Searchable abstracts of presentations at key conferences in endocrinology

ea0036oc4.9 | Oral Communications 4 | BSPED2014

Neurodevelopmental phenotypes in children with early and late presenting congenital hyperinsulinism

Mohamed Zainaba , Michaelidou Maria , Nicholson Jacqueline , Butler Thomas , Rigby Lindsey , Padidela Raja Narendra Rao , Cosgrove Karen E , Dunne Mark J , Clayton Peter , Banerjee Indraneel

Introduction: Adverse neurodevelopmental outcomes have been recognised in children with hypoglycaemia due to early and late presenting congenital hyperinsulinism (CHI). The Vineland Adaptive Behaviour Scales II (VABS-II) is a standardised measure used to assess parent reported adaptive behaviour. The test measures five domains; motor, communication, daily living skills (DLS), socialisation, and maladaptive behaviour. We have used VABS-II to identify specific neurodevelopmental...

ea0033p14 | (1) | BSPED2013

Design and validation of a severity scale for use in congenital hyperinsulinism

Most Jessica , Mohamed Zainab , Avatapalle Hima Bindu , Ehtisham Sarah , Foster Peter , Stevens Adam , Cosgrove Karen E , Dunne Mark J , Banerjee Indraneel , Clayton Peter E

Introduction: Congenital hyperinsulinism (CHI) is an important cause of hypoglycaemia in infancy requiring intensive medical and surgical support. Carbohydrate requirement (CHO) represents a simple index of severity but does not predict the failure of medical treatment and hence the requirement for pancreatectomy.Aims: To design and validate a severity tool for use in early onset CHI patients.Methods: To design the Manchester CHI s...

ea0033p16 | (1) | BSPED2013

Increasing weight in children with congenital hyperinsulinism is linked to KATP channel gene mutations

Mohamed Zainaba , Chidanandaswamy Rajesh , Swancott Abigail , Steele Caroline , Murray Philip , Rigby Lindsey , Padidela Raja , Ehtisham Sarah , Skae Mars , Patel Leena , Ellard Sian , Didi Mohammed , Cosgrove Karen E , Dunne Mark , Banerjee Indi , Clayton Peter

Introduction: Congenital hyperinsulinism (CHI) is a cause of severe hypoglycaemia due to insulin over-secretion. The medical management of CHI involves supplementary glucose, which combined with insulin excess, may be obesogenic. However, increased weight in CHI patients has not been reported. We have investigated if children with CHI increase in weight and if genetic or treatment factors influence the weight trajectory.Methods: Weights were measured and...

ea0033p17 | (1) | BSPED2013

Frequency of focal and diffuse congenital hyperinsulinism with paternally inherited mutations in ABCC8 and KCNJ11

Gopal Jaya Sujatha , Mohamed Zainaba , Padidela Raja , Patel Leena , Skae Mars , Didi Mohammed , James Jackie , Caine Louise , Rigby Lindsey , Cosgrove Karen E , Dunne Mark , Ellard Sian , Banerjee Indi , Clayton Peter

Introduction: Congenital hyperinsulinism (CHI) causes severe hypoglycaemia, which can be either focal or diffuse in aetiology. Both forms are associated with paternally inherited mutations in ABCC8/KCNJ11. Lymphocytic DNA analysis alone is inadequate to diagnose focal CHI, as pancreatic maternal allelic silencing cannot be tested prior to surgery. Additional 18-fluorodopa PET–CT scanning (PET–CT) is required for definitive diagnosis; in this study, ...

ea0033p18 | (1) | BSPED2013

Altered plasma incretin concentrations in patients with non-typical forms of congenital hyperinsulinism

Shi Yanqin , Avatapalle Hima B , Skae Mars S , Padidela Raja , Newbould Melanie , Rigby Lindsey , Flanagan Sarah E , Ellard Sian , Rahier Jacques , Clayton Peter E , Banerjee Indraneel , Dunne Mark J , Cosgrove Karen E

Introduction: Congenital hyperinsulinism (CHI) may arise due to loss-of-function mutations in ABCC8 and KCNJ11 genes which encode subunits of ATP-sensitive potassium (KATP) channels. KATP channels couple nutrient metabolism with insulin secretion in pancreatic β-cells but are also located in enteroendocrine L- and K-cells and may play a role in the control of GLP-1 and GIP secretion respectively. More than 70% of patients with CHI h...