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Clinical Chemistry 0: clinchem.2006.083170v1, 2007; 10.1373/clinchem.2006.083170
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Received on November 15, 2006
Accepted on April 5, 2007

Proteomics and Protein Markers

B-Type Natriuretic Peptide Concentrations Predict the Progression of Nondiabetic Chronic Kidney Disease: The Mild-to-Moderate Kidney Disease Study

Katharina-Susanne Spanaus 1, Florian Kronenberg 2, Eberhard Ritz 3, Ralph Schlapbach 4, Danilo Fliser 5, Martin Hersberger 1, Barbara Kollerits 2, Paul König 6, Arnold von Eckardstein 1*, for the Mild-to-Moderate Kidney Disease Study Group

1 Institute of Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland
2 Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Innsbruck, Austria
3 Department of Internal Medicine, Division of Nephrology, Ruprecht-Karls-University, Heidelberg, Germany
4 Functional Genomics Center, University of Zürich and ETH Zürich, Zürich, Switzerland
5 Division of Nephrology, Department of Internal Medicine, Hannover Medical School, Hannover, Germany
6 Innsbruck University Hospital, Department of Clinical Nephrology, Innsbruck, Austria

* To whom correspondence should be addressed. E-mail: arnold.voneckardstein{at}usz.ch.

Background: Plasma concentrations of B-type natriuretic peptide (BNP) and N-terminal proBNP (NT-proBNP) are diagnostic and prognostic biomarkers of heart failure and are also increased in patients with chronic kidney disease (CKD). We examined the relevance of BNP and NT-proBNP as predictors of CKD progression.

Methods: Of 227 nondiabetic patients with mild-to-moderate renal insufficiency, 177 patients ages 18-65 years were followed in a prospective multicenter cohort study for a period of ≤7 years. CKD progression was assessed by recording renal endpoints, defined as doubling of baseline serum creatinine or end-stage renal disease (ESRD) requiring renal replacement therapy.

Results: BNP and NT-proBNP were significantly higher among 65 patients who reached the combined renal endpoint than among the 112 who did not [median (interquartile range) 61 (27-98) ng/L vs 39 (20-70) ng/L, P = 0.023, for BNP; 320 (117-745) ng/L vs 84 (44-176) ng/L, P <0.001, for NT-proBNP)]. Each increment of 1 SD in log-transformed BNP and NT-proBNP increased the risk of CKD progression by hazard ratios of 1.38 (95% CI 1.09-1.76, P = 0.009) and 2.28 (1.76-2.95, P <0.001), respectively. After adjustment for other established prognostic factors of CKD progression, NT-proBNP but not BNP remained a significant independent predictor of the combined renal endpoint.

Conclusions: Increased BNP and NT-proBNP concentrations indicate an increased risk for accelerated progression of CKD to ESRD and may prove to be valuable biomarkers for the assessment of prognosis in patients with CKD.




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