Background: High density lipoproteins are all heterogeneous population of p
articles. Two main subpopulations have been identified, one contains Apo A-
I and APo A-II and is denominated LPA-I:A-II and another one contains only,
Apo A-I and is denominated LPA-I. Aim: To measure the concentrations of th
ese particles in patients with stable coronary artery disease. Patients and
Methods: Serum lipids, A-I and B apolipoproteins, LpA- I, LPA-I. A-I and L
PB particles were measured in 73 melt aged 33 to 82 years with angiographic
ally documented coronary artery disease (CAD) and 33 control subjects aged
39 to 76 years. LPA-I, LPA-I. A-II and LpB were measured by a noncompetitiv
e enzyme linked immunoassay using previously characterized monoclonal antib
odies against Apo A-I, APoA-II and apoB. Results: Patients with CAD had sig
nificantly higher mean levels of LDL cholesterol than the control group (p=
0.038). The mean concentration of LPA-I particles in patients with CAD was
significantly lower (p=0.031) than in control subjects, while the concentra
tion of LpA-I:A-II particles was significantly, higher (p=0.016). The perce
ntage of coronary stenosis correlated negatively with LPA-I and positively
with LPA-I:A-II. The best relative risk (RR) indicator in these patients wa
s LDL-cholesterol. The relative risk increases 2.5 fold when LPA-I falls be
low the cut-off level. Likewise, the relative risk increases 3-fold when LP
A-I:A-II raises over the cut-off level. Conclusions: Our findings indicate
that the quantification of LPA-I and LPA-I:A-II particles might allow, a mo
re accurate evaluation of the CAD risk than HDL cholesterol. LPA-I might re
present the antiatherogenic fraction of HDL.