The expression of coxsackie B virus adenovirus receptor (CAR) in viral myocarditis and dilated cardiomyopathy patients.
- Author:
Hong-yan LI
1
;
Yong-hong LI
;
Tuan-jie ZHU
Author Information
1. Forensic medicine department of Wannan Medical College, Wuhu 241001, China. hongyanli007@yahoo.com.cn
- Publication Type:Journal Article
- MeSH:
Adenovirus Infections, Human/complications*;
Cardiomyopathy, Dilated/virology*;
Case-Control Studies;
Coxsackie and Adenovirus Receptor-Like Membrane Protein;
Coxsackievirus Infections/complications*;
Death, Sudden, Cardiac;
Female;
Humans;
Immunohistochemistry;
Male;
Myocarditis/virology*;
Myocardium/pathology*;
Receptors, Virus/metabolism*
- From:
Journal of Forensic Medicine
2007;23(4):247-249
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore etiology and pathogenesis of viral myocarditis (VMC) and dilated cardiomyopathy (DCM).
METHODS:The expression of Coxsackie B virus and adenovirus receptors (CAR) were detected with modified immunohistochemical (IHC) technique in myocardium of left ventricle, right ventricle, interventricular septum, and septal papillary muscle from 28 patients with viral myocarditis, 31 patients with dilated cardiomyopathy and 17 control patients (including normal, hypertension heart disease, myocardial infarction and coronary atherosclerotic heart disease).
RESULTS:The brown staining on the cell membrane of myocardium represents positive result. 100% (28 of 28) of VMC patients (IHC surface integral: 4.3975 +/- 0.0365) and 84% (26 of 31) of DCM patients (4.2064 +/- 0.052 6) had prevalent CAR expression compared to 0% (0 of 19) control patients (0.073 1 +/- 0.0362). There were statistically significant differences between VMC/DCM and control patients (P < 0.05).
CONCLUSION:The prevalence of CAR expression was significantly higher in VMC and DCM patients (100% and 84% vs. 0% in control). In contrast, there was no difference found between VMC and DCM patients. These results suggest that both VMC and DCM involve viral etiology and could share a similar pathogenesis.
