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

被引:25
|
作者
Foo, Jared Yong Yang [1 ]
Wan, Yunxia [1 ]
Schulz, Benjamin L. [2 ]
Kostner, Karam [3 ,4 ]
Atherton, John [3 ,5 ]
Cooper-White, Justin [1 ,6 ]
Dimeski, Goce [3 ,7 ]
Punyadeera, Chamindie [1 ,6 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld, Australia
[2] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld, Australia
[3] Univ Queensland, Sch Med, Brisbane, Qld, Australia
[4] Mater Adult Hosp, Dept Cardiol, Brisbane, Qld, Australia
[5] Royal Brisbane & Womens Hosp, Dept Cardiol, Brisbane, Qld, Australia
[6] Univ Queensland, Sch Chem Engn, Brisbane, Qld, Australia
[7] Princess Alexandra Hosp, Brisbane, Qld 4102, Australia
基金
英国医学研究理事会;
关键词
SALIVA; ASSAY; CORIN; STATE;
D O I
10.1373/clinchem.2012.200204
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
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 degrees C. NT-proBNP was enriched from HF patient plasma by use of immunoprecipitation followed by mass spectrometric analysis. Customized homogeneous sandwich AlphaLISA (R) 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. (c) 2013 American Association for Clinical Chemistry
引用
收藏
页码:1523 / 1531
页数:9
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