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Journal of Lipid Research, Vol 37, 640-650, Copyright © 1996 by Lipid Research, Inc.
S Bijvoet, SE Gagne, S Moorjani, C Gagne, HE Henderson, JC Fruchart, J Dallongeville, P Alaupovic, M Prins, JJ Kastelein and MR Hayden
We have assessed the expression of heterozygosity for lipoprotein lipase
(LPL) deficiency by studying a single large French Canadian family
comprising 92 persons including 21 carriers of the catalytically defective
P207L mutation. Phenotypic changes distinguishing heterozygotes from
controls were seen early, before the age of 40 and often before 20 years of
age. In the total cohort these changes included an elevation in the mean
very low density (VLDL) and intermediate density lipoprotein (IDL)
triglyceride (+69%; P = 0.01 and +40%; P = 0.001) and cholesterol (+51%; P
= 0.03 and +67%; P = 0.007) and apoB levels but decreased HDL2 and HDL3
cholesterol, (-32%; P = 0.01 and -15%; P = 0.002 respectively). While the
lipid compositions of VLDL and IDL were similar between heterozygotes and
controls, the low density (LDL) and high density lipoproteins (HDL) of
carriers were triglyceride enriched. Heterozygotes also had a markedly
lower apoC-III ratio (apoC-III in supernatant/apoC-III in heparin
precipitate) (1.46 vs. 3.86 P = 1 x 10(-4)) indicating a substantial
enrichment of VLDL and IDL with apoC-III and depletion of HDL apoC-III
supporting this ratio as an effective index for efficiency of lipolysis.
LpA-I was markedly reduced (0.34 vs. 0.43 P = 1 x 10(-5)) showing that
levels of this particle are partly dependent on LPL catalytic activity.
Heterozygotes manifest from an early age with a markedly reduced HDL,
LpA-I, apoC-III ratio and an increased TC/HDLc ratio which would predict a
relatively increased risk of premature coronary artery disease, compared to
their normal siblings.
ARTICLES
Alterations in plasma lipoproteins and apolipoproteins before the age of 40 in heterozygotes for lipoprotein lipase deficiency
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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