OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose

Amazit, Larbi;Barbot, Mattia;Beau, Isabelle;Bouligand, Jérôme;Chasseloup, Fanny;et.al.
(2022) Annual Meeting of the Endocrine Society 2022 — Location: (United States) Atlanta, GA (11.June.2022)

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Authors
  • Amazit, Larbi
    Author
  • Barbot, Mattia
    Author
  • Beau, Isabelle
    Author
  • Bouligand, Jérôme
    Author
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  • Chasseloup, Fanny
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Abstract
CONTEXT : Primary bilateral macronodular adrenal hyperplasia (PBMAH) with glucose-dependent insulinotropic polypeptide (GIP)-dependent Cushing's syndrome is caused by ectopic expression of GIP receptor (GIPR) in the adrenal lesions. Such ectopic expression of GIPR was also reported in other endocrine neoplasm, notably in somatotroph pituitary adenomas from acromegalic patients with paradoxical increase of GH after oral glucose load, suggesting a common molecular pathogenesis. We aimed to identify the driver event responsible for GIP-dependent PBMAH with Cushing's syndrome and ectopic GIPR expression in somatotropinomas. [...]
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Amazit, L., Barbot, M., Beau, I., Bouligand, J., Bourdeau, I., Chanson, P., Cloix, L., Corbeil, G., de Herder, W., Deméocq, V., Desailloud, R., Dumontet, C., Dupeux, M., Emy, P., Fiore, F., Guiochon-Mantel, A., Kamenicky, P., Lacroix, A., Ladurelle, N., et al. (2022). OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing’s Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose. Journal of the Endocrine Society, 6(Suppl 1), A81. https://doi.org/10.1210/jendso/bvac150.168 (Original work published 2022)