Determination of sex-specific 99th percentile upper reference limits for a point of care high sensitivity cardiac troponin I assay
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Fred S. Apple
, Karen Schulz
, Trees S. Y. van Domburg
Abstract
Objectives
High sensitivity (hs) cardiac troponin (cTn) assays are defined per the IFCC Committee on Clinical Application of Cardiac Biomarker (C-CB) by the ability to measure ≥ 50% of concentrations greater than the limit of detection (LoD) with an impression of ≤10% at sex-specific 99th percentiles. Our study determined the sex-specific 99th percentile upper reference limits for males and females utilizing heparinized plasma from AACC universal sample bank for the Siemens point of care (POC) Atellica® VTLi hs-cTnI immunoassay.
Methods
Apparently healthy subjects, included overall 693, males 363, and females 330, following exclusionary surrogate biomarker use of hemoglobin A1c, NT-proBNP, and eGFR, along with statin medication. hs-cTnI was measured in a central laboratory, on multiple POC Atellica® VTLi immunoassay analyzers. The LoD was 1.24 ng/L and the 10%CV concentration was 6.7 ng/L. 99th percentile URLs were determined by the nonparametric (NP) method.
Results
Histograms of the hs-cTnI concentrations (ng/L) for males and females were used to visualize the distributions and concentrations in men and women and differed significantly (pre- and post-exclusion, both p <0.001). 99th percentile URLs were: overall 23 ng/L (90% CI 20–32 ng/L); male 27 ng/L (CI 21–37 ng/L); female 18 ng/L (CI 9–78 ng/L). The percentages of subjects having a measurable concentration ≥ the LoD were: overall 83.7%, male 87.3%, female 79.7%.
Conclusions
Our findings show the novel POC Atellica® VTLi hs-cTnI assay meets the designation of a ‘high-sensitivity’ assay using heparinized plasma.
Funding source: Hennepin Healthcare Research Institute
Award Identifier / Grant number: Funded in part
Funding source: Siemens Healthineers
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Research funding: This study was funded in part by Siemens Healthineers.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: FSA: Board of Directors, HyTest Ltd.; Honorarium Advisory Boards: Siemens Healthcare, Instrumentation Laboratory, Qorvo; Research PI through Hennepin Healthcare Research Institute (not salaried): Abbott Diagnostics, Abbott Point of Care, Roche Diagnostics, Siemens Healthcare, Quidel/Alere, Ortho-Clinical Diagnostics, Beckman Coulter; Other: Associate Editor Clinical Chemistry.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the authors’ Institutional Review Board.
References
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© 2021 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
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- General Clinical Chemistry and Laboratory Medicine
- Multicenter evaluation of use of dried blood spot compared to conventional plasma in measurements of globotriaosylsphingosine (LysoGb3) concentration in 104 Fabry patients
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- Cancer Diagnostics
- Circulating pro-gastrin releasing peptide (ProGRP) in patients with medullary thyroid carcinoma
- Cardiovascular Diseases
- Determination of sex-specific 99th percentile upper reference limits for a point of care high sensitivity cardiac troponin I assay
- Comparison of the analytical performance of the PATHFAST high sensitivity cardiac troponin I using fresh whole blood vs. fresh plasma samples
- Infectious Diseases
- Comprehensive assessment of humoral response after Pfizer BNT162b2 mRNA Covid-19 vaccination: a three-case series
- Analytical validation of an automated assay for the measurement of adenosine deaminase (ADA) and its isoenzymes in saliva and a pilot evaluation of their changes in patients with SARS-CoV-2 infection
- A new tool for sepsis screening in the Emergency Department
- Letters to the Editor
- Caveat emptor – hidden pitfalls in defining the 99th percentile of cardiac troponin assays
- Assay requirements for COVID-19 testing: serology vs. rapid antigen tests
- Stability of SARS-CoV-2 RNA in FTA card spot-prep samples derived from nasopharyngeal swabs
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- Congress Abstracts
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Articles in the same Issue
- Frontmatter
- Editorial
- High-sensitivity assay for cardiac troponins with POCT methods. The future is soon
- Review
- The assessment of circulating cell-free DNA as a diagnostic tool for breast cancer: an updated systematic review and meta-analysis of quantitative and qualitative ssays
- Mini Review
- Which laboratory technique is used for the blood sodium analysis in clinical research? A systematic review
- Guidelines and Recommendations
- IFCC interim guidelines on rapid point-of-care antigen testing for SARS-CoV-2 detection in asymptomatic and symptomatic individuals
- General Clinical Chemistry and Laboratory Medicine
- Multicenter evaluation of use of dried blood spot compared to conventional plasma in measurements of globotriaosylsphingosine (LysoGb3) concentration in 104 Fabry patients
- S100B protein, cerebral ultrasound and magnetic resonance imaging patterns in brain injured preterm infants
- Urinary exosomal CD26 is associated with recovery from acute kidney injury in intensive care units: a prospective cohort study
- Evaluation of red blood cell parameters provided by the UF-5000 urine auto-analyzer in patients with glomerulonephritis
- Reference Values and Biological Variations
- Pediatric reference interval verification for common biochemical assays on the Abbott Alinity system
- Paediatric reference range for overnight urinary cortisol corrected for creatinine
- Cancer Diagnostics
- Circulating pro-gastrin releasing peptide (ProGRP) in patients with medullary thyroid carcinoma
- Cardiovascular Diseases
- Determination of sex-specific 99th percentile upper reference limits for a point of care high sensitivity cardiac troponin I assay
- Comparison of the analytical performance of the PATHFAST high sensitivity cardiac troponin I using fresh whole blood vs. fresh plasma samples
- Infectious Diseases
- Comprehensive assessment of humoral response after Pfizer BNT162b2 mRNA Covid-19 vaccination: a three-case series
- Analytical validation of an automated assay for the measurement of adenosine deaminase (ADA) and its isoenzymes in saliva and a pilot evaluation of their changes in patients with SARS-CoV-2 infection
- A new tool for sepsis screening in the Emergency Department
- Letters to the Editor
- Caveat emptor – hidden pitfalls in defining the 99th percentile of cardiac troponin assays
- Assay requirements for COVID-19 testing: serology vs. rapid antigen tests
- Stability of SARS-CoV-2 RNA in FTA card spot-prep samples derived from nasopharyngeal swabs
- Homocysteine (Hcy) assessment to predict outcomes of hospitalized Covid-19 patients: a multicenter study on 313 Covid-19 patients
- Concomitant immune thrombocytopenia and bone marrow hemophagocytosis in a patient with SARS-CoV-2
- Procalcitonin measurement by Diazyme™ immunturbidimetric and Elecsys BRAHMS™ PCT assay on a Roche COBAS modular analyzer
- Use of Neurosoft expert system improves turnaround time in a laboratory section specialized in protein diagnostics: a two-year experience
- Impact of different sampling and storage procedures on stability of acid/base parameters in venous blood samples
- Compound heterozygotes of Hb Constant Spring and Hb Stanleyville II in HbE/β0-thalassemia
- Congress Abstracts
- 60th National Congress of the Hungarian Society of Laboratory Medicine