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Updated: May 14, 2026

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
Published on: January 28, 2021
Lipoprotein(a): Role in Cardiovascular Risk and Advances in Novel Therapeutics
Adrián Murillo Sotela1, Gloriana Orozco Loaiza1, Paula Villalobos Villalobos1
1General Medicine, Universidad de Costa Rica, San José, CRI.
Insights
Lipoprotein(a) (Lp(a)) contributes to residual cardiovascular risk. Novel therapies targeting Lp(a) show promise in clinical trials, offering new hope for managing cardiovascular disease.
Area of Science:
- Cardiology
- Genetics
- Pharmacology
Background:
- Significant residual cardiovascular risk persists despite established prevention strategies.
- Lipoprotein(a) (Lp(a)), a genetically determined lipoprotein, is increasingly recognized as a causal factor in cardiovascular disease (CVD).
- The apolipoprotein(a) (apo(a)) component of Lp(a) drives proatherogenic, proinflammatory, prothrombotic, and procalcific mechanisms contributing to CVD.
Purpose of the Study:
- To review the role of Lp(a) in residual cardiovascular risk.
- To discuss current therapeutic strategies and emerging treatments targeting Lp(a).
Main Methods:
- Literature review of studies investigating Lp(a) and cardiovascular disease.
- Analysis of clinical trial data for novel Lp(a)-targeting therapeutics.
Main Results:
- Lp(a) is a significant, genetically determined contributor to residual cardiovascular risk.
- Current management relies on aggressive control of traditional risk factors.
- Phase 2 trials of small interfering ribonucleic acids (siRNAs) and antisense oligonucleotides (ASOs) targeting Lp(a) demonstrate promising efficacy.
Conclusions:
- Novel therapeutics targeting Lp(a) are on the horizon, with multiple agents in phase 3 trials.
- These emerging therapies hold the potential to address the unmet need in managing Lp(a)-associated cardiovascular risk.
- Targeting Lp(a) represents a promising new frontier in cardiovascular disease prevention.
Abstract:
Despite adequate primary and secondary prevention of cardiovascular events, significant residual risk remains. Part of this risk has been attributed to lipoprotein(a) (Lp{a}). This is a genetically determined lipoprotein that has been linked to cardiovascular disease. Its variability and pathogenicity are attributed to the unique apolipoprotein(a) (apo{a}) within the molecule. This protein has been related to proatherogenic, proinflammatory, prothrombotic, and procalcific mechanisms that favor cardiovascular disease (CVD). Although it is recognized as a causal factor in disease, there are currently no approved therapeutics targeting this lipoprotein. Current management focuses on aggressive control of traditional cardiovascular risk factors. Novel therapeutics targeting Lp(a), including small interfering ribonucleic acids (siRNAs) and antisense oligonucleotides (ASOs), showed promising results in phase 2 trials. Multiple therapeutics are currently undergoing phase 3 trials, promising to bring a solution to this unsolved issue.
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