COMPLEX SEGREGATION ANALYSIS OF LDL PEAK PARTICLE DIAMETER

被引:30
作者
AUSTIN, MA [1 ]
JARVIK, GP [1 ]
HOKANSON, JE [1 ]
EDWARDS, K [1 ]
机构
[1] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98195
关键词
CHOLESTEROL; GENETICS; LOW-DENSITY LIPOPROTEIN; SEGREGATION ANALYSIS;
D O I
10.1002/gepi.1370100645
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A predominance of small low-density lipoprotein (LDL) particles, as determined by gradient gel electrophoresis (GGE), has been proposed to be a common genetic marker for risk of coronary heart disease. Previous analyses of the families in the Berkeley data set defined a dichotomous trait based on the LDL size distribution by GGE: subjects with a predominance of small LDL particles have LDL subclass ''pattern B,'' while those with a predominance of large LDL particles have LDL subclass ''pattern A.'' Using this definition, previous complex segregation analyses demonstrated a single major gene effect on pattern B with a dominant or additive mode of inheritance, and reduced penetrance in young males and premenopausal women. In the present analyses, a continuous variable denoted LDL peak particle diameter is used, reflecting the size (diameter in A) of the major LDL subclass, for comparison with the dichotomous LDL subclass pattern classification. After adjusting for age and gender, the results demonstrate a single major Mendelian gene effect, but the exact mode of inheritance could not be established. Thus, analysis of the continuous variable was not superior to that of the dichotomous classification in determining the mode of inheritance of the proposed single gene controlling LDL subclasses. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:599 / 604
页数:6
相关论文
共 12 条
  • [1] AUSTIN MA, 1988, AM J HUM GENET, V43, P838
  • [2] INHERITANCE OF LOW-DENSITY-LIPOPROTEIN SUBCLASS PATTERNS IN FAMILIAL COMBINED HYPERLIPIDEMIA
    AUSTIN, MA
    BRUNZELL, JD
    FITCH, WL
    KRAUSS, RM
    [J]. ARTERIOSCLEROSIS, 1990, 10 (04): : 520 - 530
  • [3] AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
  • [4] ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK
    AUSTIN, MA
    KING, MC
    VRANIZAN, KM
    KRAUSS, RM
    [J]. CIRCULATION, 1990, 82 (02) : 495 - 506
  • [5] A MIXED-MODEL LIKELIHOOD APPROXIMATION ON LARGE PEDIGREES
    HASSTEDT, SJ
    [J]. COMPUTERS AND BIOMEDICAL RESEARCH, 1982, 15 (03): : 295 - 307
  • [6] Hasstedt SJ, 1981, 13 U UT DEP MED BIOP
  • [7] KRAUSS RM, 1982, J LIPID RES, V23, P97
  • [8] LALOUEL JM, 1979, 14 U UT DEP MED BIOP
  • [9] LINDGREN FT, 1950, J PHYS COLLOID CHEM, V55, P80
  • [10] EFFECT OF GENDER, AGE, AND LIPID STATUS ON LOW-DENSITY-LIPOPROTEIN SUBFRACTION DISTRIBUTION - RESULTS FROM THE FRAMINGHAM OFFSPRING STUDY
    MCNAMARA, JR
    CAMPOS, H
    ORDOVAS, JM
    PETERSON, J
    WILSON, PWF
    SCHAEFER, EJ
    [J]. ARTERIOSCLEROSIS, 1987, 7 (05): : 483 - 490