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Traditional and Novel Markers: Target of Treatment vs Marker of Risk
G B John Mancini1, Paul Poirier2, Daniel Esau3
1Division of Cardiology, Centre for Cardiovascular Innovation, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Insights
Low-density lipoprotein cholesterol (LDL-C) alone may not fully assess cardiovascular risk. Measuring triglycerides (TGs) and lipoprotein(a) [Lp(a)] offers a more comprehensive cardiovascular risk assessment.
Area of Science:
- Cardiovascular Medicine
- Lipidology
- Preventive Cardiology
Background:
- Low-density lipoprotein cholesterol (LDL-C) is a primary marker for cardiovascular (CV) risk, directly correlating with atherosclerotic disease.
- Traditional CV risk assessment often relies on LDL-C, typically estimated by the Friedewald equation, which may not capture the complete risk profile.
- Emerging evidence highlights the importance of other lipid markers beyond LDL-C.
Purpose of the Study:
- To discuss lipid-related markers associated with cardiovascular risk.
- To emphasize the significance of non-high-density lipoprotein cholesterol and apolipoprotein B100 alongside LDL-C.
- To underscore the need for incorporating triglycerides (TGs) and lipoprotein(a) [Lp(a)] into comprehensive CV risk assessments.
Main Methods:
- Review and discussion of current literature on lipid markers and CV risk.
- Analysis of the limitations of LDL-C estimation using the Friedewald equation.
- Examination of the roles of triglycerides (TGs) and lipoprotein(a) [Lp(a)] in CV disease.
Main Results:
- Elevated TGs may indicate increased cholesterol in non-LDL particles, suggesting non-high-density lipoprotein cholesterol or apolipoprotein B100 are more accurate risk indicators.
- Lipoprotein(a) [Lp(a)], a genetically determined LDL-like particle, possesses inflammatory and prothrombotic properties contributing to CV risk.
- Novel therapies targeting Lp(a) are emerging, but their clinical benefit in preventing CV outcomes requires further validation.
Conclusions:
- While LDL-C remains important, its limitations necessitate a broader assessment.
- Triglycerides (TGs) and lipoprotein(a) [Lp(a)] are crucial emerging markers for a more accurate and comprehensive cardiovascular risk evaluation.
- Healthcare professionals should re-evaluate traditional lipid assessment strategies to include TGs and Lp(a).
Abstract:
In this article we discuss lipid-related markers associated with cardiovascular (CV) risk, and emphasize the significance of low-density lipoprotein (LDL) cholesterol (LDL-C), non-high-density lipoprotein cholesterol, and apolipoprotein B100. LDL-C, a traditional CV risk factor, correlates directly with atherosclerotic CV disease. However, LDL-C alone, usually estimated using the Friedewald equation, might not capture the entire risk profile. Therefore, triglycerides (TGs) and lipoprotein(a) [Lp(a)] should be measured as part of a complete CV risk assessment. Although TGs represent potential markers of increased CV risk, their role as direct causal agents remains inconclusive. Elevated TG levels suggest a greater cholesterol presence in non-LDL particles, necessitating the use of non-high-density lipoprotein cholesterol or apolipoprotein B100, rather than solely LDL-C, to ensure an accurate CV risk assessment. Lp(a), however, is a genetically determined particle resembling LDL, linked with various significant CV diseases. Its role in CV risk is potentially because of its added inflammatory and prothrombotic properties. Certain medications (most notably proprotein convertase subtilisin/kexin type 9 inhibitors and novel small interfering RNA molecules) can reduce Lp(a) levels. Whether this confers a benefit in preventing CV outcomes requires validation from ongoing trials. Although LDL-C remains a crucial metric, health care professionals must acknowledge its limitations and understand the emerging significance of TGs and Lp(a) in CV risk assessment. This article underscores the need to reevaluate traditional lipid markers in light of emerging evidence on TGs and Lp(a) to promote a more comprehensive approach to CV risk assessment.
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