An ecological study of association between coronary heart disease mortality rates in men and the relative frequencies of common allelic variations in the gene coding for apolipoprotein E

被引:85
作者
Stengârd, JH
Weiss, KM
Sing, CF
机构
[1] Natl Publ Hlth Inst, Dept Epidemiol & Hlth Promot, FIN-00300 Helsinki, Finland
[2] Penn State Univ, Dept Anthropol, University Pk, PA 16802 USA
[3] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
基金
英国医学研究理事会; 芬兰科学院; 美国国家卫生研究院;
关键词
D O I
10.1007/s004390050811
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Three common alleles, epsilon(2), epsilon(3), and epsilon(4), of the gene coding for apolipoprotein E (apoE) have been identified as predictors of interindividual variation in measures of lipid and lipoprotein metabolism, and ultimately risk of coronary heart disease (CHD), within many populations. Here we evaluated the utility of the geographic distribution of these alleles for prediction of interpopulation variation in average level of serum total cholesterol and other traditional risk factors, and CHD mortality rate. We employed published estimates of the relative frequencies of the three common apoE alleles, average levels of risk factors such as serum total cholesterol, systolic and diastolic blood pressure, body mass index, smoking prevalence and CHD mortality rate for nine population-based samples of middle-aged males studied by the international WHO MONICA Project. There was approximately a 10-fold difference between the highest and lowest CHD mortality rate. Of the traditional risk factors, variation in the average level of serum total cholesterol was the best predictor (approximately 33%) of the observed interpopulation variation in estimates of CHD mortality rate (Pr = 0.10). Variation in the relative frequency of the epsilon(4) allele predicted approximately 50% of interpopulation variation in average serum total cholesterol level (Pr = 0.02) and 75% of the variation in CHD mortality rate (Pr = 0.002) when information about variation in the other risk factors and the epsilon(2) and epsilon(3) alleles is ignored. Furthermore, variation in the relative frequency of the epsilon(4) allele predicted approximately 40% of the variation in CHD mortality rate (Pr = 0.02) after considering the contribution of variation in average serum total cholesterol level. Average serum total cholesterol level was estimated to increase by 0.114 mmol/l (4.405 mg/dl), and CHD mortality rate by 24.5/100,000, for an increase of 0.01 in the relative frequency of the epsilon(4) allele. The predictive utility of the epsilon(2) and epsilon(3) alleles was considerably less than that of the epsilon(4) allele. For the sample of populations considered, the geographic distribution of the apoE alleles can be a statistically significant predictor of interpopulation variation in both the average serum total cholesterol level and CHD mortality rate. In particular, the epsilon(4) allele may confer valuable ecological risk information.
引用
收藏
页码:234 / 241
页数:8
相关论文
共 36 条
  • [1] APOLIPOPROTEIN-E POLYMORPHISM AND ATHEROSCLEROSIS
    DAVIGNON, J
    GREGG, RE
    SING, CF
    [J]. ARTERIOSCLEROSIS, 1988, 8 (01): : 1 - 21
  • [2] DAVIGNON J, 1993, NEW HORIZONS CORONAR
  • [4] EKLAND I, 1993, BROKEN DICE OTHER MA
  • [5] Falconer D. S., 1996, Introduction to quantitative genetics.
  • [6] METABOLIC ABNORMALITIES OF HYPERTENSION - A LESSON IN COMPLEXITY
    FERRANNINI, E
    [J]. HYPERTENSION, 1991, 18 (05) : 636 - 639
  • [7] FIDANZA F, 1993, 7 COUNTRIES STUDY SC, P151
  • [8] APOLIPOPROTEIN-E POLYMORPHISM IN A DANISH POPULATION COMPARED TO FINDINGS IN 45 OTHER STUDY POPULATIONS AROUND THE WORLD
    GERDES, LU
    KLAUSEN, IC
    SIHM, I
    FAERGEMAN, O
    [J]. GENETIC EPIDEMIOLOGY, 1992, 9 (03) : 155 - 167
  • [9] HALLMAN DM, 1991, AM J HUM GENET, V49, P338
  • [10] IMPACT OF APOLIPOPROTEIN-E GENOTYPE VARIATION ON MEANS, VARIANCES, AND CORRELATIONS OF PLASMA-LIPID, LIPOPROTEIN, AND APOLIPOPROTEIN TRAITS IN OCTOGENARIANS
    HAVILAND, MB
    LUSSIERCACAN, S
    DAVIGNON, J
    SING, CF
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (04): : 315 - 331