Genetics
Lp(a) is higher in Black populations and in women, but a lack of standardised assays and cutoffs still limits clinical use, a review (Best Pract Res Clin Endocrinol Metab 2023)
Original title: Supporting evidence for lipoprotein(a) measurements in clinical practice
This review summarises evidence that elevated Lp(a) is causal for atherosclerotic cardiovascular disease and highly regulated by genetics, with levels higher in Black compared with White populations, and in women compared with men. Lp(a), composed mainly of apolipoprotein(a) and apoB100 (the main LDL structural protein), is linked to inflammatory, coagulation and wound-healing pathways. The field remains hampered by a lack of validated, universally accepted assays, risk cutoff values, and targeted therapies, though ongoing trials are evaluating the cardiovascular benefit of dedicated apo(a)-lowering treatments. The review summarises current evidence on Lp(a) clinical presentation, existing guidelines, and promising emerging therapies.
Original abstract
High levels of lipoprotein(a) [Lp(a)] are causal for development of atherosclerotic cardiovascular disease and highly regulated by genetics. Levels are higher in Blacks compared to Whites, and in women compared to men. Lp(a)'s main protein components are apolipoprotein (apo) (a) and apoB100, the latter being the main component of Low-Density Lipoprotein (LDL) particles. Studies have identified Lp(a) to be associated with inflammatory, coagulation and wound healing pathways. Lack of validated and accepted assays to measure Lp(a), risk cutoff values, guidelines for diagnosis, and targeted therapies have added challenges to the field. Scientific efforts are ongoing to address these, including studies evaluating the cardiovascular benefits of decreasing Lp(a) levels with targeted apo(a) lowering treatments. This review will provide a synopsis of evidence-based effects of high Lp(a) on disease presentation, highlight available guidelines and discuss promising therapies in development. We will conclude with current clinical information and future research needs in the field.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.