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Ultradian hydrocortisone replacement alters neuronal processing, emotional ambiguity, affect and fatigue in adrenal insufficiency: The PULSES trial.

Authors :
Russell, Georgina
Kalafatakis, Konstantinos
Durant, Claire
Marchant, Nicola
Thakrar, Jamini
Thirard, Russell
King, Jade
Bowles, Jane
Upton, Thomas
Thai, Ngoc Jade
Brooks, Jonathan C. W.
Wilson, Aileen
Phillips, Kirsty
Ferguson, Stuart
Grabski, Meryem
Rogers, Chris A.
Lampros, Theodoros
Wilson, Sue
Harmer, Catherine
Munafo, Marcus
Source :
Journal of Internal Medicine; Jan2024, Vol. 295 Issue 1, p51-67, 17p
Publication Year :
2024

Abstract

Background: Primary adrenal insufficiency (PAI) mortality and morbidity remain unacceptably high, possibly arising as glucocorticoid replacement does not replicate natural physiology. A pulsatile subcutaneous pump can closely replicate cortisol's circadian and ultradian rhythm. Objectives: To assess the effect of pump therapy on quality of life, mood, functional neuroimaging, behavioural/cognitive responses, sleep and metabolism. Methods: A 6‐week randomised, crossover, double‐blinded and placebo‐controlled feasibility study of usual dose hydrocortisone in PAI administered as either pulsed subcutaneous or standard care in Bristol, United Kingdom (ISRCTN67193733). Participants were stratified by adrenal insufficiency type. All participants who received study drugs are included in the analysis. The primary outcome, the facial expression recognition task (FERT), occurred at week 6. Results: Between December 2014 and 2017, 22 participants were recruited – 20 completed both arms, and 21 were analysed. The pump was well‐tolerated. No change was seen in the FERT primary outcome; however, there were subjective improvements in fatigue and mood. Additionally, functional magnetic resonance imaging revealed differential neural processing to emotional cues and visual stimulation. Region of interest analysis identified the left amygdala and insula, key glucocorticoid‐sensitive regions involved in emotional ambiguity. FERT post hoc analysis confirmed this response. There were four serious adverse events (AE): three intercurrent illnesses requiring hospitalisation (1/3, 33.3% pump) and a planned procedure (1/1, 100% pump). There was a small number of expected AEs: infusion site bruising/itching (3/5, 60% pump), intercurrent illness requiring extra (3/7, 42% pump) and no extra (4/6, 66% pump) steroid. Conclusions: These findings support the administration of hormone therapy that mimics physiology. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09546820
Volume :
295
Issue :
1
Database :
Complementary Index
Journal :
Journal of Internal Medicine
Publication Type :
Academic Journal
Accession number :
174325816
Full Text :
https://doi.org/10.1111/joim.13721