Lipid Lowering Drugs: Present Status and Future Developments

Curr Atheroscler Rep. 2021 Mar 10;23(5):17. doi: 10.1007/s11883-021-00918-3.

Abstract

Purpose of review: Based on the recent data of the DA VINCI study, it is clear that, besides utilization of statins, there is a need to increase non-statin lipid lowering approaches to reduce the cardiovascular burden in patients at highest risk.

Recent findings: For hypercholesterolemia, the small synthetic molecule bempedoic acid has the added benefit of selective liver activation, whereas inclisiran, a hepatic inhibitor of the PCSK9 synthesis, has comparable effects with PCSK9 monoclonal antibodies. For hypertriglyceridemia, cardiovascular benefit has been achieved by the use of icosapent ethyl, whereas results with pemafibrate, a selective agonist of PPAR-α, are eagerly awaited. In the era of RNA-based therapies, new options are offered to dramatically reduce levels of lipoprotein(a) (APO(a)LRX) and of triglycerides (ANGPTL3LRX and APOCIII-LRx). Despite the demonstrated benefits of statins, a large number of patients still remain at significant risk because of inadequate LDL-C reduction or elevated blood triglyceride-rich lipoproteins or lipoprotein(a). The area of lipid modulating agents is still ripe with ideas and major novelties are to be awaited in the next few years.

Keywords: ANGPTL3LRX; APOCIII-LRx; Inclisiran; Lipoprotein(a); Proprotein convertase subtilisin/kexin type 9.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anticholesteremic Agents*
  • Cholesterol, LDL
  • Humans
  • Hypercholesterolemia / drug therapy*
  • Hypertriglyceridemia / drug therapy*
  • Lipids
  • Lipoprotein(a)
  • Proprotein Convertase 9

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL
  • Lipids
  • Lipoprotein(a)
  • PCSK9 protein, human
  • Proprotein Convertase 9