The plasma LDL concentration is firmly established as a cause of coronary h
eart disease. However, the efficacy of LDL lowering may reach a limit when
it is brought well below average during treatment. The Cholesterol and Recu
rrent Events (CARE) trial compared pravastatin and placebo in patients who
had experienced myocardial infarction who had average concentrations of tot
al cholesterol < 240 mg/dl (baseline mean 209 mg/dl) and LDL cholesterol (L
DL) 115 to 174 mg/dl (mean 139 mg/dl).
Pravastatin reduced coronary death or recurrent myocardial infarction by 24
%. In multivariate analysis, the LDL concentration achieved during follow-u
p was a significant predictor of the coronary event rate. The relationship
was nonlinear since the coronary event rate declined as LDL decreased durin
g follow-up from 174 to approximately 125 mg/dl, but no further decline was
seen in the LDL range from 125 to 71 mg/dl.
A major ongoing effort in the CARE trial concerns the identification of non
-LDL mediated mechanisms of coronary events. Chronic low-grade inflammation
has recently been identified as an important new risk factor for coronary
artery disease. Two markers of inflammation, C-reactive protein (CRP) and s
erum amyloid A (SAA), were measured in patients in the CARE trial who suffe
red a recurrent myocardial infarction or coronary death and in those who di
d not have these recurrent events. Levels of both inflammatory markers were
significantly higher among post-myocardial infarction patients who subsequ
ently developed recurrent coronary events. This association was significant
in the patients who were treated with placebo but not in those in the prav
astatin group.
In conclusion, attaining an LDL of < 125 mg/dl may be sufficient treatment
of LDL concentrations, removing the adverse effect of LDL on coronary event
s. These findings also raise the possibility that the efficacy of pravastat
in may partly result from anti-inflammatory as well as lipid lowering prope
rties.