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Submitted on October 15, 2002
From Clinical Biochemistry, PathCentre, Perth, Western Australia, Australia (J.P.B., C.C.J.H., C.M.L.C., J.P.B.); Sir Charles Gairdner Hospital Campus of the Heart Research Institute of Western Australia and Department of Medicine, University of Western Australia, Nedlands (B.M.M., P.L.T., J.H.), Australia; and the Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, Mass (L.J.P.). * To whom correspondence should be addressed. E-mail: john.beilby{at}health.wa.gov.au.
Background and Purpose--Several studies have investigated the role of apolipoprotein E (apoE) polymorphisms on carotid intima-media thickness (IMT) with conflicting results. The objective of this study was to use a large, community-based population to investigate associations between apoE gene polymorphisms and cardiovascular disease-associated phenotypes: IMT, carotid artery plaque, and low- (LDL-C) and high-density lipoprotein cholesterol (HDL-C). Methods--ApoE genotypes were determined in 1109 randomly selected community subjects with an equal man-to-woman ratio and equal numbers in each age decile who were 27 to 77 years of age and had bilateral carotid B-mode ultrasound and cardiovascular risk factor measurements. Results--Multivariate analyses, stratified by sex, demonstrated an association between apoE genotypes and LDL-C levels in men (P=0.03) and women (P<0.001). A significant linear trend in increasing LDL-C ( Conclusions--Our data suggest that polymorphisms in the apoE gene are significantly associated with LDL-C levels and increased risk of carotid plaque formation in men but not IMT in either men or women.
Accepted on October 29, 2002
Apolipoprotein E Gene Polymorphisms Are Associated With Carotid Plaque Formation but Not With Intima-Media Wall Thickening. Results From the Perth Carotid Ultrasound Disease Assessment Study (CUDAS)
John P. Beilby PhD*;
=0.33 per unit change in genotype; SE=0.07; P<0.001) levels with increasing number of
4 alleles across the
3/
3,
3/
4, or
4/
4 genotypes was observed in women but not in men. The associations were independent of age, diastolic blood pressure, and history of diabetes mellitus. Multivariate analyses found a log-additive trend in risk of developing carotid plaque with increasing numbers of
4 alleles across the
3/
3,
3/
4, and
4/
4 genotypes (odds ratio [OR], 1.72 per unit change in genotype; 95% CI, 1.05 to 2.80; P=0.03) in men. There was no association between plaque frequency and the
4 allele in women. However, the
2/
3 genotype was shown to be associated with a lower OR (OR, 0.40; 95% CI, 0.17 to 0.91; P=0.03) for carotid plaques relative to the
3/
3 genotype in women. The associations were independent of age and standard vascular risk factors. There were no significant independent associations between apoE genotypes and IMT in either men or women.
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