Clinical Chemistry
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Clinical Chemistry 54: 1339-1348, 2008. First published June 6, 2008; 10.1373/clinchem.2007.101691
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Right arrow Proteomics and Protein Markers
(Clinical Chemistry. 2008;54:1339-1348.)
© 2008 American Association for Clinical Chemistry, Inc.


Proteomics and Protein Markers

N-terminal Pro-B–Type Natriuretic Peptide (NT-proBNP) Concentrations in Hemodialysis Patients: Prognostic Value of Baseline and Follow-up Measurements

Orlando M. Gutiérrez1,a, Hector Tamez1, Ishir Bhan1, James Zazra2, Marcello Tonelli3, Myles Wolf1, James L. Januzzi4, Yuchiao Chang5 and Ravi Thadhani1

1 Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA; 2 Spectra Laboratories, Rockleigh, NJ; 3 Department of Medicine, University of Alberta, Edmonton, Alberta, Canada; 4 Cardiology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA; 5 General Medicine, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA.

aAddress correspondence to this author at: University of Miami, Rosenstiel Medical Science Building, Suite 7168, 1600 NW 10th Avenue, Miami, FL 33136. Fax 305-243-3506; e-mail ogutierrez2{at}med.miami.edu.

Background: Increased N-terminal pro-B–type natriuretic peptide (NT-proBNP) concentrations are associated with increased cardiovascular mortality in chronic hemodialysis patients. Previous studies focused on prevalent dialysis patients and examined single measurements of NT-proBNP in time.

Methods: We measured NT-proBNP concentrations in 2990 incident hemodialysis patients to examine the risk of 90-day and 1-year mortality associated with baseline NT-proBNP concentrations. In addition, we calculated the change in concentrations after 3 months in a subset of 585 patients to examine the association between longitudinal changes in NT-proBNP and subsequent mortality.

Results: Increasing quartiles of NT-proBNP were associated with a monotonic increase in 90-day [quartile 1, referent; from quartile 2 to quartile 4, hazard ratio (HR) 1.7–6.3, P < 0.001] and 1-year (quartile 1, referent; from quartile 2 to quartile 4, HR 1.7–4.9, P < 0.001) all-cause mortality. After multivariable adjustment, these associations remained robust. When examined using a multivariable fractional polynomial, increased NT-proBNP concentrations were associated with increased 90-day (HR per unit increase in log NT-proBNP 1.5, 95% CI 1.3–1.7) and 1-year (HR per unit increase in log NT-proBNP 1.4, 95% CI 1.3–1.5) all-cause mortality. In addition, patients with the greatest increase in NT-proBNP after 3 months of dialysis had a 2.4-fold higher risk of mortality than those with the greatest decrease in NT-proBNP.

Conclusions: NT-proBNP concentrations are independently associated with mortality in incident hemodialysis patients. Furthermore, the observation that longitudinal changes in NT-proBNP concentrations were associated with subsequent mortality suggests that monitoring serial NT-proBNP concentrations may represent a novel tool for assessing adequacy and guiding therapy in patients initiating hemodialysis.







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