Influence of apolipoprotein E polymorphism on serum lipid and lipoprotein changes:: a 21-year follow-up study from childhood to adulthood.: The Cardiovascular Risk in Young Finns Study

被引:31
作者
Gronroos, Paula
Raitakari, Olli T.
Kahonen, Mika
Hutri-Kahonen, Nina
Marniemi, Jukka
Viikari, Jorma
Lehtimaki, Terho
机构
[1] Univ Turku, Dept Clin Chem, Turku 20521, Finland
[2] Tampere Univ Hosp, Dept Clin Chem, Lab Atherosclerosis Genet, Tampere, Finland
[3] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
[4] Univ Turku, Sch Med, SF-20500 Turku, Finland
[5] Univ Turku, Dept Clin Physiol, SF-20500 Turku, Finland
[6] Univ Turku, Dept Clin Physiol, SF-20500 Turku, Finland
[7] Tampere Univ Hosp, Dept Clin Physiol, Tampere, Finland
[8] Tampere Univ Hosp, Dept Paediat, Tampere, Finland
[9] Natl Publ Hlth Inst, Dept Hlth & Funct Capac, Populat Res Lab, Turku, Finland
[10] Univ Turku, Dept Med, SF-20500 Turku, Finland
基金
芬兰科学院;
关键词
apolipoprotein E polymorphism; cardiovascular risk factors; cholesterol; lipids; long-term follow-up; CORONARY-ARTERY DISEASE; E PHENOTYPE; MYOCARDIAL-INFARCTION; CHOLESTEROL RESPONSE; PLASMA-LIPIDS; E ALLELES; ASSOCIATION; CHILDREN; DIET; ATHEROSCLEROSIS;
D O I
10.1515/CCLM.2007.116
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
1001 ;
摘要
Background: We examined the influence of apolipoprotein E (apoE) polymorphism on longitudinal changes in serum lipids by following the subjects participating in The Cardiovascular Risk in Young Finns Study over a 21-year period. Methods: Serum lipids were determined in randomly selected Finnish children and adolescents in 1980 and the subjects were re-examined in 1983, 1986 and after 21 years in 2001. ApoE polymorphism was determined in 1736 participants, and serum lipid values and apoE phenotypes were available for 1233 subjects. Results: ApoE phenotype-related differences in serum total and low-density lipoprotein (LDL)-cholesterol were maintained throughout the 21-year follow-up from childhood to adulthood, i.e., the apoE epsilon 2 allele was consistently associated with lower and the epsilon 4 allele with higher total and LDL-cholesterol (p < 0.001 for all). In adulthood, there was also a significant apoE phenotype-related difference in high-density lipoprotein (HDL)-cholesterol (p=0.007), and the e2 allele was associated with higher and the epsilon 4 allele with lower apoA-I and HDL-cholesterol. In addition, apoB increased in the phenotype order E3/2 < E3/3 < E4 (E4/3 + E4/4) (p < 0.001). The LDL-lowering effect of the epsilon 2 allele was greater in adulthood than in childhood, i.e., there was a significant apoE phenotype x time interaction (p 0.039) with longitudinal change in LDL-cholesterol. Conclusions: ApoE polymorphism is associated with lipid levels at different ages and affects the longitudinal change in LDL-cholesterol from childhood to adulthood.
引用
收藏
页码:592 / 598
页数:7
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