In 1995, some retrospective reports showed that certain patients treat
ed with short-acting calcium antagonists were at increased risk for my
ocardial infarction and had a higher mortality rate compared with pati
ents treated with other cardiovascular drugs. Subsequent reports attem
pted to establish a connection between calcium antagonists and disorde
rs as diverse as malignancy, Parkinsonism, cognitive dysfunction, and
suicide. However, other retrospective studies and, more compelling, se
veral prospective studies have reported that calcium antagonists exert
a beneficial effect on morbidity and mortality in a variety of cardio
vascular disorders such as hypertension, ischemic heart disease after
myocardial infarction, and congestive heart failure due to dilated car
diomyopathy. Calcium antagonists are a heterogeneous drug class, and d
istinct differences have been documented between short- and long-actin
g, as well as between dihydropyridine and nondihydropyridine, agents.
Sympathetic activation, which is a risk factor for coronary events, oc
curs with short-acting agents only and is absent with long-acting calc
ium antagonists. Recent dam make it extremely unlikely that calcium an
tagonists increase the risk of malignancy by affecting apoptosis or im
munosuppression or both. Long-acting calcium antagonists have distinct
benefits in patients with hypertension and diabetes and may be more b
eneficial than other drugs in patients with diabetes and left ventricu
lar hypertrophy. (C) 1998 by Excerpta Medico, Inc.