Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study

Mary F. Feitosa, Ingrid B. Borecki, Tuomo Rankinen, Treva Rice, Jean Pierre Després, Yvon C. Chagnon, Jacques Gagnon, Arthur S. Leon, James S. Skinner, Claude Bouchard, Michael A. Province, D. C. Rao

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Genome-wide multipoint linkage analyses were performed to identify chromosomal regions harboring genes influencing 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 is linkage evidence in black families on chromosomes 1q41-q44 [at marker D1S2860, 238 centimorgan (cM), with a maximum log of the odds (LOD) score of 3.7 for LDL-apoB] and in white families on chromosome 8q24 (at marker D8S1774, 142 cM, with LOD scores 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 posttraining minus 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.

Original languageEnglish (US)
Pages (from-to)281-286
Number of pages6
JournalJournal of lipid research
Volume46
Issue number2
DOIs
StatePublished - Feb 2005

Keywords

  • Apolipoprotein B
  • Coronary heart disease
  • Exercise
  • Genetics
  • Genome scan
  • Linkage analysis
  • Lipids
  • Lipoproteins
  • Low density lipoprotein
  • Quantitative trait loci
  • Risk factors

Fingerprint Dive into the research topics of 'Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study'. Together they form a unique fingerprint.

Cite this