Performance of the 1 mg dexamethasone suppression test in patients with severe obesity

Objective To analyze the performance of the 1 mg dexamethasone suppression test (DST) in patients with obesity. Special attention was paid to the influence of interfering medication on DST. Methods In this prospective cohort study (Mannheim Obesity Study), patients with obesity were evaluated before...

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Main Authors: Lammert, Alexander (Author) , Nittka, Stefanie (Author) , Otto, Mirko (Author) , Schneider-Lindner, Verena (Author) , Krämer, Bernhard (Author) , Birck, Rainer (Author) , Hammes, Hans-Peter (Author) , Benck, Urs Tobias (Author)
Format: Article (Journal)
Language:English
Published: 7 March 2016
In: Obesity
Year: 2016, Volume: 24, Issue: 4, Pages: 850-855
ISSN:1930-739X
DOI:10.1002/oby.21442
Online Access:Verlag, Volltext: https://doi.org/10.1002/oby.21442
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/oby.21442
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Author Notes:Alexander Lammert, Stefanie Nittka, Mirko Otto, Verena Schneider‐Lindner, Anne Kemmer, Bernhard K. Krämer, Rainer Birck, Hans-Peter Hammes, and Urs Benck

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520 |a Objective To analyze the performance of the 1 mg dexamethasone suppression test (DST) in patients with obesity. Special attention was paid to the influence of interfering medication on DST. Methods In this prospective cohort study (Mannheim Obesity Study), patients with obesity were evaluated before bariatric surgery. For evaluation of hypercortisolism, a 1 mg dexamethasone-suppression test (DST) in all subjects was performed. Medication was assessed for possible interference. Results Two hundred seventy-eight patients with a mean age of 42.3 years (68.8% women) and a mean BMI of 47.9 ± 8.4 kg/m2 were screened. Insufficient suppression of cortisol after DST was found in 24 patients (8.6%). In two patients hypercortisolism was confirmed. The specificity for DST was calculated at 92.0%. Only CYP3A4 inducers (n = 22, 7.9%) and estrogen therapy (n = 17, 6.1%) were significantly associated with falsely elevated cortisol after DST. Regression analysis excluded any interrelation between DST and anthropometry. Conclusions Low prevalence of hypercortisolism (0.7 or <1.8%) was found. Specificity of DST in this cohort typically screened for hypercortisolism was 92.0% (≤ 50 nmol/L). DST should be avoided in patients taking CYP3A4 inducers or estrogen therapy, due to their significant interaction. In summary, the 1 mg DST is an adequate test for screening for hypercortisolism even in patients with extreme obesity. 
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