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3,265,266 Classical and non-classical congenital adrenal hyperplasia (CAH and NC-CAH) are autosomal recessive diseases that cause adrenal steroid 21-hydroxylase deficiency

Some patients use them together, particularly those who reach a body-composition plateau on a GLP-1 with persistent central adiposity

Discussion We used nationwide registers in three Scandinavian countries to conduct two cohort studies that assessed the risk of cholangiocarcinoma associated with use of DPP4 inhibitors and GLP-1-receptor agonists, respectively

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An Insight into Pharmaceutical Design and Pharmacokinetic Characteristics of GLP-1 RAs