11-Oxygenated androgens in health and disease

AF Turcu, J Rege, RJ Auchus, WE Rainey - Nature Reviews …, 2020 - nature.com
The adrenal gland is a source of sex steroid precursors, and its activity is particularly
relevant during fetal development and adrenarche. Following puberty, the synthesis of …

[HTML][HTML] Intracrine androgen biosynthesis, metabolism and action revisited

L Schiffer, W Arlt, KH Storbeck - Molecular and cellular endocrinology, 2018 - Elsevier
Androgens play an important role in metabolic homeostasis and reproductive health in both
men and women. Androgen signalling is dependent on androgen receptor activation, mostly …

Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia

RJ Auchus, O Hamidi, R Pivonello… - … England Journal of …, 2024 - Mass Medical Soc
Background Adrenal insufficiency in patients with classic 21-hydroxylase deficiency
congenital adrenal hyperplasia (CAH) is treated with glucocorticoid replacement therapy …

Management of endocrine disease: diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency

A Nordenström, H Falhammar - European journal of …, 2019 - academic.oup.com
Non-classic congenital adrenal hyperplasia (NCAH) is a relatively common disorder
regardless of ethnicity, but most cases are never diagnosed, especially in males. A baseline …

Testicular adrenal rest tumors: current insights on prevalence, characteristics, origin, and treatment

M Engels, PN Span, AE van Herwaarden… - Endocrine …, 2019 - academic.oup.com
This review provides the reader with current insights on testicular adrenal rest tumors
(TARTs), a complication in male patients with congenital adrenal hyperplasia (CAH). In …

A new dawn for androgens: novel lessons from 11-oxygenated C19 steroids

E Pretorius, W Arlt, KH Storbeck - Molecular and cellular endocrinology, 2017 - Elsevier
The abundant adrenal C19 steroid 11β-hydroxyandrostenedione (11OHA4) has been
written off as a dead-end product of adrenal steroidogenesis. However, recent evidence has …

[PDF][PDF] Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia

K Sarafoglou, MS Kim, M Lodish, EI Felner… - New England Journal of …, 2024 - nadf.us
BACKGROUND Children with classic congenital adrenal hyperplasia (CAH) due to 21-
hydroxylase deficiency require treatment with glucocorticoids, usually at supraphysiologic …

Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency

AM Al Alawi, A Nordenström, H Falhammar - Endocrine, 2019 - Springer
Purpose 3β-hydroxysteroid dehydrogenase type 2 deficiency (3βHSD2D) is a very rare
variant of congenital adrenal hyperplasia (CAH) causing less than 0.5% of all CAH. The aim …

The interplay between stress, circadian clocks, and energy metabolism

H Oster - Journal of Endocrinology, 2020 - joe.bioscientifica.com
Endogenous circadian clocks adapt an organism's physiology and behavior to predictable
changes in the environment as a consequence of the Earth's rotation around its axis. In …

GC/MS in recent years has defined the normal and clinically disordered steroidome: will it soon be surpassed by LC/tandem MS in this role?

C Shackleton, OJ Pozo, J Marcos - Journal of the Endocrine …, 2018 - academic.oup.com
Gas chromatography/mass spectrometry (GC/MS) has been used for steroid analysis since
the 1960s. The advent of protective derivatization, capillary columns, and inexpensive …