Effect of APOC3 Inhibition With Olezarsen on Coronary Atherosclerosis: Essence-TIMI 73b Imaging Study
Abstract
BACKGROUND: Whether lowering triglyceride-rich lipoproteins and remnant cholesterol favorably modifies coronary atherosclerosis is unclear. Olezarsen, an antisense oligonucleotide that targets apolipoprotein C-III, reduces triglycerides by ~60% and remnant cholesterol by ~70%, has a neutral effect on LDL (low-density lipoprotein) cholesterol (LDL-C), and reduces apoB (apolipoprotein B) by ~15% in moderate hypertriglyceridemia. We investigated the effect of olezarsen on coronary plaque in adults with largely moderate hypertriglyceridemia. METHODS: We conducted a coronary computed tomography angiography study within Essence-TIMI 73b, a randomized, placebo-controlled trial of olezarsen versus placebo that enrolled patients between November 2022 and February 2024. Inclusion criteria were triglycerides ≥150 mg/dL (2.26 mmol/L), presence of or high risk for cardiovascular disease, and, for this imaging study, noncalcified plaque on baseline coronary computed tomography angiography. The primary end point was percent change from baseline to 12 months in noncalcified plaque volume. RESULTS: Of 468 participants (349 olezarsen, 119 placebo), the median age was 63 years (interquartile range, 56–70); 31% were women, and 97% received lipid-lowering therapy. Median baseline triglycerides were 249 mg/dL (interquartile range, 197–331), and remnant cholesterol was 53 mg/dL (interquartile range, 38–76). Median baseline noncalcified plaque volume was 125.3 mm³ (interquartile range, 63.2–213.3). At 6 months, olezarsen reduced triglycerides by 63.9%, remnant cholesterol by 71.9%, and apoB by 16.0% over placebo, with no difference in LDL-C. The percent change in noncalcified plaque volume from baseline to month 12 did not differ between olezarsen and placebo (placebo-adjusted least-squares mean difference, 2.98% [95% CI, −3.4 to 9.3]; p=0.36). No significant differences between olezarsen and placebo were observed for changes in low-attenuation, calcified, or total plaque volumes at 12 months. CONCLUSIONS: Despite substantial triglyceride and remnant cholesterol lowering, treatment with olezarsen for 12 months on top of standard-of-care lipid-lowering therapy in patients with largely moderate hypertriglyceridemia did not affect noncalcified coronary plaque volume. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT05610280.
Article Details
Authors (25)
Nicholas A. Marston
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Brian A. Bergmark
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Thomas A. Prohaska
Ionis Pharmaceuticals, Carlsbad, CA
Filipe A. Moura
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Andre Zimerman
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Veronica J. Alexander
Ionis Pharmaceuticals, Carlsbad, CA
Yu Mi Kang
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Julia Weinland
Ionis Pharmaceuticals, Carlsbad, CA
Xinhui Ran
Thrombolysis in Myocardial Infarction Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, MA (N.A.M., B.A.B., X.R., S.A.M., S.Z., R.P.G., M.S.S.).
Sabina A. Murphy
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Shuanglu Zhang
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston
Dan Li
Maciej Banach
Erik S.G. Stroes
Robert Kiss
Military Hospital, Budapest, Hungary (R.K.).
Daniel Gaudet
Department of Medicine, Université de Montréal, Montreal
Michal Vrablík
Assen Goudev
Division of Cardiology, University Hospital Tsaritsa Yoanna, Sofia, Bulgaria
Jeroen J. Bax
Leiden University Medical Center, Leiden, the Netherlands (J.J.B.).
Matthew J. Budoff
Borek Foldyna
Michael T. Lu
Sotirios Tsimikas
Robert P. Giugliano
Marc S. Sabatine
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston