Impact of Hypertriglyceridemia on Endothelial Dysfunction During Statin ± Ezetimibe Therapy in Patients With Coronary Heart Disease

Despite the use of statin therapy and achieving the target for low-density lipoprotein cholesterol, a substantial number of coronary events are not prevented, and residual risk factors remain unsettled. Recently, ezetimibe has been shown to reduce not only low-density lipoprotein cholesterol but als...

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Veröffentlicht in:The American journal of cardiology 2011-08, Vol.108 (3), p.333-339
Hauptverfasser: Yunoki, Kei, MD, Nakamura, Kazufumi, MD, PhD, Miyoshi, Toru, MD, PhD, Enko, Kenki, MD, PhD, Kubo, Motoki, MD, Murakami, Masato, MD, PhD, Hata, Yoshiki, MD, PhD, Kohno, Kunihisa, MD, PhD, Morita, Hiroshi, MD, PhD, Kusano, Kengo F., MD, PhD, Ito, Hiroshi, MD, PhD
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Sprache:eng
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Zusammenfassung:Despite the use of statin therapy and achieving the target for low-density lipoprotein cholesterol, a substantial number of coronary events are not prevented, and residual risk factors remain unsettled. Recently, ezetimibe has been shown to reduce not only low-density lipoprotein cholesterol but also triglyceride (TG) levels. The aim of this study was to investigate the associations of residual risk factors, mainly hypertriglyceridemia, with endothelial function during statin therapy in patients with coronary heart disease and examine the effect of ezetimibe add-on therapy. A total of 109 consecutive patients with coronary heart disease during statin therapy were enrolled. Lipid profile was measured and endothelial function was assessed by flow-mediated dilation (FMD) of the brachial artery in a fasting state. Next, 32 patients with high TG levels (≥150 mg/dl) were prospectively assigned to the ezetimibe add-on group or the no-ezetimibe group, and endothelial function was assessed after 3 months. Multivariate linear regression analysis demonstrated that serum TG and high-density lipoprotein cholesterol levels were independent determinants of percentage FMD (β = −0.210 and 0.208, respectively, p
ISSN:0002-9149
1879-1913
DOI:10.1016/j.amjcard.2011.03.049