Lipoprotein (a) and lipid-lowering treatment from the perspective of a cardiac surgeon. An impact on the prognosis in patients with aortic valve replacement and after heart transplantation
- PMID: 38962113
- PMCID: PMC11219948
- DOI: 10.1016/j.ijcrp.2024.200297
Lipoprotein (a) and lipid-lowering treatment from the perspective of a cardiac surgeon. An impact on the prognosis in patients with aortic valve replacement and after heart transplantation
Abstract
Lipoprotein(a) is a recognized risk factor for ASCVD. There is still no targeted therapy for Lp(a), however, drugs such as pelacarsen, olpasiran, zerlasiran, lepodisiran and muvalaplin are in clinical trials and have been shown to be effective in significantly reducing Lp(a) levels. Moreover, elevated Lp(a) levels significantly affect the prognosis of patients after aortic valve replacement (AVR) and heart transplantation (HTx). Therefore, the assessment of Lp(a) concentration in these patients will allow for a more accurate stratification of their cardiovascular risk, and the possibility of lowering Lp(a) will allow for the optimization of this risk. In this article, we summarized the most important information regarding the role of Lp(a) and lipid-lowering treatment in patients after AVR and HTx.
Keywords: Aortic stenosis; Aortic valve replacement; Cardiovascular risk optimization; Heart transplantation; Lipoprotein (a).
© 2024 The Author(s).
Conflict of interest statement
Stanisław Surma: honoraria from: Novartis/Sandoz, Pro.Med; Michał O. Zembala: honoraria from Boston Scientific; Bogusław Okopień: honoraria from: Sanofi, Bayer, Boehringer Ingelheim; Amgen, Novartis, Viatris, Servier, Astra Zeneca; Maciej Banach: honoraria from: Amgen, Daiichi Sankyo, KRKA, Polpharma, Mylan/Viatris, Novartis, Novo-Nordisk, Pfizer, Sanofi-Aventis, Teva, Zentiva; consultant to Adamed, Amgen, Daiichi Sankyo, Esperion, NewAmsterdam, Novartis, Novo-Nordisk, Sanofi-Aventis; Grants from Amgen, Daiichi Sankyo, Mylan/Viatris, Sanofi and Valeant.
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