Searchable abstracts of presentations at key conferences in endocrinology

ea0093oc37 | Oral communication 5: Reproductive Endocrinology | EYES2023

Regulation of the postnatal activity of the HPG axis in male Callithrix jacchus – A project description

Odroniec Amadeusz , Busch Alexander

Background: The control of the Hypothalamic–Pituitary–Gonadal (HPG) axis is a highly complex process, with the hypothalamic arcuate-median eminence complex (Arc-ME) as the master regulating region. The transient activation of the HPG axis is essential for the development and function of the reproductive system. This project’s focus is the transient phase of HPG axis activation within the first weeks and months postpartum (minipuberty). The mechanisms guiding the...

ea0094p32 | Bone and Calcium | SFEBES2023

Review of current guidelines on fracture risk recommendations in patients on hormonal therapies for Breast Cancer

Busch Sophia , Higham Claire

Introduction: Women prescribed hormonal therapies for breast cancer (eg Aromatase Inhibitors (AI) and ovarian suppression therapy (OST)) are at increased risk of fracture and monitoring of Bone Mineral Density (BMD) is needed. Recommendations for BMD monitoring and treatment interval thresholds differ between guidelines which has implications for management. We compared the outcomes from the application of 3 commonly used guidelines for bone health in women wi...

ea0029p929 | Female Reproduction | ICEECE2012

Endocrine effects of the FSHB−211 promoter polymorphism in females

Busch A. , Schuring A. , Gromoll J. , Tuttelmann F.

Introduction: FSH is a key player in reproductive functions, the expression of its unique subunit FSHB is regulated by the FSHB promoter. Recently, a single nucleotide polymorphism (SNP) at a highly conserved position in the FSHB promoter (rs10835638; −211G>T) has been found to be associated with decreased serum FSH levels in men and with male infertility. Because to date no information is available on possible endocrine consequences of this SNP in women, we conducte...

ea0035p690 | Male reproduction | ECE2014

The variant FSHB −211G>T attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndrome

Gromoll Joerg , Busch Alexander , Zitzmann Michael , Kliesch Sabine , Tuettelmann Frank

Background: Klinefelter syndrome (KS) is the most frequent genetic cause of male infertility. Individuals share the endocrine hallmark of hypergonadotropic hypogonadism, displaying high gonadotropin levels due to deficient testicular function. A single-nucleotide polymorphism (SNP) located within the FSHB promoter region (−211G>T, rs10835638) was recently shown to be associated with reduced serum FSH levels and other reproductive parameters in men. The objec...

ea0032oc5.4 | Reproduction | ECE2013

Influence of variants in the FSHB and FSHR gene on reproductive parameters in males and females

Gromoll Joerg , Schuring Andreas , Busch Alexander , Kliesch Sabine , Tuttelmann Frank

Background: Recently, a single nucleotide polymorphism (SNP) in the FSHB promoter (−211G>T, rs10835638) was found to be associated with lower serum FSH levels and oligozoospermia in males. In contrast, a SNP in the FSH-receptor gene (FSHR, 2039A>G, rs6166) was previously shown to be associated with FSH levels in women only.Subjects and methods: One thousand two hundred and thirteen male partners in infertile couples without known c...

ea0070aep1018 | Hot topics (including COVID-19) | ECE2020

18 Flour-Cholin-PET-CTis the supreme tool to localize ultrasound and mibi-’negative’ parathyroid adenomas – intraoperative correlation and 12 month postoperative results

Smaxwil Constantin , Philipp Aschoff , Mirjam Busch , Joachim Wagner , Julia Altmeier , Oswald Ploner , Andreas Zielke

Background: To characterize the diagnostic performance of 18-Fluoroethylcholine-PET-CT (FCH-PET-CT) to localize parathyroid adenomas (PA) in primary hyperparathyroidism (pHPT) when ultrasound (US) and MIBI-Scan (MibiS) fail to localize – intraoperative correlation and one-year follow up.Method: Beginning in 07/2017 18-FCH-PET was employed in patients with proven pHPT in whom US and MS delivered either incongruent or negative findings. All patients ...

ea0016p230 | Diabetes and cardiovascular diseases | ECE2008

Induction of autoantigen-specific tolerance by retroviral transduction of hematopoetic stem cells with GAD65

Jaeckel Elmar , Ivanyi Philipp , Busch Markus , von Boehmer Harald , Manns Michael P

Transfer of hematopoetic stem cells from mice transgenically overexpressing the islet autoantigen insulin could prevent type I diabetes in NOD mice. We tested if such an approach of tolerance induction could be employed by means of retroviral gene transfer of autoantigens into syngeneic hematopoetic stem cells (HSCs). We used glutamic acid decarboxylase 65 (GAD) as the autoantigen as T cell responses against GAD are more easily detected in NOD mice and as it has been previousl...

ea0032p530 | Endocrine tumours and neoplasia | ECE2013

Insulinoma: is enucleation a safe option?

Jilesen Anneke , Klumpen Heinz-Josef , Bisschop Peter , Busch Olivier , van Gulik Thomas , Gouma Dirk , van Dijkum Els Nieveen

Background: Insulinomas are the most prevalent functional neuroendocrine tumors of the pancreas. Enucleation is often preferred to pancreatic resection because it’s minimally invasive nature. The aim of this study is to assess the post-operative surgical outcome in particular pancreatic fistula after resection.Methods: All patients with insulinomas were selected from a retrospective database of resected pancreatic neuroendocrine tumors (pNET). Patie...

ea0084op-01-04 | Oral Session 1: Topic Highlights | ETA2022

Selenoprotein deficiency disorder predisposes to aortic aneurysm formation

Schoenmakers Erik , Marelli Federica , Jorgensen Helle , Edward Visser W. , Moran Carla , Groeneweg Stefan , Avalos Carolina , Figg Nichola , Finigan Alison , Wali Neha , Agostini Maura , Wardle-Jones Hannah , Lyons Greta , Rusk Rosemary , Gopalan Deepa , Johannes Visser Jacob , Goddard Martin , Nashef Samer , Heijmen Robin , Clift Paul , Sinha Sanjay , Busch-Nentwich Elisabeth , Ramirez-Solis Ramiro , Persani Luca , Bennett Martin , Chatterjee Krishna

Objectives: Mutations in SECISBP2 cause deficiency of selenoproteins, resulting in a multisystem disorder with abnormal circulating thyroid hormone and selenium levels and features due to lack of specific selenoproteins or loss of antioxidant selenoenzymes. Having observed early-onset, aneurysmal thoracic aortic dilatation in four patients with this disorder, we studied zebrafish and murine Secisbp2 mutant models to determine whether the aortic phenotype and selenopro...