Pregnancy associated plasma protein-A: ultrasensitive immunoassay and determination in coronary heart disease

被引:58
作者
Khosravi, J [1 ]
Diamandi, A
Krishna, RG
Bodani, U
Mistry, J
Khaja, N
机构
[1] Diagnost Syst Labs Canada Inc, Toronto, ON, Canada
[2] Dianost Syst Labs Inc, Webster, TX USA
[3] Univ Toronto, Fac Med, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
关键词
PAPP-A; ELISA; pregnancy; MI; acute coronary syndrome; IGF; IGFBP; IGFBP-4;
D O I
10.1016/S0009-9120(02)00359-4
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
Objective: Markers of myocardial injury have been vital in the assessment of patients with coronary heart disease. Pregnancy associated plasma protein A (PAPP)-A is an insulin-like growth factor (IGF) binding protein (IGFBP)-4 protease and a potential early indicator of unstable angina. We developed an ultrasensitive enzyme-linked immunosorbent assay (ELISA) for PAPP-A and measured serum PAPP-A in patients with biochemical evidence of acute coronary syndrome. Design and Methods: Method development was based on pair-wise evaluation of a panel of antibodies and determination of PAPP-A specificity and sensitivity relative to those of a conventional method. Association of PAPP-A with myocardial damage was assessed in serum samples classified based on serum creatine kinase (CK)-MB or cardiac troponin-T levels. Results: Serum PAPP-A was significantly higher in samples with elevated CK-MB or troponin-T than in samples with normal CK-MB (p < 0.001). Marker-association studies showed strong correlation between PAPP-A and troponin-T (r = 0.59, p < 0.001) in a subset of troponin-T positive samples. Indications for both parallel as well as divergence in the expression of PAPP-A and troponin-T was also evident when serial timed samples available from a number of patients were analyzed. Conclusions: The data are consistent with the conclusion that expression of PAPP-A is enhanced in patients with biochemical evidence of acute coronary syndrome and suggest strongly that demonstration of PAPP-A association with other cardiac markers might be influenced by their relative release dynamics (timing and duration). The availability of the ultrasensitive PAPP-A ELISA should facilitate systematic investigations of PAPP-A expression in this and other pathophysiological conditions that might involve altered expression of the IGF/PAPP-A system. (C) 2002 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:531 / 538
页数:8
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