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Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia
Objectives. Nonalcoholic fatty liver disease (NAFLD) and hyperlipidemia (HL) are common metabolic disorders due to overnutrition and obesity. NAFLD is often associated with hyperlipidemia. The aim of this study was to identify and compare the erythrocyte membrane lipids profile in NAFLD patients wit...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519187/ https://www.ncbi.nlm.nih.gov/pubmed/33014047 http://dx.doi.org/10.1155/2020/9501826 |
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author | Chen, Wenbin Shao, Shanshan Cai, Hu Han, Jie Guo, Tian Fu, Yilin Yu, Chunxiao Zhao, Meng Bo, Tao Yao, Zhenyu Zhao, Jiajun Zhang, Qunye Xu, Guowang Hu, Chunxiu Gao, Ling |
author_facet | Chen, Wenbin Shao, Shanshan Cai, Hu Han, Jie Guo, Tian Fu, Yilin Yu, Chunxiao Zhao, Meng Bo, Tao Yao, Zhenyu Zhao, Jiajun Zhang, Qunye Xu, Guowang Hu, Chunxiu Gao, Ling |
author_sort | Chen, Wenbin |
collection | PubMed |
description | Objectives. Nonalcoholic fatty liver disease (NAFLD) and hyperlipidemia (HL) are common metabolic disorders due to overnutrition and obesity. NAFLD is often associated with hyperlipidemia. The aim of this study was to identify and compare the erythrocyte membrane lipids profile in NAFLD patients with or without HL. Methods. A total of 112 subjects (with similar age and body mass index) were divided into four groups: (1) normal controls, (2) NAFLD alone, (3) HL alone, and (4) NAFLD combined with HL (NAFLD + HL). Lipid was extracted from the erythrocyte membrane, and lipid profiles of subjects were analyzed by liquid chromatography mass spectrometry (LC-MS). Results. Data sets from 103 subjects were adopted for lipidomic analysis. Significant changes of lipid species were observed in patient groups, especially in the HL group and NAFLD + HL group. The HL group showed increased level of most lipid species, and decreased level of most lipid species was observed in the NAFLD + HL group. The weight percent of myristic acid, stearic acid, erucic acid, and docosahexaenoic acid also showed distinct variation between different groups. Conclusions. NAFLD, HL, and NAFLD + HL all had an impact on lipid profiling of the erythrocyte membrane. The influence of NAFLD alone is less important compared with HL. Some lipids should be highlighted because of their specific role in cell function and systemic metabolism. |
format | Online Article Text |
id | pubmed-7519187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-75191872020-10-02 Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia Chen, Wenbin Shao, Shanshan Cai, Hu Han, Jie Guo, Tian Fu, Yilin Yu, Chunxiao Zhao, Meng Bo, Tao Yao, Zhenyu Zhao, Jiajun Zhang, Qunye Xu, Guowang Hu, Chunxiu Gao, Ling Int J Endocrinol Research Article Objectives. Nonalcoholic fatty liver disease (NAFLD) and hyperlipidemia (HL) are common metabolic disorders due to overnutrition and obesity. NAFLD is often associated with hyperlipidemia. The aim of this study was to identify and compare the erythrocyte membrane lipids profile in NAFLD patients with or without HL. Methods. A total of 112 subjects (with similar age and body mass index) were divided into four groups: (1) normal controls, (2) NAFLD alone, (3) HL alone, and (4) NAFLD combined with HL (NAFLD + HL). Lipid was extracted from the erythrocyte membrane, and lipid profiles of subjects were analyzed by liquid chromatography mass spectrometry (LC-MS). Results. Data sets from 103 subjects were adopted for lipidomic analysis. Significant changes of lipid species were observed in patient groups, especially in the HL group and NAFLD + HL group. The HL group showed increased level of most lipid species, and decreased level of most lipid species was observed in the NAFLD + HL group. The weight percent of myristic acid, stearic acid, erucic acid, and docosahexaenoic acid also showed distinct variation between different groups. Conclusions. NAFLD, HL, and NAFLD + HL all had an impact on lipid profiling of the erythrocyte membrane. The influence of NAFLD alone is less important compared with HL. Some lipids should be highlighted because of their specific role in cell function and systemic metabolism. Hindawi 2020-09-16 /pmc/articles/PMC7519187/ /pubmed/33014047 http://dx.doi.org/10.1155/2020/9501826 Text en Copyright © 2020 Wenbin Chen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Wenbin Shao, Shanshan Cai, Hu Han, Jie Guo, Tian Fu, Yilin Yu, Chunxiao Zhao, Meng Bo, Tao Yao, Zhenyu Zhao, Jiajun Zhang, Qunye Xu, Guowang Hu, Chunxiu Gao, Ling Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title | Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title_full | Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title_fullStr | Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title_full_unstemmed | Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title_short | Comparison of Erythrocyte Membrane Lipid Profiles between NAFLD Patients with or without Hyperlipidemia |
title_sort | comparison of erythrocyte membrane lipid profiles between nafld patients with or without hyperlipidemia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519187/ https://www.ncbi.nlm.nih.gov/pubmed/33014047 http://dx.doi.org/10.1155/2020/9501826 |
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