Exp Mol Med.  2005 Feb;37(1):51-57.

Myocardial injury occurs earlier than myocardial inflammation in acute experimental viral myocarditis

• Lim BK
• Shin JO
• Choe SC
• Choi SW
• Jeong JO
• Seong IW
• Kim DK
• Jeon ES

Abstract

Endomyocardial biopsy often fails to show myocardial inflammation for patients with clinically suspected myocarditis. The serum isoforms of troponin T (cTnT) level is a very sensitive marker of myocardial injury and it is elevated even in the absence of myocardial inflammation. We investigated the correlations for myocardial injury, virus titers and inflammation in acute viral infection. Using the murine coxsackievirus group B3 (CVB3) myocarditis model, the histopathologic findings and virus titers in mouse hearts were compared with the serum cTnT levels measured by ELISA at various time points. Viable virus titers in the hearts peaked at 3 days after infection (8.22+/-0.13 log10 PFU/100 mg of heart); they decreased at day 7 and no viable virus was detected from day 14. Myocardial inflammation was minimal at day 3, peaked at day 7 and markedly decreased at day 14. The individual serum TnT levels were significantly increased at day 3 (7.37+/-1.46 ng/ml), persisted to day 7 (0.73+/-0.08 ng/ml), and normalized at day 14. Serum cTnT levels were correlatable with virus titers in the heart (r=0.744, P <0.01), but the serum cTnT levels were not correlated with the degrees of inflammation. Using the less myocarditic strain of CVB3, similar relationships were observed between the changes for the serum cTnT levels and the heart virus titers. During the course of viral infection, myocardial injury precedes the pathologic evidence of inflammation, and the elevated cTnT levels provide evidence of myocardial injury even in the absence of any histologic findings of myocarditis.

Keyword

inflammation; myocardial injury; troponin; viral myocarditis

MeSH Terms

Acute Disease
Animals
Coxsackievirus Infections/*pathology
Enterovirus B, Human/isolation & purification/pathogenicity/*physiology
Female
Heart/*virology
Hela Cells
Humans
Inflammation/*immunology
Mice
Mice, Inbred BALB C
Myocardial Infarction/immunology/*pathology
Myocarditis/immunology/pathology/*virology
*Myocardium/immunology/pathology
Research Support, Non-U.S. Gov't
Troponin T/blood
Virus Replication