Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5656731 | Médecine des Maladies Métaboliques | 2016 | 4 Pages |
Abstract
Ezetimibe is an agent reducing intestinal cholesterol absorption by inhibiting NPC1L1 transporter. This reduction in cholesterol absorption induces, via a decrease in the cholesterol pool in the hepatocytes, an increase in LDL receptor expression leading to enhance LDL-cholesterol (LDLc) catabolism and, as a consequence, to reduce plasma LDLc level. Recently, came out important pieces of evidence for the efficiency of ezetimibe to reduce cardiovascular risk. A large Genome Wide Association Study showed that individuals with inactivating mutations of NPC1L1 had, in parallel with a decreased LDLc plasma level, a significant reduced cardiovascular risk. The PRECISE-IVUS study demonstrated a higher rate of coronary atherosclerotic plaque regression in patients treated with atorvastatin + ezetimibe compared to those treated with atorvastatin alone. In addition, the prospective IMPROVE-IT trial, had shown a significant reduction in major cardiovascular events (P=0.016), in myocardial infarction (P=0.002), in ischemic stroke (P=0.008), in coronary mortality (P=0.02), and in cardiovascular mortality (P=0.04) in patients treated with simvastatin + ezetimibe compared to those treated with simvastatin alone.
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Authors
B. Vergès,