Searchable abstracts of presentations at key conferences in endocrinology

ea0056p489 | Diabetes therapy | ECE2018

Dulaglutide; effectiveness in a real world population with type 2 diabetes

Linares Lidia Urbon Lopez de , Soto Cristina Crespo

Diabetes is a chronic disease that is often accompanied by multiple comorbidities and health complications such as overweight/obesity. In the late years therapies improving glycemic control while reducing body weight have become a convenient choice to treat diabetes. One of those therapies are GLP 1 receptor agonists. Dulaglutide allows for a once weekly dosing which might improve compliance; moreover its new application device ease the injection. We show the results of HbA1c ...

ea0056p520 | Endocrine Disruptors | ECE2018

Cognitive impairment and nutritional status in patients admitted to the Department of Internal Medicine

Merida De la Torre Francisco J , Bel Pena Nieves

Introduction: Altered nutritional status is a problem in itself that can complicate a patient’s disease. In our hospital, the assessment of nutritional status at hospital admission is protocolized and performed by the Clinical Laboratory automatically, through the CONUT system, for three years ago. Our hospital provides assistance to a population of 120,000 patients, from rural areas and with a high average age. Hospital admissions for cognitive impairment are increasing ...

ea0056p701 | Clinical case reports - Pituitary/Adrenal | ECE2018

A case of hypothalamic-pituitary disease: who’s the deceiving suspect?

Van Meerhaeghe Tess , De Schepper Jean , Velkeniers Brigitte

Introduction: Diagnosis and treatment of neurosarcoidosis (NS) can be challenging. We describe an unsual presentation of an isolated NS in a 21 year old adult, initially presenting with central diabetes insipidus (DI) associated with a stalk thickening at the age of 14.Case description: A 21 year old patient was first seen at the department of endocrinology after a 9 years follow-up for panhypopituitarism. He presented at the age of 14 years at the pedia...

ea0002sp7 | The Endocrinology of Syndrome X | SFE2001

Sex Steroid Production in Human Adipose Tissue

Judd S , de Candia L , Lavranos T , Corbould A

There is a marked disparity between the amount of androstenedione (A) excreted in the urine as testosterone (T) glucuronide and the amount of A-T converted in the systemic circulation indicating that there is considerable production of testosterone within the portal circulation which is extracted by the liver. Our studies have examined the hypothesis that intra-abdominal fat is a major source of testosterone production which might contribute to insulin resistance.<p class=...

ea0045oc6.5 | Oral Communications 6- Endocrine | BSPED2016

A novel methodology using high resolution thermal imaging to detect vertebral fractures in children with osteogenesis imperfecta

De Salis Alexandra Fane , Saatchi Reza , Dimitri Paul

Background: Vertebral compression fractures are common in children with osteogenesis imperfecta. Current imaging methods for fracture detection (X-ray and DXA) use ionising radiation. High Resolution Thermal imaging (HRTI) is a non-invasive, non-ionising method that detects infrared radiation energy emissivity to an accuracy of 0.04 °C, providing a quantitative and qualitative map of temperature distribution. Given that the alteration in blood flow in vertebral fractures ...

ea0071030 | A rare ABCC8 gene mutation causing severe Maturity-Onset Diabetes of the Young (MODY-12): case report and mini review | BES2020

A rare ABCC8 gene mutation causing severe Maturity-Onset Diabetes of the Young (MODY-12): case report and mini review

Marijke Timmers , Eveline Dirinck , Patrick Lauwers , Christophe De Block

Context: Maturity-Onset Diabetes of the Young (MODY) refers to a group of monogenic β cell disorders1. MODY12 comprises various mutations in the ATP-binding cassette transporter subfamily C member 8 (ABCC8) gene of the ATP-sensitive potassium (K-) channel and is a condition that is not frequently encountered, comprising 1% of all MODY types1. Gain-of-function ABCC8 mutations can result in neonatal diabetes mellitus and/or MODY12, whereas loss-of-fun...

ea0073aep11 | Adrenal and Cardiovascular Endocrinology | ECE2021

The role of estimated glucose disposal rate as a predictor of insulin resistance, NAFLD and major adverse cardiovascular events in type 1 diabetes mellitus

Mertens Jonathan , Block Christophe De , Dirinck Eveline , Francque Sven

Background and AimsPeople with type 1 diabetes (T1D) have an increased risk of cardiovascular disease (CVD) despite insulin therapy to treat hyperglycaemia. Insulin resistance may be a contributing factor to CVD. Insulin resistance is strongly associated with NAFLD, which is increasingly linked to CVD. The estimated glucose disposal rate (eGDR) correlates well with the euglycemic clamp, which is the gold standard to assess insulin resistance in T1D, but ...

ea0073ep167 | Pituitary and Neuroendocrinology | ECE2021

Delayed diagnosis of acromegaly: a two-year journey

Asma Bitar De Zayas-Enriquez , Stojanovic Nemanja , Mlawa Gideon

AimsTo present the case of a 69 year-old female patient who was diagnosed with acromegaly two years following the initial onset of facial and acral symptoms, having already developed colonic hyperplastic polyps, one of the complications associated with acromegaly, one year prior to diagnosis.MaterialCase report and literature review.MethodAcromegaly was diagnosed ...

ea0074ncc12 | Highlighted Cases | SFENCC2021

A rare presentation of parathyroid carcinoma and brown tumours in a young woman with no associated genetic condition

de Bray Anne , Jones Sharon , Ahmad Ijaz , Juszczak Agata

Case history: A 34-year old Caucasian nurse presented to her GP with a 7 month history of abdominal pain. She was found to have PTH-dependent hypercalcaemia with Stage 3A chronic kidney disease (corrected calcium 3.43 mmol/l, phosphate 0.62 mmol/l, total vitamin D 32 nmol/l, PTH 214.9 pmol/l, creatinine 117 μmol/l and eGFR 45 ml/min/1.73m2). On direct questioning, she reported fatigue, generalised weakness and intermittent joint pains affecting her lower back and bo...

ea0097022 | Section | BES2023

Primary infertility: a rare presentation of adrenocortical carcinoma

S Desmedt , Vijver A Van De , E Van Caenegem , S Vandewalle

Background: Adrenocortical carcinomas (ACC) are rare and aggressive endocrine tumours with an annual incidence of 1 to 2 per million.(1) Frequently, patients present with signs of hormonal excess. The majority are cortisol excreting carcinomas, followed by aldosterone or androgen excess.(2) Estrogen secreting ACC are extremely rare. We present a case of estradiol and progesterone excess in primary infertility caused by an ACC.Cas...