Searchable abstracts of presentations at key conferences in endocrinology

ea0019p212 | Neuroendocrinology and behaviour | SFEBES2009

Stimulation of PKCβII -dependent ERK1/2 signalling by endokinin B and substance P may cause gene transcription via the tachykinin NK1 receptor in astrocytoma cells

Newton S , Walker A , Page N

Endokinin B (EKB) is a recently identified tachykinin whose role is not yet fully understood. EKB displays equivalent affinity for the three tachykinin receptors as substance P (SP) which it is often found co-expressed with. SP has been implicated in a variety of neuroendocrinological responses including stress regulation, and affective and anxiety-related behaviours. An important aspect, therefore, is to dissect a distinct role for EKB from that of SP. Here, we have attempted...

ea0011p78 | Clinical case reports | ECE2006

Synchronous malignant para-aortic phaeochromocytoma and vagal nerve paraganglioma in a patient with germline SDHB mutation

McCallum RW , Stanton P , Walker S , Parameswaran V , Greenaway T

Phaeochromocytomas and paragangliomas arising as part of familial syndromes such as multiple endocrine neoplasia (MEN)2 or von-Hippel Lindau syndrome (VHL) are more likely to be malignant and multiple. Recently the role of mutations in the SDH genes (encoding subunits of succinate dehydrogenase) have also been identified as important in the aetiology of such tumours. We report a case where identification of an apparently sporadic metastatic phaeochromocytoma was found to be co...

ea0004oc30 | Neuroendocrinology and diabetes | SFE2002

INVESTIGATION OF IMPAIRED INSULIN ACTION IN CULTURED SKELETAL MUSCLE FROM TYPE 2 DIABETES MELLITUS PATIENTS

McIntyre E , Halse R , Yeaman S , Walker M

Impaired insulin action is a characteristic feature of type 2 diabetes and skeletal muscle is the principal tissue for peripheral glucose disposal. Aims: To determine if after prolonged culture human muscle cells from characterised type 2 diabetes patients have defects of insulin action compared to controls. Design: After attaining local Ethical Committee approval six compliant type 2 diabetic patients with severe clinical insulin resistance, on greater than 100 units of insul...

ea0004dp13 | Diabetes, metabolism and cardiovascular | SFE2002

INVESTIGATION OF IMPAIRED INSULIN ACTION IN CULTURED SKELETAL MUSCLE FROM TYPE 2 DIABETES MELLITUS PATIENTS

McIntyre E , Halse R , Yeaman S , Walker M

Impaired insulin action is a characteristic feature of type 2 diabetes and skeletal muscle is the principal tissue for peripheral glucose disposal. Aims: To determine if after prolonged culture human muscle cells from characterised type 2 diabetes patients have defects of insulin action compared to controls. Design: After attaining local Ethical Committee approval six compliant type 2 diabetic patients with severe clinical insulin resistance, on greater than 100 units of insul...

ea0030oc5.3 | Oral Communications 5 | BSPED2012

A comparison of patient's preferences for attributes of GH delivery devices: children starting versus children established on GH treatment

Yaw Stephanie How , Mushtaq Talat , Alvi N S , Walker Jenny , Whitehead Amanda

Background: Several devices are available for the administration of recombinant GH. A prospective study was undertaken to look at those attributes of GH delivery device most important to patients when making their choice.Objectives: i) To understand which features of a GH device are considered most important to patients when choosing a device. ii) Comparison of patient’s device preferences at start of GH treatment and after 2 years of treatment. iii...

ea0007p223 | Steroids | BES2004

11beta-hydroxysteroid dehydrogenase type 1 and the production of cerebrospinal fluid

Rauz S , Walker E , Tomlinson J , Hughes S , Wood P , Stewart P , Murray P

The epithelial cells of the choroid plexus (CP) are responsible for cerebrospinal fluid (CSF) secretion into the ventricles of the brain, which then drains principally into the dural sinuses. The balance between production and drainage, in part, facilitates a normal intracranial pressure. The secretion of sodium and anions by the CP, creates an osmotic gradient driving the movement of water into the ventricles. This mechanism is analogous to that found in the ocular ciliary ep...

ea0003p244 | Steroids | BES2002

Expression and corticosteroid regulation of serum and glucocorticoid regulated kinase, and epithelial sodium channel subunits in human ocular ciliary epithelium

Rauz S , Walker E , Hughes S , Coca-Prados M , Hewison M , Murray P , Stewart P

Sodium transport across the human ocular non-pigmented ciliary epithelium (NPE) is fundamental to the production aqueous humour and maintenance of intraocular pressure. In sodium transporting tissues, serum and glucocorticoid regulated kinase isoform 1 (SGK1) has been identified as an early corticosteroid target gene in the activation of pre-existing epithelial sodium channels (ENaC). We previously demonstrated the presence of both the mineralocorticoid (MR) and glucocorticoid...

ea0029p1285 | Paediatric endocrinology | ICEECE2012

ACTH and cortisol are differently associated with metabolic syndrome components in a large cohort of Caucasian obese children and adolescents

Ricotti R. , Prodam F. , Bellone S. , Walker G. , Parlamento S. , Savastio S. , Genoni G. , Agarla V. , Aimaretti G. , Bona G.

Introduction: Higher cortisol levels and, in particular, hyperactivity of the HPA axis might play a role in the development of MS at least in adults. Data on the pediatric age are scanty.Aim of our study was to evaluate ACTH and cortisol association with MS, its components, phenotypic parameters, family history of metabolic derangements in pediatric obesity.Methods: Cross-sectional study. 271 Caucasian overweight or obese children ...

ea0003oc4 | Genetics: New Insights into Endocrine Disease | BES2002

Analysis of novel mutations in the HSD11B2 gene: Implications for AME and possibly IUGR

Lavery G , Ronconi V , Draper N , Chalder S , Walker E , Mcternan C , Mantero F , Hewison M , Stewart P

Mutations in the HSD11B2 gene explain the syndrome of apparent mineralocorticoid excess (AME), which is characterised by severe hypokalemic hypertension. The enzyme product of the HSD11B2 gene, 11-beta hydroxysteroid dehydrogenase type 2 (11beta HSD2), converts cortisol to its inactive form, cortisone. This reaction occurs primarily in the kidney, preventing the mineralocorticoid effects of cortisol, and in the placenta where it is believed to regulate fetal growth by protecti...

ea0034p249 | Obesity, diabetes, metabolism and cardiovascular | SFEBES2014

Derivatisation of estrogens enhances specificity and sensitivity of analysis by liquid chromatography tandem mass spectrometry

Faqehi Abdullah M M , Cobice Diego F , Naredo Gregorio , Mak Tracy C S , Walker Brian R , Homer Natalie Z M , Andrew Ruth

Physiological circulating concentrations of estrogens are very low in men and postmenopausal women (<50 pg/ml), which presenting analytical challenges. Immunoassays can detect as low as 30 pg/ml, but cross-reactivity is a concern. Liquid chromatography–tandem mass spectrometry (LC–MS/MS) offers greater specificity than immunoassays, but ionisation of estrogens is inefficient. Derivatisation, which introduces charged moieties, may enhance ionisation. Dansylated de...