Circulating Fragments of N-Terminal Pro–B-Type Natriuretic Peptides in Plasma of Heart Failure Patients

Author:

Foo Jared Yong Yang1,Wan Yunxia1,Schulz Benjamin L2,Kostner Karam34,Atherton John35,Cooper-White Justin16,Dimeski Goce37,Punyadeera Chamindie168

Affiliation:

1. The Australian Institute for Bioengineering and Nanotechnology

2. School of Chemistry and Molecular Biosciences, and

3. School of Medicine, the University of Queensland, Brisbane, Queensland, Australia

4. Department of Cardiology, Mater Adult Hospital, Brisbane, Queensland, Australia

5. Department of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

6. School of Chemical Engineering, the University of Queensland, Brisbane, Queensland, Australia

7. Chemical Pathology, Princess Alexandra Hospital, Brisbane, Queensland, Australia

8. current affiliation: Saliva Translational Research Group, The University of Queensland Diamantina Institute, Woolloongabba, Australia

Abstract

BACKGROUND The use of nonstandardized N-terminal pro–B-type natriuretic peptide (NT-proBNP) assays can contribute to the misdiagnosis of heart failure (HF). Moreover, there is yet to be established a common consensus regarding the circulating forms of NT-proBNP being used in current assays. We aimed to characterize and quantify the various forms of NT-proBNP in the circulation of HF patients. METHODS Plasma samples were collected from HF patients (n = 20) at rest and stored at −80 °C. NT-proBNP was enriched from HF patient plasma by use of immunoprecipitation followed by mass spectrometric analysis. Customized homogeneous sandwich AlphaLISA® immunoassays were developed and validated to quantify 6 fragments of NT-proBNP. RESULTS Mass spectrometry identified the presence of several N- and C-terminally processed forms of circulating NT-proBNP, with physiological proteolysis between Pro2-Leu3, Leu3-Gly4, Pro6-Gly7, and Pro75-Arg76. Consistent with this result, AlphaLISA immunoassays demonstrated that antibodies targeting the extreme N or C termini measured a low apparent concentration of circulating NT-proBNP. The apparent circulating NT-proBNP concentration was increased with antibodies targeting nonglycosylated and nonterminal epitopes (P < 0.05). CONCLUSIONS In plasma collected from HF patients, immunoreactive NT-proBNP was present as multiple N- and C-terminally truncated fragments of the full length NT-proBNP molecule. Immunodetection of NT-proBNP was significantly improved with the use of antibodies that did not target these terminal regions. These findings support the development of a next generation NT-proBNP assay targeting nonterminal epitopes as well as avoiding the central glycosylated region of this molecule.

Funder

National Health and Medical Research Council Project

National Health and Medical Research Council Career Development

Queensland Government Smart Futures

University of Queensland New Staff Research Funds

University of Queensland Foundation Research Excellence Award Scheme

Perkin Elmer

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Reference26 articles.

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3. Analytical performance of the N terminal pro B type natriuretic peptide (NT-proBNP) assay on the Elecsys 1010 and 2010 analysers;Collinson;Eur J Heart Fail,2004

4. Biochemistry of B-type natriuretic peptide: where are we now?;Mair;Clin Chem Lab Med,2008

5. Laboratory testing for B-type natriuretic peptides (BNP and NT-proBNP): clinical usefulness, utilization, and impact on hospital operations;Melanson;Am J Clin Pathol,2005

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