Your browser doesn't support javascript.
loading
Comparison of modified-release hydrocortisone capsules versus prednisolone in the treatment of congenital adrenal hyperplasia.
Rees, Dafydd Aled; Merke, Deborah P; Arlt, Wiebke; Brac De La Perriere, Aude; Hirschberg, Angelica Linden; Juul, Anders; Newell-Price, John; Prete, Alessandro; Reisch, Nicole; Stikkelbroeck, Nike M; Touraine, Philippe A; Lewis, Alex; Porter, John; Coope, Helen; Ross, Richard J.
Afiliação
  • Rees DA; Cardiff University, Cardiff, United Kingdom.
  • Merke DP; National Institutes of Health Clinical Center and the Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, USA.
  • Arlt W; MRC LMS, London, United Kingdom.
  • Brac De La Perriere A; Hospices Civils de Lyon - GHE - Endocrinologie, Bron, France.
  • Hirschberg AL; Karolinska Institute, Solna, Sweden.
  • Juul A; Department of Growth and Reproduction, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark, and Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Newell-Price J; The University of Sheffield, Sheffield, United Kingdom.
  • Prete A; University of Birmingham, Birmingham, United Kingdom.
  • Reisch N; Endokrinologie, Nephrologie und weitere Sektionen - Medizinische Klinik und Poliklinik IV - Campus Innenstadt, München, Germany.
  • Stikkelbroeck NM; Radboud University Nijmegen, Nijmegen, Netherlands.
  • Touraine PA; University Hospitals Pitié Salpêtrière - Charles Foix, Paris, France.
  • Lewis A; Neurocrine Biosciences Inc, London, United Kingdom.
  • Porter J; Neurocrine Biosciences Inc, London, United Kingdom.
  • Coope H; Neurocrine Biosciences Inc, London, United Kingdom.
  • Ross RJ; The University of Sheffield, Sheffield, United Kingdom.
Endocr Connect ; 13(8)2024 Aug 01.
Article em En | MEDLINE | ID: mdl-38934378
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 0900-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 0900 h compared to prednis(ol)one and the dose of MRHC can be down-titrated over time in the majority of patients.
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Endocr Connect Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Endocr Connect Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido