SAT-420 First Insights into the Health Status of Adults with CAH in the UK and Ireland - CaHASE2

Abstract Disclosure: I.A. Bacila: None. R. Welch: None. S. Adam: None. S.F. Ahmed: None. M. Alimussina: None. E. Chinnasamy: None. E.C. Crowne: None. J.H. Davies: None. A. Davis: None. J. Davis: None. M. Debono: None. S. Elford: None. Y. Elhassan: None. G. Gazdagh: None. H. Gleeson: None. L. James: None. M. Korbonits: None. S. Llanaha: None. J.M. Lynch: None. S. McGeoch: None. A. Mitchell: None. R.D. Murray: None. S. Nedelcu: None. G. Okoro: None. M.W. O'Reilly: None. A. Rees: None. R. Scott: None. R.H. Stimson: None. A. Thankamony: None. J.W. Tomlinson: None. B. Vaidya: None. N.P. Krone: None. Background: Congenital adrenal hyperplasia (CAH) is one of the commonest forms of primary adrenal insufficiency with an incidence of about 1 in 15,000. Previous studies have highlighted the suboptimal health status and care provision in adults with CAH and these were associated with significant co-morbidities. In 2023, we implemented CaHASE2 (https://www.endocrinology.org/clinical-practice/research-projects/cahase-2/) to develop a strategy for prospective collection of longitudinal data. Our recent CAH service evaluation suggested significant differences in the approach to CAH patients. Aim: To identify specific unmet needs in the care of people living with CAH, through standardised phenotyping across all participating centres. Methods: In September 2023, PIs agreed a minimal dataset for the collection of real-world data for participating centres. The data is collected using the international CAH registry (I-CAH; https://sdmregistries.org/). CaHASE2 was launched in November 2023. Results: To date, 351 adults (213 females, 138 males) with CAH have been recruited and 1213 clinic visits were available for analysis. There is a preponderance of younger to middle-aged adults in the currently available datasets (median age 42 years, range 23-88). Preliminary analysis suggests a temporal change in glucocorticoid choice over time with an increased use of hydrocortisone and a decreased use of prednisolone. Analysis of 17OHP concentrations shows that a significant proportion of patients are overtreated. A significant proportion of patients are overweight or obese. Currently 18 centres are actively recruiting and 5 are awaiting local approval to use the I-CAH registry. The data will be analysed in 12-month cycles, to assess the current level of care provision and inform the development of CAH standards. In addition, we will establish a report that will provide centres with information about their local care provision in relation to other centres. Conclusions: The CaHASE2 project will provide important information about the health status of adults with CAH and how this might be related to differences in health care provision. Ultimately, such data should lead to a higher degree of equality of service provision in all parts of the UK and Ireland. Presentation: Saturday, July 12, 2025

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Journal
Journal of the Endocrine Society
Published
2025-10-01
DOI
https://doi.org/10.1210/jendso/bvaf149.288
Primary Topic
Sexual Differentiation and Disorders
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article
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article

SAT-420 First Insights into the Health Status of Adults with CAH in the UK and Ireland - CaHASE2

Journal of the Endocrine Society
Sexual Differentiation and Disorders
article

SAT-420 First Insights into the Health Status of Adults with CAH in the UK and Ireland - CaHASE2

article en

Abstract

Abstract Disclosure: I.A. Bacila: None. R. Welch: None. S. Adam: None. S.F. Ahmed: None. M. Alimussina: None. E. Chinnasamy: None. E.C. Crowne: None. J.H. Davies: None. A. Davis: None. J. Davis: None. M. Debono: None. S. Elford: None. Y. Elhassan: None. G. Gazdagh: None. H. Gleeson: None. L. James: None. M. Korbonits: None. S. Llanaha: None. J.M. Lynch: None. S. McGeoch: None. A. Mitchell: None. R.D. Murray: None. S. Nedelcu: None. G. Okoro: None. M.W. O'Reilly: None. A. Rees: None. R. Scott: None. R.H. Stimson: None. A. Thankamony: None. J.W. Tomlinson: None. B. Vaidya: None. N.P. Krone: None. Background: Congenital adrenal hyperplasia (CAH) is one of the commonest forms of primary adrenal insufficiency with an incidence of about 1 in 15,000. Previous studies have highlighted the suboptimal health status and care provision in adults with CAH and these were associated with significant co-morbidities. In 2023, we implemented CaHASE2 (https://www.endocrinology.org/clinical-practice/research-projects/cahase-2/) to develop a strategy for prospective collection of longitudinal data. Our recent CAH service evaluation suggested significant differences in the approach to CAH patients. Aim: To identify specific unmet needs in the care of people living with CAH, through standardised phenotyping across all participating centres. Methods: In September 2023, PIs agreed a minimal dataset for the collection of real-world data for participating centres. The data is collected using the international CAH registry (I-CAH; https://sdmregistries.org/). CaHASE2 was launched in November 2023. Results: To date, 351 adults (213 females, 138 males) with CAH have been recruited and 1213 clinic visits were available for analysis. There is a preponderance of younger to middle-aged adults in the currently available datasets (median age 42 years, range 23-88). Preliminary analysis suggests a temporal change in glucocorticoid choice over time with an increased use of hydrocortisone and a decreased use of prednisolone. Analysis of 17OHP concentrations shows that a significant proportion of patients are overtreated. A significant proportion of patients are overweight or obese. Currently 18 centres are actively recruiting and 5 are awaiting local approval to use the I-CAH registry. The data will be analysed in 12-month cycles, to assess the current level of care provision and inform the development of CAH standards. In addition, we will establish a report that will provide centres with information about their local care provision in relation to other centres. Conclusions: The CaHASE2 project will provide important information about the health status of adults with CAH and how this might be related to differences in health care provision. Ultimately, such data should lead to a higher degree of equality of service provision in all parts of the UK and Ireland. Presentation: Saturday, July 12, 2025

Journal of the Endocrine SocietyVol. 9(Supplement_1)
Cardiff and Vale University Health Board (GB), Queen Mary University of London (GB), City, University of London (GB), Leeds Teaching Hospitals NHS Trust (GB), Southampton Hospital (US), Society for Endocrinology (GB), Royal Hospital for Children (GB), Royal Victoria Infirmary (GB), Aberdeen Royal Infirmary (GB), Royal Devon and Exeter Hospital (GB), Kingston Hospital NHS Trust (GB), Beaumont Hospital (IE), Bristol Royal Hospital for Children (GB), University of Oxford (GB), Bedford Research Foundation (US), The Christie Hospital (GB), Chelsea and Westminster Hospital (GB), NIHR Surgical Reconstruction and Microbiology Research Centre (GB), Addenbrooke's Hospital (GB), Cardiff University (GB), University of Sheffield (GB), University of Edinburgh (GB)
Partnerships for the goals
Openalex Percentile: Top 44%
Sexual Differentiation and Disorders
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