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GIP receptor antagonism eliminates paradoxical growth hormone secretion in some patients with acromegaly

Title: GIP receptor antagonism eliminates paradoxical growth hormone secretion in some patients with acromegaly
Authors: Jensen, Mette H; Gasbjerg, Lærke S; Skov-Jeppesen, Kirsa; Jacobsen, Jens C B; Poulsen, Steen S; Zhou, Cuiqi; Jakubauskaite, Ruta; Poulsen, Frantz R; Bonde, Christian; Albarazi, Mahmoud; Halle, Bo; Christiansen, Charlotte B; Sanni, Samra J; Byberg, Sarah; Hoe, Bjørn; Holst, Jens J; Dela, Flemming; Rasmussen, Aase K; Knop, Filip K; Arlien-Søborg, Mai C; Melmed, Shlomo; Jørgensen, Jens Otto L; Andersen, Marianne S; Jørgensen, Jens Otto Lunde; Hartmann, Bolette; Klose, Marianne C; Feldt-Rasmussen, Ulla; Sparre-Ulrich, Alexander H; Rosenkilde, Mette M
Source: Jensen, M H, Gasbjerg, L S, Skov-Jeppesen, K, Jacobsen, J C B, Poulsen, S S, Zhou, C, Jakubauskaite, R, Poulsen, F R, Bonde, C, Albarazi, M, Halle, B, Christiansen, C B, Sanni, S J, Byberg, S, Hoe, B, Holst, J J, Dela, F, Rasmussen, A K, Knop, F K, Arlien-Søborg, M C, Melmed, S, Jørgensen, J O L, Andersen, M S, Jørgensen, J O L, Hartmann, B, Klose, M C, Feldt-Rasmussen, U, Sparre-Ulrich, A H & Rosenkilde, M M 2025, 'GIP receptor antagonism eliminates paradoxical growth hormone secretion in some patients with acromegaly', The Journal of clinical endocrinology and ....
Publication Year: 2025
Collection: Aarhus University: Research
Subject Terms: GIP receptor antagonism; acromegaly; glucose-dependent insulinotropic polypeptide (GIP); growth hormone (GH); paradoxical GH secretion
Description: Context: About 30% of patients with active acromegaly experience paradoxically increased growth hormone (GH) secretion during the diagnostic oral glucose tolerance test (OGTT). Endogenous glucose-dependent insulinotropic polypeptide (GIP) is implicated in this paradoxical secretion. Objective: We used the GIP receptor (GIPR) antagonist GIP(3-30)NH 2 to test the hypothesis that GIP mediates this paradoxical response when GIPR is abundantly expressed in somatotropinomas. Methods: A total of 25 treatment-naive patients with acromegaly were enrolled. Each patient underwent one OGTT during simultaneous placebo infusion and one OGTT during a GIP(3-30)NH 2 infusion. Blood samples were drawn at baseline and regularly after infusions to measure GH. We assessed pituitary adenoma size by magnetic resonance imaging and GIPR expression by immunohistochemistry on resected somatotropinomas. For mechanistic confirmation, we applied in vitro and ex vivo approaches. The main outcome measure was the effect of GIP(3-30)NH 2 on paradoxical GH secretion during OGTT as a measure of GIP involvement. Results: In 4 of 7 patients with paradoxical GH secretion, GIP(3-30)NH 2 infusion completely abolished the paradoxical response (P =. 0003). Somatotrophs were available from 3 of 4 of these patients, all showing abundant GIPR expression. Adenoma size did not differ between patients with and without paradoxical GH secretion. Conclusion: Of 25 patients with acromegaly, 7 had paradoxical GH secretion during OGTT, and pharmaceutical GIPR blockade abolished this secretion in 4. Corresponding somatotroph adenomas abundantly expressed GIPR, suggesting a therapeutic target in this subpopulation of patients. In vitro and ex vivo analyses confirmed the role of GIP and the effects of the antagonist.
Document Type: article in journal/newspaper
Language: English
ISSN: 0021-972X; 1945-7197
Relation: info:eu-repo/semantics/altIdentifier/pmid/39172542; info:eu-repo/semantics/altIdentifier/pissn/0021-972X; info:eu-repo/semantics/altIdentifier/eissn/1945-7197
DOI: 10.1210/clinem/dgae583
Availability: https://pure.au.dk/portal/en/publications/a6651425-eda5-490f-ad7b-e79c199ab5c6; https://doi.org/10.1210/clinem/dgae583; https://www.scopus.com/pages/publications/85213692573
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.AB28F26F
Database: BASE