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Supporting evidence for lipoprotein(a) measurements in clinical practice.

Authors :
Matveyenko A
Pavlyha M
Reyes-Soffer G
Source :
Best practice & research. Clinical endocrinology & metabolism [Best Pract Res Clin Endocrinol Metab] 2023 May; Vol. 37 (3), pp. 101746. Date of Electronic Publication: 2023 Feb 11.
Publication Year :
2023

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.<br /> (Copyright © 2023. Published by Elsevier Ltd.)

Details

Language :
English
ISSN :
1878-1594
Volume :
37
Issue :
3
Database :
MEDLINE
Journal :
Best practice & research. Clinical endocrinology & metabolism
Publication Type :
Academic Journal
Accession number :
36828715
Full Text :
https://doi.org/10.1016/j.beem.2023.101746