Key result
Novel RNA-based therapies targeting Lp(a) advance in trials to evaluate cardiovascular risk reduction.
Why the study?
Elevated Lp(a) is an independent, causal cardiovascular risk factor without approved specific pharmacotherapies, while research into RNA-based therapies and pathogenic mechanisms is rapidly evolving.
Answers are grounded in this paper and cite their sources.
Emerging RNA-based therapies targeting elevated Lp(a) are advancing in clinical trials, potentially transforming secondary cardiovascular disease prevention strategies.
Elevated plasma lipoprotein(a) [Lp(a)] levels, which occur in as many as 1.5 billion people worldwide, are an independent and causal risk factor for atherosclerotic cardiovascular disease and calcific aortic valve disease. Unlike low-density lipoprotein cholesterol, Lp(a) levels are approximately 70-90% genetically determined. Currently, no approved pharmacological therapies specifically target lowering Lp(a) concentrations. Several drugs, mainly RNA-based therapies, that specifically and potently lower Lp(a), are under investigation. Three of these new therapeutic agents are advancing through clinical development to evaluate whether reducing Lp(a) levels can decrease cardiovascular risk. The outcomes of these trials could potentially transform cardiovascular disease prevention strategies; however, once approved, the drugs will likely be used for secondary prevention, and ongoing strategies for managing elevated Lp(a) in primary prevention will be important. Lipoprotein(a) research is a rapidly evolving field, but unanswered questions remain concerning the physiological function of Lp(a) and its true pathogenic mechanisms. This review of Lp(a) research focuses on new findings and clinical trial results that appeared in 2024.
No takes yet. Share an insight, caveat, or question.
Sosnowska et al. (2025) conducted a review in Elevated plasma lipoprotein(a). RNA-based therapies targeting Lipoprotein(a) was evaluated. A 2024 review highlights that several RNA-based therapies specifically targeting elevated lipoprotein(a) are advancing through clinical trials to evaluate their impact on cardiovascular risk.
Synapse has enriched 10 related papers. Consider them for comparative context: