Obicetrapib and ezetimibe enhance LDL receptor-mediated VLDL-clearance and regress atherosclerosis on atorvastatin background

The selective cholesteryl ester transfer protein (CETP) inhibitor obicetrapib is in clinical evaluation for dyslipidemia and cardiovascular risk reduction. This study investigated how obicetrapib alone and with ezetimibe reduces non-HDL-C, affects atherosclerotic lesion progression, and regression when added to background atorvastatin intervention. APOE*3-Leiden.CETP mice received a Western-type diet (WTD) or this diet supplemented with obicetrapib, ezetimibe or both. After 8 weeks, all interventions reduced non-HDL-C levels (obicetrapib: -53%; ezetimibe: -19%; combination: -75%). Obicetrapib mono and combination treatment blocked CETP activity (-99% and -98%), thereby increasing HDL-C levels (+286% and +256%). Very low-density lipoprotein (VLDL) cholesterol production was not affected, while obicetrapib and the combination with ezetimibe increased VLDL clearance (plasma half-life [<sup>14</sup>C]-cholesteryloleate: -44% and -57%) and LDL receptor expression (+63% and +74%), without increasing liver lipids. Atherosclerosis progression was evaluated after 28 weeks. All interventions reduced atherosclerotic lesion area (obicetrapib: -90%; ezetimibe: -50%; combination: -98%) and severity due to almost complete reductions in severe lesions (obicetrapib: -80%; combination: -98%). Non-HDL-C exposure (p<0.001) was independently associated with lesion area, in contrast to HDL-C (p=0.336). Combination treatment synergistically reduced non-HDL-C and atherosclerosis. For atherosclerosis regression, mice with advanced and established atherosclerosis received obicetrapib and ezetimibe on top of atorvastatin for 24 weeks. Triple therapy regressed lesion area (-44% versus baseline) and increased healthy vessel segments, indicating potential for complete atherosclerosis resolution. In summary, obicetrapib alone and with ezetimibe reduces non-HDL-C by enhancing LDL receptor-mediated VLDL clearance, thereby synergistically reducing atherosclerosis. Triple treatment with obicetrapib, ezetimibe and atorvastatin regresses pre-existent atherosclerotic lesions.

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Publication Details

Journal
Journal of Lipid Research
Published
2026-03-01
DOI
https://doi.org/10.1016/j.jlr.2026.101028
Citations
1
Primary Topic
Lipoproteins and Cardiovascular Health
Type
article
Field-Weighted Citation Impact
39.15
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article

Obicetrapib and ezetimibe enhance LDL receptor-mediated VLDL-clearance and regress atherosclerosis on atorvastatin background

Geurt Stokman, Elsbet Pieterman, Nanda Keijzer, José A. Inia et al.
1 citations
Journal of Lipid Research
Lipoproteins and Cardiovascular Health
39.15
article

Obicetrapib and ezetimibe enhance LDL receptor-mediated VLDL-clearance and regress atherosclerosis on atorvastatin background

Geurt Stokman, Elsbet Pieterman, Nanda Keijzer, José A. Inia, Nicole Worms, H. Princen, Anita M. van den Hoek, J Kastelein, Anita van Nieuwkoop-van Straalen, M Szarek, Marc Ditmarsch, Mathijs de Kleer, J. Wouter Jukema, Leo H. Zhang
article en
1 citations

Abstract

The selective cholesteryl ester transfer protein (CETP) inhibitor obicetrapib is in clinical evaluation for dyslipidemia and cardiovascular risk reduction. This study investigated how obicetrapib alone and with ezetimibe reduces non-HDL-C, affects atherosclerotic lesion progression, and regression when added to background atorvastatin intervention. APOE*3-Leiden.CETP mice received a Western-type diet (WTD) or this diet supplemented with obicetrapib, ezetimibe or both. After 8 weeks, all interventions reduced non-HDL-C levels (obicetrapib: -53%; ezetimibe: -19%; combination: -75%). Obicetrapib mono and combination treatment blocked CETP activity (-99% and -98%), thereby increasing HDL-C levels (+286% and +256%). Very low-density lipoprotein (VLDL) cholesterol production was not affected, while obicetrapib and the combination with ezetimibe increased VLDL clearance (plasma half-life [<sup>14</sup>C]-cholesteryloleate: -44% and -57%) and LDL receptor expression (+63% and +74%), without increasing liver lipids. Atherosclerosis progression was evaluated after 28 weeks. All interventions reduced atherosclerotic lesion area (obicetrapib: -90%; ezetimibe: -50%; combination: -98%) and severity due to almost complete reductions in severe lesions (obicetrapib: -80%; combination: -98%). Non-HDL-C exposure (p<0.001) was independently associated with lesion area, in contrast to HDL-C (p=0.336). Combination treatment synergistically reduced non-HDL-C and atherosclerosis. For atherosclerosis regression, mice with advanced and established atherosclerosis received obicetrapib and ezetimibe on top of atorvastatin for 24 weeks. Triple therapy regressed lesion area (-44% versus baseline) and increased healthy vessel segments, indicating potential for complete atherosclerosis resolution. In summary, obicetrapib alone and with ezetimibe reduces non-HDL-C by enhancing LDL receptor-mediated VLDL clearance, thereby synergistically reducing atherosclerosis. Triple treatment with obicetrapib, ezetimibe and atorvastatin regresses pre-existent atherosclerotic lesions.

Journal of Lipid Research
State University of New York (US), Netherlands Organisation for Applied Scientific Research (NL), SUNY Downstate Health Sciences University (US), Leiden University Medical Center (NL), Givaudan (Netherlands) (NL)
Zero hunger
Openalex Percentile: Top 0%
Lipoproteins and Cardiovascular Health
39.15
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