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APOE polymorphism and carotid atherosclerosis in Korean population: The Dong-gu Study and the Namwon Study
Authors:Min-Ho Shin  Jin-Su Choi  Jung-Ae Rhee  Young-Hoon Lee  Hae-Sung Nam  Seul-Ki Jeong  Kyeong-Soo Park  Hye-Yeon Kim  So-Yeon Ryu  Seong-Woo Choi  Hee Nam Kim  Hye-Rim Song  Jane A Cauley  Sun-Seog Kweon
Institution:1. Department of Preventive Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;2. Jeonnam Regional Cancer Center, Chonnam National University Hwasun, Hwasun Hospital, Republic of Korea;3. Department of Preventive Medicine & Institute of Wonkwang Medical Science, Wonkwang University College of Medicine, Iksan, Republic of Korea;4. Department of Preventive Medicine, Chungnam National University Medical School, Daejeon, Republic of Korea;5. Department of Neurology & Research Institute of Clinical Medicine, Chonbuk National University, Biomedical Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea;6. Department of Preventive Medicine, Seonam University College of Medicine, Namwon, Republic of Korea;g Department of Preventive Medicine, Chosun University Medical School, Gwangju, Republic of Korea;h Genome Research Center for Hematopoietic Diseases, Chonnam National University Hwasun Hospital, Hwasun, Jeollanam-do, Republic of Korea;i Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, USA
Abstract:

Objective

We evaluated the association between APOE polymorphism and carotid atherosclerosis in two large independent cohorts from South Korea.

Methods

The datasets were from the Dong-gu Study (N = 9056) and the Namwon Study (N = 10,158). Carotid ultrasonography was performed to measure carotid intima-media thickness (IMT) and the presence of carotid plaques. The APOE polymorphism was determined by PCR-RFLP. We performed combined and separate analyses for the two datasets.

Results

In the combined analysis, individuals with E2E2 or E2E3 genotype had a lower common carotid IMT compared with individuals with E3E3 genotype (0.684 mm vs. 0.736 mm, p = 0.007; 0.718 mm vs. 0.736 mm, p < 0.001, respectively). This association was very slightly attenuated but remained statistically significant after adjustment for blood lipids (0.690 mm vs. 0.736 mm, p = 0.033; 0.725 mm vs. 0.736 mm, p = 0.005, respectively). Compared with individuals with E3E3 genotype, individuals with E2E3 genotype had lower risk for carotid plaque (odds ratio (OR) = 0.83, 95% confidence interval (CI) = 0.75–0.93), while individuals with E3E4 genotype had a higher risk for carotid plaque (OR = 1.09, 95% CI = 1.00–1.20). After adjustment for blood lipids, ORs of E2E3 genotype for carotid plaque was slightly attenuated but remained significant (OR = 0.87 95% CI = 0.78–0.97), while OR of E3E4 genotype were slightly attenuated and not significant (OR = 1.08, 95% CI, 0.99–1.18).

Conclusions

We found that APOE polymorphism is associated with carotid atherosclerosis and this association was partly mediated through blood lipid. Our results suggest that APOE polymorphism may influence atherosclerosis through non-lipid pathways.
Keywords:Apolipoprotein E  Polymorphism  Carotid artery plaque  Intima-media thickness
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