GENETIC INFLUENCES ON AGE-RELATED CHANGE IN TOTAL CHOLESTEROL, LOW-DENSITY LIPOPROTEIN-CHOLESTEROL, AND TRIGLYCERIDE LEVELS - LONGITUDINAL APOLIPOPROTEIN-E GENOTYPE EFFECTS

被引:52
作者
JARVIK, GP
AUSTIN, MA
FABSITZ, RR
AUWERX, J
REED, T
CHRISTIAN, JC
DEEB, S
机构
[1] UNIV WASHINGTON,SCH PUBL HLTH & COMMUNITY MED,DEPT MED,DIV MED GENET,SEATTLE,WA 98195
[2] UNIV WASHINGTON,SCH PUBL HLTH & COMMUNITY MED,DEPT EPIDEMIOL,SEATTLE,WA 98195
[3] NIH,BETHESDA,MD 20892
[4] CTR BIOCHIM,BIOL REGULAT CHEZ EUCARYOTES LAB,NICE,FRANCE
[5] INDIANA UNIV,MED CTR,DEPT MOLEC & MED GENET,INDIANAPOLIS,IN
关键词
APOLIPOPROTEIN E; LONGITUDINAL; CHOLESTEROL; TRIGLYCERIDE; AGING; GENOTYPE; POLYMORPHISM;
D O I
10.1002/gepi.1370110407
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
This study addressed the possible influence of apolipoprotein E (ape E) genotype on age-related changes in total cholesterol (TC), low density lipoprotein-cholesterol (LDL-C), and triglyceride (TG) levels in older males. Apo E is a component of LDL, is a ligand for the LDL receptor, and apo E genotype has been consistently associated with variation in mean levels of TC and LDL-C, and also appears to influence TG levels. Using male twins followed longitudinally between mean ages of 48 and 63 years, the change in TC, LDL-C, and TG over time for individuals with the epsilon 3 epsilon 3 and the epsilon 3 epsilon 4 genotypes was contrasted. At exam 1 mean TC and LDL-C levels were lower in the epsilon 3 epsilon 3 group than in the epsilon 3 epsilon 4 group, but at exam 3 mean TC and LDL-C levels were significantly higher in the epsilon 3 epsilon 3 group than in the epsilon 3 epsilon 4 group. The rate of change in TC and LDL-C with age differed significantly between epsilon 3 epsilon 3 and epsilon 3 epsilon 4 groups. Results for TG were not statistically significantly. These findings suggest that the apo E genotype effects on risk of coronary artery disease may be age-dependent. This study demonstrates the value of longitudinal studies in refining models for genetic risk factors for disease. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:375 / 384
页数:10
相关论文
共 47 条
  • [1] ALLAIN CC, 1974, CLIN CHEM, V20, P470
  • [2] ALVAREZ C, 1984, CLIN CHEM, V30, P404
  • [3] HYPERCHOLESTEROLEMIA IN POSTMENOPAUSAL WOMEN - METABOLIC DEFECTS AND RESPONSE TO LOW-DOSE LOVASTATIN
    ARCA, M
    VEGA, GL
    GRUNDY, SM
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (06): : 453 - 459
  • [4] THE USE OF MEASURED GENOTYPE INFORMATION IN THE ANALYSIS OF QUANTITATIVE PHENOTYPES IN MAN .3. SIMULTANEOUS ESTIMATION OF THE FREQUENCIES AND EFFECTS OF THE APOLIPOPROTEIN E POLYMORPHISM AND RESIDUAL POLYGENETIC EFFECTS ON CHOLESTEROL, BETA-LIPOPROTEIN AND TRIGLYCERIDE LEVELS
    BOERWINKLE, E
    SING, CF
    [J]. ANNALS OF HUMAN GENETICS, 1987, 51 : 211 - 226
  • [5] APO-E ALLELE FREQUENCIES IN YOUNGER (AGE 42-50) VS OLDER (AGE 65-90) WOMEN
    CAULEY, JA
    EICHNER, JE
    KAMBOH, MI
    FERRELL, RE
    KULLER, LH
    [J]. GENETIC EPIDEMIOLOGY, 1993, 10 (01) : 27 - 34
  • [6] GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES
    CORDER, EH
    SAUNDERS, AM
    STRITTMATTER, WJ
    SCHMECHEL, DE
    GASKELL, PC
    SMALL, GW
    ROSES, AD
    HAINES, JL
    PERICAKVANCE, MA
    [J]. SCIENCE, 1993, 261 (5123) : 921 - 923
  • [7] GENETICS OF THE APOLIPOPROTEIN-E ISOPROTEIN SYSTEM IN MAN
    CUMMING, AM
    ROBERTSON, FW
    [J]. JOURNAL OF MEDICAL GENETICS, 1982, 19 (06) : 417 - 423
  • [8] CUMMING AM, 1984, CLIN GENET, V25, P310
  • [9] DALLONGEVILLE J, 1992, J LIPID RES, V33, P447
  • [10] Davignon J, 1988, Trans Am Clin Climatol Assoc, V99, P100