Why the study?
Epidemiological, genetic, and biological evidence supports a causal and independent role for Lp(a) in atherosclerotic disease and aortic valve stenosis, creating a clear need to include Lp(a) measurement in global cardiovascular risk assessment and clinical management.
This multisociety consensus document provides operational guidance for standardizing Lipoprotein(a) measurement in nmol/L and integrating it as a continuous, causal risk amplifier into global cardiovascular risk stratification.
Lipoprotein(a) [Lp(a)] is a plasma lipoprotein that shares structural elements with low-density lipoprotein (LDL), such as apolipoprotein B-100 (apoB), but differs by the presence of apolipoprotein(a) [apo(a)], which is covalently linked to apoB via a disulphide bond. In recent years, interest in Lp(a) has increased considerably, as epidemiological, genetic and biological evidence supports its causal role in cardiovascular disease. Its heterogeneous structural features, metabolic peculiarities, and ability to transport biologically active and potentially pro- atherogenic, pro-inflammatory and pro-thrombotic molecules make Lp(a) a unique lipoprotein among the apoB-containing lipoproteins. Lp(a) is now recognised as an important risk factor in cardiovascular risk assessment, as it plays a causal and independent role in the development of both atherosclerotic disease and aortic valve stenosis. Measuring Lp(a), together with other determinants of cardiovascular risk, is now recognised as essential for appropriate clinical management and the identification of new therapeutic targets. Consequently, the need to include Lp(a) in global cardiovascular risk assessment has clearly emerged, especially in individuals with a personal history of early or recurrent events, familial hypercholesterolaemia, family history of early events, or family history of high Lp(a) levels. This document, produced through the collaboration of the main Italian scientific societies in the field of cardiovascular disease management and laboratory medicine (SISA, SIC, ANMCO and SIBioC), analyses the pathogenetic role of lipoprotein(a) [Lp(a)] and the clinical significance of its measurement.
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Catapano et al. (2025) conducted a review in Atherosclerotic cardiovascular disease and calcific aortic valve stenosis. Elevated Lipoprotein(a) [Lp(a)] vs. Normal or low Lipoprotein(a) levels (<75 nmol/L or <30 mg/dL) was evaluated. Lipoprotein(a) is a continuous, causal risk factor for atherosclerotic cardiovascular disease, with levels >125 nmol/L (>50 mg/dL) indicating high risk and warranting once-in-a-lifetime measurement.
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