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Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus
OBJECTIVE: The Diabetes Prevention Program (DPP) trial investigated rates of progression to diabetes among adults with prediabetes randomized to treatment with placebo, metformin, or intensive lifestyle intervention. Among women in the DPP, diabetes risk reduction with metformin was greater in women...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964494/ https://www.ncbi.nlm.nih.gov/pubmed/24271189 http://dx.doi.org/10.2337/dc13-0700 |
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author | Sullivan, Shannon D. Jablonski, Kathleen A. Florez, Jose C. Dabelea, Dana Franks, Paul W. Dagogo-Jack, Sam Kim, Catherine Knowler, William C. Christophi, Costas A. Ratner, Robert |
author_facet | Sullivan, Shannon D. Jablonski, Kathleen A. Florez, Jose C. Dabelea, Dana Franks, Paul W. Dagogo-Jack, Sam Kim, Catherine Knowler, William C. Christophi, Costas A. Ratner, Robert |
author_sort | Sullivan, Shannon D. |
collection | PubMed |
description | OBJECTIVE: The Diabetes Prevention Program (DPP) trial investigated rates of progression to diabetes among adults with prediabetes randomized to treatment with placebo, metformin, or intensive lifestyle intervention. Among women in the DPP, diabetes risk reduction with metformin was greater in women with prior gestational diabetes mellitus (GDM) compared with women without GDM but with one or more previous live births. RESEARCH DESIGN AND METHODS: We asked if genetic variability could account for these differences by comparing β-cell function and genetic risk scores (GRS), calculated from 34 diabetes-associated loci, between women with and without histories of GDM. RESULTS: β-Cell function was reduced in women with GDM. The GRS was positively associated with a history of GDM; however, the GRS did not predict progression to diabetes or modulate response to intervention. CONCLUSIONS: These data suggest that a diabetes-associated GRS is associated with development of GDM and may characterize women at risk for development of diabetes due to β-cell dysfunction. |
format | Online Article Text |
id | pubmed-3964494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-39644942015-04-01 Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus Sullivan, Shannon D. Jablonski, Kathleen A. Florez, Jose C. Dabelea, Dana Franks, Paul W. Dagogo-Jack, Sam Kim, Catherine Knowler, William C. Christophi, Costas A. Ratner, Robert Diabetes Care Current Concepts of Type 2 Diabetes Prevention OBJECTIVE: The Diabetes Prevention Program (DPP) trial investigated rates of progression to diabetes among adults with prediabetes randomized to treatment with placebo, metformin, or intensive lifestyle intervention. Among women in the DPP, diabetes risk reduction with metformin was greater in women with prior gestational diabetes mellitus (GDM) compared with women without GDM but with one or more previous live births. RESEARCH DESIGN AND METHODS: We asked if genetic variability could account for these differences by comparing β-cell function and genetic risk scores (GRS), calculated from 34 diabetes-associated loci, between women with and without histories of GDM. RESULTS: β-Cell function was reduced in women with GDM. The GRS was positively associated with a history of GDM; however, the GRS did not predict progression to diabetes or modulate response to intervention. CONCLUSIONS: These data suggest that a diabetes-associated GRS is associated with development of GDM and may characterize women at risk for development of diabetes due to β-cell dysfunction. American Diabetes Association 2014-04 2014-03-08 /pmc/articles/PMC3964494/ /pubmed/24271189 http://dx.doi.org/10.2337/dc13-0700 Text en © 2014 by the American Diabetes Association. 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/ for details. |
spellingShingle | Current Concepts of Type 2 Diabetes Prevention Sullivan, Shannon D. Jablonski, Kathleen A. Florez, Jose C. Dabelea, Dana Franks, Paul W. Dagogo-Jack, Sam Kim, Catherine Knowler, William C. Christophi, Costas A. Ratner, Robert Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title | Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title_full | Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title_fullStr | Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title_full_unstemmed | Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title_short | Genetic Risk of Progression to Type 2 Diabetes and Response to Intensive Lifestyle or Metformin in Prediabetic Women With and Without a History of Gestational Diabetes Mellitus |
title_sort | genetic risk of progression to type 2 diabetes and response to intensive lifestyle or metformin in prediabetic women with and without a history of gestational diabetes mellitus |
topic | Current Concepts of Type 2 Diabetes Prevention |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964494/ https://www.ncbi.nlm.nih.gov/pubmed/24271189 http://dx.doi.org/10.2337/dc13-0700 |
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