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Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients
BACKGROUND: Increased plasma levels of cellular adhesion molecules (CAMs) have been shown to be predictors of all cause mortality in individuals with chronic renal failure [1,2] and patients with end-stage renal disease receiving haemodialysis [3]. In renal transplant recipients the predictive value...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120748/ https://www.ncbi.nlm.nih.gov/pubmed/21600046 http://dx.doi.org/10.1186/1471-2369-12-23 |
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author | Connolly, Grainne M Cunningham, Ronan McNamee, Peter T Young, Ian S Maxwell, Alexander P |
author_facet | Connolly, Grainne M Cunningham, Ronan McNamee, Peter T Young, Ian S Maxwell, Alexander P |
author_sort | Connolly, Grainne M |
collection | PubMed |
description | BACKGROUND: Increased plasma levels of cellular adhesion molecules (CAMs) have been shown to be predictors of all cause mortality in individuals with chronic renal failure [1,2] and patients with end-stage renal disease receiving haemodialysis [3]. In renal transplant recipients the predictive value of CAMs has not been well characterised. The aim of this study was to assess the relationship between CAMs and all-cause mortality during prospective follow-up of a renal transplant cohort. METHODS: A total of 378 renal transplant recipients were recruited between June 2000 and December 2002. Soluble vascular CAM-1 (VCAM) and soluble intercellular CAM-1 (ICAM) were measured at baseline and prospective follow-up data was collected at a median of 2441 days after enrolment. RESULTS: In univariate survival analysis the renal transplant recipients with a VCAM or ICAM concentration in the lowest third were significantly more likely to have survived at follow-up (p < 0.001 and p = 0.009 respectively). In multivariate survival analysis VCAM and ICAM remained significant independent predictors of mortality following adjustment for traditional cardiovascular risk factors, hsCRP and estimated GFR (p = 0.030 and p = 0.037 respectively). CONCLUSIONS: The results of this prospective study are the first to show that the CAMs, ICAM and particularly VCAM, are significant independent predictors of mortality in patients with a renal transplant. |
format | Online Article Text |
id | pubmed-3120748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31207482011-06-23 Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients Connolly, Grainne M Cunningham, Ronan McNamee, Peter T Young, Ian S Maxwell, Alexander P BMC Nephrol Research Article BACKGROUND: Increased plasma levels of cellular adhesion molecules (CAMs) have been shown to be predictors of all cause mortality in individuals with chronic renal failure [1,2] and patients with end-stage renal disease receiving haemodialysis [3]. In renal transplant recipients the predictive value of CAMs has not been well characterised. The aim of this study was to assess the relationship between CAMs and all-cause mortality during prospective follow-up of a renal transplant cohort. METHODS: A total of 378 renal transplant recipients were recruited between June 2000 and December 2002. Soluble vascular CAM-1 (VCAM) and soluble intercellular CAM-1 (ICAM) were measured at baseline and prospective follow-up data was collected at a median of 2441 days after enrolment. RESULTS: In univariate survival analysis the renal transplant recipients with a VCAM or ICAM concentration in the lowest third were significantly more likely to have survived at follow-up (p < 0.001 and p = 0.009 respectively). In multivariate survival analysis VCAM and ICAM remained significant independent predictors of mortality following adjustment for traditional cardiovascular risk factors, hsCRP and estimated GFR (p = 0.030 and p = 0.037 respectively). CONCLUSIONS: The results of this prospective study are the first to show that the CAMs, ICAM and particularly VCAM, are significant independent predictors of mortality in patients with a renal transplant. BioMed Central 2011-05-22 /pmc/articles/PMC3120748/ /pubmed/21600046 http://dx.doi.org/10.1186/1471-2369-12-23 Text en Copyright ©2011 Connolly 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. |
spellingShingle | Research Article Connolly, Grainne M Cunningham, Ronan McNamee, Peter T Young, Ian S Maxwell, Alexander P Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title | Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title_full | Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title_fullStr | Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title_full_unstemmed | Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title_short | Elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
title_sort | elevated soluble cellular adhesion molecules are associated with increased mortality in a prospective cohort of renal transplant recipients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120748/ https://www.ncbi.nlm.nih.gov/pubmed/21600046 http://dx.doi.org/10.1186/1471-2369-12-23 |
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