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Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease
Non-alcoholic fatty liver disease (NAFLD) is the main cause of chronic liver disease. This cross-sectional study aimed to evaluate whether parallel clinical features and serum markers are related to the severity of NAFLD. We enrolled 111 participants with different metabolic syndrome (MetS) scores (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832180/ https://www.ncbi.nlm.nih.gov/pubmed/27079922 http://dx.doi.org/10.1038/srep24031 |
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author | Shih, Kai-Lun Su, Wei-Wen Chang, Chia-Chu Kor, Chew-Teng Chou, Chen-Te Chen, Ting-Yu Wu, Hung-Ming |
author_facet | Shih, Kai-Lun Su, Wei-Wen Chang, Chia-Chu Kor, Chew-Teng Chou, Chen-Te Chen, Ting-Yu Wu, Hung-Ming |
author_sort | Shih, Kai-Lun |
collection | PubMed |
description | Non-alcoholic fatty liver disease (NAFLD) is the main cause of chronic liver disease. This cross-sectional study aimed to evaluate whether parallel clinical features and serum markers are related to the severity of NAFLD. We enrolled 111 participants with different metabolic syndrome (MetS) scores (zero, n = 22; one, n = 19; two, n = 22; and ≥ three, n = 48) and used (1)H-MRS to measure liver fat content. Biochemical profiles and potential biomarkers of NAFLD were measured in fasting plasma. We found that (1)H-MRS-measured fat content was significantly associated with MetS score ≥1, endotoxin, and hs-CRP. Ordinal logistic regression analysis revealed that MetS score ≥2 and endotoxin were predictive of NAFLD ((1)H-MRS > 5%) and that endotoxin, hs-CRP, and malondialdehyde (MDA) were predictive of NAFLD with liver injury ((1)H-MRS > 9.67%). Endotoxin plus MetS score was shown to be the most accurate predictor of overall NAFLD (AUC = 0.854; (95% CI: 0.785–0.924), P < 0.001), and endotoxin plus hs-CRP and MDA was found to be predictive of NAFLD with liver injury (0.868; (0.801–0.936), P < 0.001). These results suggest that MetS score plus certain serum biomarkers with (1)H-MRS findings may hold promise for developing an effective model for monitoring the severity of NAFLD. |
format | Online Article Text |
id | pubmed-4832180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48321802016-04-20 Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease Shih, Kai-Lun Su, Wei-Wen Chang, Chia-Chu Kor, Chew-Teng Chou, Chen-Te Chen, Ting-Yu Wu, Hung-Ming Sci Rep Article Non-alcoholic fatty liver disease (NAFLD) is the main cause of chronic liver disease. This cross-sectional study aimed to evaluate whether parallel clinical features and serum markers are related to the severity of NAFLD. We enrolled 111 participants with different metabolic syndrome (MetS) scores (zero, n = 22; one, n = 19; two, n = 22; and ≥ three, n = 48) and used (1)H-MRS to measure liver fat content. Biochemical profiles and potential biomarkers of NAFLD were measured in fasting plasma. We found that (1)H-MRS-measured fat content was significantly associated with MetS score ≥1, endotoxin, and hs-CRP. Ordinal logistic regression analysis revealed that MetS score ≥2 and endotoxin were predictive of NAFLD ((1)H-MRS > 5%) and that endotoxin, hs-CRP, and malondialdehyde (MDA) were predictive of NAFLD with liver injury ((1)H-MRS > 9.67%). Endotoxin plus MetS score was shown to be the most accurate predictor of overall NAFLD (AUC = 0.854; (95% CI: 0.785–0.924), P < 0.001), and endotoxin plus hs-CRP and MDA was found to be predictive of NAFLD with liver injury (0.868; (0.801–0.936), P < 0.001). These results suggest that MetS score plus certain serum biomarkers with (1)H-MRS findings may hold promise for developing an effective model for monitoring the severity of NAFLD. Nature Publishing Group 2016-04-15 /pmc/articles/PMC4832180/ /pubmed/27079922 http://dx.doi.org/10.1038/srep24031 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Shih, Kai-Lun Su, Wei-Wen Chang, Chia-Chu Kor, Chew-Teng Chou, Chen-Te Chen, Ting-Yu Wu, Hung-Ming Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title | Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title_full | Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title_fullStr | Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title_full_unstemmed | Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title_short | Comparisons of parallel potential biomarkers of (1)H-MRS-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
title_sort | comparisons of parallel potential biomarkers of (1)h-mrs-measured hepatic lipid content in patients with non-alcoholic fatty liver disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832180/ https://www.ncbi.nlm.nih.gov/pubmed/27079922 http://dx.doi.org/10.1038/srep24031 |
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