Lifestyle
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Lipoprotein-associated Phospholipase A2 · PLAC Test
Lp-PLA2 quantifies the enzyme activity associated with the hydrolysis of oxidized phospholipids in lipoproteins.
Reference ranges may vary based on laboratory and population-specific studies.
Lipoprotein-associated phospholipase A2 (Lp-PLA2) is an enzyme primarily associated with low-density lipoprotein (LDL) particles in the bloodstream. It plays a role in the hydrolysis of oxidized phospholipids, leading to the production of pro-inflammatory lysophosphatidylcholine and oxidized non-esterified fatty acids. These products contribute to the inflammatory processes within atherosclerotic plaques, potentially leading to plaque instability and rupture. Clinically, Lp-PLA2 is considered a significant biomarker for cardiovascular diseases, particularly in assessing the risk of coronary heart disease, ischemic stroke, and other atherosclerotic conditions. Elevated levels of Lp-PLA2 have been associated with increased risk of cardiovascular events, making it a valuable tool for risk stratification and management in patients with or at risk for cardiovascular diseases. In the context of athletic performance and biohacking, Lp-PLA2 may be of interest due to its role in inflammation and cardiovascular health. While not directly linked to athletic performance, maintaining optimal cardiovascular health is crucial for longevity and physical endurance. Biohackers may monitor Lp-PLA2 to optimize cardiovascular risk profiles and potentially enhance longevity. However, researchers have noted that Lp-PLA2 levels can be influenced by factors such as LDL cholesterol levels, inflammation, and genetic predispositions. It is important to consider these confounders when interpreting Lp-PLA2 results. Additionally, fasting is not required for Lp-PLA2 testing, and it is not significantly affected by the time of day, making it a convenient marker for routine cardiovascular risk assessment.
Klinische Bedeutung
Elevated Lp-PLA2 levels indicate increased cardiovascular risk, particularly for coronary heart disease and ischemic stroke. Lower levels may suggest reduced inflammatory activity within atherosclerotic plaques.
Rising Lp-PLA2 levels suggest increasing cardiovascular risk and may warrant lifestyle or therapeutic interventions. Re-test in 3-6 months.
Falling levels indicate reduced cardiovascular risk and effective management of inflammation.
Re-test Interval
6 months if outside optimal range
Note:
Consult a healthcare provider before starting any supplementation, especially if on medication.
Testing Frequency
Annually for individuals at risk of cardiovascular disease.
Correlated with
Current research suggests that reference ranges for Lp-PLA2 levels and the optimal targets for intervention remain debated, particularly regarding confounding factors such as lipid profiles and comorbidities. Researchers have not yet established the precise mechanisms by which Lp-PLA2 contributes to plaque instability and cardiovascular events. Additionally, unanswered clinical questions include the long-term effects of Lp-PLA2 inhibition on cardiovascular outcomes and the biomarker's role in diverse populations.
652
Total Citations
13
Human/RCT
3.2
Avg. Influence
2025
Latest
This review discussed Lp-PLA2 as an emerging biomarker for coronary heart disease. Researchers emphasized its proinflammatory role in atherosclerosis and presented a new ELISA method for measuring Lp-PLA2 levels in plasma.
Netala Vasudeva Reddy, et al. · International journal of molecular sciences · 2025
This study reviewed various cardiovascular biomarkers, highlighting their roles in diagnosing and managing cardiovascular diseases. Researchers found that biomarkers like Lp-PLA2 provide insights into lipid metabolism and atherosclerosis, aiding in risk stratification and personalized medicine.
Key findings
This study investigated the association between Lp-PLA2 activity and recurrent stroke risk. Researchers found that patients in the highest quartile of Lp-PLA2 activity had a significantly increased risk of recurrent stroke compared to those in the lowest quartile.
Zhang Ding-Ding, et al. · Stroke and vascular neurology · 2022
Researchers investigated the association between inflammatory biomarkers, including Lp-PLA2, and MRI markers of cerebral small vessel disease. They found that high levels of endothelial-related inflammatory biomarkers were linked to increased white matter hyperintensity and lacunes.
Key findings
Researchers reviewed the biochemical properties of Lp-PLA2 and its association with LDL and HDL. They found that LDL-associated Lp-PLA2 is a cardiovascular risk marker, while HDL-associated Lp-PLA2 may have protective effects.
Vittos Oana, et al. · Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals · 2012
This systematic review assessed Lp-PLA2's significance in cardiovascular diseases. Researchers found a consistent association between elevated Lp-PLA2 levels and cardiovascular events across diverse populations, confirming its role as a biomarker of vascular inflammation.
Key findings
This study examined the causal relationship between Lp-PLA2 and coronary heart disease. Researchers found that elevated levels of Lp-PLA2 are unlikely to be causal risk factors for the disease, suggesting that prior genetic studies could improve the efficiency of drug development.
Researchers identified Lp-PLA2 as a promising biomarker for chronic obstructive pulmonary disease (COPD). The study demonstrated that Lp-PLA2 levels correlate with disease severity and can effectively assess exercise tolerance in patients.
Rubinstein Ardon & Izkhakov Elena · Harefuah · 2011
Researchers examined the role of lipoprotein-associated phospholipase A2 (Lp-PLA2) as an inflammatory biomarker linked to plaque instability in coronary heart disease. They found that high levels of Lp-PLA2 are associated with increased cardiovascular risk and may indicate the need for more aggressive treatment in at-risk patients.
Key findings
This review highlighted the need for novel biomarkers like Lp-PLA2 for better cardiovascular risk assessment. Researchers noted that traditional risk algorithms may miss significant CVD events, emphasizing the potential of multi-biomarker panels for improved prediction.
8
Total Trials
3,240
Total Enrolled
Kanuni Sultan Suleyman Training and Research Hospital
80
2020
study group
Meenakshi Ammal Dental College and Hospital
75
2015
Estimation of serum Lp-PLA2
Nanjing First Hospital, Nanjing Medical University
1,713
2015
Lipoprotein-associated Phospholipase A2
Universitaire Ziekenhuizen KU Leuven
100
2015
Circulating Inflammatory Biomarkers: CRP, total cholesterol, HDL-cholesterol, triglycerides, albumin, Lp-PLA2 activity, Thrombin Activatable Fibrinolysis Inhibitor (TAFI), vitamin D
St. Petersburg State Pavlov Medical University
97
2011
Mean concentration of Lipoprotein-associated Phospholipase A2 (LP-PL-A2)
Alexhander Izhaki
40
2010
Mayo Clinic
166
2009
Lp-PLA2 Assessment
GlaxoSmithKline
969
2005
On treatment sustained inhibition of plasma Lp-PLA2 activity.
Research publications about Lp-PLA2 over time
9totalLog lab results, track trends and optimize your biomarkers over time.
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