Validation of Acute Myocardial Infarction (AMI) Cut-off Point for Troponin I on the ADVIA Centaur Assay
Authors: M.E. Salama; Carolyn S. Feldkamp; John L. Carey; James K. McCord; Mouaz Al-Mallah
Source: Journal of Clinical Ligand Assay, Volume 27, Number 1, Spring 2004 , pp. 14-17(4)
Publisher: Clinical Ligand Assay Society
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Abstract:
The preferred biomarker for myocardial damage is cardiac troponin. Any increased value exceeding the 99th percentile of a reference control group (by an assay with CV < 10%) in the appropriate clinical setting is associated with acute myocardial infarction. We evaluated an automated platform, ADVIA Centaur. An essential step in the evaluation of troponin I level is to establish a clinically relevant cut-off point for AMI diagnosis. Four hundred sixty-nine heparinized plasma samples were drawn from 161 patients presenting with symptoms suggestive of myocardial infarction. Part 1: In 80 patients, troponin I was measured on two different analytical systems (Abbott AxSYM and Bayer ADVIA Centaur). Clinical diagnosis of AMI was used as the 'gold standard' for the AMI. Results were compared using Receiver Operator Characteristic (ROC) curve analysis. Part 2: To determine the clinical sensitivity and specificity within different time intervals after presentation, an additional 81 patients, each with a series of at least 3 samples, were analyzed by ADVIA Centaur Assay. Twenty-six patients with undetermined clinical diagnosis were excluded from the analysis (17 in part 1 and 9 in part 2). Part 1: Of 63 subjects, 16 (25.4%) had AMI, 47 (74.6%) did not. Based on our data, 0.77 ng/mL (plasma) cut-off point in the Centaur assay optimizes both sensitivity and specificity (100% & 98% respectively). Our previously established cut-off in use by the AxSYM is 2.5 ng/mL (sensitivity and specificity of 94% & 81%). Part 2: Of 72 subjects, 53 (73.6%) had AMI, 19 (26.4%) did not. ROC analysis of cTnI at time intervals after presentation (T1=0, T2=>0 to <3, T3=3 to <6, T4=6 to <12, T5=>12 hours) showed maximum efficiency at cut-off points of 0.20, 0.51, 0.61 and 0.93 ng/mL respectively. We conclude that in plasma, 0.77 ng/mL is the best cut-off for the diagnosis of AMI based on the established clinical diagnosis. The precision is adequate for our clinical application in the range of the cut-off.Keywords: ACUTE MYOCARDIAL INFARCTION CUT-OFF POINT; TROPONIN I; ENZYME IMMUNOASSAY; CHEMILUMINESCENCE; ADVIA CENTAUR; AXSYM
Document Type: Research article
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