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Published in: Diagnostic Pathology 1/2013

Open Access 01-12-2013 | Research

Expression level of the growth factor progranulin is related with development of systemic lupus erythematosus

Authors: Feng Qiu, Lijun Song, Feng Ding, Huaxiang Liu, Qiang Shu, Ning Yang, Weiwei Liu, Xingfu Li

Published in: Diagnostic Pathology | Issue 1/2013

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Abstract

Background

This study is to investigate the expression of progranulin (PGRN) in systemic lupus erythematosus (SLE) patients and the effect of glucocorticoid (GC) treatment on its expression.

Methods

Thirty newly diagnosed severe SLE patients and 30 healthy subjects were enrolled in this study. The serum levels of PGRN and the inflammatory factors of SLE were detected by ELISA and the mRNA expression of these proteins were detected by real-time PCR.

Results

The serum levels of PGRN, IL-6, PR3, TNFR, TNF-α and anti-dsDNA antibody in SLE patients were increased significantly compared with healthy controls (P < 0.05). The relative expression of PGRN mRNA was increased by 4.88-fold in pre-treatment SLE patients compared with controls (P < 0.05). After prednisone treatment, the serum levels of PGRN decreased significantly, and the relative expression of PGRN mRNA was decreased by 1.34-fold compared with the untreated controls (P < 0.01). Moreover, Serum concentration of PGRN was correlated with serum levels of IL-6, TNF-α, TNFR and anti-dsDNA antibody in both pre-treatment and post-treatment SLE patients.

Conclusions

PGRN is up-regulated in the SLE patients and is correlated with pro-inflammatory cytokines and anti-dsDNA antibody. Glucocorticoids can down-regulate the expression of PGRN in SLE patients.
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Metadata
Title
Expression level of the growth factor progranulin is related with development of systemic lupus erythematosus
Authors
Feng Qiu
Lijun Song
Feng Ding
Huaxiang Liu
Qiang Shu
Ning Yang
Weiwei Liu
Xingfu Li
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Diagnostic Pathology / Issue 1/2013
Electronic ISSN: 1746-1596
DOI
https://doi.org/10.1186/1746-1596-8-88

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