Exp Clin Endocrinol Diabetes 2016; 124(04): 257-260
DOI: 10.1055/s-0035-1565172
Article
© Georg Thieme Verlag KG Stuttgart · New York

Serum Levels of Copeptin are Decreased in Gestational Diabetes Mellitus

T. Ebert*
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
,
M. Platz*
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
,
S. Kralisch
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
,
U. Lossner
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
,
B. Jessnitzer
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
,
J. Richter
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
,
M. Blüher
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
,
M. Stumvoll
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
,
M. Fasshauer
1   Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany
2   Leipzig University Medical Center, IFB AdiposityDiseases, Leipzig, Germany
› Author Affiliations
Further Information

Publication History

received 31 August 2015
first decision 31 August 2015

accepted 27 October 2015

Publication Date:
29 January 2016 (online)

Abstract

Objective: Copeptin, the c-terminal part of pro-Arginine vasopressin, has recently been introduced as a novel risk factor to develop facets of the metabolic syndrome. However, regulation of copeptin in pregnancy-associated metabolic disease, i. e., gestational diabetes mellitus (GDM), has not been fully understood, so far.

Patients and Measurements: For this study, 74 GDM patients and 74 healthy, pregnant, age-, body mass index-, and gestational age-matched controls were recruited. Serum levels of copeptin were quantified by an illuminometric assay. Furthermore, copeptin concentrations were correlated to biochemical and anthropometric markers of obesity, glucose and lipid metabolism, renal function, and inflammation.

Results: Median [interquartile range] serum copeptin levels were significantly lower in subjects with GDM (3.5 [2.0] pmol/l) as compared to controls (4.4 [3.2] pmol/l) (p<0.05). Furthermore, GDM remained an independent predictor of circulating copeptin in multivariate regression analysis (p<0.05). Moreover, copeptin was independently associated with gestational age at blood sampling (p<0.05).

Conclusions: Copeptin serum levels are significantly lower in GDM as compared to healthy pregnant controls. Further studies are needed to better clarify the pathophysiological role of copeptin in GDM.

* These authors equally contributed to this work


 
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