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Rottenkolber, M.* ; Ferrari, U. ; Holland, L. ; Aertsen, S. ; Kammer, N.N.* ; Hetterich, H.* ; Fugmann, M. ; Banning, F. ; Weise, M. ; Sacco, V. ; Kohn, D.* ; Freibothe, I. ; Hutter, S.* ; Hasbargen, U.* ; Lehmann, R.* ; Grallert, H. ; Parhofer, K.G.* ; Seissler, J. ; Lechner, A.

The diabetes risk phenotype of young women with recent gestational diabetes.

J. Clin. Endocrinol. Metab. 100, E910-E918 (2015)
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Context: The pathogenesis of type 2 diabetes (T2D) is still incompletely understood. In-depth phenotyping of young individuals at risk for T2D can contribute to the understanding of this process. Objective: To metabolically characterize women with recent gestational diabetes (GDM), an at-risk cohort for T2D. Study participants: 147 consecutively recruited women 3-16 months after pregnancy, women who had GDM and women after a normoglycemic pregnancy (controls) in a 2:1 ratio Design: Mono-center cross-sectional analysis (PPS-Diab study) Methods: 5-point OGTT with calculation of insulin sensitivity (ISI) and disposition index (DI; validation by euglycemic clamp and IVGTT), anthropometrics, medical and family history, clinical chemistry and biomarkers, statistical modelling, MRI/MRS substudy (body fat distribution, liver and muscle fat; n=66) Results: Compared to control subjects, women post GDM had a reduced DI, higher levels of plasma fetuin-A and a lower ISI. A low ISI was also the major determinant of pathologic glucose tolerance after GDM. The factors most strongly predictive of low insulin sensitivity were high plasma leptin, BMI, triglycerides, and waist circumference. Ectopic lipids showed no BMI-independent associations with having had GDM or low insulin sensitivity in an MRI substudy. Conclusions: We found that beta cell function is already impaired in women with recent GDM, a young at-risk cohort for T2D. Additionally, our data suggest that fetuin-A and leptin signaling may be important early contributors to the pathogenesis of T2D, at this disease stage equally or more relevant than ectopic lipids and low-grade inflammation.
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2015
HGF-reported in Year 2015
ISSN (print) / ISBN 0021-972X
e-ISSN 1945-7197
Journal Journal of Clinical Endocrinology & Metabolism, The
Quellenangaben Volume: 100, Issue: 6, Pages: E910-E918 Article Number: , Supplement: ,
Publisher Endocrine Society
Publishing Place Bethesda, Md.
Reviewing status Peer reviewed
Institute(s) Institute of Experimental Genetics (IEG)
CCG Nutrigenomics and Type 2 Diabetes (KKG-KDN)
Institute of Epidemiology (EPI)
POF-Topic(s) 30201 - Metabolic Health
90000 - German Center for Diabetes Research
30202 - Environmental Health
Research field(s) Genetics and Epidemiology
PSP Element(s) G-521500-002
G-501900-701
G-504091-002
G-501900-402
PubMed ID 25742512
DOI 10.1210/jc.2014-3898
WOS ID WOS:000360840000011
Scopus ID 84930814122
Erfassungsdatum 2015-04-22
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