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Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis

BACKGROUND: Glucocorticoids have been known to be less effective for treating ankylosing spondylitis (AS) patients than for treating rheumatoid arthritis (RA) patients. To elucidate the mechanisms underlying this phenomenon, we evaluated whether the glucocorticoid receptor (GR)β expression of the pe...

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Autores principales: Lee, Chang-Keun, Lee, Eun Young, Cho, You-Sook, Moon, Keun Ae, Yoo, Bin, Moon, Hee-Bom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891384/
https://www.ncbi.nlm.nih.gov/pubmed/16134770
http://dx.doi.org/10.3904/kjim.2005.20.2.146
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author Lee, Chang-Keun
Lee, Eun Young
Cho, You-Sook
Moon, Keun Ae
Yoo, Bin
Moon, Hee-Bom
author_facet Lee, Chang-Keun
Lee, Eun Young
Cho, You-Sook
Moon, Keun Ae
Yoo, Bin
Moon, Hee-Bom
author_sort Lee, Chang-Keun
collection PubMed
description BACKGROUND: Glucocorticoids have been known to be less effective for treating ankylosing spondylitis (AS) patients than for treating rheumatoid arthritis (RA) patients. To elucidate the mechanisms underlying this phenomenon, we evaluated whether the glucocorticoid receptor (GR)β expression of the peripheral blood mononuclear cells (PBMCs) in patients with AS is increased compared with patients with RA. METHODS: PBMCs were isolated from the subjects of 3 study groups: the healthy controls (n=25), the RA patients (n=25), and the AS patients (n=25). All the subjects had never taken corticosteroids and the patients with RA or AS were newly diagnosed. The expression of GRβ messenger RNA (mRNA) was determined by reverse transcription of the total RNA, and this was followed by semi-quantitative polymerase chain reaction analysis (RT-PCR). RESULTS: The level of GRα mRNA expression was not different among three groups. GRβ mRNA expression of the AS patients (2.02 [range: 0.99-7.21], median [25(th)-75(th) percentiles]) was enhanced compared with that of the controls (0.78 [range: 0.43-1.62]) and the RA patients (0.98 [range: 0.79-1.18]). The level of GRβ mRNA expression was not related to the inflammatory markers or the disease activity score 28 for the RA patients, and it was not related to the Bath ankylosing spondylitis disease activity index for the AS patients. CONCLUSION: The expression of GRβ mRNA, which is a dominant negative regulator for the glucocorticoid response, was increased in AS patients. The results suggest that the increased expression of GRβ mRNA may be related to the ineffectiveness of glucocorticoids for the treatment of AS.
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spelling pubmed-38913842014-01-16 Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis Lee, Chang-Keun Lee, Eun Young Cho, You-Sook Moon, Keun Ae Yoo, Bin Moon, Hee-Bom Korean J Intern Med Original Article BACKGROUND: Glucocorticoids have been known to be less effective for treating ankylosing spondylitis (AS) patients than for treating rheumatoid arthritis (RA) patients. To elucidate the mechanisms underlying this phenomenon, we evaluated whether the glucocorticoid receptor (GR)β expression of the peripheral blood mononuclear cells (PBMCs) in patients with AS is increased compared with patients with RA. METHODS: PBMCs were isolated from the subjects of 3 study groups: the healthy controls (n=25), the RA patients (n=25), and the AS patients (n=25). All the subjects had never taken corticosteroids and the patients with RA or AS were newly diagnosed. The expression of GRβ messenger RNA (mRNA) was determined by reverse transcription of the total RNA, and this was followed by semi-quantitative polymerase chain reaction analysis (RT-PCR). RESULTS: The level of GRα mRNA expression was not different among three groups. GRβ mRNA expression of the AS patients (2.02 [range: 0.99-7.21], median [25(th)-75(th) percentiles]) was enhanced compared with that of the controls (0.78 [range: 0.43-1.62]) and the RA patients (0.98 [range: 0.79-1.18]). The level of GRβ mRNA expression was not related to the inflammatory markers or the disease activity score 28 for the RA patients, and it was not related to the Bath ankylosing spondylitis disease activity index for the AS patients. CONCLUSION: The expression of GRβ mRNA, which is a dominant negative regulator for the glucocorticoid response, was increased in AS patients. The results suggest that the increased expression of GRβ mRNA may be related to the ineffectiveness of glucocorticoids for the treatment of AS. The Korean Association of Internal Medicine 2005-06 2005-06-30 /pmc/articles/PMC3891384/ /pubmed/16134770 http://dx.doi.org/10.3904/kjim.2005.20.2.146 Text en Copyright © 2005 The Korean Association of Internal Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Chang-Keun
Lee, Eun Young
Cho, You-Sook
Moon, Keun Ae
Yoo, Bin
Moon, Hee-Bom
Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title_full Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title_fullStr Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title_full_unstemmed Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title_short Increased Expression of Glucocorticoid Receptorβ Messenger RNA in Patients with Ankylosing Spondylitis
title_sort increased expression of glucocorticoid receptorβ messenger rna in patients with ankylosing spondylitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891384/
https://www.ncbi.nlm.nih.gov/pubmed/16134770
http://dx.doi.org/10.3904/kjim.2005.20.2.146
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