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Glucocorticoid sensitivity in Behçet's disease
OBJECTIVE: Glucocorticoid (GC) sensitivity is highly variable among individuals and has been associated with susceptibility to develop (auto-)inflammatory disorders. The purpose of the study was to assess GC sensitivity in Behçet's disease (BD) by studying the distribution of four GC receptor (...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioScientifica
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681319/ https://www.ncbi.nlm.nih.gov/pubmed/23781311 http://dx.doi.org/10.1530/EC-12-0056 |
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author | Quax, R A M van Laar, J A M van Heerebeek, R Greiner, K Ben-Chetrit, E Stanford, M Wallace, G R Fortune, F Ghabra, M Soylu, M Hazes, J M W Lamberts, S W J Kappen, J H van Hagen, P M Koper, J W Feelders, R A |
author_facet | Quax, R A M van Laar, J A M van Heerebeek, R Greiner, K Ben-Chetrit, E Stanford, M Wallace, G R Fortune, F Ghabra, M Soylu, M Hazes, J M W Lamberts, S W J Kappen, J H van Hagen, P M Koper, J W Feelders, R A |
author_sort | Quax, R A M |
collection | PubMed |
description | OBJECTIVE: Glucocorticoid (GC) sensitivity is highly variable among individuals and has been associated with susceptibility to develop (auto-)inflammatory disorders. The purpose of the study was to assess GC sensitivity in Behçet's disease (BD) by studying the distribution of four GC receptor (GR) gene polymorphisms and by measuring in vitro cellular GC sensitivity. METHODS: Healthy controls and patients with BD in three independent cohorts were genotyped for four functional GR gene polymorphisms. To gain insight into functional differences in in vitro GC sensitivity, 19 patients with BD were studied using two bioassays and a whole-cell dexamethasone-binding assay. Finally, mRNA expression levels of GR splice variants (GR-α and GR-β) were measured. RESULTS: Healthy controls and BD patients in the three separate cohorts had similar distributions of the four GR polymorphisms. The Bcll and 9β minor alleles frequency differed significantly between Caucasians and Mideast and Turkish individuals. At the functional level, a decreased in vitro cellular GC sensitivity was observed. GR number in peripheral blood mononuclear cells was higher in BD compared with controls. The ratio of GR-α/GR-β mRNA expression levels was significantly lower in BD. CONCLUSIONS: Polymorphisms in the GR gene are not associated with susceptibility to BD. However, in vitro cellular GC sensitivity is decreased in BD, possibly mediated by a relative higher expression of the dominant negative GR-β splice variant. This decreased in vitro GC sensitivity might play an as yet unidentified role in the pathophysiology of BD. |
format | Online Article Text |
id | pubmed-3681319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioScientifica |
record_format | MEDLINE/PubMed |
spelling | pubmed-36813192013-06-17 Glucocorticoid sensitivity in Behçet's disease Quax, R A M van Laar, J A M van Heerebeek, R Greiner, K Ben-Chetrit, E Stanford, M Wallace, G R Fortune, F Ghabra, M Soylu, M Hazes, J M W Lamberts, S W J Kappen, J H van Hagen, P M Koper, J W Feelders, R A Endocr Connect Research OBJECTIVE: Glucocorticoid (GC) sensitivity is highly variable among individuals and has been associated with susceptibility to develop (auto-)inflammatory disorders. The purpose of the study was to assess GC sensitivity in Behçet's disease (BD) by studying the distribution of four GC receptor (GR) gene polymorphisms and by measuring in vitro cellular GC sensitivity. METHODS: Healthy controls and patients with BD in three independent cohorts were genotyped for four functional GR gene polymorphisms. To gain insight into functional differences in in vitro GC sensitivity, 19 patients with BD were studied using two bioassays and a whole-cell dexamethasone-binding assay. Finally, mRNA expression levels of GR splice variants (GR-α and GR-β) were measured. RESULTS: Healthy controls and BD patients in the three separate cohorts had similar distributions of the four GR polymorphisms. The Bcll and 9β minor alleles frequency differed significantly between Caucasians and Mideast and Turkish individuals. At the functional level, a decreased in vitro cellular GC sensitivity was observed. GR number in peripheral blood mononuclear cells was higher in BD compared with controls. The ratio of GR-α/GR-β mRNA expression levels was significantly lower in BD. CONCLUSIONS: Polymorphisms in the GR gene are not associated with susceptibility to BD. However, in vitro cellular GC sensitivity is decreased in BD, possibly mediated by a relative higher expression of the dominant negative GR-β splice variant. This decreased in vitro GC sensitivity might play an as yet unidentified role in the pathophysiology of BD. BioScientifica 2012-10-24 /pmc/articles/PMC3681319/ /pubmed/23781311 http://dx.doi.org/10.1530/EC-12-0056 Text en © 2012 The Authors. Published by BioScientifica Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Quax, R A M van Laar, J A M van Heerebeek, R Greiner, K Ben-Chetrit, E Stanford, M Wallace, G R Fortune, F Ghabra, M Soylu, M Hazes, J M W Lamberts, S W J Kappen, J H van Hagen, P M Koper, J W Feelders, R A Glucocorticoid sensitivity in Behçet's disease |
title | Glucocorticoid sensitivity in Behçet's disease |
title_full | Glucocorticoid sensitivity in Behçet's disease |
title_fullStr | Glucocorticoid sensitivity in Behçet's disease |
title_full_unstemmed | Glucocorticoid sensitivity in Behçet's disease |
title_short | Glucocorticoid sensitivity in Behçet's disease |
title_sort | glucocorticoid sensitivity in behçet's disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681319/ https://www.ncbi.nlm.nih.gov/pubmed/23781311 http://dx.doi.org/10.1530/EC-12-0056 |
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