Searchable abstracts of presentations at key conferences in endocrinology

ea0036P18 | (1) | BSPED2014

Suppression of bone turnover and its determinants in children receiving bisphosphonate therapy

Kyriakou Andreas , McNeilly Jane D , McMillan Martin , Guftar Shaikh M , Mason Avril , Faisal Ahmed S

Introduction: Bisphosphonate therapy (BPT) reduces osteoclast activity and may be associated with adynamic bone turnover. The extent of suppression of bone turnover and its determinants are unclear.Methods: Markers of bone metabolism were evaluated in 15 children (9M/6F) receiving cyclical BPT intravenously for osteoporosis. The median age at first biochemical assessment was 10.8 years (0.16, 16.3). Serum type I collagen cross-linked C-telopeptide (CTX),...

ea0036P57 | (1) | BSPED2014

Effect of vitamin D treatment on glucose and insulin metabolism, and bone turnover in children with symptomatic vitamin D deficiency

El-Fakhri Nagla , McMillan Martin , McNeilly Jane , Ahmed S F , McDevitt Helen

Background: There are limited data in paediatric population on the association between vitamin D deficiency/treatment and glucose/insulin metabolism.Objective and hypotheses: This study aimed to investigate the effect of vitamin D therapy on glucose homeostasis, insulin resistance and bone turnover, in children with vitamin D deficiency.Method: 22 children aged 3 months to 10 years (nine males) who were diagnosed with vitamin D def...

ea0030p61 | (1) | BSPED2012

A prospective study of pubertal growth in children with inflammatory bowel disease

Mason Avril , Malik Salma , McMillan Martin , McNeilly Jane , Bishop Jonathan , McGrogan Paraic , Russell Richard , Ahmed Faisal

Background: Puberty is understood to be commonly affected in adolescents with Crohn’s disease (CD) and ulcerative colitis (UC).Objective: To determine the impact of IBD on pubertal status and pubertal growth.Methods: Single centre prospective study over 12 months of 45 adolescents (boys, 23) with CD and 18 (boys, 12) with UC with a median age of 13.4 years (10, 16.6). Assessment included details of disease, anthropometry and b...

ea0077p111 | Reproductive Endocrinology | SFEBES2021

An investigation of androgen-responsive non-coding RNAs in boys with atypical genitalia without genetic variants in the androgen receptor (AR)

Alimussina Malika , McMillan Martin , Chudleigh Sandra , McNeilly Jane D , Diver Louise A , McGowan Ruth , Tobias Edward S , Faisal Ahmed S

Introduction: Transcriptome analysis of peripheral blood mononuclear cells (PBMC) RNA has identified a set of androgen-responsive non-coding RNAs.Aim: To quantify the androgen-responsive gene expression and investigate its relationship to the testosterone (T) rise following hCG stimulation in boys with no genetic evidence of androgen insensitivity.Methods: Boys with suspected DSD who were evaluated at the Royal Hospital for Childre...

ea0078OC5.3 | Oral Communications 5 | BSPED2021

An investigation of androgen-responsive non-coding RNAs in boys with atypical genitalia without genetic variants in the androgen receptor (AR)

Alimussina Malika , McMillan Martin , Chudleigh Sandra , McNeilly Jane D , Diver Louise A , McGowan Ruth , Tobias Edward S , Ahmed S Faisal

Introduction: Transcriptome analysis of peripheral blood mononuclear cells (PBMC) RNA has identified a set of androgen-responsive non-coding RNAs.Aim: To quantify the androgen-responsive gene expression and investigate its relationship to the testosterone (T) rise following hCG stimulation in boys with no genetic evidence of androgen insensitivity. Methods: Boys with suspected DSD who were evaluated at the Royal Hospital for Childr...

ea0031oc3.4 | Reproduction, growth and development | SFEBES2013

Characterising changes in the in vivo male rodent brain using magnetic resonance spectroscopy

Rodie Martina , Welsh Michelle , Holmes William , Gallagher Lindsay , Mullin James , McMillan Martin , Macrae I Mhairi , Ahmed S Faisal

Background: By providing a non-invasive, functional insight into brain chemistry, MRS has the potential to provide objective longitudinal data on mammalian brain development.Aims: To assess the sexual dimorphism in rodent brain chemistry and development using in vivo MRS.Methods: 26 (19 males) Sprague–Dawley rats were scanned at 6 weeks and 12 male rats at 10 weeks using a 7T MRI scanner. Testosterone concentrations w...

ea0039oc6.5 | Oral Communications 6 | BSPED2015

The measurement of urinary gonadotrophins for assessment and management of pubertal disorders

Lucaccioni Laura , McNeilly Jane , McMillan Martin , Kyriakou Andreas , Wong S C , Predieri Barbara , Iughetti Lorenzo , Shaikh M Guftar , Mason Avril , Ahmed S Faisal

Objective: Prospective evaluation of the relationship between first morning urinary gonadotrophins (uGn) measured by immunoassay and corrected for creatinine (uLH:uCr and uFSH:uCr), and basal serum gonadotropins (sLH and sFSH) and in response to LHRH stimulation test. Prospective evaluation of uGn trend in patients receiving GnRH analogue (GnRH-a; decapeptyl SR, 11.25 mg, every 10–12 weeks).Methods: Enrolled 15 (12M) patients evaluated for delayed p...

ea0058oc7.3 | Oral Communications 7 | BSPED2018

The determinants of skeletal morbidity and fractures in children with type 1 diabetes

Chen Suet Ching , Shepherd Sheila , McMillan Martin , McNeilly Jane , McComb Christie , Foster John , Wong Sze Choong , Robertson Kenneth J , Ahmed S Faisal

Objective: The pathophysiology of the increased fracture risk in Type 1 Diabetes (T1D) remains unclear. Given that childhood and adolescence are important physiological periods for optimal bone development, we performed a multimodality assessment to determine the effects of T1D on bone health.Methods: Thirty two affected children at a median (range) age of 13.7 years (10.4, 16.7), were recruited for detailed assessment of bone health. Serum bone alkaline...

ea0045oc5.8 | Oral Communications 5- Endocrine | BSPED2016

Understanding the Utility of Performing Endocrine & Genetic Investigations in Boys with a Suspected Disorder of Sex Development

Nixon Rachael , Cerqueira Vera , Kyriakou Andreas , Lucas-Herald Angela , McNeilly Jane , Diver Louise , Clelland Sharleene , Baird William , McMillan Martin , Purvis Andrew , Tobias Edward , McGowan Ruth , Ahmed Syed Faisal

Introduction: Evaluation of XY DSD requires a combination of endocrine and genetic tests. It is unclear whether these two sets of investigations should be performed stepwise or in parallel.Aims: The aim of the study was to document the range of endocrine and genetic abnormalities identified in all XY boys who were investigated at one specialist multidisciplinary service.Methods: Case records were reviewed to collect information fro...