Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans

Jack W. Kent, Michael C. Mahaney, Anthony G. Comuzzie, Harald H.H. Göring, Laura Almasy, Thomas D. Dyer, Shelley A. Cole, Jean W. MacCluer, John Blangero

    Research output: Contribution to journalArticlepeer-review

    8 Scopus citations

    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 (h2 = 0.50 ± 0.06, P < 10-6). Multipoint linkage analysis using a ∼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.

    Original languageEnglish (US)
    Pages (from-to)367-373
    Number of pages7
    JournalAtherosclerosis
    Volume195
    Issue number2
    DOIs
    StatePublished - Dec 2007

    Keywords

    • Genetic heterogeneity
    • Genome scan
    • ICAM-1
    • Inflammation
    • Mexican Americans
    • Quantitative trait locus

    ASJC Scopus subject areas

    • Cardiology and Cardiovascular Medicine

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