Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep898 | Thyroid | ECE2020

Age and sex-specific TSH upper-limit reference intervals in the general French population: There is a need to adjust our actual practices

Raverot Véronique , Maxime Bonjour , Juliette Abeillon , Pauline Perrin , Florence Roucher , Hélène Lasolle , Fabien Subtil , Borson-Chazot Francoise

Background: The increasing age of the general population represents a new challenge for endocrinologists and caregivers since it is well know that the occurrence of thyroid dysfunction increases with age. It is still controversial whether or not reference values of thyrotropin (TSH) adapted to age and sex need to be used. Herein, we aimed to determine reference intervals, in males and females, suitable for thyroid disease exploration and follow-up during adult life in a tertia...

ea0081p289 | Calcium and Bone | ECE2022

Hypercalcemia with positive calcium-sensing receptor (casr) autoantibodies

Vankemmel Romain , Dupuis Hippolyte , Herman Pierre-Loup , Fabien Nicole , Vantyghem Marie-Christine

CaSR-autoantibodies may cause auto-immune hypercalcemia through either simple blocking or biased properties. The phenotype of this rare disease is most often acquired hypocalciuric hypercalcemia (AAH) (Minanbres JCEM 2020, Makita JCI insight 2022), but sometimes hyperparathyroidism (Pelletier-Morel Intern Med 2008), in elderly. Gender, auto-immune context is variable. Blood calcium may fluctuate, and acute exacerbations may be successfully treated with predni...

ea0047oc4 | Spotlight on Neuroendocrine tumours | Theranostics2016

68Ga, 64Cu labelling and affinity study of NODAGANOC, a NODAGA conjugated somatostatin analogue

Azzouna Rana Ben , Al-Shoukr Faisal , Hyafil Fabien , Rouzet Francois , Guilloteau Denis , Le Guludec Dominique

Introduction: DOTANOC is a largely used somatostatin analogue in NETs investigations. In NODAGANOC, the DOTA is replaced by NODAGA, a chelator derivative from NOTA which is the ‘gold standard’ for Ga3+ and Cu2+ chelation because it forms more stable complexes than DOTA.[1] The aim of our study is to evaluate the affinity of NODAGANOC for somatostatin receptors (sst) and to develop a 68Ga and 64Cu labelled NODAGANOC for a fu...

ea0099p599 | Late-Breaking | ECE2024

Differentiation of intra-tumoral necrosis between clusters 1 and 2 pheochromocytoma

Ronger Lise , Desailloud Rachel , Fabien Saint , Cedric Renard , Al-Salameh Abdallah

Introduction: Pheochromocytoma is a catecholamine-secreting neuroendocrine tumor arising from the chromaffin cells of the adrenal medulla. It is rare and considered benign, but can be life-threatening in the event of catecholaminergic discharge. Tumors differ in genotype, mechanism of tumorigenesis and type of secretion. On imaging, it is often characterized by central intra-tumor necrosis; there is very little data in the literature on the genesis and pathophysiological role ...

ea0090ep1151 | Late Breaking | ECE2023

Non-functioning adenomas submitted to surgery: clinical characterization and outcomes

Dias Daniela , Matos Tania , Silvestre Catarina , Serra FIlipa , Palha Ana , Lucas Neto Lia , Tavares Ferreira Joana , Subtil Joao , Tortosa Francisco , Sagarribay Amets , Sapinho Ines

Introduction: Nonfunctioning pituitary adenomas (NFPAs) are a heterogeneous group of tumors with different presentations. Clinical management of these tumors is complex. Our aim was to evaluate the clinical characteristics/postsurgical outcomes of NFPAs and to identify predictive factors of good response to surgery.Methods: Retrospective analysis of NFPA, who underwent surgery and followed in our hospital, from 2015-2022.Results: W...

ea0034p357 | Steroids | SFEBES2014

Steroid sulfatase contributes to systemic androgen activation in pre-pubertal boys: lessons from steroid sulfatase deficiency

Idkowiak Jan , Taylor Angela E , O'Neil Donna M , Subtil Sandra , Vijzelaar Raymon , Dias Renuka P , Amin Rakesh , Barrett Timothy G , Kirk Jeremy W , Shackleton Cedric H L , Moss Celia , Arlt Wiebke

Steroid sulfatase (STS) cleaves the sulfate moiety off steroid sulfates, including DHEAS, the inactive sulfate ester of the adrenal androgen precursor DHEA. Deficient DHEA sulfation, the opposite enzymatic reaction to that catalysed by STS, results in androgen excess by increased conversion of DHEA to active androgens. STS deficiency (STSD) due to deletions or inactivating mutations in the X-linked STS gene manifests with ichthyosis, but androgen homeostasis in STSD h...

ea0099oc5.5 | Oral Communications 5: Pituitary and Neuroendocrinology | Part I | ECE2024

B-RAF and MEK inhibitor argeted therapy in papillary craniopharyngiomas: results from the French national multicenter study

De Alcubierre Dario , Gkasdaris Grigorios , Briet Claire , Almairac Fabien , Boetto Julien , Mouly Celine , Larrieu-Ciron Delphine , Joncour Anthony , Mordrel Margaux , Vasiljevic Alexandre , Villa Chiara , Sergeant Camille , Ducray Francois , Feuvret Loic , Baussart Bertrand , Raverot Gerald , Jouanneau Emmanuel

Background: Papillary craniopharyngiomas (PCPs) are driven by V600E BRAF mutations in 95% of cases. Recently, combined anti-BRAF/MEK targeted therapy (TT) has emerged as a potential treatment in aggressive PCPs. However, standardized data on large cohorts are still lacking. Our study aimed to assess the real-life efficacy and safety of TT in patients with PCPs.Methods: This was a retrospective national multicenter study involving patients with V600E BRAF...

ea0063oc7.5 | Endocrine Connections 1 | ECE2019

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) syndrome: French prospective study in a cohort of 25 patients

Humbert Linda , Dubucquoi Sylvain , Kemp Helen , Veber Pascale Saugier , Fabien Nicole , Top Isabelle Raymond , Bauters Catherine Cardot , Cartigny Maryse , Delemer Brigitte , Docao Christine , Penfornis Alfred , Guignat Laurence , Kerlan Veronique , Lefevbre Herve , Chabre Olivier , Vanhove Laura , Sendid Boualem , Carel Jean-Claude , Souchon Perre-Francois , Weil Jacques , Vantyghem Marie-Christine , Wemeau Jean-Louis , Proust-Lemoine Emmanuelle

Background: APECED syndrome is a rare monogenic disease caused by homozygous mutation of AIRE gene. It classically presents with chronic mucocutaneous candidiasis (CMC), hypoparathyroidism (HP), and adrenal insufficiency (AI) with an early onset in childhood. Non-endocrine manifestations as ectodermic dystrophy, asplenism and pneumonitis are also observed but their incidence remains unknown and their mechanisms not well understood. APECED has been poorly reported in France alt...

ea0042p34 | (1) | Androgens2016

Mechanisms of radioresistance in prostate cells

Guggenberger Fabian , Erb Holger , Skvortsova Ira-Ida , Culig Zoran , Santer Frederic R.

Among androgen deprivation therapy (ADT), radiation therapy is an approved treatment either for early stage local PCa, but also for metastatic M1 stage PCa. However, tumour relapse is a frequent event that affects about 80% of patients undergoing prior treatment. There is increasing evidence that the occurrence of cancer stem cells (CSC) may play an important role in therapy resistance, in particular also in radioresistance. However, our knowledge on the mechanisms of radiores...

ea0015p127 | Diabetes, metabolism and cardiovascular | SFEBES2008

Mineralocorticoid action in essential hypertension

Hammer Fabian , Dale Jane , Ayuk John , Hobbs Richard , Stewart Paul

Primary hyperaldosteronism is now recognised as the most frequent underlying cause of hypertension. We recruited 94 patients (age (mean±S.D.) 56±11 years) with hypertension from primary care in order to study the role of corticosteroid hormone action in this cohort. Random, blood pressure (BP), plasma renin activity (PRA) and aldosterone (Aldo) was measured both on and off antihypertensive medication. In addition, a 24 h ambulatory blood pressure (ABP)...