The determination of the 99th centile level for troponin assays in an Australian reference population
Jillian R Tate1, Wendy Ferguson, Renze Bais
1Chemical Pathology Department, Pathology Queensland, Royal Brisbane and Women's Hospital, Herston, QLD 4029, Australia. jill_tate@health.qld.gov.au
Insights
Cardiac troponin (cTn) 99th centile values vary by assay and reference population, potentially impacting myocardial infarction diagnosis. This study highlights the need for consistent assay calibration and population selection for accurate clinical classification.
Area of Science:
- Clinical Chemistry
- Cardiovascular Diagnostics
- Biomarker Assay Validation
Background:
- Current myocardial infarction guidelines use a single cardiac troponin (cTn) cut-off based on the 99th centile.
- This study determined the 99th centile for eight cTn assays in an Australian reference population.
Purpose of the Study:
- To assess the 99th centile values of cardiac troponin assays.
- To evaluate the variability and concordance of cTn measurements across different methods.
Main Methods:
- Nine laboratories measured cTn in serum and plasma from 111 healthy individuals.
- Imprecision profiles and method comparisons were conducted using routine samples.
Main Results:
- 99th centile values were often lower than manufacturer levels, with imprecision at the 99th centile being 20% CV or higher.
- Significant variability in cTn concentrations above the study's 99th centile was observed across eight different assays.
Conclusions:
- Reference population selection significantly influences cTn 99th centile values.
- Observed differences in cTn method concordance at the 99th centile cut-off may lead to varied clinical classifications for myocardial infarction.
Background:
Current guidelines for the diagnosis and risk assessment of patients presenting with myocardial infarction recommend a single decision cut-off point for cardiac troponin (cTn) based on the 99th centile of a reference population. The 99th centile level for eight troponin assays was determined in an apparently cardio-healthy Australian reference population.
Methods:
Nine laboratories measured troponin in serum and plasma collected from 111 reference individuals. An imprecision profile was determined using up to 10 serum samples analysed on 10 separate days. Method comparison using 100 routinely tested plasma samples was performed to estimate method concordance.
Results:
Generally 99th centile values determined in this study were lower than, or the same as manufacturers' levels, except for cTnI by Architect (0.020 vs. 0.012 microg/L), and imprecision at the 99th centile was 20% coefficient of variation (CV) or higher. Troponin concentrations at 10% CV were greater than those quoted in the manufacturer's package insert except by AxSYM, 0.06 vs. 0.16 microg/L cTnI, and by E-170, 0.02 vs. 0.03 microg/L cTnT. In the method comparison 74, 70, 65, 75, 58, 66, 58 and 77 samples measured by Access, Architect, AxSYM, Centaur, Dimension RxL, E-170, i-STAT and Vitros ECi assays, respectively, had troponin concentrations above the study 99th centile.
Conclusions:
Depending on the selected reference population for troponin, there is likely to be variability in the 99th centile as shown in this study. Some differences in sample concordance at the 99th centile cut-off were observed between cTn methods and may result in different clinical classification.
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