To determine the clinical effect of diltiazem on the metabolism of ade
nosine, and its importance in ischemic heart disease, arterial plasma
concentrations of the purine metabolites were determined in 21 healthy
volunteers (10 female and 11 male) and 19 patients with effort-angina
(8 female and 11 male) before, during, and immediately after standard
treadmill exercise feats conducted before and after they had taken 60
mg diltiazem (Cardizem; Hoechst Marion Roussel, Laval, QC, Canada) fo
ur times a day for 1 week. The results showed that the cardiac patient
s had significantly lower mean plasma concentrations of uric acid (46.
82 +/- 25.51 versus 95.47 +/- 35.41 mu g/ml, p < 0.05), inosine (0.25
+/- 0.19 versus 0.84 +/- 0.17 mu g/ml, p < 0.05), and hypoxanthine (0.
18 +/- 0.35 versus 0.50 +/- 0.27 mu g/ml, p < 0.05), Diltiazem decreas
ed the mean resting plasma concentrations of uric acid in patients (ur
ic acid 43.47 +/- 22.26 versus 46.82 +/- 25.51 mu g/ml, p < 0.05) and
healthy volunteers (uric acid 85.68 +/- 26.71 versus 95.47 +/- 35.41 m
u g/ml, p < 0.05). There was no statistically significant change in th
e plasma concentrations of the purine metabolites during exercise (p >
0.05). Female subjects had significantly lower plasma concentrations
of uric acid than males (patients, 34.87 +/- 26.93 versus 55.78 +/- 21
.25 mu g/ml healthy volunteers, 84.79 +/- 32.07 versus 104.22 +/- 37.0
5 mu g/ml; p < 0.05 for both). Results of the study suggest that norma
l therapeutic doses of diltiazem may modulate the metabolism of adenos
ine and that some of the purine metabolites may be useful markers for
specific types of ischemic heart disease.