Why the study?
Elevated Lp(a) is an independent causative risk factor for CVD and calcific aortic valve stenosis, making therapeutic management aimed at reducing Lp(a) levels clinically relevant.
What are the current therapeutic options for the management of hyperlipoproteinemia (a)?
What are the current therapeutic options for the management of hyperlipoproteinemia (a)?
This review summarizes current and emerging therapies for elevated Lp(a), highlighting novel antisense oligonucleotides and PCSK9 inhibitors as promising interventions for severe cases.
Answers are grounded in this paper and cite their sources.
May inform initial Lp(a) management in mild cases; leaves open optimal strategies for severe elevations pending randomized trials.
Cardiovascular disease (CVD) has consistently been the leading cause of death worldwide. Several clinical and epidemiological studies have demonstrated that an elevated plasma concentration of lipoprotein (a) [Lp(a)] is a causative and independent major risk factor for the development of CVD, as well as calcific aortic valve stenosis. Thus, the therapeutic management of hyperlipoproteinemia (a) has received much attention, as significant reductions in Lp(a) levels may, potentially, favorably affect cardiovascular risk. Aspirin, niacin, estrogens, and statins, which act on different molecular pathways, may be prescribed to patients with mild or modest elevations of Lp(a) levels. Other therapeutic interventions, such as proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, Lp(a) apheresis, and the novel antisense oligonucleotides APO(a)-Rx and APO(a)-LRx, which are being evaluated in ongoing clinical trials, have provided some promising results and can potentially be used in severe cases of hyperlipoproteinemia (a). This review aims to present and discuss the current clinical and scientific data pertaining to the therapeutic options for the management of hyperlipoproteinemia (a).
No takes yet. Share an insight, caveat, or question.
Kosmas et al. (2019) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: