Cardiac troponin I (cTnI) is highly specific for cardiac muscle. In this study, we compared the utility of CK and CK-MB index versus cTnI in the assessment of myocardial infarction in 155 patients being evaluated for myocardial damage. As a cardiac marker for MI, Troponin I seems to be superior to C
Lack of Association Between Cardiac Troponin T and D-Dimer in the Evaluation of Myocardial Damage
✍ Scribed by Rafael Noal Moresco; Luís Cláudio Rosa Vargas; Ronald Halla Júnior; Lúcia Mariano da Rocha Silla
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 106 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0887-8013
No coin nor oath required. For personal study only.
✦ Synopsis
Acute myocardial infarction (AMI) disrupts cardiac cell membranes, releasing intracellular cardiac proteins into the vascular system. Some of these proteins, including the cardiac troponin subunits T and I, have proven useful for diagnosing myocardial damage. Intracoronary thrombosis plays a key role in the pathogenesis of AMI, and the formation of an occlusive thrombus usually precedes the development of myocardial damage. To evaluate whether there is an association between the size of intracoronary thrombosis and myocardial damage, we analyzed D-dimer and cTnT levels in blood samples from patients suspected to have myocardial damage. We investigated 102 patients who were admitted to emergency service for suspected myocardial damage. D-dimer was assessed with the use of the immunoassay Liatest D-dimer, and cTnT levels were measured with an electrochemiluminescence immunoassay (Troponin T STAT). D-dimer levels were lower in patients with cTnTo0.01 than in patients presenting cTnT40.01 ng/mL. We investigated the relationship between D-dimer and cTnT levels in the patients with cTnT40.01 ng/mL (0.4070.10 ng/mL), and no significant agreement (r 5 0.20, P40.05) was observed. The levels of D-dimer were not associated with the levels of cTnT in patients with cTnT40.01 ng/mL.
📜 SIMILAR VOLUMES
The purpose of this study was to evaluate diffuse myocardial fibrosis by measuring myocardial and blood T1values using contrast-enhanced Look-Locker cardiac MRI and comparing these values with left cardiac function in dilated cardiomyopathy (DCM). We also sought to assess the relation between the di
BACKGROUND: Genetic variation in the folate metabolic pathway may influence the risk of congenital heart defects. This study was undertaken to assess the associations between the inherited and maternal genotypes for variants in folate-related genes and the risk of a composite heart phenotype that in