Searchable abstracts of presentations at key conferences in endocrinology

ea0051oc8.2 | Oral Communications 8 | BSPED2017

Assessment of adrenal function and recovery of HPA axis in children with chronic asthma assessed by LDSST

Gangadharan Arundoss , Didi Mohammed , Das Urmi , Dharmaraj Poonam , Senniappan Senthil , Ramakrishnan Renuka , Blair Jo

Background: Biochemical evidence of adrenal insufficiency (AI) is reported commonly during inhaled corticosteroid (ICS) treatment for asthma. The significance of mildly abnormal results is uncertain. For this reason we adopt a stratified approach to the management of patients with impaired cortisol responses to the low dose short Synacthen test (LDSST): Patients with peak cortisol 350–499 nmol/l (‘suboptimal’) receive hydrocortisone 20 mg/m2 per day d...

ea0051p003 | Thyroid | BSPED2017

Long-term follow-up of Grave’s disease in Adolescents: a 10 year study from a single UK tertiary centre

Li Judy , Giri Dinesh , Ramakrishnan Renuka , Das Urmi , Dharmaraj Poonam , Blair Jo , Didi Mohammad , Senniappan Senthil

Introduction: Anti-thyroid medications are the first line therapy for children and young people with Grave’s disease (GD). Some studies have shown remission rates up to 40–50%; however long-term follow up studies have reported much lower remission rates in children compared to adults.Aim: To review the long-term follow up and management of adolescents with Grave’s disease in a single tertiary centre in the UK.Methods...

ea0051p019 | Miscellaneous/other | BSPED2017

Calcium/calmodulin dependent protein kinase 2 (CaMKK2) mutation – a novel genetic cause of congenital hyperinsulinism

Giri Dinesh , Scott John , Kemp Bruce , Didi Mohammed , Means Anthony , Senniappan Senthil

Background: Congenital hyperinsulinism (CHI) is a disorder of unregulated insulin secretion causing persistent hypoglycaemia. In around 50% of the patients with CHI, the underlying molecular genetic etiology is unknown. Ca2+/calmodulin-dependent protein kinase 2 (CaMKK2) belongs to the Serine/Threonine protein kinase family. Alternative splicing results in multiple transcripts encoding distinct isoforms. We report, for the first time, CaMKK2 mutati...

ea0085oc5.3 | Oral Communications 5 | BSPED2022

UK protocol for induction of puberty with gonadotropins in males with hypogonadotropic hypogonadism

Dunkel Leo , Prasad Rathi , Martin Lee , Senniappan Senthil , Butler Gary , Howard Sasha

Hypogonadotropic hypogonadism (HH) is a rare reproductive disorder that results in a lack of normal pubertal development and reduced potential for fertility in adult life. The condition is characterised by low circulating sex steroid concentrations resulting from a deficiency of pituitary gonadotropin production. HH may be congenital or acquired, most commonly due to tumour or treatment for malignant disease. When associated with anosmia it is termed Kallmann syndrome. HH is a...

ea0085oc6.4 | Oral Communications 6 | BSPED2022

A Collaborative community based approach in providing support for children and young people with severe obesity

Clarke Ellie , Jones Dani , Davies Sioned , Kenny Nicola , Fulstow Andrew , Ellis Carrigg Katie , Senniappan Senthil

Background: The highest rates of childhood obesity are among children from lower socioeconomic groups. Tier 3 weight management services for children currently rely on an MDT approach that is focused on the management of complications associated with excessive weight, but the resources are generally limited. Evidence suggests that the input in the community is key to empower children, young people, and their families to make healthy lifestyle changes, although the availability...

ea0085p12 | Bone | BSPED2022

A case series of 8 patients with pseudohypoparathyroidism and variable phenotype

Gubaeva Diliara , Makazan Nadezhda , Kareva Maria , Peterkova Valentina , Ramakrishnan Renuka , Senniappan Senthil

Introduction: Pseudohypoparathyroidism (PHP) is a group of heterogeneous disorders causing parathyroid hormone (PTH) resistance. The features could include Albright’s hereditary osteodystrophy phenotype (AHO) [brachydactyly, short stature, obesity, round face, ectopic ossifications, intellectual disability]. The condition is rare with an estimated prevalence of 0.34-1.1 in 100,000 and the clinical presentation can be variable. Herein, we present 8 patients with PHP from t...

ea0085p38 | Obesity 1 | BSPED2022

A questionnaire-based baseline evaluation of hunger in UK adolescents with severe obesity

Apperley Louise , Owens Meghan , Parkinson Jennifer , Clarke Ellie , Gubaeva Diliara , Senniappan Senthil

Introduction: Evaluating hunger and hyperphagia is an important component of assessing children and young people with obesity. Identifying increased hunger levels will help clinicians and health professionals to taper management aspects including relevant genetic testing and providing tailored dietary and pharmacological management.Aim: The aim of this study was to evaluate the baseline hunger levels in a group of UK adolescents with severe obesity.<...

ea0085p39 | Obesity 1 | BSPED2022

Baseline body composition of adolescents attending a UK tertiary weight management service

Suntharesan Jananie , Parkinson Jennifer , Apperley Louise , Clarke Ellie , Gubaeva Diliara , Senniappan Senthil

Introduction: Visceral body fat has been shown to correlate with complications related to obesity. Body mass index (BMI) is widely used to define obesity in the adolescent population; however, it does not take the overall body composition into account. We present body composition data in a group of UK adolescents attending the tertiary MDT weight management service.Methods: Data was collected on 31 patients (M:F = 15:16) attending the MDT service over a ...

ea0085p79 | Obesity 2 | BSPED2022

Baseline health-related quality of life in UK children and adolescents with severe obesity

Apperley Louise , Owens Meghan , Longworth Melissa , Parkinson Jennifer , Clarke Ellie , Gubaeva Diliara , Senniappan Senthil

Introduction: Childhood obesity is associated with several complications related to physical and mental health. Determining health-related quality of life (HRQOL) is an important outcome measure to ensure patients receive the appropriate care.Aim: We report the baseline HRQOL in a group of UK children and adolescents with severe obesity who were managed in a Tier 3 weight management service.Methods: Paediatric quality of life (Peds...

ea0066p71 | Learning from Mistakes and Miscellaneous | BSPED2019

Intracranial hypertension secondary to severe obesity: case series

Apperley Louise , Erlandson-Parry Karen , Laing Peter , Das Urmi , Senniappan Senthil

Introduction: The prevalence of childhood obesity is continuing to increase, especially in more deprived areas. It is estimated that 28% of children are overweight or obese in England. Evidence has shown that obesity is associated with increased intracranial pressure (ICP) in adult and paediatric populations. We report three patients who presented with intracranial hypertension due to severe obesity.Case 1: A fifteen-year-old girl presented with severe h...