Genetic analysis of pediatric primary adrenal insufficiency of unknown etiology: 25 years’ experience in the UK

Buonocore, F. et al. (2021) Genetic analysis of pediatric primary adrenal insufficiency of unknown etiology: 25 years’ experience in the UK. Journal of the Endocrine Society, 5(8), bvab086. (doi: 10.1210/jendso/bvab086) (PMID:34258490) (PMCID:PMC8266051)

Abstract

Context: Although primary adrenal insufficiency (PAI) in children and young people is often due to congenital adrenal hyperplasia (CAH) or autoimmunity, other genetic causes occur. The relative prevalence of these conditions is poorly understood. Objective: We investigated genetic causes of PAI in children and young people over a 25 year period. Design, Setting and Participants: Unpublished and published data were reviewed for 155 young people in the United Kingdom who underwent genetic analysis for PAI of unknown etiology in three major research centers between 1993 and 2018. We pre-excluded those with CAH, autoimmune, or metabolic causes. We obtained additional data from NR0B1 (DAX-1) clinical testing centers. Intervention and Outcome Measurements: Genetic analysis involved a candidate gene approach (1993 onward) or next generation sequencing (NGS; targeted panels, exomes) (2013-2018). Results: A genetic diagnosis was reached in 103/155 (66.5%) individuals. In 5 children the adrenal insufficiency resolved and no genetic cause was found. Pathogenic variants occurred in 11 genes: MC2R (adrenocorticotropin receptor; 30/155, 19.4%), NR0B1 (DAX-1; 7.7%), CYP11A1 (7.7%), AAAS (7.1%), NNT (6.5%), MRAP (4.5%), TXNRD2 (4.5%), STAR (3.9%), SAMD9 (3.2%), CDKN1C (1.3%), and NR5A1/steroidogenic factor-1 (SF-1; 0.6%). Additionally, 51 boys had NR0B1 variants identified through clinical testing. Although age at presentation, treatment, ancestral background, and birthweight can provide diagnostic clues, genetic testing was often needed to define the cause. Conclusions: PAI in children and young people often has a genetic basis. Establishing the specific etiology can influence management of this lifelong condition. NGS approaches improve the diagnostic yield when many potential candidate genes are involved.

• Item Type: Articles
• Additional Information: Financial Support: This research was funded in whole, or in part, by the Wellcome Trust (grants 098513/Z/12/Z and 209328/Z/17/Z).
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Shaikh, Dr Mohammed Guftar
• Authors: Buonocore, F., Maharaj, A., Qamar, Y., Koehler, K., Suntharalingham, J. P., Chan, L. F., Ferraz-de-Souza, B., Hughes, C. R., Lin, L., Prasad, R., Allgrove, J., Andrews, E. T., Buchanan, C. R., Cheetham, T. D., Crowne, E. C., Davies, J. H., Gregory, J. W., Hindmarsh, P. C., Hulse, T., Krone, N. P., Shah, P., Shaikh, M. G., Roberts, C., Clayton, P. E., Dattani, M. T., Thomas, N. S., Huebner, A., Clark, A. J., Metherell, L. A., and Achermann, J. C.
• College/School: College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
• Journal Name: Journal of the Endocrine Society
• Publisher: Oxford University Press
• ISSN: 2472-1972
• ISSN (Online): 2472-1972
• Published Online: 11 May 2021
• Copyright Holders: Copyright © The Author(s) 2021
• First Published: First published in Journal of the Endocrine Society 5(8): bvab086
• Publisher Policy: Reproduced under a Creative Commons License