Searchable abstracts of presentations at key conferences in endocrinology

ea0092op-11-05 | Oral Session 11: Autoimmunity / Hyperthyroidism | ETA2023

Association between thyroid function and osteoarthritis: a population-based cohort study

Xu Yanning , Szilagyi Ingrid , Boer Cindy , Sedaghati-Khayat Bahar , Edward Visser W. , van Meurs Joyce , Chaker Layal

Background: Previous genetic and animal studies implied a potential association between thyroid hormone and osteoarthritis (OA), but this has not been confirmed in the general population. We aim to investigate whether thyroid function is associated with hand, hip or knee OA.Methods: We included 9,054 participants from Rotterdam Study with baseline measurement of thyroid-stimulating hormone (TSH), free thyroxine (FT4) and radiographs. Joint radiographs we...

ea0099rc9.3 | Rapid Communications 9: Pituitary and Neuroendocrinology | Part II | ECE2024

Identifying potential small molecule “metabolites” as biomarkers for growth hormone deficiency (GHD): Insights from a novel mouse model

Al-Samerria Sarmed , Xu Huiting , Phelan Joseph , Diaz Rubio Maria Elena , Yamada Sayaka , Negron Ariel , Wondisford Fredric , Radovick Sally

Growth hormone deficiency (GHD) diagnosis poses a significant challenge since no test definitively diagnoses GHD. The current diagnostic approach for GHD relies on a determination of auxologic parameters followed by determining Growth Hormone (GH) levels and Insulin-like Growth Factor-I (IGF-I) in serum. However, clinical assessment and interpretation of GH and IGF-1 levels lack sensitivity. Further provocative studies of GH secretion do not have a precise cutoff level that di...

ea0099p1 | Adrenal and Cardiovascular Endocrinology | ECE2024

Reversal of cardiac damage after treatment for aldosterone-producing adenoma and idiopathic hyperaldosteronism – A Prospective Cardiac Magnetic Resonance Imaging study

Xu Chenxiao , Sun Jiayu , Wu Tao , Chen Tao , Tang Lu , Wang Wei , Zhou Fangli , Wen Deying , Ren Yan

Objective: At present, there are no studies in which authors report the use of cardiac magnetic resonance imaging (CMR) to evaluate the differences in myocardial strain between patients with aldosterone-producing adenomas (APAs) and those with idiopathic hyperaldosteronism (IHA) or the improvement in myocardial strain after treatment.Methods: In this study, 71 patients with APA and 51 patients with IHA were prospectively enrolled from the Department of E...

ea0063oc7.2 | Endocrine Connections 1 | ECE2019

Thyroid hormones are new key regulators of glucocorticoid metabolism

Bessiene Laura , Hescot Segolene , Bourdin-Pintueles Alexandra , Dumeige Laurence , Vitellius Geraldine , Perrot Julie , Xu Qiong-Yao , Vu Thi-An , Sachs Laurent , Pussard Eric , Lombes Marc , Viengchareun Say , Martinerie Laetitia

The 11-beta hydroxysteroid dehydrogenase (11βHSD) isozymes are well-known regulators of glucocorticoid hormone metabolism: 11βHSD2, mostly expressed in the distal nephron, converts cortisol [F] into cortisone [E] in humans or corticosterone into 11-dehydrocorticosterone in rodents (11-dehydro derivatives being inactive compounds), and 11βHSD1, ubiquitously expressed but predominantly in the liver, catalyzes the opposite reaction. Under pathophysiological conditi...

ea0041ep735 | Neuroendocrinology | ECE2016

Phenotype-genotype analysis in patients with GnRH deficiency in a single center

Djurdjevic Sandra Pekic , Xu Cheng , Dwyer Andrew , Cassatella Daniele , Doknic Mirjana , Miljic Dragana , Stojanovic Marko , Petakov Milan , Pitteloud Nelly , Popovic Vera

Objective: Congenital hypogonadotropic hypogonadism (CHH) results from isolated GnRH deficiency and may present with normal sense of smell (nCHH), anosmia (Kallmann syndrome, KS) or in syndromic forms. Genetic defects are identified in approximately half of CHH cases and oligogenicity is noted in almost 10%. Further, spontaneous reversal of is seen in 15% of patients.Methods: We analyzed the clinical characteristics of 37 Serbian CHH probands (34 sporadi...

ea0037gp.05.04 | Developmental and paediatric endocrinology | ECE2015

Pilot study on the effects of cross-sex hormone treatment in transsexual persons on metabolism by means of metabolomics profiling

Auer Matthias K , Xu Tao , Roepke Yasmin , Stalla Gunter K , Stieg Mareike , Van Caenegem Eva , Prehn Cornelia , Wang-Sattler Rui , Adamski Jerzy , T'sjoen Guy

Introduction: Sex steroid hormones exert a wide range of effects on metabolism. New techniques such as metabolomic profiling allow for a deeper insight into metabolic regulation. In epidemiological samples it has been demonstrated that most of these metabolites show sex-specific differences. However, if these differences are attributable to the effects of sex hormones or genetics is little understood so far.Methods: We performed targeted metabolomics pro...

ea0070aep788 | Reproductive and Developmental Endocrinology | ECE2020

Clinical and genetic overlap between congenital hypogonadotropic hypogonadism and cornelia de lange syndrome

Xu Cheng , Messina Andrea , Acierno James , Niederlander Nicolas , Santoni Federico , Papadakis Georgios , Pignatelli Duarte , Avbelj Stefanija Magdalena , Keefe Kimberly , Balasubramanian Ravikumar , Crowley William , Pitteloud Nelly

Background: Congenital hypogonadotropic hypogonadism (CHH), a clinically and genetic heterogenous sydrome, is caused by > 40 known loci whose mutations share the ability to cause defects in the ontogeny of the GnRH neuron network leading to absent/incomplete puberty and infertility. Cornelia de Lange Syndrome (CdLS) is similarly heterogenous disorder (distinctive facies, psychomotor delay, growth retardation and upper limb malformation) caused by mutations in 7 different g...

ea0029s40.1 | New familial endocrine cancer syndromes: pathophysiology and counselling | ICEECE2012

DICER1 mutations characterize a novel syndrome with endocrine features

Wu M. , Priest J. , Hamel N. , Sabbaghian N. , Xu B. , Tischkowitz M. , Choong C. , Deal C. , Albrecht S. , Charles A. , Goodyer P. , Foulkes W.

DICER1 is a microRNA processing-RNase III-type endoribonuclease and is crucial for embryogenesis and early development. Nearly 50 different heterozygous germ-line DICER1 mutations have been reported world-wide in individuals who developed, as children or young adults, pleuropulmonary blastoma, cystic nephroma, ovarian sex cord stromal tumors (especially Sertoli–Leydig cell tumor), multi-nodular goiter, embryonal rhabdomyosarcoma (of cervix and other typical sites), Wilms ...

ea0029p558 | Diabetes | ICEECE2012

Alterations in fecal lactobacillus and bifidobacterium species are associated with differences in cholesterol metabolism in type 2 diabetic patients

Hui H , Cai D , Le K , Li Y , Xu X , Liu T , Yang W , He F , Zhao X , Su K , Pandol S , Go V

Background: Type 2 diabetic (T2D) patients have alterations in the gut microbiota composition, compared to healthy individuals. Such alterations may play a role in the pathogenesis of T2D and insulin resistance. Bifidobacteria and Lactobacillus are among the most predominant bacteria found in human gut. They can also easily be added in probiotic preparations, thus making them ideal agents for therapeutic interventions. In this study, we aimed to determine if there were alterat...

ea0029p762 | Endocrine Disruptors | ICEECE2012

The effects of BPA exposure on fat mass and serum leptin concentrations have no impact on bone mineral densities in non-obese premenopausal women.

Liu J. , Zhao H. , Bi Y. , Ma L. , Zhang L. , Zhao L. , Tao B. , Sun L. , Wang T. , Zhao Y. , Wang W. , Xu M. , Chen J. , Ning G.

Objective: Bisphenol A (BPA) exposure may promote obesity, but its effect on bone mineral density (BMD) has not been reported in humans. In the present study, we aimed to examine the complex interplay between BPA exposure, fat mass, fat-free mass, serum estradiol, leptin, osteocalcin levels and BMDs in a group of premenopausal women.Methods: A total of 246 Chinese premenopausal women aged 20 years and older with regular menstrual cycles were investigated...