Genomewide Linkage Scan for Genes Influencing Plasma Triglyceride Levels in the Veterans Administration Genetic Epidemiology Study (VAGES)

  1. Dawn K. Coletta (richardsond2{at}uthscsa.edu)1,
  2. Jennifer Schneider2,
  3. Shirley L. Hu1,
  4. Thomas D. Dyer2,
  5. Sobha Puppala2,
  6. Vidya S. Farook2,
  7. Rector Arya3,
  8. Donna M. Lehman3,
  9. John Blangero2,
  10. Ralph A. DeFronzo1,4,
  11. Ravindranath Duggirala2 and
  12. Christopher P. Jenkinson1,2,4
  1. 1Division of Diabetes, Department of Medicine, University of Texas Health Science Center at San Antonio
  2. 2Southwest Foundation for Biomedical Research, San Antonio
  3. 3Division of Clinical Epidemiology, Department of Medicine, University of Texas Health Science Center at San Antonio, and
  4. 4South Texas Veterans Health Care System

    Abstract

    Objective. Elevated plasma triglyceride (TG) concentration is a component of the insulin resistance syndrome and is commonly associated with type 2 diabetes, obesity and coronary heart disease. The goal of our study was to perform a genomewide linkage scan to identify genetic regions that influence variation in plasma TG levels in families that are enriched with individuals with type 2 diabetes (T2DM).

    Research Design and Methods. We used phenotypic and genotypic data from 1,026 individuals distributed across 294 Mexican American families from the Veterans Administration Genetic Epidemiology Study (VAGES), which were ascertained for T2DM. Plasma TG values were transformed, and a variance components technique was used to conduct multipoint linkage analysis.

    Results. After adjusting for the significant effects of sex and BMI, heritability for plasma TG was estimated as 46 ± 7% (P < 0.0001). Multipoint linkage analysis yielded the strongest evidence for linkage of plasma TG near marker D12S391 on chromosome 12p (LOD = 2.4). Our linkage signal on chromosome 12p provides independent replication of a similar finding in another Mexican American sample from the San Antonio Family Diabetes Study (SAFDS). Combined multipoint linkage analysis of the VAGES and SAFDS data yielded significant evidence for linkage of plasma TG to a genetic location between markers GATA49D12 and D12S391 on 12p (LOD = 3.8, empirical P value = 2.0 x 10-5). This region on 12p harbors the gene encoding adiponectin receptor 2 (AdipoR2), where we previously have shown that multiple SNPs are associated with plasma TG concentrations in the SAFDS. In the present study, we provided suggestive evidence in favor of association for rs929434 with TG concentrations in the VAGES.

    Conclusions. Collectively, these results provide strong evidence for a major locus on chromosome 12p that influences plasma TG levels in Mexican Americans.

    Footnotes

      • Received April 10, 2008.
      • Accepted October 7, 2008.