Zhang, Wei; Nowotny, Hanna; Theodoropoulou, Marily; Simon, Julia; Hemmer, Charlotte M.; Bidlingmaier, Martin; Auer, Matthias K.; Reincke, Martin; Uhlenhaut, Henriette; Reisch, Nicole (2023): E47 as a novel glucocorticoid-dependent gene mediating lipid metabolism in patients with endogenous glucocorticoid excess. Frontiers in Endocrinology, 14: 1249863. ISSN 1664-2392
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Abstract
Purpose
E47 has been identified as a modulating transcription factor of glucocorticoid receptor target genes, its loss protecting mice from metabolic adverse effects of glucocorticoids. We aimed to analyze the role of E47 in patients with endogenous glucocorticoid excess [Cushing’s syndrome (CS)] and its association with disorders of lipid and glucose metabolism.
Methods
This is a prospective cohort study including 120 female patients with CS (ACTH-dependent = 79; ACTH-independent = 41) and 26 healthy female controls. Morning whole blood samples after an overnight fast were used to determine E47 mRNA expression levels in patients with overt CS before and 6–12 months after curative surgery. Expression levels were correlated with the clinical phenotype of the patients. Control subjects underwent ACTH stimulation tests and dexamethasone suppression tests to analyze short-term regulation of E47.
Results
E47 gene expression showed significant differences in patient cohorts with overt CS vs. patients in remission ( p = 0.0474) and in direct intraindividual comparisons pre- vs. post-surgery ( p = 0.0353). ACTH stimulation of controls resulted in a significant decrease of E47 mRNA expression 30 min after i.v. injection compared to baseline measurements. Administration of 1 mg of dexamethasone overnight in controls did not change E47 mRNA expression. E47 gene expression showed a positive correlation with total serum cholesterol ( p = 0.0036), low-density lipoprotein cholesterol ( p = 0.0157), and waist–arm ratio ( p = 0.0138) in patients with CS in remission.
Conclusion
E47 is a GC-dependent gene that is upregulated in GC excess potentially aiming at reducing metabolic glucocorticoid side effects such as dyslipidemia.
Doc-Type: | Article (LMU Hospital) |
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Organisational unit (Faculties): | 07 Medicine > Medical Center of the University of Munich > Medical Clinic and Outpatient Clinic IV (Endocrinology, nephrology, other sections) |
DFG subject classification of scientific disciplines: | Life sciences |
Date Deposited: | 05. Dec 2023 08:42 |
Last Modified: | 07. Dec 2023 12:20 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/1051 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 325768017 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 491502892 |