Searchable abstracts of presentations at key conferences in endocrinology

ea0090p575 | Calcium and Bone | ECE2023

Cardiac MRI revealed altered structural and functional myocardium in patients with primary hyperparathyroidism: preliminary results

Ozberk Uğur , Hazirolan Tuncay , Ardali Duzgun Selin , Erbaş Tomris , Nahit Sendur Suleyman

Aim: The primary objective of this study was to evaluate the structural and functional cardiac parameters with MRI in patients with primary hyperparathyroidism (pHPT) before and after successful surgery.Method: In this prospective study 16 patients with pHPT were included. Detailed cardiac magnetic resonance imaging (MRI) examinations were performed preoperatively and at six months post-surgery. Following parameters were measured: Left ventricle ejection...

ea0090p611 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Gaucher Disease Type 3c: A Rare Metabolic Disease Diagnosed In Adulthood

Tuğce Şah Unal Fatma , Demir Ozgur

Background: Gaucher disease (GD) is the most prevalent lysosomal disorder caused by GBA mutations and abnormal glucocerebrosidase function, leading to glucocerebroside accumulation mainly in the liver, spleen, bone marrow, lungs, and occasionally in the central nervous system. Gaucher disease type 3c (GD3c) is a rare subtype of the subacute/chronic neuronopathic GD3, caused by homozygosity for the GBA p. Asp448His (D409H) mutation. Case...

ea0090ep304 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Neonatal diabetes mellitus in a patient with a novel heterozygous mutation in GATA6

Sechko Elena , Raykina Elizaveta , Kuraeva Tamara , Laptev Dmitry , Bezlepkina Olga , Peterkova Valentina

Transient neonatal diabetes mellitus (TNDM) occurs in 50-60% of all cases of neonatal diabetes mellitus (NDM). The most common cause of TNDM (70%) is almost invariably associated with defect in chromosome 6 and mutations in the KCNJ11, ABCC8, INS, NHF1B etc. genes. TNDM is caused by mutations in the GATA6 gene in rare cases. This gene encodes a transcription factor that is important for the development of the hematopoietic, cardiac and gastrointestinal systems.<p ...

ea0069p23 | Poster Presentations | SFENCC2020

Myxoedema crisis: The importance of establishing cardiac baseline at admission to guide optimum thyroid function correction rate

Elias Jennifer

Case history: A 65 year old unresponsive female, admitted as a stroke call, was found to have myxoedema crisis with admission TSH level of >100 mIU/l and T4 of 0.7 pmol/l. She was known hypothyroid with poor medication compliance. ITU admission for intubation and ventilation, CVVH (renal filtration) and vasopressors was required. Total length of ITU stay was 62 days, prolonged by cardiac complications during correction. There was no known cardiac history. On Day 7 of admission...

ea0062p03 | Poster Presentations | EU2019

Secondary Takotsubo syndrome induced by Phaeochromocytoma

Dhar Mili , Lakshmipathy Kavitha , Poddar Ankur , Field Benjamin , Nayyar Vidhu , Clark James , Zachariah Sunil

Case history: We present the case of a 70-year-old female who presented to the Emergency Department with sudden onset inter-scapular and upper abdominal pain. She had been experiencing intermittent headaches, palpitations and constipation which had not previously been investigated. The only past medical history was of hypothyroidism. She had no significant family history. There was a discrepancy in the blood pressure between both arms. Admission blood pressure was elevated at ...

ea0041ep894 | Pituitary - Clinical | ECE2016

Cardiac tissue Doppler echocardiographic evaluation of patients with prolactinoma treated with cabergoline

Arikan Durmaz Senay , Rasid Tasdelen Mustafa , Yildirim Nesligul , Cifci Aydin , Gungunes Askin

Introduction and aim: There are few side effects of cabergoline which is used for medical treatment of prolactinoma. For this reason, cabergoline is considered as first-line therapy of prolactinoma. However, chronic administration of high dose cabergoline in patients with prolactinoma may be associated with valvular heart disease. The aim of this study is to evaluate left ventricular systolic and diastolic functions by conventional and tissue Doppler echocardiography in patien...

ea0037ep150 | Reproduction, endocrine disruptors and signalling | ECE2015

Serum N-terminal pro-B-type brain natriuretic peptide levels detection and cardiac interventricular septum tissue Doppler echocardiographic evaluation of women with polycystic ovary syndrome

Ayhan Mehmet Emin , Durmaz Senay Arikan , Carlioglu Ayse , Demirelli Selami

Introduction: The aim of this study, left ventricular systolic and diastolic function by echocardiography and tissue Doppler echocardiographic evaluation and relationship serum N-terminal pro-B-type brain natriuretic peptide (NT-proBNP) levels of women with polycystic ovary syndrome (PCOS).Materials and method: Thirty-two women with PCOS (age: 23.4–4.6 years; BMI: 23.8–4.8 kg/m2), similar age and BMI have features 30 healthy womens c...

ea0060oc1 | (1) | UKINETS2018

The proinflammatory molecule, VAP-1, is enriched in the stroma of midgut NETs and plaques of carcinoid heart disease valves

Sagar Vandana M , Neil Desley AH , Papakyriacou Pantelitsa , Shah Tahir , Liu Boyang , Hirschfield Gideon , Steeds Richard P , Shetty Shishir , Weston Christopher J

Background: Vascular adhesion protein-1 (VAP-1) is a novel driver of tissue inflammation and fibrosis and may contribute to fibrotic complications of neuroendocrine tumours (NETs). We studied the VAP-1 expression in midgut NETs, which are associated with desmoplasia, and carcinoid heart disease (CHD), a significant complication of metastatic midgut NETs.Methods: Immunohistochemical analysis of paraffin-embedded midgut NETs and CHD valves were stained for...

ea0070aep124 | Bone and Calcium | ECE2020

«Angio Scan-01» for extraskeletal calcification assessment in patients with mineral and bone disorders in chronic kidney disease

Maganeva Irina , Volodicheva Victoria , Eremkina Anna , Aynetdinova Alina , Mokrysheva Natalia

Background: Mineral and bone disorders in chronic kidney disease (CKD-MBD) is a systemic disorder of mineral metabolism due to CKD, which is manifestedby abnormalities of calcium, phosphorus, parathormone (PTH) and vitamin D; renal osteodystrophy; extraskeletal calcification. In patients with CKD, vascular calcification occurs 10–20 years earlier than in the general population, and is highly prevalent (40–92%) in the hemodialysis population. «AngioScan-01&#187...

ea0070aep746 | Pituitary and Neuroendocrinology | ECE2020

Preoperative pegvisomant as a potential therapeutic option to improve cardiac function in Acromegaly-induced cardiomyopathy: Two cases

Ernst Matthias E. , Anand Gurpreet , Beuschlein Felix

Introduction: Acromegaly is a rare chronic disorder caused by growth hormone hypersecretion due to GH-producing pituitary adenoma. Surgery is the first-line treatment modality. However, patients with severe cardiac involvement are high-risk candidates for pituitary surgery. These patients may benefit from rapid preoperative biochemical control of acromegaly. There is emerging evidence of efficacy of pegvisomant, a GH-receptor antagonist, (either alone or in combination with so...