Clinical trial
Evaluation of Cortisol and Bile Acids Metabolism in Obese Patients
Recruiting now · Not applicable · 1 countries · Registry ID NCT04844684
What this study is about
Bariatric surgery is currently the most efficient treatment for obesity. The sustained weight loss and metabolic improvement seen following Roux-en-Y gastric bypass (RYGB), is explained partly by modifications in hormones including bile acids (BA). After RYGB, an increased total BA pool and a reduction in hepatic cortisol exposure is observed. Hydroxysteroid 11-β dehydrogenase 1 (HSD11B1), steroid 5α-reductases (SRD5A), and steroid 5β-reductases, AKR1D1 (also a BA metabolizing enzyme), are three enzymes involved in the metabolism of cortisol in the liver and are known to participate in metabolic syndrome. Their activity has been shown to be decreased after RYGB. Interestingly, the mechanisms explaining the modification of hepatic cortisol exposure and the activity of theses enzymes after RYGB are unknown. In view of the few data suggesting a link between cortisol metabolism and bile acids, this work aim to study and characterize this link in a context of RYBP
Basic eligibility
Full registry criteria
Treatments and study arms
Blood and urine collection
Blood sampling urine collections before RYGP and 1 month and 1 year after.
Primary outcomes
Study locations
1 locations were listed when this page was built. The first 40 are shown.