Searchable abstracts of presentations at key conferences in endocrinology

ea0094p206 | Metabolism, Obesity and Diabetes | SFEBES2023

New approaches to imaging metabolic heterogeneity in cultured adipocytes

Greig Justin , Tipping William , Graham Duncan , Faulds Karen , Cunningham Margaret , Gould Gwyn

Introduction: Adipocytes have been shown to exhibit considerable heterogeneity. In humans, they vary in size from <20 to 300 µm in diameter, which equates to a several hundred-fold difference in cell volume within the same tissue. Population based studies indicate larger adipocytes are associated with metabolic diseases, but how cell size is related to metabolism is poorly understood. Recent studies measured glucose levels in individual cells in cultu...

ea0012p99 | Reproduction | SFE2006

Are anti-Müllerian hormone levels and antral follicle count related to lifestyle factors, demographics and reproductive history in subfertile women?

Nardo LG , Christodoulou D , Gould D , Fitzgerald CT , Laing I

Amongst the different markers of ovarian function, AMH levels and antral follicle count (AFC) are the most objective and reliable predictors of ovarian response in women undergoing in-vitro fertilisation (IVF). Several factors, that have been reported to interfere with ovarian response, are taken into consideration when enrolling women into an IVF programme.The aim of this prospective study was to determine the correlation, if any, between baseline AMH l...

ea0011p378 | Diabetes, metabolism and cardiovascular | ECE2006

SiRNA-mediated depletion of synaptotagmin-11 abrogates insulin-stimulated glucose uptake in 3T3-L1 adipocytes

Miller SCM , Mitra P , Connell JMC , Gould GW

The fusion of insulin-stimulated GLUT4-containing vesicles (GSV) with the plasma membrane (PM) of adipose or skeletal muscle cells is governed by regulated exocytosis. In all such membrane fusion events cognate t- and v-SNAREs interact in an ordered way to allow vesicles to first dock with, and then fuse with the plasmalemma. In neurons, the best-studied example of this well conserved process, the protein species responsible for directing the final (rate-limiting) fusion step ...

ea0014p610 | (1) | ECE2007

A comparison between the efficacy and safety of pegvisomant to that of octreotide LAR in patients with acromegaly

Harris Philip , D’Souza Gwyn , Good Anthony , Layton Gary , Colao Annamaria , Beverly Biller , Klibanski Anne , Ghigo Ezio

Two medical therapies are now available for the treatment of acromegaly. Pegvisomant is a growth hormone (GH) receptor antagonist. Somatostatin analogues, in contrast, act by inhibiting the release of GH from the pituitary. The primary objective of this study was to compare the efficacy of pegvisomant (P) to that of octreotide LAR (LAR) in terms of IGF-1 normalisation. The secondary objective was to compare safety and tolerability between the two treatments.<p class="abste...

ea0012oc4 | Young Endocrinologist prize session | SFE2006

Antral follicle count (AFC) is related to serum anti-Mullerian hormone (AMH) independent of age, FSH and body mass index (BMI) in candidates for assisted conception

Nardo LG , Gould D , Fitzgerald CT , Christodoulou D , Yates AP , Laing I

AFC is related to ovarian function and outcome in assisted reproduction programmes. Current regimens for ovulation induction consider patient age to determine initial FSH dose and may exclude patients from treatment when FSH is high. Increased BMI is also an indication to defer treatment. We aimed to investigate the relationship between AFC and other predictors of ovarian response in candidates for assisted conception.We studied 89 patients referred to a...

ea0080p6 | Abstracts | UKINETS2021

Earlier diagnosis of neuroendocrine tumours (NETs) through transformation of the south wales NET service

Gould Harriet , Amin Kapish , Karategos Thanos , Abbas Sarah , Taylor Rebecca , Cook Katherine , Powell Catherine , Hargest Rachel , Phillips Simon , Horwood James , Cornish Julie , Torkington Jared , Khan Mohid

Background: Neuroendocrine tumours (NETs) are heterogeneous cancers with varied survival, arising mainly from the gastroenteropancreatic tract. Delayed diagnosis and mislabelling are widely recognised internationally in midgut NETs with little data describing how to improve diagnosis times. In 2017, transformation of the South Wales NET Service included a change to a gastroenterology-led service model alongside education and forming working relationships with gastroenterologis...

ea0019p171 | Endocrine tumours and neoplasia | SFEBES2009

Asymptomatic children with multiple endocrine neoplasia type 1 (MEN1) mutations harbour pancreatic and pituitary tumours

Newey P , Jeyabalan J , Christie P , Shine B , Phillips R , Gleeson F , Gould S , Soonawalla Z , Johnson P , Ryan F , Thakker R

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by parathyroid, anterior pituitary and pancreatic islet tumours. Primary hyperparathyroidism is the first clinical manifestation in >85% of patients, although in some patients pancreatic and pituitary tumours may precede the occurrence of primary hyperparathyroidism. The earliest occurrence of MEN1-tumours has been reported at the age of 5 years following which the age-related penetr...