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The positive correlations of apolipoprotein E with disease activity and related cytokines in systemic lupus erythematosus
BACKGROUND: The aim of this study is to investigate the expression of apolipoprotein E (apoE) and the relationship between apoE and disease activity of SLE, and the possible effects of glucocorticoid on apoE and other cytokines activities in SLE patients. METHODS: Forty treatment-naïve SLE patients...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231472/ https://www.ncbi.nlm.nih.gov/pubmed/24144108 http://dx.doi.org/10.1186/1746-1596-8-175 |
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author | Song, Li-jun Liu, Wei-wei Fan, Yu-chen Qiu, Feng Chen, Qi-lin Li, Xing-fu Ding, Feng |
author_facet | Song, Li-jun Liu, Wei-wei Fan, Yu-chen Qiu, Feng Chen, Qi-lin Li, Xing-fu Ding, Feng |
author_sort | Song, Li-jun |
collection | PubMed |
description | BACKGROUND: The aim of this study is to investigate the expression of apolipoprotein E (apoE) and the relationship between apoE and disease activity of SLE, and the possible effects of glucocorticoid on apoE and other cytokines activities in SLE patients. METHODS: Forty treatment-naïve SLE patients and forty matched healthy controls were studied. All the SLE patients received prednisone 1 mg/kg/day for 28 consecutive days. The sera levels of apoE and related cytokines were evaluated by ELISA. The expression of apoE mRNA in peripheral blood mononuclear cells (PBMCs) was determined by real-time PCR. RESULTS: Compared with healthy controls, the relative expression levels of ApoE proteins and sera levels were significantly up-regulated in active SLE patients. ApoE sera concentrations positively correlated with SLEDAI, anti-dsDNA antibody and the related cytokines including IL-6, IFN-γ and IL-10, and uncorrelated with the concentration of total cholesterol (TC) and triglyceride (TG) in SLE patients. After 4 weeks prednisone treatment, the relative mRNA expression of apoE and the serum levels of apoE and related cytokines decreased. CONCLUSIONS: ApoE correlated with disease activity and related cytokines in SLE patients. Glucocorticoid can down-regulate the expressions of apoE and related cytokines. VIRTUAL SLIDE: The virtual slide(s) for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/1646714011077325 |
format | Online Article Text |
id | pubmed-4231472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42314722014-11-18 The positive correlations of apolipoprotein E with disease activity and related cytokines in systemic lupus erythematosus Song, Li-jun Liu, Wei-wei Fan, Yu-chen Qiu, Feng Chen, Qi-lin Li, Xing-fu Ding, Feng Diagn Pathol Research BACKGROUND: The aim of this study is to investigate the expression of apolipoprotein E (apoE) and the relationship between apoE and disease activity of SLE, and the possible effects of glucocorticoid on apoE and other cytokines activities in SLE patients. METHODS: Forty treatment-naïve SLE patients and forty matched healthy controls were studied. All the SLE patients received prednisone 1 mg/kg/day for 28 consecutive days. The sera levels of apoE and related cytokines were evaluated by ELISA. The expression of apoE mRNA in peripheral blood mononuclear cells (PBMCs) was determined by real-time PCR. RESULTS: Compared with healthy controls, the relative expression levels of ApoE proteins and sera levels were significantly up-regulated in active SLE patients. ApoE sera concentrations positively correlated with SLEDAI, anti-dsDNA antibody and the related cytokines including IL-6, IFN-γ and IL-10, and uncorrelated with the concentration of total cholesterol (TC) and triglyceride (TG) in SLE patients. After 4 weeks prednisone treatment, the relative mRNA expression of apoE and the serum levels of apoE and related cytokines decreased. CONCLUSIONS: ApoE correlated with disease activity and related cytokines in SLE patients. Glucocorticoid can down-regulate the expressions of apoE and related cytokines. VIRTUAL SLIDE: The virtual slide(s) for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/1646714011077325 BioMed Central 2013-10-21 /pmc/articles/PMC4231472/ /pubmed/24144108 http://dx.doi.org/10.1186/1746-1596-8-175 Text en Copyright © 2013 Song et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Song, Li-jun Liu, Wei-wei Fan, Yu-chen Qiu, Feng Chen, Qi-lin Li, Xing-fu Ding, Feng The positive correlations of apolipoprotein E with disease activity and related cytokines in systemic lupus erythematosus |
title | The positive correlations of apolipoprotein E with disease activity and related
cytokines in systemic lupus erythematosus |
title_full | The positive correlations of apolipoprotein E with disease activity and related
cytokines in systemic lupus erythematosus |
title_fullStr | The positive correlations of apolipoprotein E with disease activity and related
cytokines in systemic lupus erythematosus |
title_full_unstemmed | The positive correlations of apolipoprotein E with disease activity and related
cytokines in systemic lupus erythematosus |
title_short | The positive correlations of apolipoprotein E with disease activity and related
cytokines in systemic lupus erythematosus |
title_sort | positive correlations of apolipoprotein e with disease activity and related
cytokines in systemic lupus erythematosus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231472/ https://www.ncbi.nlm.nih.gov/pubmed/24144108 http://dx.doi.org/10.1186/1746-1596-8-175 |
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