Searchable abstracts of presentations at key conferences in endocrinology

ea0028se1.5 | (1) | SFEBES2012

Why does the endocrine dog not bark in the cytokine night?

Edwards Christopher

Pro-inflammatory cytokines activate the hypothalamic pituitary adrenal (HPA) axis but chronic inflammatory diseases such as Rheumatoid Arthritis (RA) do not. The axis is subtly subnormal despite nocturnal cytokine peaks. This poses the question ‘Why does the endocrine dog not bark in the cytokine night?’. Is this chronic stress adaptation similar to that seen with restraint when the normotypic stressor is reduced with decreased parvocellular CRH mRNA, a compensatory ...

ea0038p418 | Steroids | SFEBES2015

Lack of awareness contributes to delayed diagnosis and inappropriate management in men with low testosterone: findings from a UK study of men diagnosed with hypogonadism

Edwards David , Olding Laurence

Introduction: Hypogonadism is prevalent in older men and associated with various comorbidities. Despite this, it is underdiagnosed and undertreated.Aim: To identify factors associated with underdiagnosis and undertreatment of male hypogonadism.Methods: Quantitative, questionnaire-based, online survey conducted in the UK among men aged ≧40 years with hypogonadism confirmed by blood test (n=101, from N=3 871 ...

ea0028p198 | Obesity, diabetes, metabolism and cardiovascular | SFEBES2012

A novel genetic mutation causing MODY 1

Brady Sally , Edwards Mark

Maturity-onset diabetes of the young (MODY) is a group of autosomal dominant inherited disorders causing non-insulin-dependent diabetes. MODY is the most common form of monogenic diabetes, accounting for 1-2 % of diabetes in Europe; however it is often misdiagnosed as Type 1 or 2 Diabetes. MODY is caused mainly by mutations in the GCK, HNF1A or HNF4A genes, the two former accounting for 70% of all cases. A molecular genetic diagnosis is important as it can directly alter patie...

ea0011p107 | Clinical case reports | ECE2006

Co-existing hypoparathyroidism and vitamin D deficiency causing life-threatening hypocalcaemia

Edwards L , Abubaker M

We present a case of a 76-year-old Caucasian woman with combined primary hypoparathyroidism and vitamin D deficiency resulting in life-threatening hypocalcaemia.She has a history of COPD and initially presented in 2002 with an exacerbation of her airways disease. During treatment for her condition an incidental note was made of hypocalcaemia (calcium 1.62 mmol/l). PTH was minimally elevated at the time but 25-hydroxycholecalciferol was low (4.2 ng/ml). S...

ea0006p49 | Neuroendocrinology and behaviour | SFE2003

QLS-H, A MEASURE OF QUALITY OF LIFE IN ADULT UK GHD PATIENTS

Patel S , Edwards D

QLS-H is a new, weighted QoL questionnaire developed for patients with hypopituitarism. We evaluated QLS-H data from UK patients in the HypoCCs International surveillance study, and compared results with a sample of the general UK population (n=1090).The QLS-H questionnaire was administered at baseline and at yearly intervals. Scores were corrected for age and gender differences, and expressed as Z-scores based on UK-specific reference ranges. Using this...

ea0065p40 | Adrenal and Cardiovascular | SFEBES2019

The peri-operative management of diabetes in elective major vascular procedures: a completed cycle quality improvement project (QIP)

Abadi Porya Hassan , Edwards Allen

Aim: Diabetes is the most common metabolic disorder in the UK, affecting 20–30% of vascular inpatients. Diabetes is associated with increased mortality and adverse outcomes. Major vascular operations accompany an increased incidence of metabolic complications. There are trust guidelines outlining the optimal peri-operative management of diabetes. We audited compliance to this guideline in patients undergoing major vascular operations and measured patient outcomes.<p c...

ea0077cc8 | (1) | SFEBES2021

Atraumatic chylothorax due to Graves’ disease

Edwards Amy , Osman Nadia , Gunganah Kirun

Case presentation: A 40-year-old Caribbean woman presented with sudden onset palpitations. She described 3 months of progressive shortness of breath, non-productive cough and 7kg weight loss. She denied chest pain, fevers or night sweats, but reported increased stool frequency, gritty eyes, and occasional visual blurring. She appeared cachectic and had a fine tremor, left eye proptosis and a visible pulsatile goitre. She was afebrile, tachypnoeic, hypoxic, hypotensive with fas...

ea0085p26 | Gonadal, DSD and Reproduction | BSPED2022

Gonadotrophin independent puberty (GIPP) with unusually high oestradiol level in an infant with mccune albright syndrome (MAS)

Malhotra Neha , Edwards Lowri , Brain Caroline

Background: McCune Albright Syndrome (MAS) is a rare mosaic disease caused by activating mutation in GNAS, characterized by bone fibrous dysplasia, café au- lait (CAL) and hyper functional endocrinopathies (1). GIPP is the most common endocrinologic manifestation seen more frequently in girls (2). In a few studies, letrozole, tamoxifen, or fulvestrant were effective in decreasing the rate of skeletal maturation and vaginal bleeding (3,4,5).Case Repo...