Consensus document on Lipoprotein(a) from the Italian Society for the Study of Atherosclerosis (SISA)

• Published in: Nutrition, metabolism, and cardiovascular diseases Vol. 33; no. 10; pp. 1866 - 1877
• Main Authors: Chiesa, Giulia, Zenti, Maria Grazia, Baragetti, Andrea, Barbagallo, Carlo M., Borghi, Claudio, Colivicchi, Furio, Maggioni, Aldo P., Noto, Davide, Pirro, Matteo, Rivellese, Angela A., Sampietro, Tiziana, Sbrana, Francesco, Arca, Marcello, Averna, Maurizio, Catapano, Alberico L.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.10.2023
• Subjects: Antisense oligonucleotides; Aortic valve stenosis; atherosclerosis; Atherosclerotic cardiovascular disease; epidemiology; Familial hypercholesterolemia; genetics; Lipoprotein(a); low density lipoprotein; Mendelian randomization; metabolism; nutrition; oxidation; Oxidized phospholipids; patients; phospholipids; risk; Small interfering RNA; therapeutics; Lipoprotein(a); Oxidized phospholipids; Atherosclerotic cardiovascular disease; Aortic valve stenosis; Small interfering RNA; Antisense oligonucleotides; Mendelian randomization; Familial hypercholesterolemia
• ISSN: 0939-4753; 1590-3729; 1590-3729
• DOI: 10.1016/j.numecd.2023.07.019

In view of the consolidating evidence on the causal role of Lp(a) in cardiovascular disease, the Italian Society for the Study of Atherosclerosis (SISA) has assembled a consensus on Lp(a) genetics and epidemiology, together with recommendations for its measurement and current and emerging therapeutic approaches to reduce its plasma levels. Data on the Italian population are also provided. Lp(a) is constituted by one apo(a) molecule and a lipoprotein closely resembling to a low-density lipoprotein (LDL). Its similarity with an LDL, together with its ability to carry oxidized phospholipids are considered the two main features making Lp(a) harmful for cardiovascular health. Plasma Lp(a) concentrations vary over about 1000 folds in humans and are genetically determined, thus they are quite stable in any individual. Mendelian Randomization studies have suggested a causal role of Lp(a) in atherosclerotic cardiovascular disease (ASCVD) and aortic valve stenosis and observational studies indicate a linear direct correlation between cardiovascular disease and Lp(a) plasma levels. Lp(a) measurement is strongly recommended once in a patient's lifetime, particularly in FH subjects, but also as part of the initial lipid screening to assess cardiovascular risk. The apo(a) size polymorphism represents a challenge for Lp(a) measurement in plasma, but new strategies are overcoming these difficulties. A reduction of Lp(a) levels can be currently attained only by plasma apheresis and, moderately, with PCSK9 inhibitor treatment. Awaiting the approval of selective Lp(a)-lowering drugs, an intensive management of the other risk factors for individuals with elevated Lp(a) levels is strongly recommended. •Lp(a) plasma levels are generally stable during lifetime.•Lp(a) causes atherosclerotic cardiovascular disease and aortic valve stenosis.•Cardiovascular risk increases linearly with Lp(a) levels with no threshold effect.•Lp(a) measurement is strongly recommended once in a patient's lifetime.•Current Lp(a)-lowering therapies are lipoprotein apheresis and PCSK9 inhibitors.