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Published on: October 12, 2017
Lp(a): A Clinical Review
Khalil Anchouche1, Alexis Baass2, George Thanassoulis1
1McGill University Health Centre and Research Institute, Montreal, QC, Canada; McGill University, Montreal, QC, Canada.
Insights
Elevated lipoprotein(a) (Lp[a]) is a key genetic risk factor for cardiovascular disease. New Lp[a]-lowering therapies are in late-stage trials, offering hope for future clinical practice.
Area of Science:
- Cardiology
- Genetics
- Pharmacology
Background:
- Elevated lipoprotein(a) (Lp[a]) is a prevalent, genetically determined risk factor for atherosclerotic cardiovascular disease and aortic stenosis.
- Current guidelines recommend universal Lp[a] screening due to its significant impact on cardiovascular health.
Purpose of the Study:
- To provide a comprehensive review of lipoprotein(a) (Lp[a]) biology, genetics, and clinical associations.
- To highlight emerging Lp[a]-lowering therapies and their potential future clinical applications.
Main Methods:
- Literature review of Lp(a) biology, genetics, and clinical associations.
- Analysis of current drug development pipeline for Lp[a]-lowering agents.
- Discussion of the potential role of novel therapies in clinical practice.
Main Results:
- Lp(a) is a significant, inherited risk factor for cardiovascular diseases, including atherosclerotic cardiovascular disease and aortic stenosis.
- Several novel therapies targeting Lp[a) reduction are in late-stage clinical trials.
- These therapies hold promise for future management of cardiovascular risk associated with elevated Lp(a).
Conclusions:
- Universal screening for Lp(a) is increasingly recommended for cardiovascular risk assessment.
- Emerging Lp(a)-lowering therapies represent a significant advancement in managing this risk factor.
- These novel treatments are expected to play a crucial role in future cardiovascular medicine.
Abstract:
Elevated lipoprotein(a) (Lp[a]) is a genetically determined cardiovascular risk factor, linked to both atherosclerotic cardiovascular disease and aortic stenosis. Elevated Lp(a) is widely prevalent, and consequently, several cardiovascular societies now recommend performing Lp(a) screening at least once in all adults. While there are presently no approved drugs specifically aimed at lowering Lp(a), several promising candidates are currently in the drug development pipeline, and many of these are now undergoing late phase clinical trials. In this comprehensive review, we outline Lp(a) biology and genetics, describe Lp(a)'s relationship to various cardiovascular clinical phenotypes of interest, highlight novel Lp(a)-lowering therapies, and outline what role these may have in future clinical practice.
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