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Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD

Background and aims: Non-alcoholic fatty liver disease (NAFLD) associates with low levels of serum plant sterols in cross-sectional studies. In addition, it has been suggested that the hepatic sterol transport mechanisms are altered in NAFLD. Therefore, we investigated the association between serum,...

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Autores principales: Tauriainen, Milla-Maria, Männistö, Ville, Kaminska, Dorota, Vaittinen, Maija, Kärjä, Vesa, Käkelä, Pirjo, Venesmaa, Sari, Gylling, Helena, Pihlajamäki, Jussi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968183/
https://www.ncbi.nlm.nih.gov/pubmed/29540533
http://dx.doi.org/10.1042/BSR20171274
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author Tauriainen, Milla-Maria
Männistö, Ville
Kaminska, Dorota
Vaittinen, Maija
Kärjä, Vesa
Käkelä, Pirjo
Venesmaa, Sari
Gylling, Helena
Pihlajamäki, Jussi
author_facet Tauriainen, Milla-Maria
Männistö, Ville
Kaminska, Dorota
Vaittinen, Maija
Kärjä, Vesa
Käkelä, Pirjo
Venesmaa, Sari
Gylling, Helena
Pihlajamäki, Jussi
author_sort Tauriainen, Milla-Maria
collection PubMed
description Background and aims: Non-alcoholic fatty liver disease (NAFLD) associates with low levels of serum plant sterols in cross-sectional studies. In addition, it has been suggested that the hepatic sterol transport mechanisms are altered in NAFLD. Therefore, we investigated the association between serum, liver and bile plant sterols and sitostanol with NAFLD. Methods: Out of the 138 individuals (age: 46.3 ± 8.9, body mass index: 43.3 ± 6.9 kg/m², 28% men and 72% women), 44 could be histologically categorized to have normal liver, and 94 to have NAFLD. Within the NAFLD group, 28 had simple steatosis and 27 had non-alcoholic steatohepatitis. Plant sterols and sitostanol were measured from serum (n=138), liver (n=38), and bile (n=41). The mRNA expression of genes regulating liver sterol metabolism and inflammation was measured (n=102). Results: Liver and bile sitostanol ratios to cholesterol were higher in those with NAFLD compared to those with histologically normal liver (all P<0.022). Furthermore, liver sitostanol to cholesterol ratio correlated positively with histological steatosis and lobular inflammation (r(s) > 0.407, P<0.01 for both). In contrast, liver sitosterol to cholesterol ratio correlated negatively with steatosis (r(s) = −0.392, P=0.015) and lobular inflammation (r(s) = −0.395, P=0.014). Transcriptomics analysis revealed suggestive correlations between serum plant sterol levels and mRNA expression. Conclusion: Our study showed that liver and bile sitostanol ratios to cholesterol associated positively and liver sitosterol ratio to cholesterol associated negatively with liver steatosis and inflammation in obese individuals with NAFLD..
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spelling pubmed-59681832018-06-12 Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD Tauriainen, Milla-Maria Männistö, Ville Kaminska, Dorota Vaittinen, Maija Kärjä, Vesa Käkelä, Pirjo Venesmaa, Sari Gylling, Helena Pihlajamäki, Jussi Biosci Rep Research Articles Background and aims: Non-alcoholic fatty liver disease (NAFLD) associates with low levels of serum plant sterols in cross-sectional studies. In addition, it has been suggested that the hepatic sterol transport mechanisms are altered in NAFLD. Therefore, we investigated the association between serum, liver and bile plant sterols and sitostanol with NAFLD. Methods: Out of the 138 individuals (age: 46.3 ± 8.9, body mass index: 43.3 ± 6.9 kg/m², 28% men and 72% women), 44 could be histologically categorized to have normal liver, and 94 to have NAFLD. Within the NAFLD group, 28 had simple steatosis and 27 had non-alcoholic steatohepatitis. Plant sterols and sitostanol were measured from serum (n=138), liver (n=38), and bile (n=41). The mRNA expression of genes regulating liver sterol metabolism and inflammation was measured (n=102). Results: Liver and bile sitostanol ratios to cholesterol were higher in those with NAFLD compared to those with histologically normal liver (all P<0.022). Furthermore, liver sitostanol to cholesterol ratio correlated positively with histological steatosis and lobular inflammation (r(s) > 0.407, P<0.01 for both). In contrast, liver sitosterol to cholesterol ratio correlated negatively with steatosis (r(s) = −0.392, P=0.015) and lobular inflammation (r(s) = −0.395, P=0.014). Transcriptomics analysis revealed suggestive correlations between serum plant sterol levels and mRNA expression. Conclusion: Our study showed that liver and bile sitostanol ratios to cholesterol associated positively and liver sitosterol ratio to cholesterol associated negatively with liver steatosis and inflammation in obese individuals with NAFLD.. Portland Press Ltd. 2018-04-20 /pmc/articles/PMC5968183/ /pubmed/29540533 http://dx.doi.org/10.1042/BSR20171274 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Tauriainen, Milla-Maria
Männistö, Ville
Kaminska, Dorota
Vaittinen, Maija
Kärjä, Vesa
Käkelä, Pirjo
Venesmaa, Sari
Gylling, Helena
Pihlajamäki, Jussi
Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title_full Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title_fullStr Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title_full_unstemmed Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title_short Serum, liver and bile sitosterol and sitostanol in obese patients with and without NAFLD
title_sort serum, liver and bile sitosterol and sitostanol in obese patients with and without nafld
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968183/
https://www.ncbi.nlm.nih.gov/pubmed/29540533
http://dx.doi.org/10.1042/BSR20171274
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