Objective: To study the mitochondrial respiratory chain enzyme activities i
n patients with idiopathic dilated cardiomyopathy (IDC). Methods: Mitochond
rial respiratory chain enzyme activities were assessed spectrophotometrical
ly in left ventricular tissue of 17 patients with IDC undergoing cardiac tr
ansplantation, as well as in two groups of controls: a group of six patient
s suffering from ischemic dilated cardiomyopathy (IC) also undergoing cardi
ac transplantation, and a group of 17 organ donors considered normal from a
cardiac point of view. Cytochrome b gene from three IDC patients whose com
plex III activity was particularly low and from three controls was also seq
uenced. Results: We found that complex III enzymatic activity was lower not
only in IDC but also in IC patients when compared with normal controls. Wh
en analysing cytochrome b gene we only found neutral polymorphisms previous
ly described. Conclusions: In view of such results, we believe that the dec
rease of respiratory chain complex III activity found in some car;es of IDC
is a secondary phenomenon, and not due to a primary mitochondrial disease.
(C) 2000 Elsevier Science B.V. All rights reserved.