Korean J Intern Med.
2000 Jan;15(1):56-64.
Apoptosis in dilated cardiomyopathy
- Affiliations
-
- 1Cardiovascular Research Institute, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Abstract
OBJECTIVE
Cardiomyopathy, a popular diagnosis that always obscures more than it
reveals, nevertheless has several characteristic histological features. These
prominently include widespread focal myocardial fibrosis and associated
hypertrophy of surviving cardiac myocyte. In fact, focal noninflammatory
degeneration (not necrosis) has been demonstrated as a feature of many forms of
cardiac hypertrophy. We hypothesized that this loss of myocardial cells in
dilated cardiomyopathy (DCMP) may result from cell death by apoptosis. METHODS:
Endomyocardial biopsy specimens from the right ventricles of six patients who
suffered from DCMP were studied, and myocardial specimens from two persons who
died in motor vehicle accidents were used as negative controls. For
identification of apoptosis, immunohistochemistry with terminal deoxynucleotidyl
transferase (TdT)-mediated dUTP-biotin nick end-labeling was performed. In
addition, apoptosis was confirmed morphologically by confocal laser scanning
microscopy with propidium iodide. RESULTS: Apoptosis, that was represented by an
apoptotic index ranging from 19.8 to 25.4+ACU-, could be extensively seen in
myocytes and also rarely in non-myocytes of interstitium and vascular
endothelium. Morphologically, there were a lot of nuclei with clumps of
condensed chromatin, suggestive of apoptosis. CONCLUSION: The present study
demonstrated that myocyte loss in DCMP might be mainly due to the apoptosis of
myocytes and interstitial cells, rather than inflammation or cell necrosis.