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Diabetologia. 2011 Mar;54(3):535-9. doi: 10.1007/s00125-010-1982-7. Epub 2010 Nov 26.

Association testing of TCF7L2 polymorphisms with type 2 diabetes in multi-ethnic youth.

Author information

1
Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, 13001 17th Place, Aurora, CO 80045, USA. dana.dabelea@ucdenver.edu

Abstract

AIM/HYPOTHESIS:

Common variants in the transcription factor 7-like 2 (TCF7L2) gene have been associated with type 2 diabetes in adults. However, it is not known whether TCF7L2 variation increases the risk of early onset type 2 diabetes. Using a case-control design, we examined whether the reported variants [rs12255372 (T/G) and rs7903146 (T/C)] are associated with type 2 diabetes in SEARCH for Diabetes in Youth study participants.

METHODS:

Variants were genotyped in 694 non-Hispanic white (NHW) youth (86 cases, mean age 15.5 years, mean BMI 34.8; and 608 controls, mean age 14.4 years, mean BMI 22.3) and 545 African-American (AA) youth (154 cases, mean age 15.9, mean BMI 37; and 391 controls, mean age 14.8, mean BMI 23.8). Logistic regression adjusted for age, sex, BMI and West African ancestry.

RESULTS:

The association of the risk T allele with case/control status was different in AA and NHW youth (p = 0.025). Among AA youth, each copy of the T allele (rs7903146) was associated with a 1.97-fold (1.37, 2.82) increased odds for type 2 diabetes (p < 0.0001), after adjustment for age, sex, BMI and African ancestry. No significant association was detected in NHW youth (adjusted OR, 1.14; 0.73, 1.79).

CONCLUSION/INTERPRETATION:

TCF7L2 variation is associated with an increased risk of early-onset type 2 diabetes among AA youth, and the association appears to be stronger in AA than NHW youth. This suggests potential different contributions of genetic and environmental factors to early-onset type 2 diabetes by race.

PMID:
21109996
PMCID:
PMC3766323
DOI:
10.1007/s00125-010-1982-7
[Indexed for MEDLINE]
Free PMC Article

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