Authors
Luca Di Lullo, Paola Peverini, Antonio Bellasi, Andre Dello Strologo, Claudio Ronco, Pasquale Saporito, Aldo Franculli
Published in
Cardiorenal medicine. Pages 1-16. Jul 10, 2026. Epub Jul 10, 2026.
Abstract
Lipoprotein(a) [Lp(a)] is an LDL-like particle containing apolipoprotein B100 covalently bound to apolipoprotein(a). Elevated Lp(a) is now recognized as a genetically determined, independent, and likely causal risk factor for atherosclerotic cardiovascular disease, calcific aortic valve stenosis, and residual cardiovascular risk despite optimal LDL-cholesterol control. Current European and North American recommendations support measuring Lp(a) at least once in adulthood, particularly for cardiovascular risk refinement. Lp(a) levels are predominantly inherited and are only modestly influenced by lifestyle or conventional lipid-lowering therapies. Chronic kidney disease represents a clinically relevant setting in which Lp(a) levels may rise as renal function declines and may contribute to the excess cardiovascular burden. However, the causal role of Lp(a) in CKD-related cardiovascular disease remains incompletely defined. Novel RNA-based and small-molecule therapies, including pelacarsen, olpasiran, lepodisiran, zerlasiran, and muvalaplin, have shown marked Lp(a)-lowering effects, but definitive cardiovascular outcome data are still missing.
PMID:
42430287
Bibliographic data and abstract were imported from PubMed on 11 Jul 2026.
Read full publication at:
Please sign in
to see all details.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 3
- Comments 0