G-protein β3 Subunit Gene Splice Variant and Body Fat Distribution in Nunavut Inuit

  1. Robert A. Hegele1,4,
  2. Carol Anderson1,
  3. T. Kue Young2, and
  4. Philip W. Connelly3
  1. 1Robarts Research Institute and Department of Medicine, University of Western Ontario, London, Ontario, Canada N6A5K8; 2Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada R3E0W2; 3Departments of Medicine and Biochemistry, St. Michael's Hospital and University of Toronto, Toronto, Ontario, Canada M5B1A6

Abstract

The GNB3 825T allele encodes a product that has enhanced activation of heterotrimeric G proteins in vitro and could play a role in adipogenesis. We therefore evaluated the possibility that theGNB3 825T allele was associated with obesity in a sample of 213 healthy Canadian Inuit. We found that body weight, body mass index, waist girth, hip girth, subscapular skinfold thickness, and triceps skinfold thickness were significantly higher in subjects with theGNB3 825T/T genotype than in subjects with other genotypes. Furthermore, two anthropometric ratios, namely that of waist to hip circumference and that of subscapular to triceps skinfold thickness, were not significantly different across genotypes. This suggested that the increased deposition of fat in subjects with the GNB3825T/T genotype was generalized and not localized to particular subregions. There was no association of this genetic variation with blood pressure. The GNB3 825T/T genotype accounted for between 1.6% and 3.3% of the total variation (≤13% of attributable variation) of the obesity-related traits. The potential for a genetic marker of obesity creates opportunities for future studies in the Inuit, not just to confirm the associations, but also to examine prospectively the influence of interventions and possible relationships between GNB3 825T and longer term complications of obesity.

Footnotes

  • 4 Corresponding author.

  • E-MAIL robert.hegele{at}rri.on.ca; FAX (519) 663-3789.

    • Received May 4, 1999.
    • Accepted August 4, 1999.
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