HMG-CoA reductase inhibitors or statins are potent hypocholesterolemic drug
s. They associate a dose-dependent diminution of LDL-cholesterol (-25 to 60
%) to a raise of HDL-cholesterol (+5 to 12 %) and a diminution of triglyce
rides (-15 a 30 %). Important controlled clinical trials have shown the abi
lity of these drugs to reduce - coronary morbidity and mortality in seconda
ry prevention (4S study with simvastatin, CARE and LIPID studies with prava
statin). - total mortality in secondary prevention (4S and LIPID studies).
- coronary morbidity and mortality (AFCAPS/Tex-CAPS with lovastatin) and to
tal mortality in primary prevention (WOSCOPS study with pravastatin).
Questions still remain unanswered. To what extent do we have to lower LDL-c
holesterol ? What are the risks of an aggressive treatment with statins ? C
an we extrapolate the results of the large clinical trials to women, elderl
y, dyslipidemic subjects with other manifestations of atherosclerosis (i.e.
cerebro-vascular, peripheral vascular diseases) ? What are the benefits of
an early treatment by statins in acute coronary syndroms ? Can << pleiotro
pic >> effects influence the future indications of statins ? These question
s will be addressed by ongoing studies which will be published within five
years.