Can We Cure Atherosclerosis?

Rev Cardiovasc Med. 2018;19(S1):S20-S24. doi: 10.3909/ricm19S1S0003.

Abstract

Cardiovascular disease mortality rates have begun to rise in the United States. Based on the large body of supportive evidence, we propose a proof-of-concept, first-in-human trial to cure atherosclerosis: CURing Early ATHEROsclerosis (CURE ATHERO). This trial is based on a model of intensive induction therapy for extensive, if not complete, plaque regression, followed by intermittent maintenance therapy. An extensive body of evidence has demonstrated the causal role of apolipoprotein B lipoproteins in atherosclerosis progression and data suggest intensive low-density lipoprotein cholesterol (LDL-C) lowering may have a substantial impact on earlier stages of atherosclerosis. Compared with lifetime treatment to prevent atherosclerosis progression, this induction-intermittent treatment model will minimize costs and maximize adherence and safety.

Publication types

  • Review

MeSH terms

  • Anticholesteremic Agents / administration & dosage*
  • Anticholesteremic Agents / adverse effects
  • Apolipoprotein B-100 / blood
  • Atherosclerosis / blood
  • Atherosclerosis / diagnosis
  • Atherosclerosis / drug therapy*
  • Atherosclerosis / epidemiology
  • Biomarkers / blood
  • Cholesterol, LDL / blood*
  • Drug Administration Schedule
  • Drug Therapy, Combination
  • Dyslipidemias / blood
  • Dyslipidemias / diagnosis
  • Dyslipidemias / drug therapy*
  • Dyslipidemias / epidemiology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage
  • PCSK9 Inhibitors
  • Plaque, Atherosclerotic
  • Proprotein Convertase 9 / metabolism
  • Randomized Controlled Trials as Topic
  • Research Design
  • Serine Proteinase Inhibitors / administration & dosage
  • Time Factors
  • Treatment Outcome

Substances

  • APOB protein, human
  • Anticholesteremic Agents
  • Apolipoprotein B-100
  • Biomarkers
  • Cholesterol, LDL
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • PCSK9 Inhibitors
  • Serine Proteinase Inhibitors
  • PCSK9 protein, human
  • Proprotein Convertase 9