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Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD

RATIONALE: Plasma soluble Receptor for Advanced Glycation End Product (sRAGE) is considered as a biomarker in COPD. The contribution of endogenous sRAGE (esRAGE) to the pool of plasma sRAGE and the implication of both markers in COPD pathogenesis is however not clear yet. The aim of the current stud...

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Autores principales: Gopal, Poornima, Reynaert, Niki L, Scheijen, Jean L J M, Schalkwijk, Casper G, Franssen, Frits M E, Wouters, Emiel F M, Rutten, Erica P A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944004/
https://www.ncbi.nlm.nih.gov/pubmed/24564838
http://dx.doi.org/10.1186/1465-9921-15-24
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author Gopal, Poornima
Reynaert, Niki L
Scheijen, Jean L J M
Schalkwijk, Casper G
Franssen, Frits M E
Wouters, Emiel F M
Rutten, Erica P A
author_facet Gopal, Poornima
Reynaert, Niki L
Scheijen, Jean L J M
Schalkwijk, Casper G
Franssen, Frits M E
Wouters, Emiel F M
Rutten, Erica P A
author_sort Gopal, Poornima
collection PubMed
description RATIONALE: Plasma soluble Receptor for Advanced Glycation End Product (sRAGE) is considered as a biomarker in COPD. The contribution of endogenous sRAGE (esRAGE) to the pool of plasma sRAGE and the implication of both markers in COPD pathogenesis is however not clear yet. The aim of the current study was therefore to measure plasma levels of esRAGE comparative to total sRAGE in patients with COPD and a control group. Further, we established the relations of esRAGE and total sRAGE with disease specific characteristics such as lung function and D(L)CO, and with different circulating AGEs. METHODS: Plasma levels of esRAGE and sRAGE were measured in an 88 patients with COPD and in 55 healthy controls. FEV(1) (%predicted) and FEV(1)/VC (%) were measured in both groups; D(L)CO (%predicted) was measured in patients only. In this study population we previously reported that the AGE N(ϵ)-(carboxymethyl) lysine (CML) was decreased, N(ϵ)-(carboxyethyl) lysine (CEL) increased and pentosidine was not different in plasma of COPD patients compared to controls. RESULTS: Plasma esRAGE (COPD: 533.9 ± 412.4, Controls: 848.7 ± 690.3 pg/ml; p = 0.000) was decreased in COPD compared to controls. No significant correlations were observed between plasma esRAGE levels and lung function parameters or plasma AGEs. A positive correlation was present between esRAGE and total sRAGE levels in the circulation. Confirming previous findings, total sRAGE (COPD: 512.6 ± 403.8, Controls: 1834 ± 804.2 pg/ml; p < 0.001) was lower in patients compared to controls and was positively correlated FEV(1) (r = 0.235, p = 0.032), FEV(1)/VC (r = 0.218, p = 0.047), and D(L)CO (r = 0.308, p = 0.006). sRAGE furthermore did show a significant positive association with CML (r = 0.321, p = 0.003). CONCLUSION: Although plasma esRAGE is decreased in COPD patients compared to controls, only total sRAGE showed a significant and independent association with FEV(1), FEV(1)/VC and D(L)CO, indicating that total sRAGE but not esRAGE may serve as marker of COPD disease state and severity.
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spelling pubmed-39440042014-03-07 Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD Gopal, Poornima Reynaert, Niki L Scheijen, Jean L J M Schalkwijk, Casper G Franssen, Frits M E Wouters, Emiel F M Rutten, Erica P A Respir Res Research RATIONALE: Plasma soluble Receptor for Advanced Glycation End Product (sRAGE) is considered as a biomarker in COPD. The contribution of endogenous sRAGE (esRAGE) to the pool of plasma sRAGE and the implication of both markers in COPD pathogenesis is however not clear yet. The aim of the current study was therefore to measure plasma levels of esRAGE comparative to total sRAGE in patients with COPD and a control group. Further, we established the relations of esRAGE and total sRAGE with disease specific characteristics such as lung function and D(L)CO, and with different circulating AGEs. METHODS: Plasma levels of esRAGE and sRAGE were measured in an 88 patients with COPD and in 55 healthy controls. FEV(1) (%predicted) and FEV(1)/VC (%) were measured in both groups; D(L)CO (%predicted) was measured in patients only. In this study population we previously reported that the AGE N(ϵ)-(carboxymethyl) lysine (CML) was decreased, N(ϵ)-(carboxyethyl) lysine (CEL) increased and pentosidine was not different in plasma of COPD patients compared to controls. RESULTS: Plasma esRAGE (COPD: 533.9 ± 412.4, Controls: 848.7 ± 690.3 pg/ml; p = 0.000) was decreased in COPD compared to controls. No significant correlations were observed between plasma esRAGE levels and lung function parameters or plasma AGEs. A positive correlation was present between esRAGE and total sRAGE levels in the circulation. Confirming previous findings, total sRAGE (COPD: 512.6 ± 403.8, Controls: 1834 ± 804.2 pg/ml; p < 0.001) was lower in patients compared to controls and was positively correlated FEV(1) (r = 0.235, p = 0.032), FEV(1)/VC (r = 0.218, p = 0.047), and D(L)CO (r = 0.308, p = 0.006). sRAGE furthermore did show a significant positive association with CML (r = 0.321, p = 0.003). CONCLUSION: Although plasma esRAGE is decreased in COPD patients compared to controls, only total sRAGE showed a significant and independent association with FEV(1), FEV(1)/VC and D(L)CO, indicating that total sRAGE but not esRAGE may serve as marker of COPD disease state and severity. BioMed Central 2014 2014-02-25 /pmc/articles/PMC3944004/ /pubmed/24564838 http://dx.doi.org/10.1186/1465-9921-15-24 Text en Copyright © 2014 Gopal 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 credited. 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
Gopal, Poornima
Reynaert, Niki L
Scheijen, Jean L J M
Schalkwijk, Casper G
Franssen, Frits M E
Wouters, Emiel F M
Rutten, Erica P A
Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title_full Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title_fullStr Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title_full_unstemmed Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title_short Association of plasma sRAGE, but not esRAGE with lung function impairment in COPD
title_sort association of plasma srage, but not esrage with lung function impairment in copd
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944004/
https://www.ncbi.nlm.nih.gov/pubmed/24564838
http://dx.doi.org/10.1186/1465-9921-15-24
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