One-year in vitro stability of cardiac troponins and galectin-3 in different sample types
One-year in vitro stability of cardiac troponins and galectin-3 in different sample types
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DOI:
10.1016/j.cca.2017.11.018
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发表时间:
2018-01-01
影响因子:
5
通讯作者:
Mueller, Thomas
中科院分区:
文献类型:
--
作者:
Egger, Margot;Dieplinger, Benjamin;Mueller, Thomas
Background: We assessed the long-term in vitro stability of cardiac troponins and galectin-3 under different storage conditions.Methods: We used high-sensitivity cardiac troponin I (hs-cTnI) and galectin-3 assays from Abbott and a high-sensitivity cardiac troponin T (hs-cTnT) assay from Roche. The analyte concentrations of 30 patients were measured in heparin-treated plasma, EDTA-treated plasma and serum samples after the following storage conditions: 1) samples used immediately after blood collection for baseline measurements; 2) samples stored for 0.5 year at -80 degrees C after one freeze-thaw cycle; 3) samples stored for 1.0 year at -80 degrees C after two freeze-thaw cycles; and 4) samples stored for 1.0 year at -80 degrees C after one freeze-thaw cycle. According to the concept of acceptable change limits (ACL) the analytes were considered stable as long as the median concentration at a particular time point was > 80%.Results: Baseline hs-cTnI, hs-cTnT and galectin-3 concentrations ranged from 2.3 to 5436 ng/L, from 5.3 to 850 ng/L, and from 8.3 to 79.3 ng/mL, respectively. After applying the default criterion for analyte stability, the three analytes were stable for at least 1.0 year even after two freeze-thaw cycles for each sample type. We observed the following variation in analyte concentrations after storage relative to the baseline values: the interquartile range (IQR) of cardiac troponin results extended from approx. 80 to 115%, and the IQR of galectin-3 results extended from approx. 90 to 110%.Conclusion: hs-cTnI, hs-cTnT and galectin-3 were stable under the reported storage conditions irrespective of the sample type used. However, we observed a considerable variation in analyte concentrations after sample storage, which might affect the diagnostic/prognostic value of these analytes in individual patients using frozen blood samples.