Torcetrapib
CETP actually boosts the ability of HDL to block LDL oxidation, a finding that may help explain why torcetrapib failed to slow vascular disease (IUBMB Life 2011)
Original title: Cholesteryl-ester transfer protein enhances the ability of high-density lipoprotein to inhibit low-density lipoprotein oxidation
This study reports, for what the authors believe is the first time, that adding CETP to HDL enhances the capacity of HDL to inhibit LDL oxidation, by about 30% for total HDL and HDL2 (both p < 0.05) and 75% for HDL3 (p < 0.01). Because CETP inhibitors are a leading strategy for raising HDL to treat or prevent vascular disease, this finding suggests CETP inhibition could be detrimental to this particular antiatherosclerotic property of HDL. The authors propose this effect may partly explain why the CETP inhibitor torcetrapib failed to slow vascular disease despite producing large HDL increases, in addition to its known off-target toxicity, a property that appears not to be shared by other CETP inhibitors then in clinical trials.
Original abstract
Therapeutic strategies to increase high-density lipoprotein (HDL) to treat or prevent vascular disease include the use of cholesteryl-ester transfer protein (CETP) inhibitors. Here, we show, to the best of our knowledge for the first time, that addition of CETP to HDL enhances the ability of HDL to inhibit low-density lipoprotein oxidation by ∼ 30% for total HDL and HDL(2) (both P < 0.05) and 75% for HDL(3) (P < 0.01). Therefore, CETP inhibition may be detrimental to the antiatherosclerotic properties of HDL, and these findings may partly explain the failure of the CETP inhibitor, torcetrapib, treatment to retard vascular disease despite large increases in HDL, in addition to its "off target" toxicity, a property which appears not to be shared by other members of this class of CETP inhibitor currently under clinical trial. Further, detailed studies are urgently required.
HDL biologymechanismstorcetrapib
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.