Apolipoprotein E in VLDL and LDL with apolipoprotein C‐III is associated with a lower risk of coronary heart disease

CO Mendivil, EB Rimm, J Furtado… - Journal of the American …, 2013 - Am Heart Assoc
Journal of the American Heart Association, 2013Am Heart Assoc
Background Low‐density lipoprotein (LDL) with apolipoprotein C‐III (apoC‐III) is the
lipoprotein species that most strongly predicts initial and recurring coronary heart disease
(CHD) events in several cohorts. Thus, a large portion of the CHD risk conferred by LDL may
be attributable to LDL that contains apoC‐III. Very‐low‐density lipoprotein (VLDL) and LDL
with apoC‐III have varying amounts of apoE. We hypothesized that a high content of apoE
lessens the adverse influence of apoC‐III on the risk of CHD because it promotes the …
Background
Low‐density lipoprotein (LDL) with apolipoprotein C‐III (apoC‐III) is the lipoprotein species that most strongly predicts initial and recurring coronary heart disease (CHD) events in several cohorts. Thus, a large portion of the CHD risk conferred by LDL may be attributable to LDL that contains apoC‐III. Very‐low‐density lipoprotein (VLDL) and LDL with apoC‐III have varying amounts of apoE. We hypothesized that a high content of apoE lessens the adverse influence of apoC‐III on the risk of CHD because it promotes the clearance of VLDL and LDL from plasma.
Methods and Results
We studied 2 independent cohorts, the Nurses' Health Study, composed of women, and the Health Professionals Follow‐up Study, composed of men. These cohorts contributed to this study 322 women and 418 men initially free of CVD who developed a fatal or nonfatal myocardial infarction during 10 to 14 years of follow‐up and matched controls who remained free of CHD. The apoE content of LDL with apoC‐III was inversely associated with CHD after multivariable adjustment (relative risk for top versus bottom quintile 0.53, 95% CI 0.35 to 0.80). The apoE content of VLDL with apoC‐III had a similar inverse association with CHD. The highest risks were associated with a high apoB concentration and a low apoE content of LDL with apoC‐III or of VLDL+LDL with apoC‐III. The observed associations were in both male and female cohorts and independent of traditional CHD risk factors and of C‐reactive protein.
Conclusions
An increased apoE content in VLDL and LDL with apoC‐III was associated with a lower risk of CHD. Strategies to enrich VLDL and LDL in apoE are worth exploring for the prevention of CHD.
Am Heart Assoc