Kataoka Yu, Andrews Jordan, Duong MyNgan, Nguyen Tracy, Schwarz Nisha, Fendler Jessica, Puri Rishi, Butters Julie, Keyserling Constance, Paolini John F, Dasseux Jean-Louis, Nicholls Stephen J
South Australian Health & Medical Research Institute, University of Adelaide, Adelaide, Australia.
Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Cardiovasc Diagn Ther. 2017 Jun;7(3):252-263. doi: 10.21037/cdt.2017.02.01.
CER-001 is an engineered pre-beta high-density lipoprotein (HDL) mimetic, which rapidly mobilizes cholesterol. Infusion of CER-001 3 mg/kg exhibited a potentially favorable effect on plaque burden in the CHI-SQUARE (Can HDL Infusions Significantly Quicken Atherosclerosis Regression) study. Since baseline atheroma burden has been shown as a determinant for the efficacy of HDL infusions, the degree of baseline atheroma burden might influence the effect of CER-001.
CHI-SQUARE compared the effect of 6 weekly infusions of CER-001 (3, 6 and 12 mg/kg) placebo on coronary atherosclerosis in 369 patients with acute coronary syndrome (ACS) using serial intravascular ultrasound (IVUS). Baseline percent atheroma volume (B-PAV) cutoff associated with atheroma regression following CER-001 infusions was determined by receiver-operating characteristics curve analysis. 369 subjects were stratified according to the cutoff. The effect of CER-001 at different doses was compared to placebo in each group.
A B-PAV ≥30% was the optimal cutoff associated with PAV regression following CER-001 infusions. CER-001 induced PAV regression in patients with B-PAV ≥30% but not in those with B-PAV <30% (-0.45%±2.65% +0.34%±1.69%, P=0.01). Compared to placebo, the greatest PAV regression was observed with CER-001 3mg/kg in patients with B-PAV ≥30% (-0.96%±0.34% -0.25%±0.31%, P=0.01), whereas there were no differences between placebo (+0.09%±0.36%) versus CER-001 in patients with B-PAV <30% (3 mg/kg; +0.41%±0.32%, P=0.39; 6 mg/kg; +0.27%±0.36%, P=0.76; 12 mg/kg; +0.32%±0.37%, P=0.97).
Infusions of CER-001 3 mg/kg induced the greatest atheroma regression in ACS patients with higher B-PAV. These findings identify ACS patients with more extensive disease as most likely to benefit from HDL mimetic therapy.
CER-001是一种经过改造的前β高密度脂蛋白(HDL)模拟物,可快速转运胆固醇。在CHI-SQUARE(高密度脂蛋白输注能否显著加速动脉粥样硬化消退)研究中,输注3mg/kg的CER-001对斑块负荷显示出潜在的有利影响。由于基线动脉粥样硬化负荷已被证明是高密度脂蛋白输注疗效的一个决定因素,因此基线动脉粥样硬化负荷的程度可能会影响CER-001的效果。
CHI-SQUARE研究使用连续血管内超声(IVUS)比较了369例急性冠状动脉综合征(ACS)患者每周输注6次CER-001(3、6和12mg/kg)或安慰剂对冠状动脉粥样硬化的影响。通过受试者操作特征曲线分析确定与CER-001输注后动脉粥样硬化消退相关的基线粥样斑块体积百分比(B-PAV)临界值。根据该临界值对369名受试者进行分层。比较每组中不同剂量的CER-001与安慰剂的效果。
B-PAV≥30%是与CER-001输注后PAV消退相关的最佳临界值。CER-001可使B-PAV≥30%的患者的PAV消退,但不能使B-PAV<30%的患者的PAV消退(-0.45%±2.65% 对 +0.34%±1.69%,P=0.01)。与安慰剂相比,在B-PAV≥30%的患者中,3mg/kg的CER-001观察到最大的PAV消退(-0.96%±0.34% 对 -0.25%±0.31%,P=0.01),而在B-PAV<30%的患者中,安慰剂(+0.09%±0.36%)与CER-001(3mg/kg;+0.41%±0.32%,P=0.39;6mg/kg;+0.27%±0.36%,P=0.76;12mg/kg;+0.32%±0.37%,P=0.97)之间没有差异。
输注3mg/kg的CER-001可使B-PAV较高的ACS患者的动脉粥样硬化消退最大。这些发现表明,疾病更广泛的ACS患者最有可能从HDL模拟物治疗中获益。