Some epidemiological studies have shown that serum total cholesterol i
ncreases with age, especially in women. On the other hand, the risk of
coronary artery disease is smaller in women than in men. Earlier stud
ies have shown that a small dense low density lipoprotein (LDL) is mor
e atherogenic than a large LDL. We studied LDL size and apolipoprotein
E (apo E) phenotypes in premenopausal and postmenopausal women and in
men at the same age. In this study 342 subjects participating in a he
alth screening study were examined. There were four subgroups: 40-year
-old men (n = 85), 40-year-old women (n = 80), 70-year old men (n = 88
) and 70-year-old women (n = 89). In the present study LDL size was la
rger (P < 0.01) in women (26.39 +/- 0.07 nm) than in men (25.95 +/- 0.
07 nm). We found that LDL size correlated highly positively (r = 0.606
; P < 0.001) with serum high density lipoprotein (HDL) concentration a
nd inversely with serum triglyceride concentration (r = -0.627; P < 0.
001). Measuring serum HDL cholesterol and triglycerides in health scre
ening studies gives information indirectly about LDL size and its athe
rogenicity. Apo E phenotype was not significantly associated with seru
m triglycerides, but was associated with LDL size, LDL cholesterol, to
tal cholesterol and HDL cholesterol. In our sample LDL size decreased
and LDL cholesterol and total cholesterol increased according to the m
ost prevalent apo E phenotypes in the order E2/3, E3/3, E3/4 and E4/4.
Subjects with phenotype apo E4/4 had the smallest LDL size (25.70 +/-
0.19 nm), the highest total cholesterol (6.53 +/- 0.35 mmol/l) and th
e lowest HDL cholesterol values (1.28 +/- 0.04 mmol/l). We conclude th
at there was a;significant interaction between sex and age in serum to
tal cholesterol which was highest in older women. However, their LDL s
ize was larger and their LDL is less atherogenic. Apo E phenotype had
a significant influence on LDL size.