Searchable abstracts of presentations at key conferences in endocrinology

ea0032p196 | Cardiovascular Endocrinology & Lipid Metabolism | ECE2013

Perturbed sympatho-vagal balance in Turner syndrome: relation to phenotype and aortic dilation

Trolle Christian , Mortensen Kristian Havmand , Hjerrild Britta , Andersen Niels Holmark , Gravholt Claus Hojbjerg

Objective: The risk of aortic dissection is 100-fold increased in Turner syndrome (TS). Increased blood pressure (BP) and heart rate is present as well as an increased risk of ischemic heart disease and diabetes. This study aimed to prospectively assess heart rate variability (HRV) in TS and its relation to aortic dimensions.Methods: Adults with TS (n=91, aged 37.4±10.4 years) recruited through the Danish National Society of Turner Syndrome...

ea0032p627 | Growth hormome IGF axis – basic | ECE2013

Preclinical characterisation of NNC0195-0092, a long-acting GH

Thygesen Peter , Sune Andersen Henrik , Rischel Christian , Josef Fels Johannes , Langeland Johansen Nils

GH is an important regulator of longitudinal growth in children and metabolism in adults. GH is used for treatment deficiency disorders in both children and adults. GH treatment is safe and well tolerated. However, its clinical use is limited to daily s.c. injections which poses a challenge for both the patients and the physicians and has prompted research into alternative approaches to GH treatment.NNC0195-0092 is a hGH derivative conjugated with an alb...

ea0032p711 | Neuroendocrinology | ECE2013

Infrasellar gangliocytoma causing cushing's disease: a case report

Domingue Marie-Eve , Marbaix Etienne , Godfraind Catherine , Col Vincent , Raftopoulos Christian , Maiter Dominique

Gangliocytomas are uncommon neuronal tumors that can sometimes cause endocrine syndromes. A few such cases have been reported in association with Cushing’s disease. In most instances, the tumor contained CRH and was associated with pituitary corticotroph hyperplasia or adenoma (mixed lesion). Only one case of isolated gangliocytoma causing Cushing’s disease per se has been described.We report the case of a 62 year-old woman whose clinical pictu...

ea0032p875 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Thirty-day mortality in acute non-surgical patients admitted with hyponatremia

Holland-Bill Louise , Christiansen Christian , Ring Troels , Toft Sorensen Henrik , Lunde Jorgensen Jens Otto

Introduction: Hyponatremia (serum sodium ≤135 mmol/l), the most common electrolyte disorder encountered, has been associated with increased mortality in patients with particularly cancer, heart failure, chronic kidney and liver disease. However, evidence of the clinical implications in broader populations is scarce, and uncertain due to confounding from preexisting disease. We aimed to examine the association between admission-hyponatremia and 30-day mortality in acute n...

ea0022s1.6 | European networks | ECE2010

The European Registry on Cushing's syndrome (ERCUSYN) database: first year experience

Webb Susan , Santos Alicia , Trainer Peter , Strasburger Christian , Lamberts Steven , Wass John , Feelders Richard , Franz Holger

The ERCUSYN (European Registry on Cushing’s syndrome (CS)) study is a project funded by the European Commission Public Health Program (PHP 800200), of which the ESE is one of the 41 Partners from 25 countries. The aims include obtaining prospective and follow-up data at EU level on epidemiology, mortality, outcome of therapies, co-morbidities, assessment of diagnostic and therapeutic strategies, quality of life evaluation using a disease-generated questionnaire (CushingQo...

ea0022p141 | Cardiovascular endocrinology and lipid metabolism | ECE2010

Serum IGF1 levels correlate to improvement of functional independence after ischemic stroke

Aberg Daniel , Jood Katarina , Blomstrand Christian , Jern Christina , Ladenvall Claes , Nilsson Michael , Isgaard Jorgen , Aberg David

Context and objective: GH and IGF1 both have neuroprotective and regenerative effects in experimental stroke. Our aim was to investigate whether the endogenous serum-IGF1 (s-IGF1) levels were correlated to recovery of functional independence in stroke patients.Subjects and methods: The analysis of s-IGF1 was performed in 400 patients of both sexes, aged 18–69 years old, and 40 controls previously included in the Sahlgrenska Academy Study on Ischemic...

ea0022p224 | Clinical case reports and clinical practice | ECE2010

Graves' disease, systemic lupus erythematosus, hypoparathyroidism: autoimmune polyglandular syndrome or coincidence?

Melcescu Eugen , Kemp Elizabeth H , Majithia Vikas , Vijayakumar Vani , Uwaifo Gabriel I , Koch Christian A

Data on coexisting Graves’ disease (GD), systemic lupus erythematosus (SLE), and hypoparathyroidism (hypop) are limited. Scanty case reports have described hypoparathyr or hypothyroidism (late complication) following external irradiation to the neck. The thyroid and parathyroid glands may be sensitive to the immunologic or irradiation damage.A 34-year old AA woman presented with tetanic-like cramps, easy skin bruising, fatigue, weight gain, nocturia...

ea0022p429 | Endocrine tumours &amp; neoplasia (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Ectopic Cushing’s syndrome caused by a well differentiated ACTH-secreting neuroendocrine carcinoma of the ileum

Singer Joerg , Koch Christian A , Bartels Michael , Aigner Thomas , Lincke Thomas , Fasshauer Mathias , Paschke Ralf

Cushing’s syndrome can be caused by adrenocorticotropic hormone-secreting solid tumors. We report a rare case of an ileal endocrine carcinoma that produced ACTH and induced hypercortisolism. A now 47-year-old male patient presented at the age of 41 with perspiration, weight gain, tremor and general fatigue. Diabetes mellitus and hypercortisolism was diagnosed by laboratory testing. Further examinations revealed ectopic Cushing’s syndrome. The search for the location ...

ea0022p503 | Growth factors | ECE2010

Acromegaly: a prospective analysis of the oral and maxillofacial pathologies and its impact of disease duration

Herrmann Burkhard , Mortsch Florentine , Berg Christian , Weischer Thomas , Mohr Christopher , Mann Klaus

Context: It is well established that clinical features of acromegaly concern the teeth and the jaw, but less is known about the degree of oral and maxillofacial pathologies and its impact of the disease duration.Patients: Twenty-eight acromegalics (13 females, 15 males) with a mean age 49±11 (mean±S.D.) years (range 31–70) were included in the study. Thirty-two percent had active disease, 39% were well-controlled under the s...

ea0022p637 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Rapid bone loss 23 years after diagnosis for childhood acute lymfoblastic leukaemia (ALL) in spite of GH therapy

Follin Cecilia , Link Katarina , Wiebe Thomas , Moell Christian , Bjork Jonas , Erfurth Eva Marie

Context: Acute lymphoblastic leukaemia (ALL) is the most common pediatric malignancy and its treatment includes many known risk factors for low bone mineral density (BMD), e.g. glucocorticosteroids, methotrexat and cranial radiotherapy (CRT).Objective: To evaluate bone mineral density (BMD) and markers of bone turn over in a group of adults with childhood onset ALL, treated with CRT and to evaluate the effect of 5 years with, and 8 years without GH thera...