| Literature DB >> 34356902 |
Gabriella Iannuzzo1, Maria Tripaldella1, Vania Mallardo1, Mena Morgillo1, Nicoletta Vitelli1, Arcangelo Iannuzzi2, Emilio Aliberti3, Francesco Giallauria4, Anna Tramontano4, Raffaele Carluccio4, Ilenia Calcaterra1, Matteo Nicola Dario Di Minno1, Marco Gentile1.
Abstract
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.Entities:
Keywords: antisense oligonucleotide APO(a)Lrx; cardiovascular risk; lipoprotein apheresis; lipoprotein(a)
Year: 2021 PMID: 34356902 DOI: 10.3390/biomedicines9070838
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059