Addressing residual risk beyond statin therapy: New targets in the management of dyslipidaemias-A report from the European Society of Cardiology Cardiovascular Round Table

J Clin Lipidol. 2024 Sep-Oct;18(5):e685-e700. doi: 10.1016/j.jacl.2024.07.001. Epub 2024 Jul 6.

Abstract

Cardiovascular (CV) disease is the most common cause of death in Europe. Despite proven benefits, use of lipid-lowering therapy remains suboptimal. Treatment goals are often not achieved, even in patients at high risk with atherosclerotic CV disease (ASCVD). The occurrence of CV events in patients on lipid-lowering drugs is defined as "residual risk", and can result from inadequate control of plasma lipids or blood pressure, inflammation, diabetes, and environmental hazards. Assessment of CV risk factors and vascular imaging can aid in the evaluation and management decisions for individual patients. Lifestyle measures remain the primary intervention for lowering CV risk. Where drug therapies are required to reach lipid treatment targets, their effectiveness increases when they are combined with lifestyle measures delivered through formal programs. However, lipid drug dosage and poor adherence to treatment remain major obstacles to event-free survival. This article discusses guideline-supported treatment algorithms beyond statin therapy that can help reduce residual risk in specific patient profiles while also likely resulting in substantial healthcare savings through better patient management and treatment adherence.

Keywords: Angiopoietin-like protein 3 (ANGPTL3); Antisense oligonucleotides (ASO); Apolipoprotein C-III (ApoCIII); Atherosclerotic cardiovascular disease (ASCVD); Familial hypercholesterolaemia; Lifestyle; Nutrition; Proprotein convertase subtilisin/kexin type 9 (PCSK9); Small interfering RNA (siRNA).

Publication types

  • Review

MeSH terms

  • Cardiovascular Diseases* / drug therapy
  • Cardiovascular Diseases* / prevention & control
  • Dyslipidemias* / drug therapy
  • Europe
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / therapeutic use
  • Risk Factors
  • Societies, Medical

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors