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Published in: Diabetologia 8/2005

01-08-2005 | Short Communication

The –174 IL-6 GG genotype is associated with a reduced risk of type 2 diabetes mellitus in a family sample from the National Heart, Lung and Blood Institute’s Framingham Heart Study

Authors: A. Herbert, C. Liu, S. Karamohamed, J. Schiller, J. Liu, Q. Yang, P. W. F. Wilson, L. A. Cupples, J. B. Meigs

Published in: Diabetologia | Issue 8/2005

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Abstract

Aims/hypothesis

We evaluated the –174 IL-6 gene polymorphism as a risk factor for type 2 diabetes mellitus in a family-based analysis.

Methods

We tested for associations between the –174 IL-6 G/C promoter polymorphism and fasting plasma glucose (FPG) and type 2 diabetes in a sample of 1,428 individuals from the largest 182 families in the National Heart, Lung and Blood Institute’s Framingham Heart Study population.

Results

A significant association was found with FPG (p=0.01) and log (FPG) (p=0.005) using a modified family-based transmission disequilibrium test, the family-based association test (FBAT). The association between IL-6 genotype and FPG (p=0.035) and log (FPG) (p=0.03) was also found in the subset of families that were informative in FBAT using a mixed-effects regression model and strengthened after adjustment for potential confounders (p=0.008 for log [FPG]). The mean glucose level estimated from models with log (FPG) as the dependent variable for the GG genotype in the informative families was significantly lower (5.20±0.06 mmol/l) than for the GC (5.41±0.06 mmol/l) and CC (5.38±0.06 mmol/l) genotypes (p=0.03 for contrast between GG and GC genotypes). In the subset of informative families, the risk of type 2 diabetes associated with the GG genotype was lower relative to the GC and CC genotypes combined (potential confounder-adjusted, mixed-effects odds ratio 0.35, 95% CI 0.14–0.88, p=0.026, unaffected n=391, affected n=32).

Conclusions/interpretation

These results are consistent with a protective role for the –174 IL-6 G allele against type 2 diabetes and warrant further analysis of this polymorphism.
Literature
1.
go back to reference Fernandez-Real JM, Broch M, Vendrell J et al (2000) Interleukin-6 gene polymorphism and insulin sensitivity. Diabetes 49:517–520PubMed Fernandez-Real JM, Broch M, Vendrell J et al (2000) Interleukin-6 gene polymorphism and insulin sensitivity. Diabetes 49:517–520PubMed
2.
go back to reference Vozarova B, Fernandez-Real JM, Knowler WC et al (2003) The interleukin-6 (–174) G/C promoter polymorphism is associated with type-2 diabetes mellitus in native Americans and Caucasians. Hum Genet 112:409–413PubMed Vozarova B, Fernandez-Real JM, Knowler WC et al (2003) The interleukin-6 (–174) G/C promoter polymorphism is associated with type-2 diabetes mellitus in native Americans and Caucasians. Hum Genet 112:409–413PubMed
3.
go back to reference Kubaszek A, Pihlajamaki J, Punnonen K, Karhapaa P, Vauhkonen I, Laakso M (2003) The C-174G promoter polymorphism of the IL-6 gene affects energy expenditure and insulin sensitivity. Diabetes 52:558–561PubMed Kubaszek A, Pihlajamaki J, Punnonen K, Karhapaa P, Vauhkonen I, Laakso M (2003) The C-174G promoter polymorphism of the IL-6 gene affects energy expenditure and insulin sensitivity. Diabetes 52:558–561PubMed
4.
go back to reference Mohlig M, Boeing H, Spranger J et al (2004) Body mass index and C-174G interleukin-6 promoter polymorphism interact in predicting type 2 diabetes. J Clin Endocrinol Metab 89:1885–1890CrossRefPubMed Mohlig M, Boeing H, Spranger J et al (2004) Body mass index and C-174G interleukin-6 promoter polymorphism interact in predicting type 2 diabetes. J Clin Endocrinol Metab 89:1885–1890CrossRefPubMed
5.
go back to reference Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA (2002) A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: the Framingham Offspring Study. Diabetes 51:833–840PubMed Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA (2002) A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: the Framingham Offspring Study. Diabetes 51:833–840PubMed
6.
go back to reference Kannel WB, Feinleib M, McNamara PM, Garrison RJ, Castelli WP (1979) An investigation of coronary heart disease in families. The Framingham Offspring Study. Am J Epidemiol 110:281–290PubMed Kannel WB, Feinleib M, McNamara PM, Garrison RJ, Castelli WP (1979) An investigation of coronary heart disease in families. The Framingham Offspring Study. Am J Epidemiol 110:281–290PubMed
7.
go back to reference Buetow KH, Edmonson M, MacDonald R et al (2001) High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci U S A 98:581–584CrossRefPubMed Buetow KH, Edmonson M, MacDonald R et al (2001) High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci U S A 98:581–584CrossRefPubMed
8.
go back to reference Meigs JB, Cupples LA, Wilson PW (2000) Parental transmission of type 2 diabetes: the Framingham Offspring Study. Diabetes 49:2201–2207PubMed Meigs JB, Cupples LA, Wilson PW (2000) Parental transmission of type 2 diabetes: the Framingham Offspring Study. Diabetes 49:2201–2207PubMed
9.
go back to reference Horvath S, Xu X, Laird NM (2001) The family based association test method: strategies for studying general genotype–phenotype associations. Eur J Hum Genet 9:301–306 Horvath S, Xu X, Laird NM (2001) The family based association test method: strategies for studying general genotype–phenotype associations. Eur J Hum Genet 9:301–306
10.
go back to reference White H (1980) A heteroskedasticity-consistent covariance matrix estimator and a direct test for heteroskedasticity. Econometrica 48:817–838 White H (1980) A heteroskedasticity-consistent covariance matrix estimator and a direct test for heteroskedasticity. Econometrica 48:817–838
Metadata
Title
The –174 IL-6 GG genotype is associated with a reduced risk of type 2 diabetes mellitus in a family sample from the National Heart, Lung and Blood Institute’s Framingham Heart Study
Authors
A. Herbert
C. Liu
S. Karamohamed
J. Schiller
J. Liu
Q. Yang
P. W. F. Wilson
L. A. Cupples
J. B. Meigs
Publication date
01-08-2005
Publisher
Springer-Verlag
Published in
Diabetologia / Issue 8/2005
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-005-1830-3

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