Multicenter evaluation of a second-generation assay for cardiac troponin T

Author:

Baum Hannsjörg1,Braun Siegmund2,Gerhardt Willie3,Gilson Georges4,Hafner Gerd5,Müller-Bardorff Margit6,Stein Wolfgang7,Klein Gerhard8,Ebert Christoph8,Hallermayer Klaus8,Katus Hugo A6

Affiliation:

1. Institut für Klinische Chemie und Pathobiochemie, Klinikum rechts der Isar der TU München, Ismaningerstr. 22, D-81675 München, Germany

2. Institut für Laboratoriumsmedizin, Deutsches Herzzentrum, München, Germany

3. Department of Clinical Chemistry, Lasarettet Helsingborg, Sweden

4. Laboratoire de Biochimie–Immunopathologie, Centre Hospitalier de Luxembourg

5. Abteilung für Klinische Chemie und Laboratoriumsmedizin der Universität Mainz, Mainz, Germany

6. Medizinische Klinik II, Medizinische Universität Lübeck, Lübeck, Germany

7. Abteilung für Laboratoriumsmedizin/Klinische Chemie, Krankenhaus St. Georg, Hamburg, Germany

8. Boehringer Mannheim, Mannheim, Germany

Abstract

Abstract We report on the evaluation of the second-generation assay for cardiac troponin T (cTnT) on the Enzymun®system. This new assay is completely specific for the cardiac isoform of TnT, utilizing two cardiospecific monoclonal antibodies. The assay time is reduced to 45 min. The interassay precision shows a median CV of 5.5%; 20% interassay CV was found between 0.05 and 0.1 μg/L. The cardiosensitivity of the second-generation cTnT assay in patients with ischemic myocardial injury appears equivalent when compared with the first-generation assay. We found no falsely positive results in patients with skeletal muscle damage including multitraumas, surgery patients, and marathon runners who showed highly increased values with the unspecific first-generation assay. In Duchenne disease cTnT was still increased, but to a much lower extent. cTnT remains increased in renal failure, but to a lesser degree than with the first-generation assay. The cause of this increase remains unclear. Although a cross-reactivity of skeletal muscle TnT in the second-generation assay could be excluded by our findings, minor myocardial damage or expression of the cardiac isoform of TnT in regenerating muscles cannot be ruled out in those cases with apparently falsely increased cTnT values. The second-generation cTnT assay is a step forward in the combination of cardiosensitivity and cardiospecificity in biochemical markers for diagnosis of heart disease.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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