Skip to main content

Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.

Publication ,  Journal Article
Palmer, ND; Hester, JM; An, SS; Adeyemo, A; Rotimi, C; Langefeld, CD; Freedman, BI; Ng, MCY; Bowden, DW
Published in: Diabetes
February 2011

OBJECTIVE: Variation in the transcription factor 7-like 2 (TCF7L2) locus is associated with type 2 diabetes across multiple ethnicities. The aim of this study was to elucidate which variant in TCF7L2 confers diabetes susceptibility in African Americans. RESEARCH DESIGN AND METHODS: Through the evaluation of tagging single nucleotide polymorphisms (SNPs), type 2 diabetes susceptibility was limited to a 4.3-kb interval, which contains the YRI (African) linkage disequilibrium (LD) block containing rs7903146. To better define the relationship between type 2 diabetes risk and genetic variation we resequenced this 4.3-kb region in 96 African American DNAs. Thirty-three novel and 13 known SNPs were identified: 20 with minor allele frequencies (MAF) >0.05 and 12 with MAF >0.10. These polymorphisms and the previously identified DG10S478 microsatellite were evaluated in African American type 2 diabetic cases (n = 1,033) and controls (n = 1,106). RESULTS: Variants identified from direct sequencing and databases were genotyped or imputed. Fifteen SNPs showed association with type 2 diabetes (P < 0.05) with rs7903146 being the most significant (P = 6.32 × 10(-6)). Results of imputation, haplotype, and conditional analysis of SNPs were consistent with rs7903146 being the trait-defining SNP. Analysis of the DG10S478 microsatellite, which is outside the 4.3-kb LD block, revealed consistent association of risk allele 8 with type 2 diabetes (odds ratio [OR] = 1.33; P = 0.022) as reported in European populations; however, allele 16 (MAF = 0.016 cases and 0.032 controls) was strongly associated with reduced risk (OR = 0.39; P = 5.02 × 10(-5)) in contrast with previous studies. CONCLUSIONS: In African Americans, these observations suggest that rs7903146 is the trait-defining polymorphism associated with type 2 diabetes risk. Collectively, these results support ethnic differences in type 2 diabetes associations.

Duke Scholars

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

February 2011

Volume

60

Issue

2

Start / End Page

662 / 668

Location

United States

Related Subject Headings

  • Transcription Factor 7-Like 2 Protein
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Male
  • Linkage Disequilibrium
  • Humans
  • Haplotypes
  • Genotype
  • Genetic Variation
  • Genetic Predisposition to Disease
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Palmer, N. D., Hester, J. M., An, S. S., Adeyemo, A., Rotimi, C., Langefeld, C. D., … Bowden, D. W. (2011). Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes, 60(2), 662–668. https://doi.org/10.2337/db10-0134
Palmer, Nicholette D., Jessica M. Hester, S Sandy An, Adebowale Adeyemo, Charles Rotimi, Carl D. Langefeld, Barry I. Freedman, Maggie C. Y. Ng, and Donald W. Bowden. “Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.Diabetes 60, no. 2 (February 2011): 662–68. https://doi.org/10.2337/db10-0134.
Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD, et al. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes. 2011 Feb;60(2):662–8.
Palmer, Nicholette D., et al. “Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.Diabetes, vol. 60, no. 2, Feb. 2011, pp. 662–68. Pubmed, doi:10.2337/db10-0134.
Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD, Freedman BI, Ng MCY, Bowden DW. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes. 2011 Feb;60(2):662–668.

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

February 2011

Volume

60

Issue

2

Start / End Page

662 / 668

Location

United States

Related Subject Headings

  • Transcription Factor 7-Like 2 Protein
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Male
  • Linkage Disequilibrium
  • Humans
  • Haplotypes
  • Genotype
  • Genetic Variation
  • Genetic Predisposition to Disease