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Tsimikas marks Lp(a)'s 61st birthday with an ATVB Centennial essay on six decades of discovery and three ongoing outcome trials (Arterioscler Thromb Vasc Biol 2024)

Original title: Lipoprotein(a) in the Year 2024: A Look Back and a Look Ahead

Arterioscler Thromb Vasc Biol · · 8

Tsimikas S

Written for the American Heart Association's 100th anniversary and the ATVB Centennial Collection, this essay by a leading Lp(a) researcher marks Lp(a)'s 61st birthday since its November discovery, reviewing six decades of progress in understanding its biology and pathophysiology. It traces Lp(a)'s identification as a unique beta-lipoprotein bearing the pathognomonic apolipoprotein(a) moiety covalently bound to apoB-100, its independent monogenetic association with cardiovascular disease and calcific aortic valve disease, its elevated content of pro-atherogenic, pro-inflammatory oxidized phospholipids relative to other lipoproteins, and the subsequent development of RNA therapeutics to lower it. The essay frames the central open question, the "Lp(a) hypothesis" that lowering plasma Lp(a) will yield clinical benefit, as currently being tested in three ongoing outcome trials, and closes with a look ahead to the field's remaining unanswered questions.

Read the paper (DOI)PubMed

Original abstract

In fitting with the American Heart Association’s 100th anniversary of its founding and Arteriosclerosis, Thrombosis and Vascular Biology organizing a Centennial Collection to celebrate this event, lipoprotein(a) [Lp(a)] celebrates its 61st birthday in November 2024. There has been substantial progress in understanding the biology and pathophysiology of Lp(a) in the last 6 decades, including its discovery as a unique β-lipoprotein containing the pathognomonic apolipoprotein(a) moiety covalently bound to apolipoprotein B-100, its independent monogenetic association with cardiovascular disease and calcific aortic valve disease, its increased content of pro-atherogenic and pro-inflammatory of oxidized phospholipids relative to other lipoproteins and the development of RNA therapeutics to lower plasma Lp(a) levels. The validation or refutation of the “Lp(a) hypothesis”, namely that lowering plasma Lp(a) will lead to clinical benefit, is ongoing in 3 clinical outcomes trials. This essay reviews the discovery of Lp(a), summarizes the seminal pathophysiological findings since its discovery, discusses ongoing clinical trials with novel drugs and approaches, and provides a look ahead to unanswered questions.

guidelinesmechanismsRNA therapeutics

Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.