Postprandial metabolism of apolipoprotein B-48-and B-100-containing particles in type 2 diabetes mellitus: relations to angiographically verified severity of coronary artery disease
N. Mero et al., Postprandial metabolism of apolipoprotein B-48-and B-100-containing particles in type 2 diabetes mellitus: relations to angiographically verified severity of coronary artery disease, ATHEROSCLER, 150(1), 2000, pp. 167-177
Citations number
61
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
The aim of the present cross-sectional angiographic study was to examine if
there is a relationship between the severity of CAD and postprandial lipem
ia in patients with type 2 diabetes mellitus. Special emphasis was directed
to determining the contribution of apolipoprotein B-48 (apoB-48)-containin
g and B-100 (apoB-100)-containing triglyceride-rich particles to the magnit
ude of postprandial lipemia and degree of CAD. The role of apolipoprotein E
(apoE) phenotype as a modulator of postprandial lipemia was also evaluated
. The severity of CAD was determined by a quantitative coronary angiography
and the subjects were classified into two groups based on the presence (se
vere CAD) or absence (mild CAD) of at least 50% stenosis in a major coronar
y vessel. The study population consisted of 43 subjects (31 men and 12 wome
n) with fair glycemic control and comparable fasting lipids and body mass i
ndex. Postprandial responses of TG, apoB-48 and apoB-100 in lipoprotein sub
fractions (chylomicrons, VLDL1, VLDL2 and IDL) were determined after a fat
load. Type 2 diabetic patients exhibited the classical dyslipidemia of the
insulin resistance syndrome and delayed clearance of both hepatic and intes
tinal particles. Fasting or postprandial lipid or lipoprotein measurements,
including apoB-48 and apoB-100 concentrations, did not differ between the
groups. The presence or absence of apoE-4 allele did not significantly infl
uence postprandial lipemia. The severity of the most significant coronary s
tenosis in angiography correlated with plasma and with chylomicron area und
er curve (AUC) for TG (n = 27) and chylomicron AUC for apoB-48 (n = 20). Th
e strongest correlate of maximal stenosis was area under incremental curve
(AUIC) for apoB-100 in IDL fraction (r=0.548, P=0.012, n=20). In conclusion
, postprandial apoB-48 and apoB-100 metabolism in triglyceride rich lipopro
teins is distorted in type 2 diabetic patients, even in those with only mil
d CAD. The data suggest that postprandial change in small remnant particle
numbers may contribute to the severity of CAD in type 2 diabetes. (C) 2000
Elsevier Science Ireland Ltd. All rights reserved.