Integrating provision of specialist lipid services with cascade testing for familial hypercholesterolaemia

Curr Opin Lipidol. 2010 Aug;21(4):366-71. doi: 10.1097/MOL.0b013e32833c14e2.

Abstract

Purpose of review: To highlight the unmet need for identifying individuals with familial hypercholesterolaemia and exploring the implications that this will have for local and national healthcare services.

Recent findings: A pathway utilising DNA testing for the diagnosis of familial hypercholesterolaemia, and subsequent cascade testing has been developed in Wales.

Summary: Undiagnosed familial hypercholesterolaemia carries a high risk of cardiovascular disease, which is easily preventable with pharmacotherapy, if individuals are appropriately diagnosed, and affected family members identified. The use of DNA testing is cost-effective and allows for efficient cascade testing. This has implications for local services and highlights unmet educational and clinical requirements in clinical lipidology.

Publication types

  • Review

MeSH terms

  • Humans
  • Hyperlipoproteinemia Type II / diagnosis*
  • Hyperlipoproteinemia Type II / metabolism
  • Lipid Metabolism
  • Lipids*
  • Mass Screening / methods*
  • Medicine*

Substances

  • Lipids