Searchable abstracts of presentations at key conferences in endocrinology

ea0044pl10 | Clinical Endocrinology Trust Lecture | SFEBES2016

Endocrine development is for life: looking beyond paediatrics

Achermann John

It is well established that certain endocrine disorders can progress over time, such as autoimmune endocrinopathies or the multiple pituitary hormone insufficiency following cranial irradiation. Although most developmental endocrine disorders are widely considered to be paediatric conditions, milder “non-classic” variants may first present to adult endocrinologists or long-term monitoring may be needed of established conditions as additional endocrine features may on...

ea0044se1.3 | Senior Endocrinologists' Session | SFEBES2016

Gut Dysbiosis and Hypertension – new or resurrected

Honour John

New research claims, for the first time, that gut microbiota affect hypertension in rats but authors were unaware of historical research indicating this link. The urine steroid metabolome by gas chromatography of a patient with congenital adrenal hyperplasia from 17-hydroxylase (CYP17) deficiency was reported in 1978. Many of the steroids were 21-deoxy products of corticosterone and could be hypertensinogenic or glycerrhitinic acid like factors. Further studies in CYP17 defici...

ea0041s25.3 | What's new and exciting in nuclear receptor action? | ECE2016

Molecular battles between corticosteroid receptors in the heart

Cidlowski John

Heart failure is a leading cause of death in man, and stress is increasingly associated with adverse cardiac outcomes. Glucocorticoids are primary stress hormones, but their direct role in cardiovascular health and disease is poorly understood. To determine the in vivo function of glucocorticoid signaling in the heart, we generated mice with cardiomyocyte-specific deletion of the glucocorticoid receptor (GR). The cardioGRKO mice appear normal early in life but die pre...

ea0038n1.1 | Nurse Session 1: Multiple Endocrine Neoplasia | SFEBES2015

Overview of multiple endocrine neoplasia

Ayuk John

Multiple endocrine neoplasia (MEN) syndromes are rare autosomal-dominant disorders that predispose affected individuals to benign and malignant tumours involving two or more endocrine glands. Four major forms of MEN are recognised, each associated with the occurrence of specific tumours. MEN1 is due to germline-inactivating mutations of the MEN1 tumour-suppressor gene, and is associated with the occurrence of parathyroid, pancreatic islet and anterior pituitary tumours. MEN2 (...

ea0037s21.2 | Thyroid hormone in pregnancy | ECE2015

Consequences of maternal thyroid dysfunction for offspring

Lazarus John

Treatment of hyperthyroidism with antithyroid drugs has recently been shown to have an effect on MMI/Carbimazole embryopathy at a specific early window in gestation. This has important implications for management.There is agreement that untreated overt gestational hypothyroidism is associated with significant adverse obstetric and fetal/neonatal effects. Although there is also substantial evidence that gestational subclinical hypothyroidism (SCH) is asso...

ea0036s2.1 | Symposia 2 Recent advances in adrenal disease | BSPED2014

Adrenal development and adrenal insufficiency

Archermann John

The human adrenal gland develops from around 4 weeks post conception and undergoes rapid growth and differentiation in early fetal life. At birth, the adrenal gland consists of a mature adult type cortex capable of mineralocorticoid and glucocorticoid production, as well as a fetal zone that involutes in the first few months. Disruption of the HPA axis development can cause adrenal hypoplasia. This is classically broken down into secondary causes (ACTH insufficiency); ACTH-res...

ea0035s24.2 | Nutrient regulation of metabolism and endocrine systems | ECE2014

Metabolic consequences of a high-fat diet on mouse models of GH action

Kopchick John

GH receptor-binding protein gene disrupted mice GHR(−/−) are dwarf, obese, insulin sensitive, and long-lived whereas GH transgenic mice are giant, glucose intolerant, lean, and short lived. When challenged with a high-fat (HF) diet, all mice became hyperinsulinemic with similar percent weight gains and increases in percent body fat and size of the epididymal, retroperitoneal, and subcutaneous fat depots. For GH mice, the increase in adipose tissue was relatively sm...

ea0035mte13 | (1) | ECE2014

Pituitary apoplexy: diagnosis and management

Wass John

Pituitary apoplexy is an uncommon emergency. It presents often with sudden thunder clap headaches and requires multidisciplinary team involvement. This includes an experienced neurosurgeon, endocrinologist, radiologist – the pituitary multidisciplinary team.Urgent treatment should be given often involving steroids (after a blood cortisol has been taken). Assessment includes neurological signs which if severe may merit urgent surgery.<p class="ab...

ea0061ou1 | A year in review: what are the highlights? | OU2019

Is obesity pharmacotherapy finally coming of age?

Wilding John

Obesity is a chronic relapsing disease with significant adverse implications for current and future health. Whilst guidelines recommend first line treatment with lifestyle interventions that include restriction of energy intake, increased physical activity and behavioural modification, these only demonstrate an average decrease of 3–5% initial body weight over 12 months, and weight regain is common. Bariatric surgery is effective, but is generally only offered to people w...