AKT1 polymorphisms are associated with risk for metabolic syndrome

Devaney, J. M. et al. (2011) AKT1 polymorphisms are associated with risk for metabolic syndrome. Human Genetics, 129(2), pp. 129-139. (doi: 10.1007/s00439-010-0910-8)

Abstract

Converging lines of evidence suggest that AKT1 is a major mediator of the responses to insulin, insulin-like growth factor 1 (IGF1), and glucose. AKT1 also plays a key role in the regulation of both muscle cell hypertrophy and atrophy. We hypothesized that AKT1 variants may play a role in the endophenotypes that make up metabolic syndrome. We studied a 12-kb region including the first exon of the AKT1 gene for association with metabolic syndrome-related phenotypes in four study populations [FAMUSS cohort (n = 574; age 23.7 +/- 5.7 years), Strong Heart Study (SHS) (n = 2,134; age 55.5 +/- 7.9 years), Dynamics of Health, Aging and Body Composition (Health ABC) (n = 3,075; age 73.6 +/- 2.9 years), and Studies of a Targeted Risk Reduction Intervention through Defined Exercise (STRRIDE) (n = 175; age 40–65 years)]. We identified a three SNP haplotype that we call H1, which represents the ancestral alleles at the three loci and H2, which represents the derived alleles at the three loci. In young adult European Americans (FAMUSS), H1 was associated with higher fasting glucose levels in females. In middle age Native Americans (SHS), H1 carriers showed higher fasting insulin and HOMA in males, and higher BMI in females. In older African-American and European American subjects (Health ABC) H1 carriers showed a higher incidence of metabolic syndrome. Homozygotes for the H1 haplotype showed about twice the risk of metabolic syndrome in both males and females (p greater than 0.001). In middle-aged European Americans with insulin resistance (STRRIDE) studied by intravenous glucose tolerance test (IVGTT), H1 carriers showed increased insulin resistance due to the Sg component (p = 0.021). The 12-kb haplotype is a risk factor for metabolic syndrome and insulin resistance that needs to be explored in further populations.

• Item Type: Articles
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Lindsay, Dr Robert
• Authors: Devaney, J. M., Gordish-Dressman, H., Harmon, B. T., Bradbury, M. K., Devaney, S. A., Harris, T. B., Thompson, P. D., Clarkson, P. M., Price, T. B., Angelopoulos, T. M., Gordon, P. M., Moyna, N. M., Pescatello, L. S., Visich, P. S., Zoeller, R. F., Seip, R. L., Seo, J., Kim, B. H., Tosi, L. A., Garcia, M., Li, R., Zmuda, J. M., Delmonico, M. J., Lindsay, R. S., Howard, B. V., Kraus, W. E., and Hoffman, E. P.
• College/School: College of Medical Veterinary and Life Sciences; College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
• Journal Name: Human Genetics
• Publisher: Springer Berlin / Heidelberg
• ISSN: 0340-6717
• ISSN (Online): 1432-1203
• Published Online: 09 November 2010
• Copyright Holders: Copyright © 2011 The Authors
• First Published: First published in Human Genetics
• Publisher Policy: Reproduced under a Creative Commons License