| Literature DB >> 28203441 |
Kazuhiko Kotani1, Maciej Banach2.
Abstract
Lipoprotein(a) [Lp(a)] has been identified as a risk factor for cardiovascular disease. Lp(a) levels are also high under certain clinical conditions, including familial hypercholesterolemia and high blood low-density lipoprotein (LDL) cholesterol levels. Few effective generic therapies for modulating Lp(a) have been developed. However, new therapies involving inhibitors of proprotein convertase subtilisin/kexin type 9 (PCSK9) using monoclonal antibodies have markedly reduced the blood LDL levels-and the Lp(a) levels as well. Much attention has therefore been focused on this therapy and its utility. The mechanism by which PCSK9 inhibitors reduce the Lp(a) levels remains unclear. We here describe the effects of PCSK9 inhibitors on Lp(a) and discuss potential mechanisms and perspectives of this topic.Entities:
Keywords: Apolipoprotein(a) [apo(a)]; LDL receptor; LDL receptor-related protein (LRP); apolipoprotein B (apoB); familiar hypercholesterolemia; scavenger receptor (SR)
Year: 2017 PMID: 28203441 PMCID: PMC5303088 DOI: 10.21037/jtd.2017.01.40
Source DB: PubMed Journal: J Thorac Dis ISSN: 2072-1439 Impact factor: 2.895