HYPERCHOLESTEROLEMIA IN 5 ISRAELI CHRISTIAN-ARAB KINDREDS IS CAUSED BY THE LEBANESE ALLELE AT THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE LOCUS AND BY AN ADDITIONAL INDEPENDENT MAJOR FACTOR

被引:18
作者
OPPENHEIM, A
FRIEDLANDER, Y
DANN, EJ
BERKMAN, N
SCHWARTZ, SP
LEITERSDORF, E
机构
[1] HADASSAH UNIV HOSP, DEPT MED B, LIPID RES LAB, POB 12000, JERUSALEM, ISRAEL
[2] HEBREW UNIV JERUSALEM, HADASSAH MED SCH, FAC MED, DEPT SOCIAL MED, IL-91010 JERUSALEM, ISRAEL
关键词
D O I
10.1007/BF00204933
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Segregation analyses were performed for plasma low density lipoprotein cholesterol (LDL-C), triglycerides (TG) and high density lipoprotein cholesterol (HDL-C) in five Christian Arab kindreds identified through probands with familial hypercholesterolemia. In this subset of the Christian Arab community, the results were consistent with major gene determination of LDL-C with allele frequency (q) of 0.042 (95% confidence interval 0.008-0.079) in addition to polygenic transmission (h2 = 0.34). The "Lebanese" allele was identified directly by polymerase chain reaction and HinfI restriction analysis. Analysis of this mutation permits direct diagnosis of familial hypercholesterolemia in most affected individuals although our results indicated the possible existence of an additional independent factor leading to elevated LDL-C levels. The segregation results for TG indicated the presence of a major effect, although the existence of a major gene could not be demonstrated. There was also no evidence of a major locus effect on HDL-C levels.
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页码:75 / 84
页数:10
相关论文
共 47 条
[1]   FINNISH TYPE OF LOW-DENSITY LIPOPROTEIN RECEPTOR GENE MUTATION (FH-HELSINKI) DELETES EXONS ENCODING THE CARBOXY-TERMINAL PART OF THE RECEPTOR AND CREATES IN INTERNALIZATION-DEFECTIVE PHENOTYPE [J].
AALTOSETALA, K ;
HELVE, E ;
KOVANEN, PT ;
KONTULA, K .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (02) :499-505
[2]  
Brown M.S, 1980, METABOLIC CONTROL DI, P393
[3]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[4]  
CANNINGS C, 1977, CLIN GENET, V12, P208
[5]   HDL CHOLESTEROL AND OTHER LIPIDS IN CORONARY HEART-DISEASE - COOPERATIVE LIPOPROTEIN PHENOTYPING STUDY [J].
CASTELLI, WP ;
DOYLE, JT ;
GORDON, T ;
HAMES, CG ;
HJORTLAND, MC ;
HULLEY, SB ;
KAGAN, A ;
ZUKEL, WJ .
CIRCULATION, 1977, 55 (05) :767-772
[6]   A BIVARIATE PROBLEM IN HUMAN-GENETICS - ASCERTAINMENT OF FAMILIES THROUGH A CORRELATED TRAIT [J].
DAWSON, DV ;
ELSTON, RC .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (03) :435-448
[7]  
DEMENAIS F, 1986, AM J HUM GENET, V38, P228
[8]   GENERAL MODEL FOR GENETIC ANALYSIS OF PEDIGREE DATA [J].
ELSTON, RC ;
STEWART, J .
HUMAN HEREDITY, 1971, 21 (06) :523-&
[9]   A-IMILANO APOPROTEIN - DECREASED HIGH-DENSITY LIPOPROTEIN CHOLESTEROL LEVELS WITH SIGNIFICANT LIPOPROTEIN MODIFICATIONS AND WITHOUT CLINICAL ATHEROSCLEROSIS IN AN ITALIAN FAMILY [J].
FRANCESCHINI, G ;
SIRTORI, CR ;
CAPURSO, A ;
WEISGRABER, KH ;
MAHLEY, RW .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 66 (05) :892-900
[10]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499