Searchable abstracts of presentations at key conferences in endocrinology

ea0038p10 | Bone | SFEBES2015

A mutation in the calcium sensing receptor (previously known to cause neonatal severe hyperparathyroidism in the homozygote state) causing familial benign hypocalciuric hypercalcaemia in the heterozygote

Hinnie John , Gallagher Andrew , Collie Angela

Familial Benign Hypocalciuric Hypercalcaemia (FBHH) is a benign autosomal dominant condition characterised by elevated serum calcium and parathyroid hormone (PTH) and low urine calcium. It is a genetically heterogeneous disorder but the majority of cases (type 1 FBHH) can be shown to be due inactivating mutations in the Calcium Sensing Receptor (CASR). This is a guanine nucleotide-binding-protein (G-protein) coupled receptor that signals through the G-protein subunit α11 ...

ea0034p4 | Bone | SFEBES2014

An audit of the clinical indications for initiation of Denosumab as a treatment for Osteoporosis in a secondary care clinic

Collie Angela , Phyomaung Khun , Shahim Menai , Gallacher Stephen , Gallagher Andrew , McLean Fergus , Ahukannah John , Hinnie John

Objective: Denosumab is a highly specific MAB, which binds to RANK Ligand thus inhibiting osteoclast formation, function and survival1.It’s efficacy in the treatment of osteoporosis was demonstrated in the FREEDOM trial which was an international, randomised, placebo controlled trial involving 7686 post menopausal women. The trial demonstrated a reduction in risk for vertebral fractures (68%), non vertebral fractures (20%), and hip fractu...