Abstract |
Circulating soluble intercellular adhesion molecule-1 (sICAM-1) is a biochemical marker of inflammation. We performed variance-components-based quantitative genetic analyses in SOLAR of sICAM-1 in 1170 individuals from Mexican American families in the San Antonio Family Heart Study. The trait is heritable (h(2)=0.50+/-0.06, P<10(-6)). Multipoint linkage analysis using a approximately 10-cM microsatellite map revealed a region on Chromosome 19p near marker D19S586 showing strong evidence of linkage for sICAM-1 (empirically adjusted univariate-equivalent LOD=4.95), coincident with the structural gene ICAM1. This region has been identified previously as a QTL for inflammatory, autoimmune, and metabolic syndrome traits. There is significant evidence (P=0.0023) of locus heterogeneity for sICAM-1 in this sample: a subset of pedigrees contributes most of the linkage signal for sICAM-1 on Chromosome 19, suggesting a logical focus for future genetic dissection of the trait.
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Authors | Jack W Kent Jr, Michael C Mahaney, Anthony G Comuzzie, Harald H H Göring, Laura Almasy, Thomas D Dyer, Shelley A Cole, Jean W MacCluer, John Blangero |
Journal | Atherosclerosis
(Atherosclerosis)
Vol. 195
Issue 2
Pg. 367-73
(Dec 2007)
ISSN: 1879-1484 [Electronic] Ireland |
PMID | 17112530
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Intercellular Adhesion Molecule-1
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Topics |
- Adult
- Bayes Theorem
- Chromosomes, Human, Pair 19
(genetics)
- Cohort Studies
- Female
- Humans
- Inflammation
- Intercellular Adhesion Molecule-1
(genetics)
- Male
- Mexican Americans
(genetics)
- Middle Aged
- Quantitative Trait Loci
(genetics)
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