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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
Published on: January 28, 2021
Protective effect of apolipoprotein E2 on coronary artery disease in African Americans is mediated through
Erdembileg Anuurad1, Jill Rubin, Guijing Lu
1Department of Medicine, University of California, Davis, CA, USA.
Insights
The apolipoprotein E (apoE) epsilon 2 allele shows a protective effect against coronary artery disease (CAD) in African Americans, linked to lower LDL cholesterol. This effect is not observed in Caucasians, as apoE2 does not impact their lipid profiles.
Area of Science:
- Genetics and Cardiovascular Health
- Human Population Studies
- Biochemistry and Lipid Metabolism
Background:
- Apolipoprotein E (apoE) is crucial for lipid metabolism.
- Different apoE isoforms (epsilon 2, epsilon 3, epsilon 4) may influence cardiovascular disease risk.
- Understanding these relationships across diverse populations is important.
Purpose of the Study:
- To investigate the association between apoE isoforms and coronary artery disease (CAD) prevalence.
- To examine potential differences in this association between African Americans and Caucasians.
- To explore the role of lipid profiles in mediating the apoE-CAD relationship.
Main Methods:
- Coronary angiography was performed on 224 African Americans and 326 Caucasians.
- CAD was defined as >50% stenosis in at least one coronary artery.
- ApoE allele frequencies and lipid levels (LDL cholesterol) were analyzed in relation to CAD presence.
Main Results:
- In African Americans, apoE epsilon 2 allele carriers had significantly lower CAD prevalence (26%) compared to epsilon 3 (48%) and epsilon 4 (47%) carriers.
- This protective effect of apoE2 in African Americans was associated with lower LDL cholesterol levels (106 mg/dl vs. 127-134 mg/dl).
- No significant association between apoE isoforms and CAD was observed in Caucasians, nor did apoE2 significantly alter their lipid profiles.
Conclusions:
- The apoE epsilon 2 allele appears to have a protective effect against CAD in African Americans, primarily mediated by a favorable impact on LDL cholesterol levels.
- This protective association was not evident in Caucasians, suggesting population-specific effects of apoE isoforms on cardiovascular health.
- The findings highlight the importance of considering genetic background and lipid metabolism when assessing cardiovascular risk associated with apoE genotypes.
Abstract:
We studied the relationship of apolipoprotein E (apoE) isoforms and coronary artery disease (CAD) in 224 African Americans and 326 Caucasians undergoing diagnostic coronary angiography. The presence of CAD was defined as >50% stenosis in at least one artery. ApoE allele frequencies were 0.12, 0.62, and 0.26 for epsilon 2, epsilon 3, and epsilon 4, respectively, in African Americans and 0.08, 0.78, and 0.14 for epsilon 2, epsilon 3, and epsilon 4, respectively, in Caucasians. Among African Americans, CAD was present in 9 of 34 epsilon 2 carriers (26%), significantly smaller (P < 0.05) in proportion compared with 39 of 82 epsilon 3 carriers and 43 of 92 epsilon 4 carriers (48% and 47%, respectively), suggesting a protective effect of the epsilon 2 allele. No such difference was seen in Caucasians. In African Americans but not Caucasians, LDL cholesterol was lower in epsilon 2 carriers than in epsilon 3 and epsilon 4 carriers (106 vs. 127 and 134 mg/dl, respectively; P < 0.005). After adjusting for lipid levels, the association between apoE2 and CAD was no longer significant. Thus, the protective effect of apoE2 seen in African Americans could be explained by a favorable lipid profile in epsilon 2 carriers, whereas in Caucasians, the absence of such a protective effect could be attributable to the lack of effect of apoE2 on the lipid profile.
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