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Updated: May 13, 2026

High-Density Lipoprotein-Specific Phospholipid Efflux Assay
Published on: September 30, 2025
Lipoprotein-associated phospholipase A2 (Lp-PLA(2)): a novel and promising biomarker for cardiovascular risks
Anping Cai1, Dongdan Zheng, Ruofeng Qiu
1Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China.
Insights
Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a key biomarker for vascular inflammation and atherosclerosis. This review summarizes Lp-PLA2
Area of Science:
- Biochemistry
- Cardiology
- Biomarker Discovery
Background:
- Cardiovascular diseases (CVD) remain a leading global cause of mortality.
- Residual cardiovascular risk persists despite current interventions.
- Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a specific biomarker for vascular inflammation and atherosclerosis.
Purpose of the Study:
- To review the biochemical characteristics of Lp-PLA2.
- To summarize the role of Lp-PLA2 in atherosclerosis.
- To discuss the clinical significance of Lp-PLA2 in risk stratification and prognosis.
Main Methods:
- Literature review of scientific and clinical studies.
- Analysis of data on Lp-PLA2 biochemical properties.
- Evaluation of Lp-PLA2's correlation with cardiovascular events.
Main Results:
- Lp-PLA2 exhibits pro-atherogenic properties and correlates with cardiovascular events.
- Lp-PLA2 is recommended as an adjunct risk assessment tool in ATP III guidelines.
- Darapladib, an Lp-PLA2 inhibitor, shows promising preclinical results with ongoing Phase III trials.
Conclusions:
- Lp-PLA2 holds significant potential for cardiovascular risk stratification.
- Therapeutic strategies targeting Lp-PLA2, like darapladib, warrant further investigation.
- Understanding Lp-PLA2's role is crucial for managing atherosclerosis and reducing CV risk.
Abstract:
Atherosclerosis and its manifestations namely cardiovascular diseases (CVD) are still the leading cause of morbidity and mortality worldwide. Although intensified interventions have been applied, the residual cardiovascular (CV) risks are still very high. Lipoprotein-associated phospholipase A2 (Lp-PLA(2)) is a novel and unique biomarker highly specific for vascular inflammation and atherosclerosis. Both pro-atherogenic property of Lp-PLA(2) and positive correlation with CV events have already been demonstrated by a large number of scientific and clinical studies. Currently, in the Adult Treatment Panel III (ATP III) guideline, Lp-PLA(2) has been recommended as an adjunct to traditional risk factors in assessing future CV risks. Encouragingly, darapladib, an orally Lp-PLA(2) specific inhibitor, has been tested in basic research and preclinical trials and the outcomes are quite striking. Additionally, there are two phase III ongoing clinical trials in evaluating the efficacy and safety of darapladib on cardiovascular outcomes. With regard to the potential values of Lp-PLA(2) in risk stratification, therapeutic regimen establishment and prognosis evaluation in patients with moderate or high risk, our present review is going to summarize the relevant data about the bio-chemical characteristics of Lp-PLA(2), the actions of Lp-PLA(2) on atherosclerosis and the results of Lp-PLA(2) in scientific research and clinical studies.
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