Lipoprotein(a)--An independent causal risk factor for cardiovascular disease and current therapeutic options

Atheroscler Suppl. 2015 May:18:263-7. doi: 10.1016/j.atherosclerosissup.2015.02.039.

Abstract

It is widely accepted that elevated levels of lipoprotein(a) (Lp(a)) are associated with an increased risk for cardiovascular diseases. Several studies have identified Lp(a) as independent cardiovascular risk factor. Consequently, therapeutic concepts are targeting at lowering Lp(a) serum levels. To date, in Europe no pharmaceutical treatment to lower levels of Lp(a) is available. Current developments of pharmaceutical agents like the apolipoprotein-(B-100)-antisense mipomersen, inhibitors of PCSK9 and apolipoprotein-(a)-antisense have shown promising results in lowering Lp(a). Presently, the only available therapy to effectively reduce levels of Lp(a) is regular extracorporeal lipoprotein apheresis. Different apheresis methods show a similar lowering effect of about 60-70 % by a single session. Apart from one small-scale study there has been no randomized, controlled study which could prove that lowering Lp(a) will result in a risk reduction for cardiovascular disease. This review looks into the current scientific evidence of.

Keywords: Cardiovascular disease; Lipoprotein apheresis; Lipoprotein(a).

Publication types

  • Review

MeSH terms

  • Biomarkers / blood
  • Blood Component Removal / methods*
  • Cardiovascular Diseases / diagnosis
  • Cardiovascular Diseases / epidemiology
  • Cardiovascular Diseases / prevention & control*
  • Humans
  • Hyperlipoproteinemias / blood
  • Hyperlipoproteinemias / diagnosis
  • Hyperlipoproteinemias / epidemiology
  • Hyperlipoproteinemias / therapy*
  • Hypolipidemic Agents / therapeutic use*
  • Lipoprotein(a) / blood*
  • Risk Factors
  • Treatment Outcome

Substances

  • Biomarkers
  • Hypolipidemic Agents
  • Lipoprotein(a)