Authors |
Yunoki
K, Nakamura K, Miyoshi T, Enko K, Kohno K, Morita H, Kusano KF,
Ito H.
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Abstract
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OBJECTIVE: Postprandial hyperlipemia has been shown to impair
endothelial function and contribute to the development of atherosclerosis.
We investigated the association between postprandial lipid profiles
and endothelial function, and we examined the effects of ezetimibe
on postprandial hyperlipemia and lipemia-induced endothelial dysfunction.
METHODS: A randomized prospective trial in which 10mg/day of ezetimibe
was administered to 10 subjects for 4 weeks and not administered
to 10 subjects (control group) was performed. Lipid profiles and
endothelial function, assessed by brachial artery flow-mediated
dilation (FMD) during a fasting state and at 2, 4, 6 and 8h after
an oral cookie loading test, were determined before and after
treatment for 4 weeks.
RESULTS: In all subjects before treatment, the maximum reduction
in postprandial %FMD was significantly correlated with the maximum
increases in postprandial triglyceride (TG) (r=-0.499, P<0.05)
and apolipoprotein B-48 (apoB-48) concentrations (r=-0.551, P<0.05).
Ezetimibe treatment for 4 weeks significantly suppressed postprandial
elevation in TG (area under the incremental curve, from 1419±594
to 968±321mgh/dl, P<0.05), remnant lipoprotein cholesterol
(from 66.9±27.6 to 38.9±15.4mgh/dl, P<0.01) and
apoB-48 (from 58.8±27.5 to 36.2±17.0µgh/ml,
P<0.05) concentrations, and postprandial endothelial dysfunction
assessed by %FMD (maximum reduction in %FMD, from -2.6±1.1%
to -1.2±0.8%, P<0.05), whereas no significant changes
were observed in the control group.
CONCLUSION: Postprandial hyperlipemia is closely correlated with
transient endothelial dysfunction. Ezetimibe improves postprandial
hyperlipemia and its induced endothelial dysfunction.
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