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B型利钠肽检测的特异性:与不同的B型利钠肽、N末端B型利钠肽原及B型利钠肽原肽的交叉反应性

Specificity of B-Type Natriuretic Peptide Assays: Cross-Reactivity with Different BNP, NT-proBNP, and proBNP Peptides.

作者信息

Saenger Amy K, Rodriguez-Fraga Olaia, Ler Ranka, Ordonez-Llanos Jordi, Jaffe Allan S, Goetze Jens Peter, Apple Fred S

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.

Laboratory Medicine Department, Hospital Universitario La Paz, Madrid, Spain.

出版信息

Clin Chem. 2017 Jan;63(1):351-358. doi: 10.1373/clinchem.2016.263749. Epub 2016 Nov 15.

Abstract

BACKGROUND

B-type natriuretic peptides (BNPs) are used clinically to diagnose and monitor heart failure and are present in the circulation as multiple proBNP-derived fragments. We investigated the specificity of BNP immunoassays with glycosylated and nonglycosylated BNP, N-terminal proBNP (NT-proBNP), and proBNP peptides to probe the cross-reactivity of each assay.

METHODS

Nine B-type natriuretic peptides were studied,including synthetic and recombinant BNP (Shionogi, Scios, Mayo), human and synthetic glycosylated and nonglycosylated NT-proBNP (HyTest, Roche Diagnostics), and human glycosylated and nonglycosylated proBNP (HyTest, Scios). Five BNP [Abbott, Abbott POC, Alere, Beckman Coulter, Siemens (Centaur)], 9 NT-proBNP [Ortho-Clinical Diagnostics, Roche, Response, bioMerieux, Siemens (Dimension, Immulite, Stratus CS), Mitsubishi] and 3 research-use-only proBNP immunoassays [Biosite (Alere), Bio-Rad, Goetze] were evaluated. Specificity was assessed by calculating the recovery between baseline and peptide-spiked human plasma pools at target concentrations of 100 ng/L BNP, 300 ng/L proBNP, or 450 ng/L NT-proBNP. All assays were performed in duplicate.

RESULTS

BNP and NT-proBNP assays demonstrated substantial cross-reactivity with proBNP peptides. NT-proBNP assays do not detect glycosylated forms of either NT-proBNP or proBNP. proBNP assays preferentially detect the BNP 1-32 peptide and have minimal cross-reactivity with BNP peptides and glycosylated proBNP.

CONCLUSIONS

BNP or NT-proBNP results are not transferable among the current existing immunoassays owing to their differences in cross-reactivity and ability to detect various glycosylated forms of proBNP-derived fragments. Opportunities remain to standardize and harmonize BNP and NT-proBNP assays, as well as to develop specific proBNP assays, to widen their clinical scope of use.

摘要

背景

B型利钠肽(BNP)在临床上用于诊断和监测心力衰竭,并且以多种来源于proBNP的片段形式存在于循环系统中。我们研究了BNP免疫测定法对糖基化和非糖基化的BNP、N末端proBNP(NT-proBNP)以及proBNP肽段的特异性,以探究每种测定法的交叉反应性。

方法

研究了9种B型利钠肽,包括合成及重组的BNP(盐野义制药、Scios公司、梅奥诊所)、人源及合成的糖基化和非糖基化NT-proBNP(HyTest公司、罗氏诊断公司),以及人源糖基化和非糖基化proBNP(HyTest公司、Scios公司)。评估了5种BNP测定法[雅培公司、雅培即时检验、Alere公司、贝克曼库尔特公司、西门子公司(Centaur)]、9种NT-proBNP测定法[奥森多临床诊断公司、罗氏公司、Response公司、生物梅里埃公司、西门子公司(Dimension、Immulite、Stratus CS)、三菱公司]以及3种仅用于研究的proBNP免疫测定法[Biosite公司(Alere公司)、伯乐公司、Goetze公司]。通过计算在目标浓度为100 ng/L BNP、300 ng/L proBNP或450 ng/L NT-proBNP时,基线水平与添加肽段的人血浆池之间的回收率来评估特异性。所有测定均重复进行。

结果

BNP和NT-proBNP测定法显示与proBNP肽段存在显著交叉反应性。NT-proBNP测定法无法检测到糖基化形式的NT-proBNP或proBNP。proBNP测定法优先检测BNP 1-32肽段,并且与BNP肽段和糖基化proBNP的交叉反应性最小。

结论

由于目前现有的免疫测定法在交叉反应性以及检测proBNP衍生片段各种糖基化形式的能力方面存在差异,因此BNP或NT-proBNP的检测结果在这些测定法之间不可通用。仍有机会对BNP和NT-proBNP测定法进行标准化和统一,以及开发特异性的proBNP测定法,以拓宽它们的临床应用范围。

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