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Anti-Lipoprotein Lipase Antibody as a Useful Marker for Plaque Vulnerability in Patients with Stable Angina
Miyu Yoshinaga1, Eika Yuasa1, Tetsuro Matsuoka2
1Department of Biomedical Informatics, Division of Health Sciences, Osaka University Graduate School of Medicine.
Insights
Serum anti-lipoprotein lipase antibody (anti-LPL Ab) levels indicate plaque instability in coronary artery disease (CAD) patients. Combining anti-LPL Ab with anti-apolipoprotein B-100 autoantibody (anti-apoB-100 Ab) levels identifies higher-risk individuals.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Atherosclerosis Research
Background:
- Identifying vulnerable plaque in coronary artery disease (CAD) is critical for prognosis and treatment.
- Low anti-apolipoprotein B-100 autoantibody (anti-apoB-100 Ab) levels are linked to unstable plaques in male CAD patients.
- Lipoprotein lipase (LPL) is involved in triglyceride metabolism and atherosclerosis.
Purpose of the Study:
- To investigate the association between autoantibodies against lipoprotein lipase (anti-LPL Ab) and coronary plaque characteristics in male CAD patients.
- To determine if anti-LPL Ab levels can serve as a marker for plaque instability.
- To assess the combined utility of anti-LPL Ab and anti-apoB-100 Ab levels in identifying high-risk CAD patients.
Main Methods:
- Serum anti-LPL Ab levels were measured using a homemade enzyme-linked immunosorbent assay in 80 male CAD patients.
- Coronary plaque properties were assessed using iMAP®-intravascular ultrasound.
- Patients were stratified based on anti-LPL Ab levels, particularly those with low anti-apoB-100 Ab.
Main Results:
- Serum anti-LPL Ab levels did not correlate with plaque burden.
- Anti-LPL Ab levels showed significant negative correlation with fibrotic plaques and positive correlation with necrotic plaques.
- CAD patients with low anti-apoB-100 Ab and high anti-LPL Ab levels had more necrotic plaques, fewer fibrotic plaques, and higher remnant-like lipoprotein particle levels.
Conclusions:
- Serum anti-LPL Ab levels are a potential marker for coronary plaque instability in CAD.
- The combination of anti-LPL Ab and anti-apoB-100 Ab levels can enhance the identification of high-risk CAD patients.
- Further research may elucidate the role of anti-LPL Ab in atherosclerosis progression and plaque vulnerability.
Aims:
Identifying patients with vulnerable plaque who have poor prognosis among those with coronary artery disease (CAD) is crucial to deciding future therapeutic interventions. We previously reported that male CAD patients with low anti-apolipoprotein B-100 autoantibody (anti-apoB-100 Ab) levels were at an increased risk of developing unstable plaque lesions. This study focused on the autoantibodies against lipoprotein lipase (LPL), a key enzyme in triglyceride metabolism, which is another risk factor for atherosclerosis, and investigated their association with plaque characteristics.
Methods:
We measured serum anti-LPL Ab levels using a homemade enzyme-linked immunosorbent assay in 80 male CAD patients. Coronary plaque properties were evaluated using iMAP®-intravascular ultrasound.
Results:
Serum anti-LPL Ab levels were not correlated with plaque burden but were significantly negatively and positively correlated with fibrotic and necrotic plaques, respectively. High-risk patients with low anti-apoB-100 Ab levels were divided into groups according to their anti-LPL Ab levels. The group with high anti-LPL Ab levels exhibited more necrotic plaques and fewer fibrotic plaques as well as higher remnant-like lipoprotein particle levels than the group with low anti-LPL Ab levels.
Conclusions:
Serum anti-LPL Ab levels can serve as a marker of plaque instability in CAD patients and can help identify higher-risk cases when combined with anti-apoB-100 Ab levels.
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