Genetics of the quantitative Lp(a) lipoprotein trait |
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Authors: | Eric Boerwinkle Hans Jürgen Menzel Hans Georg Kraft Gerd Utermann |
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Affiliation: | (1) Center for Demographic and Population Genetics, The University of Texas Health Science Center at Houston, Houston, Texas, USA;(2) Institut für Medizinische Biologie und Genetik der Universität, Schöpfstrasse 41, A-6020 Innsbruck, Austria |
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Abstract: | Summary Apolipoprotein(a) [apo(a)] is a large serum glycoprotein with several genetically determined isoforms differing in their apparent molecular weight. We determined the effects of the apo(a) isoforms on total cholesterol, high-density lipo-protein (HDL)-cholesterol, lipoprotein(a), and triglyceride levels in a sample of 473 unrelated Tyrolean adults. Average lipoprotein(a) and total cholesterol levels were significantly different among apo(a) types. These significant differences were found among the 13 apo(a) isoform patterns observed in this sample and among several logical subsets of the isoform patterns (e.g. considering only the single band types). The data suggest that the effects of apo(a) alleles on Lp(a) levels are additive. The effects of apo(a) on total cholesterol levels cannot be entirely explained by the cholesterol fraction estimated to be contained in the lipoprotein(a) particle. We estimate that the apo(a) glycoprotein polymorphism accounts for 41.9% and 9.6% of the variability in lipoprotein(a) and total cholesterol levels, respectively. This is the strongest effect of a single polymorphic gene on plasma lipid and lipoprotein levels reported so far. |
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