Weekly and 90-Minute Biological Variations in Cardiac Troponin T and Cardiac Troponin I in Hemodialysis Patients and Healthy Controls

Author:

Aakre Kristin M12,Røraas Thomas3,Petersen Per Hyltoft3,Svarstad Einar45,Sellevoll Hilde5,Skadberg Øyvind6,Sæle Kristin5,Sandberg Sverre13

Affiliation:

1. Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway

2. Norwegian Clinical Chemistry EQA Program, Bergen, Norway

3. Norwegian Quality Improvement of Primary Care Laboratories (NOKLUS), Department of Public Health and Primary Health Care, University of Bergen, Bergen, Norway

4. Department of Clinical Medicine, University of Bergen, Bergen, Norway

5. Department of Medicine, Haukeland University Hospital, Bergen, Norway

6. Laboratory of Clinical Biochemistry, Stavanger University Hospital, Stavanger, Norway

Abstract

Abstract BACKGROUND Myocardial infarction (MI) is diagnosed by the finding of a single cardiac troponin value above the 99th percentile and a significant time-dependent change in cardiac troponin concentration. The aim of this study was to determine the 90-min and weekly biological variations, the reference change value (RCV), and the index of individuality (II) of high-sensitivity cardiac troponin T (hs-cTnT) (Roche Diagnostics) and hs-cTnI (Abbott Diagnostics) in patients receiving hemodialysis (HD) and in healthy individuals. METHOD Blood samples were collected from 19 HD patients (on an HD-free day) and 20 healthy individuals at 90-min intervals over a 6-h period (between 08:30 and 14:30) and before the midweek HD treatment for 10 weeks. The within-person variation (CVi), between-person variation, RCV, and II were calculated. RESULTS During the 6-h sampling period, the concentrations of hs-cTnT (both groups) and hs-cTnI (HD patients only) decreased on average by 0.8% to 1.7% per hour, respectively. These declining trends were included in the calculation of a 90-min asymmetric RCV: −8%/+5% in HD patients (hs-cTnT), −18%/+21% in HD patients (hs-cTnI), −27%/+29% in healthy individuals (hs-cTnT), and −39%/+64% in healthy individuals (hs-cTnI). The II was low in both groups for both assays. The weekly CVi values were approximately 8% (hs-cTnT) and 15% (hs-cTnI) in both groups. CONCLUSIONS When using a cardiac troponin change of 20%–50% to diagnose an MI, the false-positive rate is likely to be lower for the hs-cTnT assay than for the hs-cTnI assay. The low II suggests that use of a diagnostic cutoff value can be omitted.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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