SMALL, DENSE LOW-DENSITY-LIPOPROTEIN PARTICLES AS A PREDICTOR OF THE RISK OF ISCHEMIC-HEART-DISEASE IN MEN - PROSPECTIVE RESULTS FROM THE QUEBEC CARDIOVASCULAR STUDY
B. Lamarche et al., SMALL, DENSE LOW-DENSITY-LIPOPROTEIN PARTICLES AS A PREDICTOR OF THE RISK OF ISCHEMIC-HEART-DISEASE IN MEN - PROSPECTIVE RESULTS FROM THE QUEBEC CARDIOVASCULAR STUDY, Circulation, 95(1), 1997, pp. 69-75
Background Case-control studies have reported that patients with ische
mic heart disease (IHD) have a higher proportion of small, dense LDL p
articles than do healthy control subjects. The extent to which the ris
k attributed to small LDL particles may be independent of concomitant
variations in plasma lipoprotein-lipid concentrations remains to be cl
early determined, however, particularly through prospective studies. M
ethods and Results Baseline characteristics were obtained in 2103 men
initially free of IHD, among whom 114 developed IHD during a 5-year fo
llow-up period. These 114 case patients were matched with healthy cont
rol subjects for age, body mass index, smoking habits, and alcohol int
ake. LDL peak particle diameter (PPD) was measured a posteriori in 103
case-control pairs by nondenaturing gradient gel electrophoresis of w
hole plasma. Conditional logistic regression analysis of the case-cont
rol status revealed that men in the first tertile of the control LDL-P
PD distribution (LDL-PPD less than or equal to 25.64 nm) had a 3.6-fol
d increase in the risk of MD (95% CI, 1.5 to 8.8) compared with those
in the third tertile (LDL-PPD>26.05 nm). statistical adjustment for co
ncomitant variations in LDL cholesterol, triglycerides, HDL cholestero
l, and apolipoprotein B concentrations had virtually no impact on the
relationship between small LDL particles and the risk of IHD. Conclusi
ons These results represent the first prospective evidence suggesting
that the presence of small, dense LDL particles may be associated with
an increased risk of subsequently developing IHD in men. Results also
suggest that the risk attributed to small LDL particles may be partly
independent of the concomitant variation in plasma lipoprotein-lipid
concentrations.