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Diabetes Care. Jun 2010; 33(6): 1233–1235.
Published online Mar 18, 2009. doi:  10.2337/dc09-1690
PMCID: PMC2875429

Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort

Abstract

OBJECTIVE

To assess whether TCF7L2 polymorphism has a role in the deterioration of glycemic control.

RESEARCH DESIGN AND METHODS

Metabolic variables were evaluated at baseline and after 6-year follow-up in 1,480 Caucasian subjects from a population-based cohort.

RESULTS

At baseline, T-allele carriers showed significantly lower BMI and homeostasis model assessment for β-cell function (HOMA-B) values and higher fasting glycemia and diabetes prevalence. At follow-up, fasting glucose and HOMA-B index were increased and reduced, respectively, in carriers of the T-allele. Incident impaired fasting glucose (IFG) and incident diabetes were 5.7, 10.7, 16.9% and 1.6, 1.7, 3.0% in the CC, CT, and TT genotypes, respectively. In a multiple logistic regression model, the association between incident IFG and the T-allele was significant (odds ratio [OR] 2.08 [95% CI 1.35–3.20] and 3.56 [2.11–5.98] in CT and TT genotypes, respectively).

CONCLUSIONS

The T-allele of TCF7L2 rs7903146 polymorphism was independently associated with increasing fasting glucose values toward hyperglycemia in the follow-up.

Among the variety of TCF7L2 polymorphisms correlating with type 2 diabetes, the single nucleotide polymorphism (SNP) rs7903146 has shown the strongest association with the disease (1). We investigated the association of the SNP rs7903146 with 1) type 2 diabetes or 2) impaired fasting glucose (IFG) or 3) the metabolic syndrome (MS) in an adult Italian population-based cohort both cross-sectionally and after 6-year follow-up.

RESEARCH DESIGN AND METHODS

All 1,877 Caucasians aged 45–64 years and representative of the province of Asti (Italy) were invited to participate in a metabolic survey in 2001–2003; 1,658 (88.3%) agreed to participate by written informed consent. Both participants and nonparticipants were similar to the resident population of corresponding age with respect to sex composition, level of education, prevalence of known diabetes, and living in a rural area (2). Diabetes and MS were diagnosed according to published recommendations and criteria (3,4); the homeostasis model assessment-insulin resistance (HOMA-IR) index and the HOMA for β-cell (HOMA-B) function were calculated (5).

Genotyping for TCF7L2 SNP rs7903146 utilized the real-time allele discrimination method (Applied Biosystems, Foster City, CA). All procedures were in accordance with the Declaration of Helsinki and approved by the local ethics committee.

HOMA-IR, HOMA-B, insulin, and triglyceride values were log-transformed and used in all analyses. Multiple regression analyses (for continuous variables) or multiple logistic regression analyses (for dichotomic variables) were used to evaluate the associations between each variable and the presence of the CT or TT genotypes (introduced in the model as dummy variables) after adjustments for age, sex, familial diabetes, BMI, and waist circumference. The capacity of the TT genotype for predicting incident IFG and diabetes was examined by calculating the receiver operating characteristics (ROC) curves and the area under the curve (AUC).

RESULTS

From January to November 2008, patients were contacted for a follow-up visit: 1,480/1,658 (89.3%) were evaluated after excluding those who died (n = 61) and those whose blood samples were not available for genotyping (n = 117). Mean follow-up was 6.1 ± 0.34 years. At baseline, 25.1% of patients were on anti-hypertensive treatment and 4.7% were on hypoglycemic drugs.

Characteristics at baseline and follow-up of subjects grouped by genotypes are presented in Table 1. The rs7903146 genotypic distribution was in Hardy-Weinberg equilibrium.

Table 1
Characteristics at baseline and follow-up by TCF7L2 rs7903146 genotypes

At baseline, carriers of the T-allele showed significantly higher values of fasting glucose and lower BMI and HOMA-B index values in a regression model (Table 1). Prevalence of diabetes was significantly higher in subjects carrying the minor T-allele in a multiple logistic regression model, while no significant differences were detected for prevalence of IFG and MS.

At follow-up, fasting glucose and HOMA-B values were increased and reduced, respectively, in T-allele carriers. In these patients, prevalence of IFG, diabetes, and MS were significantly higher in a multiple logistic regression model in both CT and TT genotypes (OR 1.78 [95% CI 1.06–2.99] and 3.10 [1.63–5.91] for diabetes; 1.81 [1.31–2.51] and [1.90–4.39] for IFG; 1.34 [1.02–1.75] and 1.79 [1.22–2.64] for MS in CT and TT genotypes, respectively). The association between T-allele and MS was exclusively due to the higher prevalence of hyperglycemia in these subjects.

Incident diabetes was almost double in homozygous for the T-allele, but the association was not significant due to the low case number. Incident IFG was twofold and threefold higher in the heterozygous and homozygous T carriers, respectively (OR 2.08 [95% CI 1.35–3.20] and 3.56 [2.11–5.98] in CT and TT genotypes, respectively). Adjustments for smoking habits, lipid parameters, or HOMA-B values did not significantly affect the results. The AUCs of the ROC curves for the TT genotype were 0.56 for incident IFG and 0.54 for incident diabetes.

CONCLUSIONS

The major findings of the present study are: 1) a high prevalence of the defective T-allele in an Italian population-based cohort; 2) a significant association between the T-allele and hyperglycemia and β-cell dysfunction at baseline and follow-up; 3) a two- to threefold higher risk of incident IFG in the T-allele carriers at follow-up; and 4) an increased prevalence of MS in the T-allele carriers.

The minor T-allele is strongly associated with reduced HOMA-B levels, suggesting that the polymorphism could affect the ability of the β-cells to secrete insulin. These data indicate that SNP rs7903146 polymorphism may modulate the degree of insulin secretion to offset the prevailing level of insulin resistance without being a cause of insulin resistance. SNP rs7903146 acts like other TCF7L2 polymorphisms, such as rs12255372 (6). The T-allele is significantly associated with lower BMI, so we can confirm recent studies that suggest that the variants do not have a primary effect on adiposity (7). These studies showed that individuals with the highest risk genotype and the lowest birth weight had the greatest risk of type 2 diabetes (8).

It has been reported that TCF7L2 exerts its influence through an impairment of insulin secretion. This impairment was reportedly due to a functional defect in the glucagon-like peptide-1 (GLP-1) signaling in β-cells and not due to defective/failing GLP-1 secretion (9). It is unlikely that the pathway of incretins by itself can play a central role in the pathophysiology of type 2 diabetes. We reported that TCF7L2 may impact β-cell function both directly through modulating β-cell response to glucose and indirectly by modulating incretin action or secretion (10).

The prevalence of MS in subjects carrying the TT genotype was about twofold higher at follow-up when compared with the prevalence at baseline. This increment was almost exclusively due to the significantly higher prevalence of hyperglycemia in this subgroup. The AUC values are similar to those reported in literature dealing with one single SNP (11).

Our study confirms an effect of the widely replicated TCF7L2 rs7903146 polymorphism on hyperglycemia in an adult Italian population-based cohort both in cross-sectional and longitudinal evaluation. The independent association of TCF7L2 polymorphism with increasing fasting glucose values in the follow-up may represent a marker for higher metabolic risk, which is useful for developing more closely tailored lifestyle preventive approaches as we have recently reported (12).

Acknowledgments

This work was supported by a grant “Progetto di Ricerca Sanitaria Finalizzata, Regione Piemonte, 2008” [DD n.12 del 14.01.2008].

No potential conflicts of interest relevant to this article were reported.

Footnotes

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

References

1. Helgason A, Pálsson S, Thorleifsson G, Grant SF, Emilsson V, Gunnarsdottir S, Adeyemo A, Chen Y, Chen G, Reynisdottir I, Benediktsson R, Hinney A, Hansen T, Andersen G, Borch-Johnsen K, Jorgensen T, Schäfer H, Faruque M, Doumatey A, Zhou J, Wilensky RL, Reilly MP, Rader DJ, Bagger Y, Christiansen C, Sigurdsson G, Hebebrand J, Pedersen O, Thorsteinsdottir U, Gulcher JR, Kong A, Rotimi C, Stefánsson K.: Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution. Nat Genet 2007;39:218–225 [PubMed]
2. Bo S, Gentile L, Ciccone G, Baldi C, Benini L, Dusio F, Lucia C, Forastiere G, Nuti C, Cassader M, Pagano G.: The metabolic syndrome and high C-reactive protein: prevalence and difference by sex in a southern-European population-based cohort. Diabete Metab Research Rev 2005;21:515–524 [PubMed]
3. The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care 2003;26(Suppl. 1):5–20 [PubMed]
4. The Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) Final Report. Circulation 2002, 106:3143–3421 [PubMed]
5. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC.: Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985;28:412–419 [PubMed]
6. Munoz J, Lok KH, Gower BA, Fernandez JR, Hunter GR, Lara-Castro C, De Luca M, Garvey WT.: Polymorphism in the transcription factor 7-like 2 (TCF7L2) gene is associated with reduced insulin secretion in nondiabetic women. Diabetes 2006;55:3630–3634 [PubMed]
7. Kimber CH, Doney AS, Pearson ER, McCarthy MI, Hattersley AT, Leese GP, Morris AD, Palmer CN.: TCF7L2 in the Go-DARTS study: evidence for a gene dose effect on both diabetes susceptibility and control of glucose levels. Diabetologia 2007;50:1186–1191 [PubMed]
8. Pulizzi N, Lyssenko V, Jonsson A, Osmond C, Laakso M, Kajantie E, Barker DJ, Groop LC, Eriksson JG.: Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes. Diabetologia 2009;52:825–829 [PubMed]
9. Schäfer SA, Tschritter O, Machicao F, Thamer C, Stefan N, Gallwitz B, Holst JJ, Dekker JM, 't Hart LM, t'Hart LM, Nijpels G, van Haeften TW, Häring HU, Fritsche A.: Impaired glucagon-like peptide-1-induced insulin secretion in carriers of transcription factor 7-like 2 (TCF7L2) gene polymorphisms. Diabetologia 2007;50:2443–2450 [PMC free article] [PubMed]
10. Musso G, Gambino R, Pacini G, Pagano G, Durazzo M, Cassader M.: Transcription factor 7-like 2 polymorphism modulates glucose and lipid homeostasis, adipokine profile, and hepatocyte apoptosis in NASH. Hepatology 2009;49:426–435 [PubMed]
11. Weedon MN.: The importance of TCF7L2. Diabet Med 2007;24:1062–1066 [PubMed]
12. Bo S, Gambino R, Ciccone G, Rosato R, Milanesio N, Villois P, Pagano G, Cassader M, Gentile L, Durazzo M, Cavallo-Perin P.: Effects of TCF7L2 polymorphisms on glucose values after a lifestyle intervention. Am J Clin Nutr 2009;90:1502–1508 [PubMed]

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