Searchable abstracts of presentations at key conferences in endocrinology

ea0026p120 | Female reproduction | ECE2011

Smoking is associated with increased adrenal responsiveness, decreased prolactin levels and a more adverse lipid profile in 650 Caucasian patients with polycystic ovary syndrome

Glintborg D , Mumm H , Hougaard D M , Ravn P , Andersen M

Objective: Smoking may be associated with changes in metabolic risk factors and sex hormones in PCOS.Design: Retrospective trans-sectional study.Patients: Six hundred and fifty caucasian premenopausal women with the diagnoses hirsutism or PCOS were divided according to smoking status: Non-smokers (NS-PCOS=390) and smokers (S-PCOS=260). 119 healthy women were studied as controls (NS-Control=105, S-Control=14)....

ea0026p305 | Obesity | ECE2011

Testosterone therapy increased muscle mass and lipid oxidation in ageing men

Frederiksen L , Hojlund K , Hougard D M , Brixen K , Andersen M

Background: The indication for testosterone therapy in ageing hypogonadal men without hypothalamic, pituitary or testicular disease remains to be elucidated. The aim of this study was to investigate the effect of testosterone therapy on insulin sensitivity, substrate metabolism, body composition and lipids in ageing men with relative hypogonadism using a predefined cut-off level for bioavailable testosterone.Methods: A randomized, double-blinded, placebo...

ea0075t07 | Thyroid | EYES2021

Thyrotoxic storm and Hypercalcemia: A Graves’ complication

D M Lavanya , Acharya Himamshu , K M Suryanarayana , Kulkarni Sanjay V

Introduction: Graves’ disease is associated with mild hypercalcemia in about 1/5th of cases. T3, through its nuclear receptor activates osteoclasts resulting in accelerated bone turnover. Although mild hypercalcemia is common in Graves’ disease, symptomatic hypercalcemia is rare. We describe a case who presented with thyrotoxic storm and hypercalcemia.Case report: 52-year-old lady presented with thyrotoxic symptoms of weight loss, dysphagia for...

ea0077op2.2 | Adrenal and Cardiovascular | SFEBES2021

Single-centre analysis of 900 short synacthen tests: do pre-test clinical or biochemical variables predict failure?

Dilrukshi M D S A , Beck K J , Loo H , May C , Jafar-Mohammadi B , Pofi R , Tomlinson J W , Pal A

Short synacthen test (SST) is the most widely used dynamic test of hypothalamic-pituitary-adrenal (HPA) axis function. It’s simple to conduct but requires nursing time and is relatively costly given 15-fold price increase in synacthen since 2015. We audited our SST use with the aim of reviewing clinical indications for testing and identifying useful predictors of test outcome. Baseline referral, clinical and biochemical data were retrospectively collected for individuals ...

ea0049ep1179 | Male Reproduction | ECE2017

Leptin modulates Sertoli cells mitochondrial function and biogenesis with implications for the nutritional support of spermatogenesis

Moreira Bruno M , D Martins Ana , Monteiro Mariana P , Sousa Mario , Alves Marco G , Oliveira Pedro F

Current lifestyle, characterized by physical inactivity and a poor diet, is heavily linked with an increased incidence of metabolic diseases. One of the most serious silent co-morbidities of those diseases is infertility. The hormonal link between food intake and energy homeostasis is mediated by the leptin ghrelin axis. Compelling evidence suggests that direct leptin’s action regulates cellular glucose homeostasis and mitochondrial biogenesis. We have recently shown that...

ea0034p136 | Clinical practice/governance and case reports | SFEBES2014

The H-syndrome and next generation sequencing for molecular genetic diagnosis

Thomas Nihal , Mahesh D M , Chapla Aaron , Asha H S , Shetty Shrinath , Shetty Sahana , Lydia M , George Renu

Background: The H-syndrome is a recently described very rare monogenic systemic autoinflammatory autosomal-recessive genodermatosis with young onset of diabetes without evidence of autoimmunity. It is caused by mutations in the SLC29A3 gene, which encodes the equilibrative nucleoside transporter hENT3.Objectives: To study the clinical features and confirm the genetic diagnosis in a subject with young onset of diabetes.Subject and m...

ea0027p78 | (1) | BSPED2011

Audit of Endocrine Adolescent Transition Clinic, RHSC Glasgow, 2008–2010

Mason Avril , Ahmed S F , Donaldson M D , McNeill E , Campbell V , Perry C , Shaikh M G

Introduction: A multi-disciplinary endocrine Adolescent Transition Clinic (ATC), with key professionals from paediatric and adult services, was instituted at the Royal Hospital for Sick Children, Glasgow, in October 2008 serving young people in the West of Scotland. A good transition should improve clinic attendance, health outcomes and quality of life into adulthood.Aim: To systematically review the success of ATC in engaging young people following thei...

ea0026p502 | Bone/calcium/Vitamin D | ECE2011

Serum testosterone and estradiol in relation to bone mineral density, muscle strength and body composition in elderly men

Hammad A A , Hassan Z A , Hamad F K , Abaza D M , Abdel Hamid K M , El Wakeel M E K

Objective: Sex steroids play an important role in the maintenance of bone health. However, there is limited information on the association between sex hormones and age-related bone loss in men. Our objective was to study the relationship between sex steroid levels and the changes accompanying aging process, including bone mineral density (BMD), muscle strength and body composition in elderly Egyptian men.Methods: Free testosterone (FT), estradiol (E...

ea0090oc6.2 | Oral Communications 6: Endocrine-related Cancer | ECE2023

Aminoacyl-tRNA synthetases as diagnostic, prognostic, and therapeutic tools in MAFLD-derived hepatocellular carcinoma

Herman-Sanchez Natalia , Lopez-Canovas Juan L. , Amado Victor , Zamora-Olaya Javier M , Rodriguez-Peralvarez Manuel , Luque Raul M , D. Gahete Manuel

Metabolic dysfunction-associated fatty liver disease (MAFLD) is a growing cause of hepatocellular carcinoma (HCCs); however, the molecular characteristics of MAFLD-derived HCCs are still to be elucidated. To provide novel insights in this field, we performed the first quantitative proteomic analysis of HCC samples from different aetiologies. Particularly, cytosolic and nuclear proteome of liver tissues from HCC patients (n=42; HCC vs adjacent tissue) and healthy contr...

ea0031oc2.4 | Steroids and thyroid | SFEBES2013

THRA or DIO2 mutations are not a common cause of high bone mass in humans

Gogakos A I , Bassett J H D , Gluer C C , Reid D M , Felsenberg D , Roux C , Eastell R , Williams G R

Mice with dominant-negative mutations of thyroid hormone receptor α1 (TRα1) are euthyroid but display growth retardation and delayed bone age as juveniles and increased bone mass during adulthood, indicating impaired skeletal thyroid hormone responsiveness. The first autosomal dominant mutations affecting TRα1 in humans were recently described in two unrelated children and one parent who were euthyroid apart from a low T4:T3 ratio. Consiste...