The Association Between Apolipoprotein E Genotype and Lipid Profiles in Healthy Woman Workers.
10.3961/jpmph.2010.43.3.213
- Author:
Kieun MOON
1
;
Sook Hee SUNG
;
Youn Koun CHANG
;
Il Keun PARK
;
Yun Mi PAEK
;
Soo Geun KIM
;
Tae In CHOI
;
Young Woo JIN
Author Information
1. Division of Health Management, Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., LTD., Korea.
- Publication Type:Original Article ; English Abstract
- Keywords:
Apolipoprotein E;
Cardiovascular disease;
Cholesterol;
Triglyceride;
Koreans;
Women's health
- MeSH:
Adult;
Apolipoproteins E/blood/*genetics/metabolism;
Cardiovascular Diseases/epidemiology/prevention & control;
Cholesterol, HDL/genetics;
Female;
*Genotype;
Humans;
Lipid Metabolism/*genetics;
Polymerase Chain Reaction;
Primary Prevention
- From:Journal of Preventive Medicine and Public Health
2010;43(3):213-221
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVES: Plasma lipid profiles and Apolipoprotein E (ApoE) are established risk factors for cardiovascular disease (CVD). The knowledge of lipid profile may estimate the potential victims of cardiovascular disease before its initiation and progression and offers the opportunity for primary prevention. The most common ApoE polymorphism has been found to influence plasma lipid concentrations and its correlation with CVD has been extensively investigated in the last decade. METHODS: The ApoE polymorphism and its influence on plasma lipid were investigated in healthy woman workers. The information on confounding factors was obtained through a self-administered questionnaire and ApoE polymorphism was investigated using PCR. RESULTS: The relative frequencies of alleles E2, E3 and E4 for the study population (n=305) were 0.127, 0.750 and 0.121, respectively. ApoE polymorphism was associated with variations in plasma HDL-cholesterol lipid profile. In order to estimate the independent effects of alleles E2 and E4, as compared with E3, on lipid profile, multiple regression was performed after adjustment for confounding variables such as age, BMI, blood pressure, education status, insulin, fasting glucose, HOMA-IR, menopause. ApoE2 had a negative association with HDL cholesterol and ApoE4 had a positive association with LDL cholesterol. CONCLUSIONS: This study identified that the ApoE and CVD risk factors contribute to the lipid profiles, similar to other studies. The analysis including dietary intake and other gene in further studies may help to identify clear effects on lipid profiles as risk factor for CVD.
