Abstract

Background and aimsInfusion of high-density lipoprotein (HDL) mimetics failed to induce regression of atherosclerosis in recent randomized clinical trials. However, patients in these previous trials had normal levels of HDL-cholesterol, which potentially limited efficacy. Patients with very low levels of HDL-cholesterol and impaired cholesterol efflux capacity can be expected to derive the most potential benefit from infusion of HDL mimetics. This randomized clinical trial evaluated the efficacy of infusions of the HDL mimetic CER-001 in patients with genetically determined very low levels of HDL cholesterol. MethodsIn this multicenter, randomized clinical trial, we recruited patients with familial hypoalphalipoproteinemia (due to ABCA1 and/or APOA1 loss-of-function variants). Participants were randomized to intravenous infusions of 8 mg/kg CER-001 or placebo (2:1 ratio), comprising 9 weekly infusions followed by infusions every two weeks. Patients underwent repeated 3T-MRI to assess mean vessel wall area and 18F-FDG PET/CT to quantify arterial wall inflammation. ResultsA total of 30 patients with a mean age of 52.7 ± 7.4 years and HDL-cholesterol of 0.35 ± 0.25 mmol/L were recruited. After 24 weeks, the absolute change in mean vessel wall area was not significantly different in the CER-001 group compared with placebo (n = 27; treatment difference: 0.77 mm2, p = 0.21). Furthermore, there was no significant difference in carotid arterial wall inflammation (n = 24, treatment difference: 0.10 target-to-background ratio of the most diseased segment, p = 0.33) after 24 weeks. ConclusionIn patients with genetically determined very low HDL-cholesterol, 24 weeks of treatment with HDL mimetic CER-001 did not reduce carotid vessel wall dimensions or arterial wall inflammation, compared with placebo.

Highlights

  • High-density lipoprotein (HDL) cholesterol is inversely correlated with atherosclerotic cardiovascular disease (ASCVD) risk in population studies [1] and remains an important predictor in ASCVD risk assess­ ment algorithms [2]

  • Patients in the CER-001 treatment group were well balanced compared with the placebo group with respect to tradi­ tional ASCVD risk factors, baseline high-density lipoprotein (HDL)-cholesterol and apoA-I levels

  • All patients were characterized by the presence of ASCVD, with a diagnosis of subclinical atherosclerosis in 6 (30%) participants in the CER-001 treatment group and 7 (70%) in the placebo group

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Summary

Introduction

High-density lipoprotein (HDL) cholesterol is inversely correlated with atherosclerotic cardiovascular disease (ASCVD) risk in population studies [1] and remains an important predictor in ASCVD risk assess­ ment algorithms [2]. One of the putative atheroprotective effects of HDLs is attributed to their role in mediating reverse cholesterol transport from peripheral tissues, including macro­ phages in the atherosclerotic vessel wall, to the liver for elimination [6] This property of HDL can be probed by measuring cholesterol efflux capacity – an independent biomarker for cardiovascular events [7]. Infusion of high-density lipoprotein (HDL) mimetics failed to induce regression of atherosclerosis in recent randomized clinical trials Patients in these previous trials had normal levels of HDL-cholesterol, which potentially limited efficacy. Conclusion: In patients with genetically determined very low HDL-cholesterol, 24 weeks of treatment with HDL mimetic CER-001 did not reduce carotid vessel wall dimensions or arterial wall inflammation, compared with placebo

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