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Therapeutic management of hyperlipoproteinemia (a)

Cardiovascular disease (CVD) has consistently been the leading cause of death worldwide. Several clinical and epidemiological studies have demonstrated that an elevated plasma concentration of lipoprotein (a) [Lp(a)] is a causative and independent major risk factor for the development of CVD, as wel...

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Autores principales: Kosmas, Constantine E, Sourlas, Andreas, Mallarkey, Gordon, Silverio, Delia, Ynoa, Domingo Y, Montan, Peter D, Guzman, Eliscer, Garcia, Mario J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752750/
https://www.ncbi.nlm.nih.gov/pubmed/31555339
http://dx.doi.org/10.7573/dic.212609
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author Kosmas, Constantine E
Sourlas, Andreas
Mallarkey, Gordon
Silverio, Delia
Ynoa, Domingo Y
Montan, Peter D
Guzman, Eliscer
Garcia, Mario J
author_facet Kosmas, Constantine E
Sourlas, Andreas
Mallarkey, Gordon
Silverio, Delia
Ynoa, Domingo Y
Montan, Peter D
Guzman, Eliscer
Garcia, Mario J
author_sort Kosmas, Constantine E
collection PubMed
description Cardiovascular disease (CVD) has consistently been the leading cause of death worldwide. Several clinical and epidemiological studies have demonstrated that an elevated plasma concentration of lipoprotein (a) [Lp(a)] is a causative and independent major risk factor for the development of CVD, as well as calcific aortic valve stenosis. Thus, the therapeutic management of hyperlipoproteinemia (a) has received much attention, as significant reductions in Lp(a) levels may, potentially, favorably affect cardiovascular risk. Aspirin, niacin, estrogens, and statins, which act on different molecular pathways, may be prescribed to patients with mild or modest elevations of Lp(a) levels. Other therapeutic interventions, such as proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, Lp(a) apheresis, and the novel antisense oligonucleotides APO(a)-Rx and APO(a)-LRx, which are being evaluated in ongoing clinical trials, have provided some promising results and can potentially be used in severe cases of hyperlipoproteinemia (a). This review aims to present and discuss the current clinical and scientific data pertaining to the therapeutic options for the management of hyperlipoproteinemia (a).
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spelling pubmed-67527502019-09-25 Therapeutic management of hyperlipoproteinemia (a) Kosmas, Constantine E Sourlas, Andreas Mallarkey, Gordon Silverio, Delia Ynoa, Domingo Y Montan, Peter D Guzman, Eliscer Garcia, Mario J Drugs Context Review Cardiovascular disease (CVD) has consistently been the leading cause of death worldwide. Several clinical and epidemiological studies have demonstrated that an elevated plasma concentration of lipoprotein (a) [Lp(a)] is a causative and independent major risk factor for the development of CVD, as well as calcific aortic valve stenosis. Thus, the therapeutic management of hyperlipoproteinemia (a) has received much attention, as significant reductions in Lp(a) levels may, potentially, favorably affect cardiovascular risk. Aspirin, niacin, estrogens, and statins, which act on different molecular pathways, may be prescribed to patients with mild or modest elevations of Lp(a) levels. Other therapeutic interventions, such as proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, Lp(a) apheresis, and the novel antisense oligonucleotides APO(a)-Rx and APO(a)-LRx, which are being evaluated in ongoing clinical trials, have provided some promising results and can potentially be used in severe cases of hyperlipoproteinemia (a). This review aims to present and discuss the current clinical and scientific data pertaining to the therapeutic options for the management of hyperlipoproteinemia (a). BioExcel Publishing Ltd 2019-09-04 /pmc/articles/PMC6752750/ /pubmed/31555339 http://dx.doi.org/10.7573/dic.212609 Text en Copyright © 2019 Kosmas CE, Sourlas A, Mallarkey G, Silverio D, Ynoa DY, Montan PD, Guzman E, Garcia MJ. Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Review
Kosmas, Constantine E
Sourlas, Andreas
Mallarkey, Gordon
Silverio, Delia
Ynoa, Domingo Y
Montan, Peter D
Guzman, Eliscer
Garcia, Mario J
Therapeutic management of hyperlipoproteinemia (a)
title Therapeutic management of hyperlipoproteinemia (a)
title_full Therapeutic management of hyperlipoproteinemia (a)
title_fullStr Therapeutic management of hyperlipoproteinemia (a)
title_full_unstemmed Therapeutic management of hyperlipoproteinemia (a)
title_short Therapeutic management of hyperlipoproteinemia (a)
title_sort therapeutic management of hyperlipoproteinemia (a)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752750/
https://www.ncbi.nlm.nih.gov/pubmed/31555339
http://dx.doi.org/10.7573/dic.212609
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