K. Honda et T. Murase, EFFECTS OF APOLIPOPROTEIN-E PHENOTYPE ON SERUM-CHOLESTEROL LEVEL AND CHOLESTEROL RESPONSE TO DIET THERAPY IN PATIENTS WITH HYPERCHOLESTEROLEMIA, Endocrine journal, 44(3), 1997, pp. 425-429
We investigated the association of the apolipoprotein (apo) E isoform
phenotype with the basal serum cholesterol level and cholesterol respo
nse to diet therapy in outpatients with primary hypercholesterolemia.
The basal levels of serum cholesterol, triglyceride and HDL-cholestero
l in the 132 subjects were 286+/-26 mg/dl, 154+/-83mg/dl and 54+/-14 m
g/dl, respectively. The frequencies of apo E 3/2, 3/3, 4/2, 4/3 and 4/
4 were 1, 104, 2, 24 and 1, respectively. There were no differences in
serum lipids between subjects with the two most common apo E phenotyp
es, i.e., apoE 3/3 (n=104) and apoE 4/3 (n=24). The serum cholesterol
response to diet therapy was evaluated by measuring the serum lipids o
f 52 participants before and 2-3 months after diet therapy. After diet
ary counselling, serum cholesterol values were reduced significantly f
rom 293+/-27 to 256+/-36 mg/dl (P<0.01) in the total group of study su
bjects. There was no significant difference in serum cholesterol reduc
tion in response to diet therapy between subjects with apoE4 (E4/2, E4
/3 and E4/4, n=12) and without apoE4 (E3/3 and E3/2, n=40). Following
dietary counselling, patients who lost a large amount of body weight (
BM I greater than or equal to 1.0) exhibited a greater reduction in se
rum cholesterol than those who showed less weight loss. In conclusion,
the results of our study demonstrated the primary importance of diet
therapy in the treatment of hypercholesterolemia, although other inves
tigators have suggested that apo E phenotypes influence the response o
f serum cholesterol to dietary changes.