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Expanding genetic spectrum and discriminatory role of steroid profiling by LC-MS/MS in 11β-hydroxylase deficiency
- Source :
- Clinical endocrinologyREFERENCES. 94(4)
- Publication Year :
- 2020
-
Abstract
- Objective To report clinical, hormonal and structural effects of CYP11B1 pathogenic variations in Indian patients with 11β-hydroxylase deficiency (11βOHD) and find hormonal criteria that accurately distinguish 11βOHD from 21α-hydroxylase deficiency (21OHD). Design Retrospective record review of genetically diagnosed patients with 11βOHD. Patients and measurements Clinical features, hormonal parameters at diagnosis (by immunoassay) and recent follow-up of 13 genetically proven 11βOHD patients managed at our centre were retrospectively reviewed. ACTH-stimulated serum adrenal steroids (measured by LC-MS/MS) of 11βOHD were compared with those of simple virilizing and non-classic 21OHD. Structural analysis of the observed pathogenic variations was performed by computational modelling. Results Nine (four females) and four (all females) patients had classic and non-classic disease, respectively. All 11βOHD patients had elevated ACTH-stimulated serum 11-deoxycortisol (26.5-342.7 nmol/L) whereas none had elevated serum 17-hydroxyprogesterone (4.2-21.2 nmol/L); both hormonal parameters distinguished 11βOHD from 21OHD with 100% accuracy. ACTH-stimulated serum cortisol, but not 11-deoxycortisol, clearly distinguished classic ( 160 nmol/L) disease. Thirteen (eight novel, two recurrent) pathogenic variants were observed. Only missense mutations were observed among patients with non-classic disease. Computational modelling predicted the possible affection of enzyme structure and function for all the observed missense mutations. Conclusions This first Indian study describes 13 11βOHD patients, including four with the rarer non-classic variant. A total of eight novel pathogenic variants were identified in our study, highlighting regional genetic heterogeneity. Measurement of ACTH-stimulated adrenal steroids by LC-MS/MS will help avoid the misdiagnosis of 11βOHD as 21OHD and has potential to distinguish classic from non-classic 11βOHD.
- Subjects :
- Male
medicine.medical_specialty
Endocrinology, Diabetes and Metabolism
030209 endocrinology & metabolism
Disease
Gastroenterology
03 medical and health sciences
0302 clinical medicine
Endocrinology
Tandem Mass Spectrometry
Internal medicine
medicine
Missense mutation
Humans
Congenital adrenal hyperplasia
Steroid 11-beta-hydroxylase
Retrospective Studies
medicine.diagnostic_test
Adrenal Hyperplasia, Congenital
business.industry
Genetic heterogeneity
medicine.disease
Enzyme structure
030220 oncology & carcinogenesis
Immunoassay
Mutation
Steroid 11-beta-Hydroxylase
Female
Steroids
business
Hormone
Chromatography, Liquid
Subjects
Details
- ISSN :
- 13652265
- Volume :
- 94
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Clinical endocrinologyREFERENCES
- Accession number :
- edsair.doi.dedup.....3033b389b422cf8ab338b0885e22003f