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. 2017 Sep 21:11:1179546817731110.
doi: 10.1177/1179546817731110. eCollection 2017.

Influence of Apolipoprotein E on the Lipid Profile and Postprandial Triglyceride Levels in Brazilian Postmenopausal Women With Artery Disease

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Influence of Apolipoprotein E on the Lipid Profile and Postprandial Triglyceride Levels in Brazilian Postmenopausal Women With Artery Disease

Lúcia Helena Bonalume Tácito et al. Clin Med Insights Cardiol. .

Abstract

This study confirms the association of risk factors for coronary artery disease (CAD) and the apoE polymorphisms, specifically related to the APOE*4 allele, with coronary disease in postmenopausal women. Significantly altered values of the lipid profile were found in patients when compared with controls, independent of the presence of the APOE*4 allele. However, the controls showed higher high-density lipoprotein cholesterol (HDL-C) levels and reduced triglyceride (TG) levels, differing significantly from patients. In this case, the study of subgroups, considering the APOE*3/3 and APOE*3/4 genotypes, suggests that the APOE*4 allele is not implicated in the variations of the lipid profile of patients and determined an increase in the production levels of HDL-C and a reduction in TG highly benefiting the control group compared with APOE*3/3 genotype. The metabolic kinetics of TG, although with the same pattern between groups, and the presence of the APOE*4 allele are suggested to be associated with accelerated clearance compared with APOE*3 allele in non-CAD group.

Keywords: Coronary artery disease; apolipoprotein E; cholesterol; postmenopause; postprandial triglycerides.

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Conflict of interest statement

Declaration of Conflicting Interests:The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Significantly greater areas under the curve in the patients with CAD (1606) compared with non-CAD group (1447; P < .001).
Figure 2.
Figure 2.
Areas under the curve in relation to the APOE*3/3 and _/APOE*4 genotypes in postmenopausal women. Thus, the area under the curve is significantly higher in patients with CAD compared with controls both with _/APOE*4 genotypes (area = 1720 versus 1243; P < .001), whereas there was no difference between the groups in respect to the APOE*3/3 genotype (area = 1.518 versus 1.487, respectively; P > .05).

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