Searchable abstracts of presentations at key conferences in endocrinology

ea0029s14.1 | Wnt/Beta-catenin in pituitary development and disease | ICEECE2012

β-catenin deficiency disrupts patterning of the ventral diencephalon, causing adenohypophysis over growth and dysmorphology

Camper S. , Mortensen A. , Davis S.

β-catenin is thought to play an important, intrinsic role in early pituitary development by regulating adenohypophysis (anterior pituitary) transcription factor activity. Expression of β-catenin is detected in the adenohypophysis, rostral mesenchyme, and neural ectoderm, including the area that develops into the infundibulum and neurohypophysis, and nearby regions. The importance of β-catenin expression in the neural ectoderm and mesenchyme has not been addresse...

ea0056gp174 | Parathyroid | ECE2018

The design and preliminary results of a phase 1 TransCon PTH trial in healthy volunteers

Karpf David , Mortensen Eva , Sprogoe Kennett , Pihl Susanne , Leff Jonathan

Background: Hypoparathyroidism (HP), a condition of parathyroid hormone (PTH) deficiency, leads to abnormal calcium metabolism. Standard of care (SOC), ie, large amounts of calcium and active vitamin D, leads to hypercalciuria and increased calcium x phosphate. Daily Natpara, PTH(1-84), injections reduced calcium and active vitamin D doses but not 24-hour urinary calcium (uCa) excretion or incidence of hypo- and hypercalcemia due to its 3-hour half-life (Natpara label). NIH st...

ea0032p196 | Cardiovascular Endocrinology & Lipid Metabolism | ECE2013

Perturbed sympatho-vagal balance in Turner syndrome: relation to phenotype and aortic dilation

Trolle Christian , Mortensen Kristian Havmand , Hjerrild Britta , Andersen Niels Holmark , Gravholt Claus Hojbjerg

Objective: The risk of aortic dissection is 100-fold increased in Turner syndrome (TS). Increased blood pressure (BP) and heart rate is present as well as an increased risk of ischemic heart disease and diabetes. This study aimed to prospectively assess heart rate variability (HRV) in TS and its relation to aortic dimensions.Methods: Adults with TS (n=91, aged 37.4±10.4 years) recruited through the Danish National Society of Turner Syndrome...

ea0022p482 | Female reproduction | ECE2010

Ascending aortic dilatation in Turner syndrome: the natural history

Mortensen Kristian , Hjerrild Britta , Stochholm Kirstine , Andersen Niels , Soerensen Keld , Lundorf Erik , Christiansen Jens , Gravholt Claus

Background: Aortic dissection causes excess mortality in Turner syndrome, and this increased risk is associated with aortic dilation, congenital cardiovascular abnormalities, karyotype, and blood pressure. But risk factor identification is inadequate, and the natural course of aortopathy in Turner syndrome is poorly investigated.Design and methods: Prospective follow-up study in women with Turner syndrome (n=102, examined twice) and healthy age-ma...

ea0090p170 | Reproductive and Developmental Endocrinology | ECE2023

RANKL signalling in female reproduction: a novel role of RANKL outside the skeleton?

Bech Arting Liv , Kooij Ireen , Krarup Knudsen Nadia , Hjorth Andreassen Christine , Juel Mortensen Li , Juul Anders , Blomberg Jensen Martin

Background and Purpose: Infertility affects 15% of couples globally, and only few treatment options are available. Gonadotropins are classic and potent regulators of ovarian and female reproductive function, but novel endocrine crosstalk appears to exist between gonads and the skeleton that may influence female fertility. One of the new players include the RANKL signalling system, which consists of the receptor activator of nuclear factor κβ ligand (RANKL), the recep...

ea0032p176 | Cardiovascular Endocrinology & Lipid Metabolism | ECE2013

Long QT interval in Turner syndrome: a high prevalence of LQTS gene mutations

Trolle Christian , Mortensen Kristian Havmand , Pedersen Lisbeth Norum , Jensen Henrik Kjaerulf , Andersen Niels Holmark , Gravholt Claus Hojbjerg

Objective: QT interval prolongation of unknown aetiology is common in Turner syndrome (TS). This study set out to explore the presence of known pathogenic long QT (LQT) mutations in TS and to examine the corrected QT interval (QTc) over time and relate the findings to the TS phenotype.Methods: Adult females with TS (n=102) were examined thrice with a mean follow-up of 4.7±0.5 years, and 68 age-matched healthy controls were examined once. QT...

ea0090oc4.2 | Oral Communications 4: Reproductive and Developmental Endocrinology | ECE2023

Inhibition of RANKL in the testis increased the number of motile sperm in a sub-group of infertile men with preserved Sertoli cell function

Hjorth Andreassen Christine , Mortensen Li Juel , Holt Rune , Knudsen Nadia Krarup , Nielsen John Erik , Juul Anders , Jorgensen Anne , Jensen Martin Blomberg

Currently, no treatment options exist to improve semen quality for the majority of infertile men. Proper interaction between germ and Sertoli cells in the testis is critical for sperm production, and a recent study suggested that Denosumab, an inhibitor of RANKL signaling, may stimulate sperm production in some infertile men. Here, we show in animal and human studies how expression of the RANKL signaling system is critical for both Sertoli cell function and the testicular resp...