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Segregation analysis of plasma lipoprotein(a) levels in pedigrees with molecularly defined familial hypercholesterolemia
Author(s) -
Friedlander Yechiel,
Leitersdorf Eran
Publication year - 1995
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.1370120203
Subject(s) - polygene , allele , pedigree chart , familial hypercholesterolemia , genetics , lipoprotein , biology , lipoprotein(a) , mutant , ldl receptor , quantitative trait locus , medicine , endocrinology , cholesterol , gene
The role of genetic and environmental factors in determining the variability in plasma lipoprotein(a) [Lp(a)] levels was investigated in 220 members of 14 families with familial hypercholesterolemia (FH) whose plasma Lp(a) levels were previously reported [Leitersdorf et al. (1991) J Lipid Res 32:1513–1519]. One hundred four subjects harbored a mutant low density lipoprotein (LDL) receptor allele as confirmed by the identification of the specific mutations in addition to the haplo‐type analysis reported before. Four different mutant alleles were identified, each in a defined genetic group—Druze, Christian‐Arabs, Ashkenazi, and Sephardic Jews. Sex‐ and age‐adjusted mean plasma Lp(a) levels were significantly higher in FH family members (34.0 mg/dl) than in non‐FH family members (21.1 mg/dl). Lp(a) levels were further adjusted for lipid levels and apo(a) isoforms. A mixture of two normal distributions fitted the adjusted Lp(a) levels better than did a single normal distribution. Segregation analysis indicated that a major effect of a non‐transmitted environmental factor explained the mixture of distributions in addition to polygenic loci which influenced Lp(a) levels within each distribution. The major environmental factor and the polygenic loci accounted for 45% and 20% of the adjusted Lp(a) variation, respectively. Furthermore, sex, age, lipid levels, apo(a) isoform, the major environmental effect, and the unmeasured polygenes could account for 80% of the unadjusted variation of plasma Lp(a) in these families. © 1995 Wiley‐Liss, Inc.