Rees, Aled Daffyd ORCID: https://orcid.org/0000-0002-1165-9092, Merke, Deborah P., Arlt, Wiebke, Brac de la Perrière, Aude, Linden-Hirschberg, Angelica, Juul, Anders, Newell-Price, John, Prete, Alessandro, Reisch, Nicole, Stikkelbroeck, Nike M., Touraine, Philippe, Lewis, Alex, Porter, John, Coope, Helen and Ross, Richard J. 2024. Comparison of modified-release hydrocortisone capsules versus prednisolone in the treatment of congenital adrenal hyperplasia. Endocrine Connections 13 (8) , e240150. 10.1530/EC-24-0150 |
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Abstract
Background: Prednisolone and prednisone are recommended treatment options for adults with congenital adrenal hyperplasia (CAH); however, there is no randomised comparison of prednis(ol)one with hydrocortisone. Design: Six-month open-label randomised phase 3 study and interim analysis of a single-arm extension study was the design of the study. Methods: The method of the study was hydrocortisone dose equivalent and 09:00-h 17-hydroxyprogesterone (17OHP) from 48 patients taking prednis(ol)one at baseline. Results: At baseline, the median hydrocortisone dose equivalent was 30 mg/day and 17OHP was < 36 nmol/L (3× upper limit of normal) in 56% of patients. Patients were randomised to continue prednis(ol)one or switch to modified-release hydrocortisone capsule (MRHC) at the same hydrocortisone-equivalent dose. At 4 weeks, 94% on MRHC and 71% on prednis(ol)one had 17OHP < 36 nmol/L. At 18 months in the extension study of MRHC, the median MRHC dose was 20 mg/day and 82% had 17OHP < 36 nmol/L. The per cent of patients with 17OHP < 36 nmol/L on a hydrocortisone dose equivalent ≤ 25 mg/day was greater at 18 months in the extension study on MRHC than while on prednis(ol)one at baseline: 57% vs 27%, P = 0.04. In the randomised study, no patients had an adrenal crisis on MRHC and one on prednisolone. In the extension study (221 patient years), there were 12 adrenal crises in 5 patients (5.4/100 patient years). Conclusion: MRHC reduces 17OHP at 09:00 h compared to prednis(ol)one and the dose of MRHC can be down-titrated over time in the majority of patients.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) |
Publisher: | BioScientifica |
ISSN: | 2049-3614 |
Date of First Compliant Deposit: | 10 July 2024 |
Date of Acceptance: | 27 June 2024 |
Last Modified: | 18 Jul 2024 11:30 |
URI: | https://orca.cardiff.ac.uk/id/eprint/170485 |
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