Back to Search
Start Over
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
- Source :
- Diabetes Care. 37:909-911
- Publication Year :
- 2014
- Publisher :
- American Diabetes Association, 2014.
-
Abstract
- 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.
- Subjects :
- Advanced and Specialized Nursing
medicine.medical_specialty
Pregnancy
endocrine system diseases
business.industry
Endocrinology, Diabetes and Metabolism
Case-control study
nutritional and metabolic diseases
Type 2 diabetes
Placebo
medicine.disease
3. Good health
Metformin
Gestational diabetes
Endocrinology
Diabetes mellitus
Internal medicine
Internal Medicine
Medicine
Prediabetes
business
medicine.drug
Subjects
Details
- ISSN :
- 19355548 and 01495992
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- Diabetes Care
- Accession number :
- edsair.doi...........9cd271226c848378724a10e66b113faa
- Full Text :
- https://doi.org/10.2337/dc13-0700