Searchable abstracts of presentations at key conferences in endocrinology

ea0007p24 | Cytokines and growth factors | BES2004

Excessive daytime sleepiness associated with hypercytokinaemia in POEMS

Wong S , Cresswell P , English P , Wilding J , Huda M , Pazmany L , Pinkney J , Hart I

The multisystem disorder POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is a rare plasma cell dyscrasia. Elevated cytokines may contribute to its pathogenesis. We describe a POEMS patient with elevated plasma cytokines and excessive daytime sleepiness (EDS).A 39-year-old white woman with IgA lambda and IgG kappa paraproteinaemia, peripheral axonal sensorimotor neuropathy, moderate anascara, skin thickening a...

ea0009p196 | Clinical | BES2005

A case of an angry old man

Grainge C , English P

A 92-year-old man presented with a one-month history of episodic aggression, confusion, urinary incontinence and auditory hallucinations. Episodes lasted 30 - 150 minutes, occurred daily and were abruptly self-terminating. Between episodes he was cognitively intact and lived independently. Initial investigations revealed a plasma glucose of 11.0 millimoles per litre, other biochemical tests were normal.He was known to have a pleural mass at the left lung...

ea0004p41 | Diabetes, metabolism and cardiovascular | SFE2002

PLASMA ADIPONECTIN RISES POST-PRANDIALLY IN OBESE BUT NOT IN LEAN SUBJECTS

English P , Coughlin S , Hayden K , Malik I , Wilding J

Introduction. Adiponectin is a novel circulating adipocyte derived protein, whose plasma concentrations paradoxically decrease with increasing fat mass. Adiponectin has been shown to improve both glucose and lipid metabolism, and circulating concentrations are inversely correlated with insulin resistance. The factors regulating adiponectin expression and secretion are poorly understood. No study has previously examined the acute post-prandial regulation of adiponectin s...

ea0003p266 | Steroids | BES2002

Testosterone exhibits a calcium antagonistic action upon store operated calcium channels in cultured vascular smooth muscle cells

Jones R , Ruban L , Pugh P , English K , Channer K , Jones T

Background: Testosterone acts as a coronary vasodilator, and improves myocardial ischaemia in men with coronary artery disease. The dilatory mechanism of testosterone is independent of the classical androgen receptor and also of the release of endothelial-derived vasodilators. The aim of the present study was to determine whether testosterone has any demonstrable calcium antagonistic action, and if so to determine whether this is via inhibition of voltage-operated calcium chan...

ea0003p267 | Steroids | BES2002

Testosterone does not increase the production of cyclic AMP (cAMP) in cultured vascular smooth muscle cells

Ruban L , Jones R , Pugh P , English K , Channer K , Jones T

Background: Testosterone is a coronary vasodilator, and improves myocardial ischaemia in men with coronary artery disease. The dilatory mechanism of testosterone is independent of the classical androgen receptor and endothelial-derived vasodilators. The aim of this study was to determine whether testosterone increases cAMP production in vascular smooth muscle cells (VSMCs) derived from the primary culture of rat thoracic aortae or in a VSMC cell line (A7r5).<p class="abste...

ea0003p268 | Steroids | BES2002

Circulating steroid levels in the testicular feminised (Tfm) mouse

Jones R , Hall J , Pugh P , English K , Channer K , Jones T

Background: The testicular feminised (Tfm) mouse exhibits an X-linked single base-pair deletion in the gene encoding the androgen receptor. Gene transcription produces a truncated form of the receptor protein, which has a conformational change in the androgen binding site, preventing androgen binding. Affected male animals (XTfmY) are rendered androgen insensitive and 17-alpha hydroxylase deficient, a key enzyme in the steroidogenesis pathway. XTfmY males have reduced circulat...

ea0002p49 | Genetics | SFE2001

A Case of Mu1tiple Endocrine Neoplasia Type 1 (MEN1) Caused By A New Genetic Mutation

Soran H , Murray L , Ellis I , Ellard S , English P , Jones I

Introduction: The MEN1 is inherited as autosomal dominant trait. In MEN 1 families a deletional mechanism of the regulatory gene appears to be the base of the syndrome.Case 1: 40-year-old lady presented with a two-day history of headaches, blurred vision and funny turns, culminating in loss of consciousness and a generalised tonic-clonic seizure. Her GCS was 3; she was intubated, ventilated and referred to ICU. U+Es normal, Calcium high, phosphate low, a...