ANALYSIS OF FORMALIN-FIXED AND FROZEN MYOCARDIAL AUTOPSY SAMPLES FOR VIRAL GENOME IN CHILDHOOD MYOCARDITIS AND DILATED CARDIOMYOPATHY WITH ENDOCARDIAL FIBROELASTOSIS USING POLYMERASE CHAIN-REACTION (PCR)
Ld. Griffin et al., ANALYSIS OF FORMALIN-FIXED AND FROZEN MYOCARDIAL AUTOPSY SAMPLES FOR VIRAL GENOME IN CHILDHOOD MYOCARDITIS AND DILATED CARDIOMYOPATHY WITH ENDOCARDIAL FIBROELASTOSIS USING POLYMERASE CHAIN-REACTION (PCR), Cardiovascular pathology, 4(1), 1995, pp. 3-11
Viral infection of the myocardium is implicated in the pathogenesis of
myocarditis and dilated cardiomyopathy (DCM). Enteroviruses have been
considered the most common viral etiologic agents, based on periphera
l culture and serologic methods. Recently, polymerase chain reaction (
PCR) has been shown to be useful in the detection of viral genomes fro
m various infected organs and body fluids. In this study, myocardial s
amples from autopsy specimens (formalin fixed and fresh frozen) were e
xamined for enteroviral and DNA viral (adenovirus, herpes simplex viru
s [HSV], and cytomegalovirus (CMV]) genome by PCR. The specimens studi
ed were from 58 patients with myocarditis, 28 patients with DCM and en
docardial fibroelastosis [EFE], and 22 controls. Viral genome was dete
ctable in 34 of the 58 (59%) autopsy-proven myocarditis samples (18 ad
enovirus, 12 enterovirus, 2 CMV, 2 HSV) and 6 of the 28 samples from p
atients with DCM and EFE (6 adenovirus). We conclude that PCR is effec
tive in the rapid amplification of virus from frozen and formalin-fixe
d myocardial samples and that adenovirus is an important etiologic age
nt in viral myocarditis as well as DCM with EFE.