Polycystic Ovary Syndrome (PCOS) in Juvenile and Adult Type 1 Diabetes in a German/Austrian Cohort

Author:

Reinauer Christina1,Bollow Esther2,Fröhlich-Reiterer Elke3,Laubner Katharina4,Bergis Dominik5,Schöfl Christof6,Kempe Hans-Peter7,Hummel Michael8,Hennes Pia9,Gollisch Katja10,Haberland Holger11,Datz Nicolin12,Meissner Thomas1,Holl Reinhard2

Affiliation:

1. Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich Heine University Düsseldorf, Düsseldorf, Germany

2. Institute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Ulm, Germany

3. Department of Paediatrics, Medical University of Graz, Austria

4. Division of Endocrinology and Diabetology, Department of Internal Medicine II, University Hospital of Freiburg, Freiburg, Germany

5. Department of Internal Medicine 1, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany

6. Centres of Endocrinology and Metabolism, Bamberg and Erlangen, Germany

7. Specialized Diabetes Practice Diabetologikum, Ludwigshafen, Germany

8. Specialized Diabetes Practice, Rosenheim, Germany

9. Department of Pediatrics, Saarland University, Homburg, Germany

10. Clinic for Gastroenterology and Gastrointestinal Oncology, Endocrine Unit, University Medical Center Göttingen, Göttingen, Germany

11. Hospital for Children and Adolescents, Sana Hospital Berlin Lichtenberg, Berlin, Germany

12. Diabetes Center for Children and Adolescents, Children's Hospital Auf der Bult, Hannover, Germany

Abstract

Abstract Context While an association between PCOS and type 2 diabetes is well established, to date there have been few data on clinical care of type 1 diabetes (T1D) patients with PCOS. Objective The aim of our study was to characterize T1D patients with the comorbidity of PCOS within the DPV cohort with regard to diabetes phenotype, therapy and metabolic control. Design and Setting Clinical data from the prospective German/Austrian DPV cohort on patients with T1D and documented PCOS (n=76) were compared to female T1D controls (n=32,566) in reproductive age. Results The age at T1D manifestation in PCOS patients was later than in the control group (14.9±8.2 vs. 11.8±7.0 years, p<0.001). PCOS patients had higher BMI-SDS (0.92±0.11 vs. 0.38±0.01, p<0.001), metformin and oral contraceptives were used more frequently (p<0.001). A1c levels were significantly lower (7.92 +/− 0.23% vs. 8.43±0.01%, p<0.05) despite of lower insulin requirements (0.76±0.04 IU/kg/d vs. 0.84±0.00 IU/kg/d, p<0.05). In the PCOS group, higher rates of dyslipidemia (63.4 vs. 48.7%, p =0.032) and thyroid disorders (42.2% vs. 21.2%, p<0.001) were present. Discussion While patients with T1D and comorbid PCOS showed features of a “type 1.5 diabetes” phenotype, insulin requirements per kg body weight were not higher and metabolic control was better, which could be explained only partially by additional metformin therapy. A more precise genetic and metabolic characterisation of these patients is needed to answer open questions on the underlying autoimmune process and residual ß-cell function.

Publisher

Georg Thieme Verlag KG

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

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