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

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 carr...

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Autores principales: Gambino, Roberto, Bo, Simona, Gentile, Luigi, Musso, Giovanni, Pagano, Gianfranco, Cavallo-Perin, Paolo, Cassader, Maurizio
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875429/
https://www.ncbi.nlm.nih.gov/pubmed/20299486
http://dx.doi.org/10.2337/dc09-1690
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author Gambino, Roberto
Bo, Simona
Gentile, Luigi
Musso, Giovanni
Pagano, Gianfranco
Cavallo-Perin, Paolo
Cassader, Maurizio
author_facet Gambino, Roberto
Bo, Simona
Gentile, Luigi
Musso, Giovanni
Pagano, Gianfranco
Cavallo-Perin, Paolo
Cassader, Maurizio
author_sort Gambino, Roberto
collection PubMed
description 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.
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spelling pubmed-28754292011-06-01 Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort Gambino, Roberto Bo, Simona Gentile, Luigi Musso, Giovanni Pagano, Gianfranco Cavallo-Perin, Paolo Cassader, Maurizio Diabetes Care Original Research 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. American Diabetes Association 2010-06 2009-03-18 /pmc/articles/PMC2875429/ /pubmed/20299486 http://dx.doi.org/10.2337/dc09-1690 Text en © 2010 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details.
spellingShingle Original Research
Gambino, Roberto
Bo, Simona
Gentile, Luigi
Musso, Giovanni
Pagano, Gianfranco
Cavallo-Perin, Paolo
Cassader, Maurizio
Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title_full Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title_fullStr Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title_full_unstemmed Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title_short Transcription Factor 7-Like 2 (TCF7L2) Polymorphism and Hyperglycemia in an Adult Italian Population-Based Cohort
title_sort transcription factor 7-like 2 (tcf7l2) polymorphism and hyperglycemia in an adult italian population-based cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875429/
https://www.ncbi.nlm.nih.gov/pubmed/20299486
http://dx.doi.org/10.2337/dc09-1690
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