RNA therapeutics
Apheresis remains the only proven Lp(a)-lowering therapy in Europe, cutting levels by 60-70% per session, a review of current treatment options (Atheroscler Suppl 2015)
Original title: Lipoprotein(a)--An independent causal risk factor for cardiovascular disease and current therapeutic options
This review by Kassner, Schlabs, Rosada and Steinhagen-Thiessen covers current therapeutic options for elevated Lp(a), an independent cardiovascular risk factor for which no pharmaceutical treatment is yet available in Europe. Emerging drugs, including the antisense agent mipomersen, PCSK9 inhibitors, and apolipoprotein(a) antisense therapy, have shown promising Lp(a)-lowering results in development. Currently, regular extracorporeal lipoprotein apheresis is the only available therapy proven to effectively reduce Lp(a), with different apheresis methods lowering levels by about 60-70% per session. Aside from one small-scale study, no randomised controlled trial has yet proven that lowering Lp(a) reduces cardiovascular disease risk, a gap the review examines.
Original 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.
apheresisPCSK9 inhibitionRNA therapeutics
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.