| Literature DB >> 32858625 |
Arturo Cesaro1,2, Alessandra Schiavo1,2, Elisabetta Moscarella1,2, Silvio Coletta1,2, Matteo Conte1,2, Felice Gragnano1,2, Fabio Fimiani3,4, Emanuele Monda2,3, Martina Caiazza4, Giuseppe Limongelli1,3,4, Laura D'Erasmo5, Carmine Riccio2, Marcello Arca5, Paolo Calabrò1,2.
Abstract
Lipoprotein(a) [Lp(a)] is an established cardiovascular risk factor, and growing evidence indicates its causal association with atherosclerotic disease because of the proatherogenic low-density lipoprotein (LDL)-like properties and the prothrombotic plasminogen-like activity of apolipoprotein(a) [apo(a)]. As genetics significantly influences its plasma concentration, Lp(a) is considered an inherited risk factor of atherosclerotic cardiovascular disease (ASCVD), especially in young individuals. Moreover, it has been suggested that elevated Lp(a) may significantly contribute to residual cardiovascular risk in patients with coronary artery disease and optimal LDL-C levels. Nonetheless, the fascinating hypothesis that lowering Lp(a) could reduce the risk of cardiovascular events - in primary or secondary prevention - still needs to be demonstrated by randomized clinical trials. To date, no specific Lp(a)-lowering agent has been approved for reducing the lipoprotein levels, and current lipid-lowering drugs have limited effects. In the future, emerging therapies targeting Lp(a) may offer the possibility to further investigate the relation between Lp(a) levels and cardiovascular outcomes in randomized controlled trials, ultimately leading to a new era in cardiovascular prevention. In this review, we aim to provide an updated overview of current evidence on Lp(a) as well as currently investigated therapeutic strategies that specifically address the reduction of the lipoprotein.Entities:
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Year: 2021 PMID: 32858625 DOI: 10.2459/JCM.0000000000001077
Source DB: PubMed Journal: J Cardiovasc Med (Hagerstown) ISSN: 1558-2027 Impact factor: 2.160