; Abelló, S; Durán-Bertran, J; Aguilar, C; Martinez, S; Sabench, F; Correig, X; Yanes, O; Auguet, T; Richart, C
Source :
International Journal Of Molecular Sciences; 10.3390/ijms24129789; International Journal Of Molecular Sciences. 24 (12):
Publication Year :
2023

Abstract

This study investigated the importance of a metabolomic analysis in a complex disease such as nonalcoholic steatohepatitis (NASH) associated with obesity. Using an untargeted metabolomics technique, we studied blood metabolites in 216 morbidly obese women with liver histological diagnosis. A total of 172 patients were diagnosed with nonalcoholic fatty liver disease (NAFLD), and 44 were diagnosed with normal liver (NL). Patients with NAFLD were classified into simple steatosis (n = 66) and NASH (n = 106) categories. A comparative analysis of metabolites levels between NASH and NL demonstrated significant differences in lipid metabolites and derivatives, mainly from the phospholipid group. In NASH, there were increased levels of several phosphatidylinositols and phosphatidylethanolamines, as well as isolated metabolites such as diacylglycerol 34:1, lyso-phosphatidylethanolamine 20:3 and sphingomyelin 38:1. By contrast, there were decreased levels of acylcarnitines, sphingomyelins and linoleic acid. These findings may facilitate identification studies of the main pathogenic metabolic pathways related to NASH and may also have a possible applicability in a panel of metabolites to be used as biomarkers in future algorithms of the disease diagnosis and its follow-up. Further confirmatory studies in groups with different ages and sexes are necessary.

Details

Database :
OAIster
Journal :
International Journal Of Molecular Sciences; 10.3390/ijms24129789; International Journal Of Molecular Sciences. 24 (12):
Publication Type :
Electronic Resource
Accession number :
edsoai.on1443596831
Document Type :
Electronic Resource