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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Myeloperoxidase, subclinical atherosclerosis, and cardiovascular disease events
Nathan D Wong1, Heidi Gransar, Jagat Narula
1Division of Cardiology, University of California, Irvine, California, USA.
Objectives:
We evaluated whether myeloperoxidase (MPO) predicts future cardiovascular disease (CVD) events in asymptomatic adults and whether subclinical atherosclerosis may affect this relation.
Background:
Myeloperoxidase is a leukocyte-derived enzyme-generating reactive oxidant species that has been shown to predict risk of CVD in selected populations.
Methods:
We studied 1,302 asymptomatic adults (mean age 59 years, 47% women) without known CVD who were followed for 3.8 years. We measured MPO by the use of immunoassay. Coronary artery calcium (CAC), a measure of subclinical atherosclerosis, was measured by computed tomography with the Agatston score categorized as none/minimal (0 to 9), mild (10 to 99), and moderate/significant (> or = 100). Cox regression, adjusted for age, sex, and other risk factors, examined the relation of CAC and/or MPO with incident CVD events.
Results:
Persons with MPO levels at or above compared with below the median (257 pM) were more likely (p < 0.05 to p < 0.001) to be women, have a higher body mass index, greater low-density lipoprotein cholesterol, greater systolic and diastolic blood pressure, and lower high-density lipoprotein cholesterol. Mean MPO levels increased according to CAC categories (p trend = 0.02). Incident CVD events were more likely in those at or above versus below the median MPO level (4.6% vs. 2.3%, p = 0.02), even after adjustment for age, sex, CAC, and risk factors (hazard ratio [HR]: 1.9, 95% confidence interval: 1.0 to 3.6, p = 0.04). Combining CAC and MPO categories, CVD incidence ranged from 0.6% in those with a CAC score of 0 to 9 to 7.1% (adjusted HR: 9.2, p < 0.001) in those with CAC scores of > or = 100 and MPO below the median and 14.0% (adjusted HR: 19.5, p < 0.0001) in those with CAC scores of > or = 100 and MPO at or above the median.
Conclusions:
Our study suggests persons with both increased levels of both MPO and CAC are at an increased risk of CVD events. Imaging of subclinical atherosclerosis combined with assessment of biomarkers of plaque vulnerability may help improve CVD risk stratification.
Insights
Myeloperoxidase (MPO) and coronary artery calcium (CAC) together predict cardiovascular disease (CVD) events in asymptomatic adults. Combining these markers, especially elevated MPO with significant CAC, indicates a substantially higher CVD risk.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Preventive Cardiology
Background:
- Myeloperoxidase (MPO) is an enzyme linked to cardiovascular disease (CVD) risk.
- Its role in asymptomatic individuals and interaction with atherosclerosis needs further clarification.
Purpose of the Study:
- To assess if myeloperoxidase (MPO) predicts future cardiovascular disease (CVD) events in asymptomatic adults.
- To determine if subclinical atherosclerosis influences the MPO-CVD relationship.
Main Methods:
- 1,302 asymptomatic adults without known CVD were followed for 3.8 years.
- Myeloperoxidase (MPO) levels and coronary artery calcium (CAC) scores were measured.
- Cox regression analysis examined the association of MPO and CAC with incident CVD events.
Main Results:
- Higher MPO levels were associated with traditional CVD risk factors.
- Incident CVD events were more frequent in individuals with MPO levels at or above the median (4.6% vs. 2.3%, p=0.02).
- The combination of elevated MPO and high CAC scores (>=100) showed a significantly increased risk of CVD events (adjusted HR: 19.5).
Conclusions:
- Elevated myeloperoxidase (MPO) and coronary artery calcium (CAC) are strong predictors of future cardiovascular events in asymptomatic adults.
- Combining biomarker assessment (MPO) with imaging of subclinical atherosclerosis (CAC) can enhance CVD risk stratification.
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