Searchable abstracts of presentations at key conferences in endocrinology

ea0090p147 | Pituitary and Neuroendocrinology | ECE2023

Baseline clinical and treatment characteristics of dopamine agonist treated patients in a Dutch national cohort of patients with prolactinoma

Zandbergen Ingrid , Pelsma Iris , van Furth Wouter , Biermasz Nienke

Introduction: Dopamine agonists (DA) are first-line treatment for prolactinomas and effectively control hyperprolactinemia in most patients. However, side effects may negatively impact health-related quality of life; and post-withdrawal remission rates are low, resulting in prolonged DA treatment.Methods: Dutch multicenter prospective observational cohort study mapping standard care for 316 prolactinoma patients. Baseline clinical characteristics and tre...

ea0099p320 | Pituitary and Neuroendocrinology | ECE2024

Impact of clinical and treatment characteristics on HR-QoL in patients with prolactinoma - cross-sectional analysis of a dutch multicenter prospective cohort study

Zandbergen Ingrid , Pelsma Iris , van Furth Wouter , Biermasz Nienke

Introduction: Patients with prolactinomas suffer from a wide range of symptoms, of which the effect on health-related quality of life (HR-QoL) needs further investigation. Moreover, the first-line treatment for patients with prolactinomas, dopamine agonists (DAs), albeit being effective in lowering prolactin levels, might further hamper HR-QoL due to side effects. To assess the impact of symptoms and treatment modality on HR-QoL, a cohort of patients with prolactinoma was cros...

ea0081ep51 | Adrenal and Cardiovascular Endocrinology | ECE2022

Is there a difference in symptoms, catecholamine release and tumor size in pheochromocytomas diagnosed due to initially symptoms or incidenthalomas

Nermoen Ingrid , Korneliussen Marte Henriksen

Background: Pheochromocytoma is a rare adrenal tumor that can present with a variety of different symptoms. The cardinal symptoms are paroxysmal palpitations, headaches and sweating together with paroxysmal or persistent hypertension. Increasing use of CT scan contribute to the discovery of more adrenal incidentalomas and therefore more pheochromocytomas due to the workup of the incidentalomas. We intended to investigate if the presentation of the pheochromocytoma was differen...

ea0045p62 | Pituitary and growth | BSPED2016

Clinical characteristics of Cornelia de Lange Syndrome due to an HDAC8 mutation

Wilkinson Ingrid , Thalange Nandu , Hammond Peter

J was born at term (2.62 kg). She presented aged six months with severe faltering growth, (weight 5.1 kg, length 57.3 cm, OFC 39.0 cm). Investigations showed elevated prolactin (1838 mIU/l) and undetectable IGF1 but were otherwise normal. Her karyotype was 46XX. A brain MRI was normal. By 11 months of age she had evident developmental delay and dysmorphic features (triangular face; hypertelorism; synophrys; broad nasal root; short nose with rounded tip; carp like mouth; short ...

ea0081p406 | Pituitary and Neuroendocrinology | ECE2022

GLP-1 receptor agonists stimulate growth hormone release

Reppo Ingrid , Heinla Keiu , Sedman Tuuli , Volke Vallo

The secretion of growth hormone (GH) is under the feedback control of numerous nutritional and endocrine factors. The most widely used endocrine dynamic tests used to diagnose GH deficiency, insulin hypoglycemia test, and glucagon test, are time-consuming and cumbersome both for patients and medical personnel. There is an unmet need for easier to conduct, shorter, and safer diagnostic tests. We and other groups have previously demonstrated that acute administration of glucagon...

ea0063p1039 | Interdisciplinary Endocrinology 2 | ECE2019

The role of the growth hormone – insulin-like growth factor 1 axis in primary osteoarthritis

Pelsma Iris , Claessen Kim , Ramos Yolande , Meulenbelt Ingrid , Biermasz Nienke

Introduction: Increased insulin-like growth factor 1 (IGF-1) levels in patients with acromegaly are associated with clinical and radiological osteoarthritis (OA). We aimed to elucidate whether serum IGF-1 levels differ in patients with primary OA as compared to healthy controls and whether genetic variants known to affect serum IGF-1 levels are also associated with primary OA.Methods: Patients from the GARP study with familial generalized OA (n=...

ea0041ep332 | Clinical case reports - Thyroid/Others | ECE2016

A novel clinical phenotype of acquired partial lipodystrophy associated with intensive childhood cytostatic treatment

Nijhoff Michiel , Corssmit Eleonora , Louwerens Marloes , Jazet Ingrid , Pereira Alberto

Context: Lipodystrophy is characterized by subcutaneous fat loss, fat maldistribution, and metabolic syndrome. We present a novel phenotype of partial acquired lipodystrophy, possibly associated with childhood chemotherapy.Case reports: Two adult female patients that had been exposed to intensive cytostatic treatment in childhood for leukemia and aplastic anemia, respectively, were referred for therapy resistant diabetes. Both patients had distinct parti...

ea0037ep164 | Reproduction, endocrine disruptors and signalling | ECE2015

Prevalence of vitamin D deficiency in Slovak women with polycystic ovary syndrome and its relation to metabolic and reproductive abnormalities

Figurova Jana , Dravecka Ingrid , Javorsky Martin , Petrikova Jana , Lazurova Ivica

Objective: Polycystic ovary syndrome (PCOS) is the most common endocrine disorder characterised by menstrual dysfunction, infertility, presence of polycystic ovaries and biochemical and clinical hyperandrogenism affecting up to 4–18% women of reproductive age. Vitamin D is thought to influence the development of PCOS through gene transcription and hormonal modulation of insulin metabolism and fertility regulation. The aim of this prospective case–control study was to...

ea0037ep1156 | Clinical Cases–Pituitary/Adrenal | ECE2015

Phaeochromocytoma and hypoglycaemic fits: a case report

Folling Ivar , Olsen Anne Lise , Nermoen Ingrid , Thorsby Per Medboe

Introduction: Phaeochromocytomas often induce hyperglycaemia. Few cases are reported with hypoglycaemic fits. The mechanism is unknown. Our findings may indicate a mechanism.The patient: A 37 year old female had a phaeochromocytoma, with typical characteristics: attacks of headache, nausea and sweating. High blood pressures, up to 237/134. Electrocardiogram indicated ischemia, normal coronary arteries on dynamic CT, normal Echo-Doppler heart examination....

ea0014p150 | (1) | ECE2007

Adrenal incidentalomas and insulin sensitivity – are there any differences between adenomas and hyperplasia?

Dudasova Daniela , Lazurova Ivica , Wagnerova Hedviga , Dravecka Ingrid

It is well known that adrenal masses, particularly adenomas are frequently related to metabolic syndrome and insulin resistance. However, there are no reported data about the differences between adenomas and hyperplasia.Authors examined the prevalence of symptoms of the metabolic syndrome and insulin resistance in 25 patients with adrenal incidentalomas (10 men, 15 women) of the mean age 57.9+15 years. 15 patients had adrenal adenoma determined by CT or ...