Searchable abstracts of presentations at key conferences in endocrinology

ea0090p545 | Late-Breaking | ECE2023

AMH in men: Higher serum levels associated with healthy male aging

Tandl Veronika , Haudum Christoph W. , Eberhard Katharina , Hutz Barbara , Kolesnik Ewald , Schmidt Albrecht , Zirlik Andreas , von Lewinski Dirk , Scherr Daniel , Verheyen Nicolas , Pieber Thomas R. , Obermayer-Pietsch Barbara

Anti-Müllerian hormone (AMH), known for its role in fetal development and female reproduction, is also present in adult and elderly men in considerable amounts. In recent years, controversial findings regarding relations to age, other hormones, and BMI (possibly based on a dilutional effect due to higher blood volume) have been discussed. To date, little is known of its clinical relevance in this population. We aimed to further investigate AMH levels in an aging male popu...

ea0063p1005 | Environment, Society and Governance | ECE2019

Genetic associations of vitamin D increase after supplementation

Trummer Olivia , Schweighofer Natascha , Haudum Christoph W , Trummer Christian , Lerchbaum Elisabeth , Pieber Thomas R , Colantonio Caterina , Kolesnik Ewald , Schmidt Albrecht , Pieske Burkert , Obermayer-Pietsch Barbara

Apart from the crucial effects of vitamin D on bone health, vitamin D deficiency has been associated with various chronic conditions such as metabolic or reproductive disturbances. The polycystic ovary syndrome (PCOS) represents the most common endocrine disorder among women of reproductive age. Women affected by PCOS frequently suffer from oligo- or anovulation as well as from obesity and insulin resistance. There is accumulating evidence showing an association of vitamin D s...

ea0041gp40 | Bone & Calcium Homeostasis | ECE2016

Severe osteomalacia caused by a phosphaturic mesenchymal tumor secreting fibroblast growth factor 23: a case report

Ravarani Lisa , Faust Michael , Quaas Alexander , Bludau Marc , Schmidt Matthias , Allendorf Inka , Topuzoglu-Muller Tengu , Hanszen Ruth , Schary Oliver , Bruning Jens C

Tumor-induced osteomalacia (TIO) is a rare acquired paraneoplastic syndrome clinically presenting with recurring fractures, muscular weakness and pain. Laboratory values of affected patients are characterized by renal phosphate wasting and hypophosphatemia caused by an overexpression of fibroblast growth factor 23 (FGF- 23), a hormone belonging to the group of phosphatonins regulating phosphate and vitamin D homeostasis. Pathologically, it is secreted especially by small (and ...

ea0070oc3.7 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Efficacy and safety of volanesorsen for the treatment of metabolic complications in patients with familial partial lipodystrophy: results of the BROADEN study

O’Dea Louis , Tami Joseph , Alexander Veronica , Watts Lynnetta , Hurh Eunju , Hubbard Brant , Schmidt Hartmut , Tiulpakov Anatoly , Mertens Ann , Garg Abhimanyu , Oral Elif

Introduction: Familial Partial Lipodystrophies (FPLD) are rare genetic disorders characterized by marked loss of subcutaneous fat from the extremities with variable fat loss from the face and trunk. Patients with FPLD develop metabolic abnormalities including hypertriglyceridemia, insulin resistance, and diabetes mellitus, which are difficult to manage with conventional therapies including fibrates, statins and insulin. The BROADEN study evaluated the efficacy a...

ea0070aep269 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Characterizing familial partial lipodystrophy: Baseline data of the BROADEN study

O’Dea Louis , Tami Joseph , Alexander Veronica , Watts Lynnetta , Hurh Eunju , Hubbard Brant , Schmidt Hartmut , Tiulpakov Anatoly , Mertens Ann , Garg Abhimanyu , Oral Elif

Introduction: Familial Partial Lipodystrophy (FPLD) is a rare genetic disorder characterized by marked loss of subcutaneous adipose tissue from the extremities and is associated with a variety of metabolic abnormalities. While phenotypic elements of the disorder can vary across genotypes, symptomatic presentation, disease severity, and onset can also vary among individuals with the same disease-causing variant, or even among family members. Due to this variabili...

ea0029oc11.2 | Thyroid Clinical 2 | ICEECE2012

Subclinical thyroid disease and risk of new-onset atrial fibrillation

Selmer C. , Olesen J. , Lindhardsen J. , Olsen A. , Madsen J. , Schmidt U. , Faber J. , Hansen P. , Pedersen O. , Hansen M. , Torp-Pedersen C. , Gislason G.

Background: It is still uncertain if subclinical thyroid disease or ‘high-normal’ thyroid function are risk-factors for atrial fibrillation (AF).Objectives: To examine the risk of AF in relation to thyroid function.Methods: Patients consulting their general practitioner from 2000–2009 in Copenhagen, Denmark, who underwent thyroid blood tests, were identified by individual-level linkage of nationwide registries. Patie...

ea0011p75 | Clinical case reports | ECE2006

About three cases of Riedel thyroiditis

Vantyghem MC , Marcelli-Tourvieille S , Schmidt J , Néraud B , Perimenis P , Leteurtre E , Cardot-Bauters C , Pattou F , Carnaille B , Wémeau JL

Riedel thyroiditis is an uncommon form of chronic thyroiditis in which the thyroid gland is replaced by fibrous tissue. The etiological mechanism underlying RT are unclear. The prevailing view is that it is part of a generalized fibro-inflammatory process also involving other organs. Therapeutic options are not standardized (surgery, corticosteroids, and more recently tamoxifene). The aim of this work is to present three new cases, and the favourable evolution observed in one ...

ea0056gp189 | Pituitary / Growth Hormone ' IGF Axis | ECE2018

Association of IGF1 receptor autoantibodies with height and body size

Haudum Christoph , Minich Waldemar , Munzker Julia , Groselj-Strele Andrea , Kolesnik Ewald , Mursic Ines , Schwiebert Christian , Welsink Tim , Schmidt Albrecht , Pieber Thomas , Schomburg Lutz , Obermayer-Pietsch Barbara

Objective: Insulin-like growth factor 1 (IGF1) has a crucial role in growth and metabolism. A specifically designed autoantibody (aAb) assay against the IGF1 receptor (IGF1R-aAb) is able to detect IGF1R-aAb in serum. As the IGF1R has shown involvement in many functional pathologies (e.g. in the Laron syndrome), we aimed to investigate the role of IGF1R-aAb in a large population-based cohort of middle-aged volunteers and their potential effects on anthropometric, osteological a...

ea0073aep6 | Adrenal and Cardiovascular Endocrinology | ECE2021

Salivary profiles of 11-oxygenated androgens follow a diurnal rhythm in patients with congenital adrenal hyperplasia

Nowotny Hanna F. , Auer Matthias K. , Lottspeich Christian , Schmidt Heinrich , Dubinski Ilja , Bidlingmaier Martin , Adaway Jo , Hawley James , Keevil Brian , Reisch Nicole

BackgroundRoutine biochemical assessment in patients with congenital adrenal hyperplasia (CAH) includes measurement of serum 17–hydroxyprogesterone (17OHP), androstenedione (A4) and testosterone (T) and their metabolites in urine. Several studies have also described 11–oxygenated 19–carbon (110 × C19) steroids as a clinically relevant androgenetic source and highlighted their potential as markers for evaluation of adrenal androgen exc...

ea0081rc11.7 | Rapid Communications 11: Thyroid 2 | ECE2022

Altered expression profiles of miR-22-5p and miR-142-3p display Hashimoto´s disease and are associated with thyroid antibodies

Trummer Olivia , Foszl Ines , Schweighofer Natascha , Arifi Edi , Haudum Christoph , Reintar Sharmaine , Pilz Stefan , Theiler-Schwetz Verena , Trummer Christian , Zirlik Andreas , Schmidt Albrecht , Colantonio Caterina , Kolesnik Ewald , Verheyen Nicolas , Pieber Thomas , Obermayer-Pietsch Barbara

Background: Hashimoto’s thyroiditis (HT), the most prevalent autoimmune disorder of the thyroid (AITD) is characterized by the presence of circulating autoantibodies, induced by a not fully understood dysregulation of the immune system. MicroRNAs (miRNAs) are small noncoding RNAs, which can play a pivotal role in immune functions and the development of autoimmunity. The aim of the present investigation was to evaluate whether a panel of nine selected miRNAs differs in ser...