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Papers In Press, published online ahead of print December 1, 2004
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Division of Biostatistics, Washington University, School of Medicine, St. Louis, MO 63110-1093
Corresponding Author: maryf{at}wubios.wustl.edu
Genome-wide multipoint linkage analyses were performed to identify chromosomal regions harboring genes influencing low density lipoprotein (LDL)-cholesterol, total apolipoprotein B (apoB) and LDL-apoB levels using 654 markers. They were assessed in a sedentary state (baseline) and after a 20-week endurance training program. Strong evidence for two quantitative trait loci (QTLs) for baseline levels was found. There are linkage evidence in Black families on chromosomes 1q41-q44 (at marker D1S2860, 238 cM, with a maximum lod score (LOD) of 3.7, for LDL-apoB) and in White families on chromosome 8q24 (at marker D8S1774, 142 cM, with LODs of 3.6, 3.3 and 2.5 for baseline LDL-cholesterol, LDL-apoB and apoB, respectively). There were no strong signals for the lipoprotein training responses (as computed as the difference in post-training baseline levels). In conclusion, QTLs for baseline apoB and LDL-cholesterol levels on chromosomes 1q41-q44 (in Blacks) and 8q24 (in Whites) were found. As there are no known strong candidate genes in these regions for lipids, follow-up studies to determine the source of those signals are needed.
Revised on November 17, 2004
Accepted on November 17, 2004
Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study
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