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11β-HSD1 inhibition in men mitigates prednisolone-induced adverse effects in a proof-of-concept randomised double-blind placebo-controlled trial

Nantia Othonos, Riccardo Pofi, Anastasia Arvaniti, Sarah White, Ilaria Bonaventura, Nikolaos Nikolaou, Ahmad Moolla, Thomas Marjot, Roland H. Stimson, André P. Beek, Martijn Faassen, Andrea M. Isidori, Elizabeth Bateman, Ross Sadler, Fredrik Karpe, Paul M. Stewart, Craig Webster, Joanne Duffy, Richard Eastell, Fatma Gossiel, Thomas Cornfield, Leanne Hodson, K. Jane Escott, Andrew Whittaker, Ufuk Kirik, Ruth L. Coleman, Charles A. B. Scott, Joanne E. Milton, Olorunsola Agbaje, Rury R. Holman and Jeremy W. Tomlinson ()
Additional contact information
Nantia Othonos: Churchill Hospital
Riccardo Pofi: Churchill Hospital
Anastasia Arvaniti: Churchill Hospital
Sarah White: Churchill Hospital
Ilaria Bonaventura: Churchill Hospital
Nikolaos Nikolaou: Churchill Hospital
Ahmad Moolla: Churchill Hospital
Thomas Marjot: Churchill Hospital
Roland H. Stimson: University of Edinburgh
André P. Beek: University Medical Center Groningen
Martijn Faassen: University Medical Center Groningen
Andrea M. Isidori: Sapienza University of Rome
Elizabeth Bateman: Churchill Hospital
Ross Sadler: Churchill Hospital
Fredrik Karpe: Churchill Hospital
Paul M. Stewart: University of Leeds
Craig Webster: NHS Foundation Trust
Joanne Duffy: NHS Foundation Trust
Richard Eastell: Dentistry & Health, University of Sheffield
Fatma Gossiel: Dentistry & Health, University of Sheffield
Thomas Cornfield: Churchill Hospital
Leanne Hodson: Churchill Hospital
K. Jane Escott: BioPharmaceuticals R&D, AstraZeneca
Andrew Whittaker: BioPharmaceuticals R&D, AstraZeneca
Ufuk Kirik: BioPharmaceuticals R&D AstraZeneca
Ruth L. Coleman: Churchill Hospital
Charles A. B. Scott: Churchill Hospital
Joanne E. Milton: Churchill Hospital
Olorunsola Agbaje: Churchill Hospital
Rury R. Holman: Churchill Hospital
Jeremy W. Tomlinson: Churchill Hospital

Nature Communications, 2023, vol. 14, issue 1, 1-12

Abstract: Abstract Glucocorticoids prescribed to limit inflammation, have significant adverse effects. As 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) regenerates active glucocorticoid, we investigated whether 11β-HSD1 inhibition with AZD4017 could mitigate adverse glucocorticoid effects without compromising their anti-inflammatory actions. We conducted a proof-of-concept, randomized, double-blind, placebo-controlled study at Research Unit, Churchill Hospital, Oxford, UK (NCT03111810). 32 healthy male volunteers were randomized to AZD4017 or placebo, alongside prednisolone treatment. Although the primary endpoint of the study (change in glucose disposal during a two-step hyperinsulinemic, normoglycemic clamp) wasn’t met, hepatic insulin sensitivity worsened in the placebo-treated but not in the AZD4017-treated group. Protective effects of AZD4017 on markers of lipid metabolism and bone turnover were observed. Night-time blood pressure was higher in the placebo-treated but not in the AZD4017-treated group. Urinary (5aTHF+THF)/THE ratio was lower in the AZD4017-treated but remained the same in the placebo-treated group. Most anti-inflammatory actions of prednisolone persisted with AZD4017 co-treatment. Four adverse events were reported with AZD4017 and no serious adverse events. Here we show that co-administration of AZD4017 with prednisolone in men is a potential strategy to limit adverse glucocorticoid effects.

Date: 2023
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DOI: 10.1038/s41467-023-36541-w

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