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Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy

A number of epidemiologic studies have demonstrated a strong association between increasing lipoprotein a [Lp(a)] and cardiovascular disease. This correlation was demonstrated independent of other known cardiovascular (CV) risk factors. Screening for Lp(a) in the general population is not recommende...

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Autores principales: Iannuzzo, Gabriella, Tripaldella, Maria, Mallardo, Vania, Morgillo, Mena, Vitelli, Nicoletta, Iannuzzi, Arcangelo, Aliberti, Emilio, Giallauria, Francesco, Tramontano, Anna, Carluccio, Raffaele, Calcaterra, Ilenia, Di Minno, Matteo Nicola Dario, Gentile, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301358/
https://www.ncbi.nlm.nih.gov/pubmed/34356902
http://dx.doi.org/10.3390/biomedicines9070838
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author Iannuzzo, Gabriella
Tripaldella, Maria
Mallardo, Vania
Morgillo, Mena
Vitelli, Nicoletta
Iannuzzi, Arcangelo
Aliberti, Emilio
Giallauria, Francesco
Tramontano, Anna
Carluccio, Raffaele
Calcaterra, Ilenia
Di Minno, Matteo Nicola Dario
Gentile, Marco
author_facet Iannuzzo, Gabriella
Tripaldella, Maria
Mallardo, Vania
Morgillo, Mena
Vitelli, Nicoletta
Iannuzzi, Arcangelo
Aliberti, Emilio
Giallauria, Francesco
Tramontano, Anna
Carluccio, Raffaele
Calcaterra, Ilenia
Di Minno, Matteo Nicola Dario
Gentile, Marco
author_sort Iannuzzo, Gabriella
collection PubMed
description A number of epidemiologic studies have demonstrated a strong association between increasing lipoprotein a [Lp(a)] and cardiovascular disease. This correlation was demonstrated independent of other known cardiovascular (CV) risk factors. Screening for Lp(a) in the general population is not recommended, although Lp(a) levels are predominantly genetically determined so a single assessment is needed to identify patients at risk. In 2019 ESC/EAS guidelines recommend Lp(a) measurement at least once a lifetime, fo subjects at very high and high CV risk and those with a family history of premature cardiovascular disease, to reclassify patients with borderline risk. As concerning medications, statins play a key role in lipid lowering therapy, but present poor efficacy on Lp(a) levels. Actually, treatment options for elevated serum levels of Lp(a) are very limited. Apheresis is the most effective and well tolerated treatment in patients with high levels of Lp(a). However, promising new therapies, in particular antisense oligonucleotides have showed to be able to significantly reduce Lp(a) in phase II RCT. This review provides an overview of the biology and epidemiology of Lp(a), with a view to future therapies.
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spelling pubmed-83013582021-07-24 Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy Iannuzzo, Gabriella Tripaldella, Maria Mallardo, Vania Morgillo, Mena Vitelli, Nicoletta Iannuzzi, Arcangelo Aliberti, Emilio Giallauria, Francesco Tramontano, Anna Carluccio, Raffaele Calcaterra, Ilenia Di Minno, Matteo Nicola Dario Gentile, Marco Biomedicines Review A number of epidemiologic studies have demonstrated a strong association between increasing lipoprotein a [Lp(a)] and cardiovascular disease. This correlation was demonstrated independent of other known cardiovascular (CV) risk factors. Screening for Lp(a) in the general population is not recommended, although Lp(a) levels are predominantly genetically determined so a single assessment is needed to identify patients at risk. In 2019 ESC/EAS guidelines recommend Lp(a) measurement at least once a lifetime, fo subjects at very high and high CV risk and those with a family history of premature cardiovascular disease, to reclassify patients with borderline risk. As concerning medications, statins play a key role in lipid lowering therapy, but present poor efficacy on Lp(a) levels. Actually, treatment options for elevated serum levels of Lp(a) are very limited. Apheresis is the most effective and well tolerated treatment in patients with high levels of Lp(a). However, promising new therapies, in particular antisense oligonucleotides have showed to be able to significantly reduce Lp(a) in phase II RCT. This review provides an overview of the biology and epidemiology of Lp(a), with a view to future therapies. MDPI 2021-07-19 /pmc/articles/PMC8301358/ /pubmed/34356902 http://dx.doi.org/10.3390/biomedicines9070838 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Iannuzzo, Gabriella
Tripaldella, Maria
Mallardo, Vania
Morgillo, Mena
Vitelli, Nicoletta
Iannuzzi, Arcangelo
Aliberti, Emilio
Giallauria, Francesco
Tramontano, Anna
Carluccio, Raffaele
Calcaterra, Ilenia
Di Minno, Matteo Nicola Dario
Gentile, Marco
Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title_full Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title_fullStr Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title_full_unstemmed Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title_short Lipoprotein(a) Where Do We Stand? From the Physiopathology to Innovative Terapy
title_sort lipoprotein(a) where do we stand? from the physiopathology to innovative terapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301358/
https://www.ncbi.nlm.nih.gov/pubmed/34356902
http://dx.doi.org/10.3390/biomedicines9070838
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