Searchable abstracts of presentations at key conferences in endocrinology

ea0026p287 | Pituitary | ECE2011

Tumor size and parasellar extension influence on macroprolactinomas’ outcome

Trifanescu R A , Mihaila V , Serban A , Hortopan D , Dumitrascu A , Caragheorgheopol A , Coculescu M

Introduction: Parasellar extension of macroprolactinomas defined on imaging criteria was reported to be an independent predictor of hormonal resistance to dopamine agonists (DA).Methods: Two hundred and twelve patients with macroprolactinomas (87 M/125 F), treated with DA for 5 years median period; prolactin (fluoroimmunoassay or chemiluminescence), CT scan and/or MRI with contrast agents were performed; maximum diameter evolution was reported.<p cla...

ea0031p298 | Pituitary | SFEBES2013

Steroid regulation of gene and protein expression of osteopontin and αvβ3 integrin in ovine endometrium

Tremaine Tina , Fouladi-Nashta Ali , Khalid Mohammed , Wathes Claire

At implantation, the ability of an embryo to successfully attach to the luminal epithelium is dependent on the receptive phenotype the endometrium must acquire. This spatially and temporally restricted period of uterine receptivity is defined by endometrial molecular adaptations, highly regulated by embryonic-derived signals and ovarian steroids. Critical to this isthe expression of adhesivemoleculesintegrins and osteopontin (OPN) at the foetal-maternal interface which facilit...

ea0081rc3.6 | Rapid Communications 3: Thyroid 1 | ECE2022

The mRNA of fibronectin 1 and of the integrin subunit alpha V are powerful prognostic indicators in papillary thyroid carcinoma

Vitale Mario , Marotta Vincenzo , Tortora Anna , Izzo Giulia , Rocco Domenico

Integrins are cell-extracellular matrix adhesion molecules considered functionally related to the development of cancer metastasis. Starting from the dataset of mRNA-seq of papillary thyroid carcinoma (PTC) from the TCGA, we determined the expression of fibronectin 1 (FN1) and fibronectin-binding integrins in PTC. We then analyzed the association of the expression of these two genes with the driver genes, the stage of the disease and its outcome. 355 PTCs and 58 normal thyroid...

ea0070aep227 | Bone and Calcium | ECE2020

Osteogenesis imperfecta type V due to a rare mutation c.119C> T in the IFITM5: A case report

Grebennikova Tatiana , Gavrilova Alina , Tiulpakov Anatoly , Tarbaeva Natalia , Melnichenko Galina , Belaya Zhanna

Osteogenesis imperfecta (OI) is a heritable skeletal disorder caused by defective bone formation. OI type V (MIM#:614757) develops due to mutation in the IFITM. Mutation c.-14C >T in the IFITM5 is more common whereas only five reported patientshave a c.119C >T mutation. Patients with IFITM5:c.119C >T mutation usually have low-traumatic fractures in the prenatal period of development, severe limb and chest deformities, short height, verteb...

ea0012oc7 | Young Endocrinologist prize session | SFE2006

T3 stimulation of MAP kinase and cell proliferation in human osteoblast-like cells is initiated at integrin αVβ3

Scarlett AL , Parsons MP , Hanson PL , Sidhu KK , Milligan TP , Burrin JM

T3 and T4 rapidly activate intracellular signalling cascades via thyroid hormone receptor (TR)-independent actions, suggesting the existence of a plasma membrane receptor. Recent studies support a role for the RGD recognition site of integrin, a transmembrane glycoprotein, as a cell surface TR. We have demonstrated, using PCR and Western blotting, the expression of integrin αVβ3 mRNA and protein in the transformed human osteosarcoma cell line MG...

ea0034p218 | Obesity, diabetes, metabolism and cardiovascular | SFEBES2014

Young women with polycystic ovary syndrome have increased concentrations of circulating annexin V-positive microparticles derived predominantly from platelets

Willis Gareth , Connolly Katherine , Ladell Kristin , Miners Kelly , Price David , Guschina Irina , Clayton Aled , James Philip , Rees Aled

Background: Women with polycystic ovary syndrome (PCOS) may have increased cardiovascular (CV) risk but the mechanisms are unclear. Microparticles (MP), small circulating vesicles released from platelets, monocytes and endothelial cells, are elevated in patients with CV disease, and may increase CV risk through altered cell content and/or increased surface exposure of procoagulant phosphatidylserine (PS).Aims: To compare MP characteristics between women ...

ea0035p384 | Diabetes (epidemiology, pathophysiology) | ECE2014

Translating the A1C assay into estimated average fasting glucose values: Data from the 2011 Korea National Health and Nutrition Examination Survey V

Kang Jun Goo , Ohn Jung Hun , Park Ju Ri , Yu Sung Hoon , Ryu Ohk Hyun , Kim Chul Sik , Lee Seong Jin , Hong Eun Gyoung , Kim Doo-Man , Yoo Jae Myung , Ihm Sung Hee , Choi Moon Gi , Yoo Hyung Joon

Aim: An international expert committee, after considering data on association of HbA1c and retinopathy, recommended that diabetes be diagnosed when HbA1c is more than 48 mmol/mol (>6.5%), provided this assay is done in a standardized laboratory. However, the performance of HbA1c in detecting diabetes in the Korean population remains unknown. The purpose of this study was to evaluate the efficiency of HbA1c in diagnosing diabetes and to identify the optimal threshold in the...

ea0019p7 | Bone | SFEBES2009

A mouse model, Hcalc1, for autosomal dominant hypercalciuria is due to a transient receptor potential cation channel, subfamily V, member 5 (Trpv5) mutation

Loh N , Stechman M , Ahmad B , Hannan F , Hough T , Chiev K-P , Stewart M , Bentley L , Cox R , Brown S , Thakker R

To identify genes causing hypercalciuria, we screened male offspring of C57BL/6J male mice mutagenised by N-ethyl-N-nitrosourea (ENU) for this abnormality. Mice were kept in accordance with UK Home Office welfare guidelines and project licence restrictions. Metabolic cage studies were performed to collect 24-hour urine samples, and this revealed one mouse with hypercalciuria (Hcalc1). Inheritance testing demonstrated that Hcalc1 was inherited as an autosomal domi...

ea0032p184 | Cardiovascular Endocrinology &amp; Lipid Metabolism | ECE2013

Adults with GH deficiency have subclinical longitudinal left ventricular dysfunction, without significant vascular function impairment, suggesting intrinsic myocardial disease

Badiu Corin , Mihaila Sorina , Mincu Raluca , Dobrescu Ruxandra , Vinereanu Dragos

Aims: GH deficiency (GHD) is associated with increased cardiovascular events. We aimed to evaluate cardiac, arterial, and endothelial function, by conventional and 2D speckle tracking echocardiography (STE), and biomarkers (proBNP and troponin I), in GHD patients by comparison with normal individuals with similar cardiovascular risk profile.The study included 52 GHD patients (46.9±15.6, 36 males), free of cardiovascular disease, severe hypertension ...

ea0038pl4biog | Society for Endocrinology Dale Medal Lecture | SFEBES2015

Society for Endocrinology Dale Medal Lecture

Thakker Rajesh V

Rajesh Thakker is the May Professor of Medicine at the University of Oxford, UK. He received his medical degree from the University of Cambridge in 1980, and from 1981 to 1988 he undertook postgraduate clinical and research training at The Middlesex Hospital, The Hammersmith (Royal Postgraduate Medical School, RPMS), Hospital, and Northwick Park (MRC Clinical Research Centre) Hospital (London). In 1988, he was appoint...