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Lipoprotein-associated phospholipase A2, high-sensitivity C-reactive protein, and risk for incident coronary heart
Christie M Ballantyne1, Ron C Hoogeveen, Heejung Bang
1Section of Atherosclerosis and Lipoprotein Research, Department of Medicine, Baylor College of Medicine, and Methodist DeBakey Heart Center, Houston, Tex 77030, USA. cmb@bcm.tmc.edu
Lipoprotein-associated phospholipase A2 (Lp-PLA2) and C-reactive protein (CRP) can help identify individuals at high risk for coronary heart disease (CHD), especially those with low LDL cholesterol. These markers may be complementary for risk assessment.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Epidemiology
Background:
- C-reactive protein (CRP) is recommended for identifying coronary heart disease (CHD) risk in patients with low LDL cholesterol.
- Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a proinflammatory enzyme linked to LDL.
Purpose of the Study:
- To examine the relationship between Lp-PLA2, CRP, traditional risk factors, and CHD risk.
- To assess the combined utility of Lp-PLA2 and CRP in identifying high-risk individuals, particularly those with low LDL cholesterol.
Main Methods:
- Prospective case cohort study of 12,819 apparently healthy middle-aged men and women.
- Analysis using a proportional hazards model, stratified by LDL cholesterol levels.
- Assessment of Lp-PLA2, CRP, and traditional risk factors over approximately 6 years.
Main Results:
- Lp-PLA2 and CRP levels were higher in CHD cases compared to noncases.
- Both Lp-PLA2 and CRP were associated with incident CHD after adjustments.
- For individuals with LDL cholesterol below 130 mg/dL, Lp-PLA2 and CRP were independently associated with CHD risk.
- The association of Lp-PLA2 with CHD was attenuated when adjusted for LDL-C in the overall cohort.
Conclusions:
- Lp-PLA2 and CRP may serve as complementary biomarkers.
- These markers can help identify individuals with low LDL cholesterol who are at high risk for CHD.
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