Measurement of Salivary Adrenal-Specific Androgens as Biomarkers of Therapy Control in 21-Hydroxylase Deficiency

Author:

Bacila Irina1,Adaway Jo2,Hawley James2,Mahdi Sundus1,Krone Ruth3,Patel Leena4,Alvi Sabah5,Randell Tabitha6,Gevers Evelien7,Dattani Mehul8,Cheetham Timothy9,Kyriakou Andreas10,Schiffer Lina11,Ryan Fiona12,Crowne Elizabeth13,Davies Justin H14,Ahmed Syed Faisal10,Keevil Brian15,Krone Nils1ORCID

Affiliation:

1. Academic Unit of Child Health, Department of Oncology and Metabolism, University of Sheffield, Sheffield, United Kingdom

2. Department of Biochemistry, Manchester University NHS Foundation Trust, Manchester, United Kingdom

3. Birmingham Women’s & Children’s Hospital, Birmingham, United Kingdom

4. University of Manchester, Manchester, United Kingdom

5. Leeds General Infirmary, Leeds, United Kingdom

6. Nottingham Children’s Hospital, Nottingham, United Kingdom

7. Queen Mary University London and Barts Health NHS Trust, The Royal London Hospital, London, United Kingdom

8. Great Ormond Street Hospital, London, United Kingdom

9. Great North Children’s Hospital, University of Newcastle, Newcastle, United Kingdom

10. Developmental Endocrinology Research Group, University of Glasgow, Glasgow, United Kingdom

11. Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom

12. Oxford Children's Hospital, Oxford, United Kingdom

13. Bristol Royal Hospital for Children, University Hospitals Bristol Foundation Trust, Bristol, United Kingdom

14. University Hospital Southampton, Southampton, United Kingdom

15. Department of Clinical Biochemistry, Wythenshawe Hospital, Manchester, United Kingdom

Abstract

AbstractBackgroundMonitoring of hormonal control represents a key part of the management of congenital adrenal hyperplasia (CAH). Monitoring strategies remain suboptimal because they rely on frequent blood tests and are not specific for adrenal-derived hormones. Recent evidence suggests the crucial role of adrenal-specific 11-oxygenated-C19 androgens in the pathogenesis of CAH.ObjectiveTo establish a correlation between plasma and salivary adrenal-specific androgens in CAH as a noninvasive monitoring strategy.DesignThis prospective cross-sectional study recruited patients between 2015 and 2018.SettingMulticenter study including 13 tertiary centers in the United Kingdom.ParticipantsSeventy-eight children with CAH and 62 matched healthy controls.MethodsUsing liquid chromatography–tandem mass spectrometry, plasma and salivary concentrations of five steroids were measured: 17-hydroxyprogesterone (17OHP), androstenedione (A4), testosterone (T), 11-hydroxyandrostenedione (11OHA4), and 11-ketotestosterone (11KT). The correlation between plasma and salivary steroids was analyzed to assess their use in clinical practice.ResultsStrong correlations between plasma and salivary steroid concentrations in patients with CAH were detected: 17OHP (rs = 0.871; P < 0.001), A4 (rs = 0.931; P < 0.001), T (rs = 0.867; P < 0.001), 11OH4A (rs = 0.876; P < 0.001), and 11KT (rs = 0.944; P < 0.001). These results were consistent for patient subgroups based on sex and age. Analysis of patient subgroups based on 17OHP concentrations established clear correlations between plasma and salivary concentrations of the adrenal-specific androgen 11KT.ConclusionsThe current study identified tight correlations between plasma and saliva for the adrenal-derived 11-oxygenated C19 androgen 11KT, as well as 17OHP and A4, which are widely used for monitoring treatment in CAH. This combination of steroid hormones will serve as an improved noninvasive salivary test for disease monitoring in patients with CAH.

Funder

National Institutes of Health Research Rare Disease Translational Research Collaboration

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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