Analyses of interaction effect between apolipoprotein E polymorphism and alcohol use as well as cholesterol concentrations on spontaneous deep intracerebral hemorrhage in the Taiwan population

被引:10
作者
Chen, Yi-Chun [1 ,2 ]
Lee-Chen, Guey-Jen [3 ]
Wu, Yih-Ru [1 ,2 ]
Hu, Fen-Ju [3 ]
Wu, Hsiu-Chuan [1 ,2 ]
Kuo, Hung-Chou [1 ,2 ]
Chu, Chun-Che [1 ,2 ]
Ryu, Shan-Jin [1 ,2 ]
Chen, Sien-Tsong [1 ,2 ]
Chen, Chiung-Mei [1 ,2 ]
机构
[1] Chang Gung Univ, Dept Neurol, Linkou Med Ctr, Chang Gung Mem Hosp, Kueishan Taoyuan 333, Taiwan
[2] Chang Gung Univ, Coll Med, Kueishan Taoyuan 333, Taiwan
[3] Natl Taiwan Normal Univ, Dept Life Sci, Taipei, Taiwan
关键词
Apolipoprotein E; Cholesterol; Genetics; Intracerebral hemorrhage; Alcohol; Polymorphism and disease association; DENSITY-LIPOPROTEIN-CHOLESTEROL; ANGIOTENSIN-CONVERTING-ENZYME; CORONARY-HEART-DISEASE; E EPSILON-2 ALLELE; E GENOTYPE; RISK-FACTORS; STROKE SUBTYPES; HIGH-FREQUENCY; APOE GENOTYPE; E PHENOTYPE;
D O I
10.1016/j.cca.2009.08.004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
100118 [医学信息学]; 100208 [临床检验诊断学];
摘要
Background: To determine the interaction effect between APOE polymorphism and lipid concentrations and alcohol use on spontaneous deep intracerebral hemorrhage (SDICH) risks. Methods: We enrolled 217 SDICH patients and 280 controls. Anthropometrics, personal history, and concentrations of total cholesterol (TC), high-density lipoprotein cholesterol, low-density lipoprotein cholesterol (LDL-c), and triglyceride were collected. Genotyping was determined by PCR-based restriction and electrophoresis assay. Associations were tested adjusting for multiple covariables. Results: Compared with the commonest genotype epsilon 3 epsilon 3, epsilon 2 epsilon 3 was inversely associated with TC (p = 0.023) and LDL-c concentrations (p = 0.005) in women. No APOE-alcohol interaction effect on lipids concentration was found. However, in men, there was a marginal effect of interaction between alcohol and APOE genotype epsilon 2 epsilon 3 vs. epsilon 3 epsilon 3 on SDICH risks (p = 0.003), which is independent of TC concentration. In the male non-alcohol group, SDICH proportion was lower in the subjects carrying APOE epsilon 2 epsilon 3 (27.6%) than in those with epsilon 3 epsilon 3 (41.1%). In contrast, in the male alcohol consumption group, APOE epsilon 2 epsilon 3 was associated with a higher SDICH rate (77.8%) compared to epsilon 3 epsilon 3 (58.0%). Conclusions: Male subjects carrying genotype epsilon 2 epsilon 3 tend to have a higher SDICH risk than those who have epsilon 3 epsilon 3 when they have alcohol exposure, but may have more benefit from alcohol abstinence. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 132
页数:5
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