Searchable abstracts of presentations at key conferences in endocrinology

ea0020p274 | Clinical case reports and clinical reports | ECE2009

Hypopituitarism revealed after repetitive hyponatremia as complication of hemorrhagic fever

Zavrsnik Matej , Kok Tanja

Six years after hemorrhagic fever with renal syndrome (HFRS) 73 years old man was admitted in hospital because of hyponatremia (Na 129 mmol/l) and abdominal pain. Before HFRS he was treated for pancreatitis, hypertension, ulcerative colitis and gallstones. In the year 2002 he was admitted with fiver, vomiting, diarrhoea, headache and blurred vision. Serologic immunoflourescence testing was positive for Hantaan (Puumala) virus. During the hospital course haemodialysis was neces...

ea0038p268 | Obesity, diabetes, metabolism and cardiovascular | SFEBES2015

Prediabetes incidence and risk of developing cardiovascular disease in women with polycystic ovary syndrome

Asimi Zelija Velija , Semiz Sabina , Dujic Tanja

Objective: In this study we analysed the prediabetes incidence in women with polycystic ovary syndrome (PCOS), as well as prediabetes and cardiovascular disease (CVD) risk factors in women with PCOS.Methods: This study included 148 women with PCOS, with no type 2 diabetes mellitus (T2DM) and CVD present at the baseline. We determined a comprehensive panel of biochemical parameters, including lipid profile, glucose and insulin levels during oral glucose t...

ea0070aep190 | Bone and Calcium | ECE2020

Multiple endocrinopathies associated with myotonic dystrophy type 1 – case report

Miličević Tanja , Novak Anela

Introduction: Myotonic dystrophy type 1 (DMT1) is the most prevalent muscular dystrophy that affects 1 in 8000 individuals. Disease is caused by CTG repeat expansion of the DMPK gene located on chromosome 19. Beside neuromuscular involvement, studies have found an increased prevalence of endocrinopathies such as diabetes, hyperparathyroidism and hypogonadism. The exact underlying mechanism of endocrine dysfunction remains unclear. Moreover, endocrine dysfunction is progressive...

ea0081p108 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Prevalence of autosomal dominant mutations of Familial hypercholesterolemia in Finnish patients with premature coronary artery disease and elevated LDL-C levels

Jokiniitty Antti , Eskola Markku , Saarela Tanja , Metso Saara

Background and aims: To assess the prevalence and variability of pathogenic or likely pathogenic autosomal dominant mutations (ADM) of Familial Hypercholesterolemia (FH) in a Finnish cohort of patients with premature coronary artery disease (CAD) and elevated LDL-C levels.Methods: Study population was enrolled from 162 patients diagnosed with premature CAD (men < 55 years and women < 60 years) and history of high LDL-C (≥ 5 mmol/l) levels, ...

ea0081p109 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Maternal triglyceride levels, and not fructosamine, in early pregnancy are associated with birth weight

Clinck Isabel , Verelst Faro , Twickler Marcel , Vrijkotte Tanja

Objectives: Maternal metabolism has a major impact on foetal growth, and the risk of developing obesity, cardiovascular disease and diabetes in later life. Identification of maternal metabolic parameters in early pregnancy that predict birth weight (BW), is pivotal in the prevention of these diseases. We evaluated whether maternal triglyceride (TG) or fructosamine levels in early pregnancy, as possible reflectors of maternal insulin resistance (IR), could predominantly contrib...

ea0070aep345 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Role of an automated screening tool in familial hypercholesterolemia

Jokiniitty Antti , Metso Saara , Saarela Tanja , Eskola Markku

Familial hypercholesterolemia (FH) remains underdiagnosed in general population. Screening programs in unselected individuals have shown modest results in identifying patients with FH. Incidence of FH is higher in young patients with coronary artery disease (CAD), especially when associated with high LDL-cholesterol levels. Targeted screening in this population could add value to FH-index patient identification. We have established an IT-based automated screening tool to enhan...

ea0016s20.2 | Translational highlights | ECE2008

SF-1 knockout mice as a model for hormone independent brain sexual differentiation

Spanic Tanja , Budefeld Tomaz , Grgurevic Neza , Tobet Stuart , Majdic Gregor

Animals that are not exposed to endogenous sex steroids during development provide an important model for studying hormone independent development of brain sex differences. Due to gonadal agenesis, male and female steroidogenic factor 1 knockout (SF-1 KO) mice are born phenotypically female. Normally, they die shortly after birth due to adrenal insufficiency. Early corticosteroid injections followed by adrenal transplantation can maintain SF-1 KO mice into adulthood. As severa...

ea0067gp5 | Poster Presentations | EYES2019

Vandetanib in medullary thyroid cancer-related Cushing syndrome: a case report

Režić Tanja , Matijaca Ana , Polovina Tanja Škorić , Marušić Srećko , Jakšić Vlatka Pandžić

Background: Medullary thyroid cancer is a rare neuroendocrine neoplasm that can secrete variety of hormones, including ACTH. Cushing syndrome due to ectopic ACTH secretion is a rare complication of medullary thyroid cancer, usually accociated with metastatic disease. Around 50 percent of patients with medullary thyroid carcinoma and ectopic Cushing syndrome die due to complications of hypercortisolism. Based on the aforementioned, efficient management of hypercortisolism is cr...

ea0070ep313 | Pituitary and Neuroendocrinology | ECE2020

Radiotherapy in acromegaly: a single centre experience

Rezic Tanja , Skoric Polovina Tanja , Kraljevic Ivana , Solak Mirsala , Zibar Tomšić Karin , Balasko Anne-Marie , Dusek Tina , Heinrich Zdravko , Kastelan Darko

Background: Radiotherapy (conventional and/or radiosurgery) is an effective treatment option in patients with acromegaly when biochemical control of the disease cannot be achieved by medication and/or surgery. Purpose: The aim of our study was to evaluate the efficacy of gamma-knife radiosurgery or conventional radiotherapy in the treatment of GH-secreting pituitary adenomas.Materials and methods: We conducted a retrospective analysis of 22 acromegaly pa...

ea0081p216 | Thyroid | ECE2022

Keep calm and call the surgeon: a case series of urgent thyroidectomy in thyrotoxicosis

Rezic Tanja , Novosel Tomislav , Kardum-Pejic Mirjana , Oreski Ivan , Boscic Drago , Marusic Srecko , Pandzic Jaksic Vlatka

Introduction: The standard management of Graves’ disease includes initial use of antithyroid drugs, while radioactive iodine ablation or thyroid surgery are later definitive treatment options. Management of thyrotoxicosis secondary to the use of amiodarone can be challenging as patients may not promptly respond to antithyroid or corticosteroid therapy, and thyrotoxicosis may be more harmful in those patients owing to the underlying cardiac disease. In rare thyrotoxicosis ...