Searchable abstracts of presentations at key conferences in endocrinology

ea0011p126 | Clinical case reports | ECE2006

Megadenoma

Field BCT , Barnes SC , Wheeler MJ , Powell MP , Thomas SM , Carroll PV

A 44-year-old woman presented to an emergency department with ear pain and worsening of longstanding headache. There was no history of menstrual disturbance, galactorrhoea, tiredness or weight gain and physical examination demonstrated only a left homonymous hemianopia. CT head scan revealed a brightly enhancing, enormous, lobulated mass arising from the pituitary fossa and causing obstructive hydrocephalus through compression of the fourth ventricle. Following collection of b...

ea0011p205 | Clinical practise and governance | ECE2006

Comparison of the effects of transdermal and oral oestrogen treatments on serum and salivary cortisol concentrations

Bahri A , Breen L , Barnes S , Powrie JK , Thomas SM , Carroll PV

Objective: To determine whether transdermal oestrogen (E2) preparations alter total cortisol and cortisol binding globulin (CBG) concentration similarly to oral E2 treatment.Methods: This cross-sectional, observational study compared levels of total serum cortisol, CBG, the free cortisol index (FCI) and salivary cortisol levels (as a measure of free cortisol) in oestrogen naïve women (n=15), women taking oral oestrogen (...

ea0044p139 | Neuroendocrinology and pituitary | SFEBES2016

LGR4 and EAP1 mutations are implicated in the phenotype of self-limited delayed puberty

Mancini Alessandra , Howard Sasha R , Ruiz-Babot Gerard , Cabrera Claudia P , Barnes Michael R , Guasti Leonardo , Dunkel Leo

Background: Aberrations in the timing of puberty may result in significant adverse health outcomes, including cancers, cardiovascular and neurological pathologies. Self-limited delayed puberty (DP) (i.e. constitutional delay of puberty) runs in families with either autosomal dominant or complex inheritance patterns in >70% of families, indicating a strong genetic basis of the trait. However, only a few genes have been identified underlying DP so far....

ea0038oc6.3 | Advances in reproduction and signalling | SFEBES2015

Mutations in HS6ST1 are causal in self-limited delayed puberty as well as idiopathic hypogonadotropic hypogonadism

Howard Sasha , Poliandri Ariel , Storr Helen , Metherell Louise , Cabrera Claudia , Barnes Michael , Warren Helen , Wehkalampi Karoliina , Guasti Leo , Dunkel Leo

Background: Self-limited delayed puberty (DP) often segregates in an autosomal dominant pattern, suggesting that inheritance is conferred by a small number of genes. However, the underlying genetic background is mostly unknown. By comparison, many genes have been identified where loss-of-function mutations lead to hypogonadotropic hypogonadism (HH). Despite likely overlap between the pathophysiology of delayed puberty and conditions of GnRH deficiency, few studies have examine...

ea0034p158 | Growth and development | SFEBES2014

A novel gene affecting the timing of puberty

Howard Sasha , Guasti Leo , Storr Helen , Metherell Lou , Cariboni Anna , Barnes Michael , Cabrera Claudia , Wehkalampi Karoliina , Dunkel Leo

Background: Disturbances of pubertal timing affect >4% of the population and are associated with adverse health outcomes. Studies estimate 60–80% of variation in pubertal onset is genetically determined, but few genetic factors are known. We hypothesise that causal variants will be low-frequency, intermediate-impact variants and will be enriched in populations at the extremes of normal pubertal timing. Families with constitutional delay in growth and puberty (CDGP) ha...

ea0003oc16 | Endocrine Neoplasia | BES2002

BPDZ-154 is a potent activator of ATP-sensitive potassium channels in pancreatic beta-cells

Lee A , Cosgrove K , Barnes P , Lindley K , Aynsley-Green A , de Tullio P , Pirotte B , Lebrun P , Dunne M

Diazoxide is an agonist of ATP sensitive K+ (KATP) channels in beta-cells and is used in the treatment of hyperinsulinism caused by insulinomas or Hyperinsulinism in Infancy (HI). The responsiveness of patients to diazoxide is highly variable and complicated by side-effects which include hypertension and hypertrichosis. The aim of this study was to examine the actions of a novel benzothiadiazine-derivative, BPDZ-154, on beta-cell KATP channels and insulin release. W...

ea0073pep1.2 | Presented ePosters 1: Adrenal and Cardiovascular Endocrinology | ECE2021

Tildacerfont for the treatment of patients with classic congenital adrenal hyperplasia: results from a 12-week phase 2 clinical trial in adults with classic CAH

Auchus Richard , Merke Deborah , Ivy-Joan Madu , Nakhle Samer , Sarafoglou Kyriakie , Huang Michael , Moriarty David , Barnes Chris , Newfield Ron

BackgroundCongenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disorder characterized by insufficient cortisol production resulting in excess adrenocorticotropic hormone (ACTH) and adrenal androgen production. Standard-of-care therapy with glucocorticoids (GC) is suboptimal due to the difficulty of balancing control of the ACTH-driven androgen excess against the serious long-term side effects associated...

ea0019p129 | Diabetes, Metabolism and Cardiovascular | SFEBES2009

Muscarinic acetylcholine receptors and adipogenesis

Stephens M , Rees D , Ludgate M

The rising prevalence of type 2 diabetes can be directly related to increasing levels of population obesity and associated insulin resistance. Adipose tissue has neuroanatomically well characterized sympathetic innervation (with activation initiating lipid mobilization), but little evidence to support the presence of a (putatively counter-regulatory) parasympathetic input (Bartness & Song 2007). Parasympathetic actions are mediated through muscarinic acetylcholine receptor...

ea0090p300 | Calcium and Bone | ECE2023

Bioluminescence and autofluorescence of parathyroid glands to identify an intra-thyroidal parathyroid tumour

Lin Zhimin , Wai Kit Lee James , Yuan Ngiam Kee

Bioluminescence is bringing new and exciting possibilities to the field of endocrine surgery, because we are able to better harness the property of autofluorescence of the parathyroid glands. Parathyroid glands have an inherent ability to produce infra-red autofluorescence at the wavelength of 820 nm to 830 nm, if the gland absorbs light at the wavelength of 750 nm. With highly sensitive technology and the ability to filter out other reflected light and noise, it is now possib...

ea0059s5.2 | Breast cancer | SFEBES2018

Metabolic pathways regulating breast cancer in obesity

Brown Kristy

Obesity is associated with an increased risk of hormone receptor positive breast cancer after menopause. The aromatase enzyme catalyzes the conversion of androgens into oestrogens and the breast adipose-specific expression of aromatase is hypothesized to be a major driver of breast cancer growth when ovarian oestrogen biosynthesis has ceased. We have found that aromatase is elevated in breast adipose stromal cells in relation to obesity and menopausal status. Furthermore, obes...