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Updated: May 5, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Lipoprotein(a): a promising marker for residual cardiovascular risk assessment
Anping Cai1, Liwen Li, Ying Zhang
1Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.
Insights
Lipoprotein(a) (Lp(a)) is a significant risk factor for atherosclerotic cardiovascular diseases (CVD) even with optimal medical therapy. Elevated Lp(a) may indicate residual cardiovascular risk, suggesting potential benefits from more aggressive LDL-C lowering.
Area of Science:
- Cardiology
- Atherosclerosis Research
- Lipidology
Background:
- Atherosclerotic cardiovascular diseases (CVD) remain a leading global cause of death and disability.
- Optimal medical therapy often fails to eliminate residual cardiovascular risk in certain patient groups, particularly those with normal low-density lipoprotein-cholesterol (LDL-C) levels.
- Lipoprotein(a) (Lp(a)) has emerged as a key independent risk factor for CVD due to its proatherogenic and prothrombotic properties.
Purpose of the Study:
- To highlight the significance of lipoprotein(a) (Lp(a)) as a marker for residual cardiovascular risk.
- To discuss the challenges in developing effective Lp(a)-lowering therapies.
- To propose potential therapeutic strategies for patients with high Lp(a) levels.
Main Methods:
- Review of clinical trials and meta-analyses on Lp(a) and cardiovascular risk.
- Analysis of Lp(a)'s role in atherosclerosis and thrombosis.
- Evaluation of current treatment guidelines and their limitations.
Main Results:
- Compelling evidence identifies Lp(a) as a significant contributor to residual cardiovascular risk.
- The lack of specific Lp(a)-lowering medications hinders large-scale clinical trials.
- Lp(a) can identify individuals at high risk, even with controlled LDL-C.
Conclusions:
- Lipoprotein(a) is a crucial factor in assessing residual cardiovascular risk.
- Aggressively lowering LDL-C may be beneficial for patients with high Lp(a) levels.
- Further research into Lp(a)-targeted therapies is warranted.
Abstract:
Atherosclerotic cardiovascular diseases (CVD) are still the leading cause of morbidity and mortality worldwide, although optimal medical therapy has been prescribed for primary and secondary preventions. Residual cardiovascular risk for some population groups is still considerably high although target low density lipoprotein-cholesterol (LDL-C) level has been achieved. During the past few decades, compelling pieces of evidence from clinical trials and meta-analyses consistently illustrate that lipoprotein(a) (Lp(a)) is a significant risk factor for atherosclerosis and CVD due to its proatherogenic and prothrombotic features. However, the lack of effective medication for Lp(a) reduction significantly hampers randomized, prospective, and controlled trials conducting. Based on previous findings, for patients with LDL-C in normal range, Lp(a) may be a useful marker for identifying and evaluating the residual cardiovascular risk, and aggressively lowering LDL-C level than current guidelines' recommendation may be reasonable for patients with particularly high Lp(a) level.
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