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. 2024 Jun 6:22:200297.
doi: 10.1016/j.ijcrp.2024.200297. eCollection 2024 Sep.

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

Affiliations

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

Stanisław Surma et al. Int J Cardiol Cardiovasc Risk Prev. .

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).

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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.

Figures

Fig. 1
Fig. 1
The role of lipoprotein (a) and lipid-lowering treatment in patients after AVR or HTx. Based on information from Refs. [[1], [2], [3], [4], [5],[14], [15], [16], [17], [18], [19], [20], [21], [22], [23], [24], [25], [26],[32], [33], [34], [35], [36], [37],[44], [45], [46], [47], [48], [49], [50]]. The elements of the figure were created using SERVIER MEDICAL ART (CC BY 4.0). CAV photos used from: Das B.B. et al. Transplantology 2022; 3(3): 241–256 - CC BY license - no permission required. Other photos used are the property of the authors - no permission required. Details about Lp(a)-targeted drugs in the text of the article. Abbreviations: Lp(a) – lipoprotein (a); AS – aortic stenosis; HR – hazard ratio; TAVI - transcatheter aortic valve implantation; AVR – aortic valve replacement; MACE – major adverse cardiovascular event; SAVR – surgical aortic valve replacement; ASCVD – atherosclerotic cardiovascular disease; PCSK9 - proprotein convertase subtilisin-kexin type 9; Apo(a) – apolipoprotein (a); LDL – low-density lipoprotein; ApoB100 – apolipoprotein B100; oxPL - oxidized phospholipids; Lp-PLA2 - lipoprotein‐associated phospholipase A2; HFpEF – heart failure with preserved ejection fraction; HFrEF – heart failure with reduced ejection fraction; HTx - heart transplantation; CAV - cardiac allograft vasculopathy.

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References

    1. Kronenberg F., Mora S., Stroes E.S.G., Ference B.A., Arsenault B.J., Berglund L., et al. Frequent questions and responses on the 2022 lipoprotein(a) consensus statement of the European Atherosclerosis Society. Atherosclerosis. 2023;374:107–120. - PubMed
    1. Sosnowska B., Stępińska J., Mitkowski P., Bielecka-Dąbrowa A., Bobrowska B., Budzianowski J., et al. Recommendations of the experts of the polish cardiac society (PTK) and the polish lipid society (PTL) on the diagnosis and management of elevated lipoprotein (a) levels. Arch. Med. Sci. 2024;20:8–27. - PMC - PubMed
    1. Banach M., Surma S., Toth P.P. The year in cardiovascular disease - the year of new and prospective lipid lowering therapies. Can we render dyslipidemia a rare disease by 2024? Arch. Med. Sci. 2023;19:1602–1615. 2023. - PMC - PubMed
    1. Björnson E., Adiels M., Taskinen M.R., Burgess S., Chapman M.J., Packard C.J., et al. Lipoprotein(a) is markedly more atherogenic than LDL: an apolipoprotein B-based genetic analysis. J. Am. Coll. Cardiol. 2024;83:385–395. - PMC - PubMed
    1. Berman A.N., Biery D.W., Besser S.A., Singh A., Shiyovich A., Weber B.N., et al. Lipoprotein(a) and major adverse cardiovascular events in patients with or without baseline atherosclerotic cardiovascular disease. J. Am. Coll. Cardiol. 2024;83:873–886. - PubMed

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