Abstract

BackgroundIncreased 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.MethodsA 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.ResultsIn 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).ConclusionsThe 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.

Highlights

  • 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]

  • The predictive value of CAMs has not been well defined in renal transplant recipients

  • 243 (64%) were male, 72 (19%) were smokers and 54 (14%) had diabetes. 12 (3%) participants had received a pre-emptive renal transplant and 366 (97%) participants had been on dialysis prior to renal transplantation

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Summary

Introduction

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]. Soluble cellular adhesion molecules (CAMs) represent promising biomarkers that may reflect underlying endothelial activation and vascular inflammation [9]. Many factors have been shown to alter expression of cellular adhesion molecules. These include hypertension [10] immunosuppressive therapy [11], autoimmune disease [11,12,13] and cell mediated allograft rejection [14,15]

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