Searchable abstracts of presentations at key conferences in endocrinology

ea0035p676 | Growth hormone IGF axis basic | ECE2014

GH replacement therapy affects the morphology and function of the left ventricle in patients with adult-onset GH deficiency

Dlesk Anton , Kamensky Gabriel , Lazurova Ivica , Kuzma Martin , Jackuliak Peter , Payer Juraj

Background: GH plays an important role in maintaining physiological morphology and function of the left ventricle (LV). In GH deficient (GHD) patients a systolic and/or diastolic LV dysfunction has been documented. LV systolic dysfunction results from reduced LV mass (LVM), which subsequently leads to a decrease of the LV ejection fraction (EF). Results from clinical trials evaluating the effect of GH replacement therapy on the morphological and functional changes of the LV in...

ea0070ep322 | Pituitary and Neuroendocrinology | ECE2020

Heart failure as a first manifestation of acromegaly - A case report

Sagova Ivana , Pavai Dusan , Dragula Milan , Kantarova Daniela , Vanuga Anton , Vaňuga Peter

Acromegaly is a rare disease, which is mainly caused by benign tumour of the pituitary gland. Long-term presence of elevated growth hormone (GH) and insulin like growth factor 1 (IGF-1) levels accompanying this disease is associated with rheumatologic, cardiovascular, pulmonary and metabolic complications. Cardiovascular complications of acromegaly include a cardiomyopathy, arterial hypertension, arrhytmias, valvulopathy as well as endothelial dysfunction. Cardiovascular disea...

ea0032p728 | Obesity | ECE2013

Serum- and glucocorticoid-regulated kinase 1 in obesity-related adipose tissue and peripheral inflammation

Reiter Marie Helene , Kiefer Florian , Zeyda Maximilian , Kopecky Chantal , Stulnig Thomas , Luger Anton , Vila Greisa

The serum- and glucocorticoid-regulated kinase 1 (Sgk1) is a direct transcriptional target of glucocorticoids and is post-translationally activated by the insulin/IGF1 pathway. Distinct polymorphisms in the Sgk1 gene are associated with increased body weight and type 2 diabetes. Here we investigate the expression and regulation of Sgk1 in human obesity.In both omental and subcutaneous human adipose tissue, Sgk1 expression is significantly increased in 20...

ea0032p826 | Pituitary–Basic (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

The role of GLI1 in pituitary tumor formation and pituitary cell survival

Lampichler Katharina , Ferrer Patricio , Vila Greisa , Luger Anton , Knosp Engelbert , Wagner Ludwig , Baumgartner-Parzer Sabina

The transcription factor and proto-oncogene GLI1 is the terminal mediator of the Hedgehog signalling pathway which is involved in developmental processes, stem cell maintenance and cell proliferation. Although the pathway is mainly active during embryogenesis and tissue repair, it is frequently reactivated in several cancer types.Based on these findings we investigated the potential role of GLI1 in the pathogenesis of pituitary adenomas. GLI1 expression ...

ea0029p1643 | Thyroid (non-cancer) | ICEECE2012

Control of 217 hypothyroid women during pregnancy

Familiar C. , Anton T. , Marco A. , Tapia M. , Villa M. , Ramos A. , Moraga I.

Introduction: The new guidelines for the management of hypothyroidism (HP) during pregnancy recommend a tighter treatment with levothyroxine (Lt4) to reach TSH values similar to those of pregnant women without thyroid dysfunction (TSH <2.5 mU/l in the 1st trimester-T- and TSH <3mu/l in the 2nd and 3rd T).Objectives: To assess the degree of control of HP in women followed during pregnancy according to the current criteria and the possible associat...

ea0025p271 | Reproduction | SFEBES2011

Increased epididymal Rnase9 expression in Rnase10 (−/−) mice

Sharp Victoria , Krutskikh Anton , Dacheux Jean-Louis , Poutanen Matti , Huhtaniemi Ilpo

Spermatozoa are dependent on the proximal epididymis environment to complete their maturation. However, no single specific factor crucial for this process has been identified. Rnase9 and Rnase10 are expressed specifically in the murine proximal epididymis. Located on chromosome 14C1 only 28 kb apart, they do not show high homology with each other. An orthologue of both genes exist in the rat and human, and ‘Train A’ (porcine orthologue) is the most abun...

ea0022p106 | Bone/Calcium | ECE2010

Osteocalcin, OPG and RANKL circulating levels in adolescent idiopathic scoliosis

Popa Oana , Chiru Anton Mariana , Vladoiu Susana , Manda Dana , Ianas Olga

Background: Idiopathic scoliosis is a pathological entity of unknown etiology, characterized by a three-dimensional deformity of the spine and a low bone mass. The exact mechanism of bone loss in idiopathic scoliosis is unknown yet. However is well known that RANKL is a potent stimulator of bone resorption by binding receptor activator of nuclear factor-kB (RANK) in the osteoclasts cell membrane. OPG is a decoy receptor for RANKL, which interferes with RANKL/RANK binding and i...

ea0022p585 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

The metabolic syndrome (MetS) in 2610 GH deficient (GHD) subjects before GH replacement: a KIMS (Pfizer International Metabolic Database) analysis

Verhelst Johan , Mattsson Anders F , Luger Anton , Thunander Maria , Goth Miklos , Koltowska-Haggstrom Maria , Abs Roger

Objective: To identify MetS and non-MetS in subjects with adult-onset GHD before start of GH replacement and to compare prevalence of cardiovascular risk factors.Subjects and methods: MetS was defined (IDF criteria) by the obligatory presence of increased waist circumference (WC) and presence of at least two of following components: hypertension, decreased HDL-cholesterol, increased triglycerides, diabetes mellitus. The complementary group was defined as...

ea0022p623 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Circadian rhythmicity changes of gonadal and growth axis in adolescent idiopathic scoliosis

Manda Dana , Chiru Anton Mariana , Vladoiu Suzana , Popa Oana , Ianas Olga

Adolescent idiopathic scoliosis (IS) represents an evolutive disease that occurs in puberty and progresses till the skeletal maturation. The neuroendocrine hypothesis involving a melatonin deficiency as the source for IS is one of the proposed causes of this plurifactorial disease.Objective: To investigate the hormonal changes of both the gonadal and growth axis and circadian rhythmicity in subjects with adolescent idiopathic scoliosis compared to age ma...