Genetic influences on serum bilirubin in American Indians: The strong heart family study

Phillip E. Melton, Karin Haack, Harald H. Göring, Sandy Laston, Jason G. Umans, Elisa T. Lee, Richard R. Fabsitz, Richard B. Devereux, Lyle G. Best, Jean W. Maccluer, Laura Almasy, Shelley A. Cole

    Research output: Contribution to journalArticlepeer-review

    7 Scopus citations

    Abstract

    Objective: To identify genetic variation influencing serum bilirubin levels in American Indians, we performed genome-wide screening and association analyses in the Strong Heart Family Study. Bilirubin is an endogenous antioxidant that has demonstrated an inverse relationship with cardiovascular disease. Genetic variation within the promoter region of uridine diphosphate glucuronosyltransferase (UGT1A1) on chromosome 2q has been associated with elevated serum bilirubin levels in European populations. However, no study has investigated the UGT1A1 promoter in American Indians. Methods: Statistical analyses were carried out with 3,484 participants aged 14 to 93 years recruited from three geographic areas in the United States; Arizona, Oklahoma, and North and South Dakota. Results: Variance components linkage analysis detected a quantitative trait locus (QTL) for bilirubin on chromosome 2q in the combined centers (LOD = 6.61, P = 4.24 × 10-6) and in Oklahoma (LOD = 5.65, P = 4.57 24 × 10-5). Genetic association of the UGT1A1 promoter polymorphism was significant for all geographic locations. After adjustment using conditional linkage for UGT1A1 promoter variance, the linkage signal dropped to 1.10 in the combined sample and to 3.32 (P = 0.02) in Oklahoma, indicating this polymorphism is not completely responsible for the linkage signal in American Indians. We also detected suggestive linkage signals in the Dakotas on chromosome 10p12 (LOD = 2.18) and in the combined centers (LOD = 2.24) on chromosome 10q21. Conclusions: Replication of a serum bilirubin QTL on chromosome 2q in American Indians implicates UGT1A1 but further genotyping is warranted to identify additional causative polymorphisms. Evidence also supports a potential novel locus for bilirubin on chromosome 10.

    Original languageEnglish (US)
    Pages (from-to)118-125
    Number of pages8
    JournalAmerican Journal of Human Biology
    Volume23
    Issue number1
    DOIs
    StatePublished - Jan 2011

    ASJC Scopus subject areas

    • Anatomy
    • Ecology, Evolution, Behavior and Systematics
    • Anthropology
    • Genetics

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