ESPE Abstracts (2018) 89 P-P1-005

ESPE2018 Poster Presentations Adrenals and HPA Axis P1 (24 abstracts)

Elevated Concentrations of Adrenal Steroid Precursors with Glucocorticoid Activity Might Prevent Addisonian Crisis in Untreated Patients with Classic Congenital Adrenal Hyperplasia

Manon Engels a, , Karijn Pijnenburg-Kleizen a , Agustini Utari c, , Sultana Faradz c , Joop Heuvel b , Teun van Herwaarden b , Paul Span e , Fred Sweep b & Hedi Claahsen-van der Grinten a

aDepartment of Pediatrics, Radboud University Medical Center, Radboud Amalia Children’s Hospital, Nijmegen, Netherlands; bDepartment of Laboratory Medicine, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands; cDiponegoro University Faculty of Medicine, Center for Biomedical Research (CEBIOR), Semarang, Indonesia; dDepartment of Pediatric Endocrinology, Diponegoro University Faculty of Medicine, Division of Pediatric Endocrinology, Semarang, Indonesia; eDepartment of Radiation Oncology, Radiotherapy & OncoImmunology Laboratory, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands

Introduction: Congenital adrenal hyperplasia (CAH) is most often caused by 21-hydroxylase deficiency (21OHD: 95%) or by 11-hydroxylase deficiency (11OHD). Classic CAH results in impaired cortisol production and consequently elevated ACTH concentrations leading to chronic adrenal stimulation with strongly elevated adrenal steroid precursors before the enzymatic defect. In contrast to other forms of adrenal insufficiency, some untreated classic CAH patients seem to have less clinical signs of cortisol deficiency.

Hypothesis: Elevated adrenal steroid precursors have agonistic glucocorticoid receptor (GR) activity, thereby compensating for the cortisol deficiency in CAH patients.

Methods: Clinical data of untreated classic CAH patients (age 3–46 years) from Indonesia (n=22) were collected. Adrenal steroids and precursors were measured by LC-MS/MS before and after ACTH stimulation. In vitro GR transactivation studies were performed using a dual luciferase assay in HEK293 cells transfected with the GR, that were incubated for 24 hours with increasing concentrations of steroids.

Results: Thirteen untreated classic CAH patients (59%) reported severe stress situations in the past: genital surgery (n=6), vomiting and/or seizures (n=5) or dengue or typhoid fever (n=3). All patients improved without application of glucocorticoid medication. Serum morning cortisol concentrations (before 9.00 am) were low without any increase after ACTH stimulation (median 73 (21OHD) and 180 (11OHD) nmol/l). Adrenal steroid precursors were strongly elevated (in 21OHD: 17-hydroxyprogesterone, 21-deoxycortisol, progesterone and in 11OHD: 11-deoxycortisol, deoxycorticosterone) without increase after ACTH stimulation. In vitro exposure of HEK293 cells showed that the GR was activated with similar potency to cortisol by corticosterone and 21-deoxycortisol. 11β-hydroxyprogesterone, 11-deoxycortisol, aldosterone, deoxycorticosterone, progesterone and 17-hydroxyprogesterone also led to GR transactivation, with a 4-100x lower potency than cortisol.

Conclusion: Untreated classic CAH patients may survive in severe stress situations even without application of stress-dosing of glucocorticoids. The elevated concentrations of adrenal steroid precursors, which are able to activate the GR, might compensate for the cortisol deficiency. Further studies have to be performed to study the clinical consequences of these findings.

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