Apoptosis in the myocardium is complex and often difficult to recognise. My
ocyte apoptosis is scattered across the myocardial wall and is restricted t
o individual cells. In the present study, we describe the amount of apoptos
is in 50 endomyocardial biopsies taken from 50 patients with dilated cardio
myopathy, in 14 hearts with hypertrophic cardiomyopathy and in five hearts
with arrhythmogenic dysplasia of the right ventricle. As a control group, 1
5 endomyocardial biopsies from 15 transplanted hearts (of live patients) we
re used. Apoptosis was immunohistochemically determined in paraffin section
s with the TUNEL method. In each specimen the TUNEL index was calculated as
the percentage of TUNEL-positive nuclei among a total number of 200 counte
d nuclei. Cellular morphology was assessed in conjunction with TUNEL staini
ng. The mean percentage of TUNEL-positive myocardial cells varied from 4% f
or dilated cardiomyopathy to 17.5% for arrhythmogenic right ventricle dyspl
asia and 18.5% for hypertrophic cardiomyopathy, whereas no signs of apoptot
ic myocardial cell death were found in normal subjects. The numbers of apop
totic cells in dilated cardiomyopathy specimens were significantly lower by
comparison with both those of hypertrophic cardiomyopathy and those of arr
hythmogenic right ventricular dysplasia specimens. it is evident that apopt
osis constitutes a major biological phenomenon in the development of at lea
st some heart diseases, but its role in their pathophysiology has yet to be
delineated.