Searchable abstracts of presentations at key conferences in endocrinology

ea0016p34 | Adrenal | ECE2008

Renal excretion rates of free cortisol, free cortisone and dehydroepiandrosterone metabolites, but not renal indices of cortisol secretion are associated with urinary volume in healthy children

Shi Lije , Wudy Stefan A , Maser-Gluth Christiane , Hartmann Michaela F , Remer Thomas

Background: In experimental studies, a high fluid intake and a corresponding high urine volume have been shown to increase renal excretion rates of urinary free cortisol (UFF) and cortisone (UFE) in adults. We aimed to examine whether 24-h urinary steroid excretion rates are also affected by urine volume in children.Methods: In 24-h urine samples of 100 prepubertal and 100 pubertal healthy children UFF, UFE, tetrahydrocortisol, 5α-tetrahydrocortisol...

ea0041ep710 | Male Reproduction | ECE2016

Androgen profiling in males of two high-fertility mouse models does not reveal a distinct phenotype but provides new reference values for androgens in mice

Weitzel Joachim M , Michaelis Marten , Sobczak Alexander , Langhammer Martina , Nurnberg Gerd , Reinsch Norbert , Hartmann Michaela F , Wudy Stefan A , Schon Jennifer

Animal models are valuable tools in fertility research. Worldwide, there are more than 1000 transgenic or knockout mouse models available showing a reproductive phenotype; almost all of them exhibit an infertile or at least subfertile phenotype. By contrast, animal models revealing an improved fertility phenotype are barely described. We developed two outbred mouse models exhibiting a ‘high-fertility’ phenotype. These mouse lines were generated via selection over a t...

ea0090oc5.1 | Oral Communications 5: Adrenal and Cardiovascular Endocrinology 1 | ECE2023

CYP21A2-R484Q mice, a humanized mutant animal model for congenital adrenal hyperplasia

Ramkumar Thirumalasetty Shamini , Schubert Tina , Naumann Ronald , Reichardt Ilka , Rohm Marie Luise , Landgraf Dana , Gembardt Florian , Peitzsch Mirko , Hartmann Michaela F , Sarov Mihail , Wudy Stefan A , Reisch Nicole , Huebner Angela , Koehler Katrin

Congenital Adrenal hyperplasia (CAH) refers to a group of autosomal-recessive inherited disorders of impaired adrenal steroidogenesis. The most common form is 21-hydroxylase deficiency (21-OHD) caused by mutations in the CYP21A2 gene. Patients lack glucocorticoids and in some cases mineralocorticoids, and present with androgen excess causing hypoglycemia, live-threatening salt wasting, virilisation, and precocious puberty. Treatment includes the replacement of deficie...