Abstract 4368587: Obicetrapib in combination with ezetimibe on top of atorvastatin regresses atherosclerotic plaque lesions in APOE*3-Leiden.CETP mice

Background and aims: Regression of pre-existing atherosclerotic vascular disease has only been observed with aggressive lipid lowering therapy. Therefore, the aim of the present study is to evaluate the effect of the novel cholesterol ester transfer protein (CETP) inhibitor obicetrapib in combination with the intestinal cholesterol absorption inhibitor ezetimibe on top of high dose atorvastatin as a potent combination for regression of established atherosclerosis in APOE*3Leiden.CETP mice, a translational mouse model for hyperlipidemia and atherosclerosis. Methods: Female APOE*3-Leiden.CETP transgenic mice were fed a Western-type diet (WTD) with 0.3% w/w cholesterol for 12 weeks to induce atherosclerosis. Hereafter, an initial/baseline control group was sacrificed and the remaining mice were divided into 4 groups and treated with WTD with 0.05% w/w cholesterol (equivalent to daily human intake) or this diet containing atorvastatin (5 mg/kg bw/d), obicetrapib (2 mg/kg/day) + ezetimibe (0.6 mg/kg/day) or the combination of atorvastatin, obicetrapib and ezetimibe for 24 weeks. Effects on plasma lipids and atherosclerotic lesion size were assessed. Results: After 24 weeks of treatment atorvastatin alone, the combo treatment of obicetrapib + ezetimibe and the triple combo treatment of obicetrapib + ezetimibe + atorvastatin reduced total plasma cholesterol levels (-40%, -58% and -76%, all p<0.001; respectively), mainly attributed to a decrease in non-HDL-C levels (-41%, -73% and -88%, all p<0.001; respectively). Triple combo treatment decreased non-HDL-C to 50 mg/dL. Obicetrapib + ezetimibe combo and the triple combo treatment nearly completely blocked CETP activity resulting in increased HDL-C levels (+161% and +95%, all p <0.001; respectively). Mono-treatment with atorvastatin reduced progression of atherosclerosis (-28%, p=0.001, versus control) and the obicetrapib + ezetimibe combo treatment completely blocked progression. Obicetrapib + ezetimibe + atorvastatin triple combo treatment regressed lesion size as compared to baseline (-44%, p=0.032), thereby diminishing lesion severity and increasing the lesion-free area. Compared to atorvastatin monotreatment, triple combo treatment further reduced lesion size (-60%, p<0.001). Conclusions: High-intensive cholesterol-lowering triple combo treatment with obicetrapib + ezetimibe on top of atorvastatin robustly decreases non-HDL-C and regresses atherosclerotic lesion area in APOE*3Leiden.CETP mice.

Authors

Institutions

Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4368587
Primary Topic
Lipoproteins and Cardiovascular Health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 4368587: Obicetrapib in combination with ezetimibe on top of atorvastatin regresses atherosclerotic plaque lesions in APOE*3-Leiden.CETP mice

J. Wouter Jukema, P. Hans, Geurt Stokman, Elsbet Pieterman et al.
Circulation
Lipoproteins and Cardiovascular Health
article

Abstract 4368587: Obicetrapib in combination with ezetimibe on top of atorvastatin regresses atherosclerotic plaque lesions in APOE*3-Leiden.CETP mice

J. Wouter Jukema, P. Hans, Geurt Stokman, Elsbet Pieterman, Nanda Keijzer, José A. Inia, Anita van Nieuwkoop, Nicole Worms, John J.P. Kastelein, Marc Ditmarsch, A van den Hoek, Mathijs de Kleer
article en

Abstract

Background and aims: Regression of pre-existing atherosclerotic vascular disease has only been observed with aggressive lipid lowering therapy. Therefore, the aim of the present study is to evaluate the effect of the novel cholesterol ester transfer protein (CETP) inhibitor obicetrapib in combination with the intestinal cholesterol absorption inhibitor ezetimibe on top of high dose atorvastatin as a potent combination for regression of established atherosclerosis in APOE*3Leiden.CETP mice, a translational mouse model for hyperlipidemia and atherosclerosis. Methods: Female APOE*3-Leiden.CETP transgenic mice were fed a Western-type diet (WTD) with 0.3% w/w cholesterol for 12 weeks to induce atherosclerosis. Hereafter, an initial/baseline control group was sacrificed and the remaining mice were divided into 4 groups and treated with WTD with 0.05% w/w cholesterol (equivalent to daily human intake) or this diet containing atorvastatin (5 mg/kg bw/d), obicetrapib (2 mg/kg/day) + ezetimibe (0.6 mg/kg/day) or the combination of atorvastatin, obicetrapib and ezetimibe for 24 weeks. Effects on plasma lipids and atherosclerotic lesion size were assessed. Results: After 24 weeks of treatment atorvastatin alone, the combo treatment of obicetrapib + ezetimibe and the triple combo treatment of obicetrapib + ezetimibe + atorvastatin reduced total plasma cholesterol levels (-40%, -58% and -76%, all p<0.001; respectively), mainly attributed to a decrease in non-HDL-C levels (-41%, -73% and -88%, all p<0.001; respectively). Triple combo treatment decreased non-HDL-C to 50 mg/dL. Obicetrapib + ezetimibe combo and the triple combo treatment nearly completely blocked CETP activity resulting in increased HDL-C levels (+161% and +95%, all p <0.001; respectively). Mono-treatment with atorvastatin reduced progression of atherosclerosis (-28%, p=0.001, versus control) and the obicetrapib + ezetimibe combo treatment completely blocked progression. Obicetrapib + ezetimibe + atorvastatin triple combo treatment regressed lesion size as compared to baseline (-44%, p=0.032), thereby diminishing lesion severity and increasing the lesion-free area. Compared to atorvastatin monotreatment, triple combo treatment further reduced lesion size (-60%, p<0.001). Conclusions: High-intensive cholesterol-lowering triple combo treatment with obicetrapib + ezetimibe on top of atorvastatin robustly decreases non-HDL-C and regresses atherosclerotic lesion area in APOE*3Leiden.CETP mice.

CirculationVol. 152(Suppl_3)
Netherlands Organisation for Applied Scientific Research (NL), Leiden University Medical Center (NL)
Openalex Percentile: Top 50%
Lipoproteins and Cardiovascular Health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.