DIFFERENCES IN THE PHENOTYPIC CHARACTERISTICS OF SUBJECTS WITH FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 AND FAMILIAL HYPERCHOLESTEROLEMIA

被引:82
作者
MISEREZ, AR
KELLER, U
机构
[1] UNIV BASEL HOSP, DEPT RES, CH-4031 BASEL, SWITZERLAND
[2] UNIV BASEL HOSP, DEPT INTERNAL MED, CH-4031 BASEL, SWITZERLAND
关键词
APOLIPOPROTEIN B-100; LDL RECEPTOR MUTATIONS; GENOTYPE; PHENOTYPE;
D O I
10.1161/01.ATV.15.10.1719
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Familial defective apolipoprotein B-100 (FDB) is a recently identified autosomal-dominantly inherited disorder caused by a point mutation in the apolipoprotein (apo) B gene. To determine whether the phenotypic characteristics in FDB subjects are similar to those in subjects with familial hypercholesterolemia (FH), 76 kindreds fulfilling the clinical criteria for heterozygous FH/FDB were characterized using molecular biological techniques. Allele-specific polymerase chain reaction (PCR) at the apoB locus was used for diagnosis or exclusion of FDB. PCR-based methods for detection of two point mutations (V408M and P664L) at the LDL receptor (LDLR) locus, cosegregation analysis using eight restriction fragment length polymorphisms (RFLPs) at the LDLR locus, or the exclusion of FDB confirmed the clinical diagnosis of FH. Three kindreds were not included because of a missing cosegregation between a particular haplotype and the FH phenotype. We predicted that a similar number of kindreds would be detected in the two groups, assuming comparable prevalences of the diseases in our population and similar phenotypic characteristics. However, only nine kindreds were identified with the FDB mutation compared with 64 kindreds with FH (P<.0001). From these 73 kindreds, 28 FDB heterozygotes and 129 FH heterozygotes were compared using multivariate analysis. There were no differences between these two groups with respect to age, sex, and apoE genotype distribution, lipoprotein(a) concentrations, body mass index, blood pressure, and smoking habits. However, FDB subjects demonstrated significantly lower concentrations of total cholesterol (8.1 versus 10.2 mmol/L, P<.001), LDL cholesterol (6.3 versus 8.2 mmol/L, P<.001), and triglycerides (1.3 versus 1.8 mmol/L, P=.025) and higher concentrations of HDL cholesterol (1.4 versus 1.2 mmol/L, P=.015) than subjects with FH. In contrast to FH, female FDB subjects tended to have higher concentrations of total cholesterol (8.9 versus 7.5 mmol/L, P=.032) and LDL cholesterol (7.1 versus 5.7 mmol/L, P=.026) than FDB males. The same results regarding total and LDL cholesterol and sex differences were observed when individual data of 238 FDB and 415 FH subjects from the literature were compared. In addition, FDB subjects showed much larger total cholesterol fluctuations than FH subjects (median of intraindividual coefficients of variation: FDB, 14.5%. FH, 5.3%; P<.001). In summary, these results demonstrate that FDB subjects tend to have a milder form of hyperlipoproteinemia than FH subjects and that only a part of the subjects with FDB fulfill the established criteria for identifying FH.
引用
收藏
页码:1719 / 1729
页数:11
相关论文
共 68 条
[1]  
BERSOT TP, 1993, J LIPID RES, V34, P1149
[2]  
BERTOLINI S, 1992, AM J HUM GENET, V51, P123
[3]   DAY-TO-DAY VARIABILITY OF SERUM-CHOLESTEROL, TRIGLYCERIDE, AND HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL LEVELS - IMPACT ON THE ASSESSMENT OF RISK ACCORDING TO THE NATIONAL CHOLESTEROL EDUCATION-PROGRAM GUIDELINES [J].
BOOKSTEIN, L ;
GIDDING, SS ;
DONOVAN, M ;
SMITH, FA .
ARCHIVES OF INTERNAL MEDICINE, 1990, 150 (08) :1653-1657
[4]   TYPE-III HYPERLIPOPROTEINEMIA - DIAGNOSIS, MOLECULAR DEFECTS, PATHOLOGY, AND TREATMENT [J].
BREWER, HB ;
ZECH, LA ;
GREGG, RE ;
SCHWARTZ, D ;
SCHAEFER, EJ .
ANNALS OF INTERNAL MEDICINE, 1983, 98 (05) :623-640
[5]  
Brown M. S., 1994, HARRISONS PRINCIPLES, V2, P2058
[6]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[7]  
BURNAND B, 1993, SCHWEIZ MED WOCH S48, V123, P29
[8]   FAMILIAL DEFECTIVE APO-B-100, CHARACTERIZATION OF AN ITALIAN FAMILY [J].
CORSINI, A ;
MCCARTHY, BJ ;
GRANATA, A ;
SORIA, LF ;
FANTAPPIE, S ;
BERNINI ;
ROMANO, C ;
ROMANO, L ;
FUMAGALLI, R ;
CATAPANO, AL .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1991, 21 (04) :389-397
[9]   FAMILIAL HYPERCHOLESTEROLEMIA IN FRENCH-CANADIANS - TAKING ADVANTAGE OF THE PRESENCE OF A FOUNDER EFFECT [J].
DAVIGNON, J ;
ROY, M .
AMERICAN JOURNAL OF CARDIOLOGY, 1993, 72 (10) :D6-D10
[10]   FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 IS CLINICALLY INDISTINGUISHABLE FROM FAMILIAL HYPERCHOLESTEROLEMIA [J].
DEFESCHE, JC ;
PRICKER, KL ;
HAYDEN, MR ;
VANDERENDE, BE ;
KASTELEIN, JJP .
ARCHIVES OF INTERNAL MEDICINE, 1993, 153 (20) :2349-2356