Y. Hattori et al., DEVELOPMENT OF APPROXIMATE FORMULA FOR LDL-CHOL, LDL-APO-B AND LDL-CHOL LDL-APO-B AS INDEXES OF HYPERAPOBETALIPOPROTEINEMIA AND SMALL DENSELDL/, Atherosclerosis (Amsterdam), 138(2), 1998, pp. 289-299
Estimation of LDL-chol and LDL-apo B is useful for the diagnosis of hy
perapobetalipoproteinemia (normal LDL-chol with increased LDL-apo B),
which is one of the most commonly occurring lipoprotein disorders asso
ciated with atherosclerotic cardiovascular diseases. The LDL-chol/LDL-
apo B ratio reflects the level of small dense LDL, which is an importa
nt risk factor for IHD, CVD and ASO. In order to estimate LDL-apo B an
d LDL-chol/LDL-apo B ratio from blood chol, TG, HDL-chol and apo B val
ues, we developed a formula for LDL-chol {0.94Chol-0.94HDL-chol-0.19TG
}, LDL-apo B {apo B-0.09Chol+0.09HDL-chol-0.08TG}, and LDL-chol/LDL-ap
o B [{0.94Chol-0.94HDL-chol-0.19TG}/{apo B-0.09Chol + 0.09HDL-chol-0.0
8TG}], using ultracentrifugal data from 2179 subjects. These were calc
ulated by the least squares method on the assumption that a certain co
mpositional relationship exists between Chol, TG and apo B in VLDL, ID
L and LDL. Friedewald's formula for LDL-chol (Chol-HDL-chol-0.2TG) inc
ludes IDL-chol, but the present new formula theoretically excludes IDL
-chol. It suggests a better estimation for the correct LDL-chol. Estim
ated LDL-apo B is useful for the diagnosis of hyperapobetalipoproteine
mia and detection of small dense LDL. Without performing ultracentrifu
ge, additional information is obtained for the quantitative and qualit
ative alteration of LDL, such as small dense LDL. The above formulae a
nd a new classification of lipoproteinemia including apo B were applie
d to the analyses of lipoprotein profiles of subjects with cardiovascu
lar diseases, which were compared with those in the general population
. Hyperapobetalipoproteinemia with high TG was observed 2-3 times more
frequently in subjects with CAD, MI and ASO than in the Suita populat
ion. Lower ratios of LDL-chol/LDL-apo B, reflecting preponderance of s
mall dense LDL, were observed in the above three groups. Type IIb and
combined low HDL-chol were also frequent phenotypes in CAD, A-Th and A
SO. The present formulae are useful for the detailed analyses of lipop
rotein disorders in both qualitative as well as quantitative aspects.
(C) 1998 Elsevier Science Ireland Ltd. All rights reserved.