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DOI 10.1186/1471-2369-12-23

Медицинская библиотека · BMC nephrology · 2011

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

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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 12 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.

Для цитирования: 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.. BMC nephrology. 2011. DOI: 10.1186/1471-2369-12-23.

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