Osteopontin predicts survival in critically ill patients with acute kidney injury.

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Osteopontin predicts survival in critically ill patients with acute kidney injury.

Nephrol Dial Transplant. 2010 Aug 23;

Authors: Lorenzen JM, Hafer C, Faulhaber-Walter R, Kümpers P, Kielstein JT, Haller H, Fliser D

BACKGROUND: The cytokine osteopontin is involved in the pathophysiology of experimental acute kidney injury. We have tested the hypothesis that osteopontin levels might serve as a biomarker predicting outcome in critically ill patients requiring renal replacement therapy after acute kidney injury. METHODS: We measured circulating plasma osteopontin levels in 109 critically ill patients with acute kidney injury at inception of renal replacement therapy and 4 weeks thereafter. Critically ill patients without acute kidney injury served as controls. Osteopontin was measured with ELISA. RESULTS: Baseline osteopontin levels in patients with acute kidney injury were significantly higher compared with controls (P < 0.0001). Baseline osteopontin levels in patients recovering from acute kidney injury were significantly elevated compared with patients with permanent loss of kidney function after acute kidney injury (P = 0.01). In addition, in patients recovering from acute kidney injury without further need for renal replacement therapy, osteopontin levels were significantly lower 4 weeks after initiation of renal replacement therapy (P = 0.0005). Moreover, multivariate Cox analysis revealed osteopontin levels at renal replacement therapy inception as an independent and powerful predictor of mortality (P < 0.0001). In the ROC-curve analysis, an osteopontin cut-off value of 577 ng/mL separated survivors from non-survivors with a sensitivity of 100% and a specificity of 61% (AUC 0.82; 95% confidence interval: 0.74-0.89; P < 0.0001). CONCLUSIONS: Osteopontin may serve as a novel biomarker for both, overall survival and renal outcome in critically ill patients with acute kidney injury, that require renal replacement therapy.

PMID: 20732925 [PubMed - as supplied by publisher]

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