Effect of APOC3 Inhibition with Olezarsen on Coronary Atherosclerosis: Essence-TIMI 73b Imaging Study.

IF 38.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Nicholas A Marston,Brian A Bergmark,Thomas A Prohaska,Filipe A Moura,Andre Zimerman,Veronica J Alexander,Yu Mi Kang,Julia Weinland,Xinhui Ran,Sabina A Murphy,Shuanglu Zhang,Dan Li,Maciej Banach,Erik S G Stroes,Robert Kiss,Daniel Gaudet,Michal Vrablik,Assen Goudev,Jeroen J Bax,Matthew J Budoff,Borek Foldyna,Michael T Lu,Sotirios Tsimikas,Robert P Giugliano,Marc S Sabatine
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引用次数: 0

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 cholesterol (LDL-C), and reduces apolipoprotein B (apoB) 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 (CCTA) study within Essence-TIMI 73b, a randomized, placebo-controlled trial of olezarsen vs. placebo that enrolled patients between November 2022 and February 2024. Inclusion criteria were triglycerides ≥150 mg/dL (2.26 mmol/L), presence or high risk for cardiovascular disease, and non-calcified plaque on baseline CCTA. The primary endpoint was percent change from baseline to 12 months in non-calcified plaque volume (NCPV). RESULTS Of 468 participants (349 olezarsen, 119 placebo), the median age was 63 years (IQR 56-70); 31% were women, and 97% received lipid-lowering therapy. Median baseline triglycerides were 249 mg/dL (IQR 197-331), and remnant cholesterol was 53 mg/dL (IQR 38-76). Median baseline NCPV was 125.3 mm³ (IQR 63.2-213.3). At 6 months, olezarsen reduced triglycerides by 63.9%, remnant cholesterol by 71.9%, and apolipoprotein B by 16.0% over placebo, with no difference in LDL-C. The percent change in NCPV with olezarsen 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.
Olezarsen抑制apo3对冠状动脉粥样硬化的影响:essence - timi73b成像研究。
背景:降低富含甘油三酯的脂蛋白和残余胆固醇是否有利于改变冠状动脉粥样硬化尚不清楚。Olezarsen是一种针对载脂蛋白C-III的反义寡核苷酸,可降低甘油三酯约60%,残余胆固醇约70%,对低密度脂蛋白胆固醇(LDL- c)有中性作用,并可降低中度高甘油三酯血症的载脂蛋白B (apoB)约15%。我们研究了olezarsen对中度高甘油三酯血症成人冠状动脉斑块的影响。我们在Essence-TIMI 73b中进行了一项冠状动脉ct血管造影(CCTA)研究,这是一项随机、安慰剂对照试验,在2022年11月至2024年2月期间招募了olezarsen和安慰剂。纳入标准为甘油三酯≥150mg /dL (2.26 mmol/L),存在或高危心血管疾病,基线CCTA无钙化斑块。主要终点是非钙化斑块体积(NCPV)从基线到12个月的百分比变化。结果468名参与者(349名奥勒扎森,119名安慰剂),中位年龄为63岁(IQR 56-70);31%为女性,97%接受降脂治疗。中位基线甘油三酯为249 mg/dL (IQR 197-331),残余胆固醇为53 mg/dL (IQR 38-76)。中位基线NCPV为125.3 mm³(IQR为63.2-213.3)。6个月时,olezarsen与安慰剂相比,甘油三酯降低63.9%,残余胆固醇降低71.9%,载脂蛋白B降低16.0%,LDL-C无差异。从基线到第12个月,olezarsen和安慰剂组NCPV的百分比变化没有差异(安慰剂校正最小二乘平均差2.98%;95% CI -3.4至9.3;p=0.36)。在12个月时,olezarsen和安慰剂在低衰减、钙化或总斑块体积的变化方面没有观察到显著差异。结论:对于中度高甘油三酯血症患者,在标准降脂治疗的基础上,奥勒扎森治疗12个月,对非钙化冠状动脉斑块体积没有影响。
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来源期刊
Circulation
Circulation 医学-外周血管病
CiteScore
45.70
自引率
2.10%
发文量
1473
审稿时长
2 months
期刊介绍: Circulation is a platform that publishes a diverse range of content related to cardiovascular health and disease. This includes original research manuscripts, review articles, and other contributions spanning observational studies, clinical trials, epidemiology, health services, outcomes studies, and advancements in basic and translational research. The journal serves as a vital resource for professionals and researchers in the field of cardiovascular health, providing a comprehensive platform for disseminating knowledge and fostering advancements in the understanding and management of cardiovascular issues.
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