Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep291 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Nesfatin-1, an appetite-suppressing and anti-obesogenic neuropeptide, is decreased in the human brainstem of obese subjects.

Psilopanagioti Aristea , Makrygianni Maria , Nikou Sofia , Logotheti Souzana , Chartoumpekis Dionysios , Papadaki Helen

Background/Aims: Food intake is orchestrated by complex neuronal networksresiding in the forebrain, hypothalamus, and brainstem, via orexigenic and anorexigenic neuropeptides. Nesfatin-1, the amino-terminal fragment of nucleobindin 2, is a potent anorexigenic and anti-obesogenic neuropeptide, with widespread central distribution in rodents. In obese humans, our research group has recently reported reduced nesfatin-1 protein expression in the lateral hypothalamic area, a brain ...

ea0070aep486 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Glycemic variability in type 1 diabetes

Santos Tiago , Inácio Isabel , Soares Bruno , Vilaverde Joana , Teixeira Sofia , Cardoso Helena

Introduction: Glycemic variability (GV) is emerging as a measure of glycemic control in type 1 diabetic patients (T1DM) given that it provides an integrated picture of postprandial hyperglycemia and hypoglycemic episodes and is associated with diabetic complications and mortality. However, little is known about the best way to address this problem in clinical practice.Aim: To characterize GV in T1DM patients followed in our center and to identify clinica...

ea0070aep580 | Pituitary and Neuroendocrinology | ECE2020

Real life efficiency of pegvisomant therapy in acromegaly

Maria Lider Burciulescu Sofia , Livia Gheorghiu Monica , Caragheorgheopol Andra , Purice Mariana , Badiu Corin

Introduction: Pegvisomant (PEG) is an efficient treatment for acromegaly but the recommendation for this treatment is less active due to its high cost. In Romania it is reimbursed in doses up to 30 mg s.c/day or as 40 or 80 mg/week in combination with a somatostatin analog (SSA).Design: Retrospective analysis of 18 consecutive patients treated with PEG for acromegaly (either as monotherapy, or in combination with SSA and/or cabergoline (CAB...

ea0070aep1010 | Hot topics (including COVID-19) | ECE2020

Clinical presentation variations of pheochromocytomas

Maria Lider Burciulescu Sofia , Livia Gheorghiu Monica , Bojoga Andreea , Badiu Corin

Introduction: Pheochromocytoma (PCC) has a wide spectrum of clinical manifestations, from insidious disease to extreme symptoms. Various mechanisms of catecholamine and other mediators actions were related to the diversity of PCC presentation.Aim: We describe a retrospective study, of patients with PCC from a tertiary hospital, focusing on clinical and biochemical characteristics of PCC depending on means of discovery.Material and ...

ea0070ep235 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Flash glucose monitoring in type 1 diabetes: Real world data

Borges Duarte Diana , Santos Tiago , Fonseca Liliana , Teixeira Sofia , Vilaverde Joana , Cardoso Maria Helena

Introduction: Clinical trial data demonstrate improved glycemic control in individuals with type 1 diabetes (T1D),especially, reduction of time in hypoglycaemia with flash glucose monitoring (FGM);however real-life conditions can modify this scenario.Aim: To examine real world use and glycemic control following a standardized initiation process of FGM.Methods: Individuals aged 18 years or older with T1D were prospectively recruited...

ea0070ep466 | Thyroid | ECE2020

Quality of life in patients with Graves’ orbitopathy

Boutzios Georgios , Kouvelioti Sofia , Papaoiconomou Eleni , Koukoulioti Eleni , Miliou Myrto , Tzioufas Athanasios

Introduction: Graves’ disease (GD) is an autoimmune thyroiditis frequently associated with development of Graves’ orbitopathy (GO). As a consequence, patients with GO experience impairment of quality of life (QoL) and social function. The aim of our study was to assess quality of life in patients with GO.Methods: This is a single-center observational study in an outpatient clinic of autoimmune endocrinopathies at a Tertiary, General, Universi...

ea0032p40 | Adrenal cortex | ECE2013

Autoimmune polyglandular syndrome on a cohort of patients with primary adrenocortical insufficiency

Gouveia Sofia , Ribeiro Cristina , Alves Marcia , Saraiva Joana , Moreno Carolina , Guelho Daniela , Carrilho Francisco

Introduction: On average, 40 to 50% of the patients with autoimmune adrenocortical insufficiency will eventually develop an autoimmune polyglandular syndrome (APS). Our aim was to characterize a population with primary adrenocortical insufficiency (AI) and determine the prevalence of other autoimmune disorders that might establish the diagnosis of APS.Materials and methods: We included patients with primary AI under surveillance at our Department. Those ...

ea0032p78 | Bone and Osteoporosis | ECE2013

Effects of Denosumab treatment on insulin resistance in postmenopausal women with osteoporosis

Tzioras Konstantinos , Mizamtsidi Maria , Chronaiou Aikaterini , Vasiliou Georgia , Tagara Sofia , Vryonidou Andromachi

Introduction: Denosumab is a new pharmacotherapy option for postmenopausal osteoporosis. It is a human monoclonal antibody against RANKL, acting as an osteoprotegerin (OPG) analog. Recently, osteoprotegerin levels were found to be elevated in type two diabetes while insulin resistance was shown to be positively associated with decreased serum OPG levels, in healthy obese subjects. However, no study has been conducted in order to clarify the effect of anti-RANKL factors adminis...

ea0032p89 | Bone and Osteoporosis | ECE2013

Association of the (TTTA)n repeat polymorphism of CYP19 gene with bone mineral density in Greek peri- and postmenopausal women

Markatseli Anastasia , Lazaros Leandros , Kostoulas Harilaos , Sakaloglou Prodromos , Markoula Sofia , Tigas Stelios , Georgiou Ioannis , Tsatsoulis Agathocles

Introduction: Aromatase is encoded by the CYP19 gene and catalyzes the conversion of androgens to estrogens, which in turn regulate skeletal homeostasis. Polymorphisms in the CYP19 gene have been studied for their association with bone mineral density (BMD) in the general population with mixed results.Objectives: To explore the influence of the CYP19 (TTTA)n repeat polymorphism on BMD and serum levels of osteoprotegerin (OPG), receptor activator...

ea0032p107 | Bone and Osteoporosis | ECE2013

Resolution of anaemia after curative parathyroidectomy in a patient with primary hyperparathyroidism

Anagnostis Panagiotis , Adamidou Fotini , Agapidou Alexandra , Vakalopoulou Sofia , Garipidou Vasilia , Kita Marina

Introduction: Despite the coexistence of secondary hyperparathyroidism with anaemia, hematological manifestations of primary hyperparathyroidism (PHPT) are rare.Case report: A 67-year-old Caucasian female was admitted to the Department of Internal Medicine due to normocytic anemia and hypercalcemia, diagnosed on occasion of muscle weakness and fatigability for 3 months.Her medication included: alendronate 70 mg/week, alphacalcidol ...