ESPE2014

18 September 2014

07:00-17:00Registration Opens
08:00-11:00ESPE Bone and Growth Plate Working Group (BGP)
Chair(s): Part 1: Ola Nilsson (Stockholm, Sweden) & Gabrielle Hausler (Vienna, Austria) Part 2: Serap Turan (Istanbul, Turkey) & Ollie Semler (Cologne, Germany) Debate: Malachi McKenna (Dublin, Ireland) & Ciara McDonnell (Dublin, Ireland)
Wicklow Hall 1
08:00 - 08:30WG1.1Unravelling GH actions on the growth plate and its promotion of linear growth
08:30 – 09:00WG1.2The effect of stimulatory G proteins on differentiation within the growth plate
09:10 – 09.30 Coffee Break
09:30 – 10.00WG1.3Denosumab as an emerging therapy in pediatric metabolic bone diseases
10:00 – 10:30WG1.4New therapies in Metabolic bone disease: PTH
10:30 – 11:00 Debate: Bisphosphonates – will drug holidays avoid atypical femoral fractures?
08:00-11:00ESPE Working Group on Diabetes Technology and Therapeutics
Chair(s): Tadej Battelino (Ljubljana, Slovenia)
Auditorium
08:00 - 08:15WG2.1 Technological horizon for diabetes treatment
08:15 - 08:40WG2.2Non-Insulin Glucoregulatory therapy for type 1 diabetes
08:40 - 09:15WG2.3Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
08:40 - 09:15WG2.4Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
09:15 - 09:40Coffee Break
09:40 - 10:15WG2.5Debate: Sensor/pump therapy from onset of diabetes?
09:40 - 10:15WG2.6Debate: Sensor/pump therapy from onset of diabetes?
10:15 - 10:50WG2.7Debate: Do we need long acting insulin analogs?
10:15 - 10:50WG2.8Debate: Do we need long acting insulin analogs?
08:00-11:00ESPE Disorders of Sex Development Working Group (DSD)
Chair(s): Part 1: Christa Flück (Bern, Switzerland) and PM Holterhus (Kiel, Germany) Part 2: Anna Nordenström (Stockholm, Sweden)
Liffey A
08:00 - 08:30WG3.1Genetic variation in human SF-1 (NR5A1): clinical consequences for individuals, families and populations
08:30 - 08:50WG3.2The potential role of the alternative ‘backdoor’ pathway for androgen synthesis and virilisation in CAH
08:50 - 09:15WG3.3Long term outcome of prenatal CAH- therapy
09:15 - 09:45Coffee Break
09:45 - 10:05WG3.4Detailed phenotyping of DSD: external virilisation
10:05 - 10:25WG3.5Imaging of the urogenital tract
10:25 - 10:35WG3.6I-DSD and I-CAH registry update
10:35 - 10:45WG3.7DSDlife
10:45 - 10:55WG3.8DSDnet: A COST Action on the systematic elucidation of differences of sex development
10:55 - 11:00Open Business meeting
08:00-11:00ESPE Obesity Working Group (OWG)
Chair(s): Bessie E. Spiliotis (Patras, Greece) and Jesus Argente (Madrid, Spain)
Wicklow Hall 2
08:00 - 08:30WG4.1Metabolic syndrome in youth: current insights and novel serum biomarkers
08:30 - 09:00WG4.2Type 2 diabetes in children and adolescents
09:00 - 09:30Coffee Break
09:30 - 10:00WG4.3Making a diagnosis in Severe Complex Obesity
10:00 - 10:30WG4.4Identification of fatty acid binding protein 4 as an adipokine that regulates insulin secretion during obesity
10:30 - 11:00Research and Business Meeting
08:00-11:00ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Chair(s): Part 1: Feyza Darendeliler & Marco Cappa Part 2: Lucia Ghizzoni & Jean-Pierre Bourguignon
Liffey B
08:00 - 08:25WG5.1New markers of Ovarian Function
08:25 - 08:50WG5.2Lessons drawn from gynecological disorders in relation with hypothalamic-pituitary malfunction
08:50 - 09:15WG5.3Delay or advancement of female puberty after early life exposure to Bisphenol A and neuroendocrine mechanism
09:15 - 09:45Coffee Break
09:45 - 10:10WG5.4Contraception in Adolescence from a Public Health Perspective
10:10 - 10:35WG5.5Contraception in adolescence: current options
10:35 - 11:00WG5.6Lessons drawn from rare gynecological disorders in relation with ovarian malfunction
08:00-11:00ESPE Turner Syndrome Working Group (TS)
Chair(s): Part 1: Berit Kriström & Laura Mazzanti Part 2: Aneta Gawlik & Theo Sas
Liffey Hall 2
08:00 - 08.45WG6.1Liver involvement in Turner syndrome
08:45 - 09:15WG6.2Gastrointestinal disease in TS
09:15 - 09:45Coffee Break
09:45 - 10:15WG6.4Motor performance in TS
10:15 – 11:00WG6.3Autism and the X-chromosome
09:00-11:00Education and Training Update
Chair(s): Part 1: Malcolm Donaldson & Jan Lebl Part 2: Rasa Verkauskiene & John Gregory
Liffey Hall 1
Welcome and meeting new ESPE members and trainees
Update of the 28th ESPE Summer School
The Winter School journey – past, present and future
Seminars in Developmental Endocrinology: Diving in Paediatric Endocrinology sea
ESPE Science School: the past and the future
Harmonization of Paediatric Endocrinology training in EU
Drop on behalf of e-learning team - the espe-elearning.org portal: Learning and teaching paediatric endocrinology on demand
ESPE Clinical Fellowship programme: starting opportunity for young Paediatric Endocrinologists
Paediatric Endocrinology in the Middle East & North Africa; future plans and collaboration
ESPE Maghreb School: training in French
Reflections on an African (PETCA) safari
ESPE Caucasus and Central Asia School: starting in 2014
ESPE Research Fellowship programme
11:15-11:30Opening Ceremony
Welcome and Opening Speech - ESPE President 2014
Auditorium
Session head(s): Hilary Hoey (Ireland)
11:30-12:30Plenary Session 1 & 2
Chair(s): Carine de Beaufort (Luxembourg City, Luxembourg) & David Dunger (Cambridge, UK)
Auditorium
11:30PL1Closed-Loop System: Dream or Reality?
12:00PL2Learning from histopathology to design novel immune-therapies for type 1 and 2 diabetes
12:30-13:30Lunch
Visit to the Posters and Exhibition
12:45-13:45Industry-sponsored Satellite Symposium 1
Liffey A
14:00-15:30Symposium 1 - Disorders of Gsalpha Signaling
Chair(s): Serap Turan (Istanbul, Turkey) & Dov Tosiano (Haifa, Israel)
Wicklow Hall 2
14:00S1.1Pseudohypoparathyroidism
14:30S1.2McCune Albright Syndrome
15:00S1.3Acrodysostosis
14:00-15:30Symposium 2 - Endocrine Cancer Syndromes: An Update
Chair(s): Helen Spoudeas (London, UK) & Hermann Mueller (Oldenburg, Germany)
Liffey B
14:00S2.1PTEN: A Gene Involved in Overgrowth and Cancer
14:30S2.2MEN1 in Children and Adolescents
15:00S2.3DICER1 syndrome: a erview of the syndrome with a focus on endocrine aspects
14:00-15:30Symposium 3 - Novel Insights into Monogenic Diabetes
Chair(s): Zdenek Sumnik (Prague, Czech Republic) & George Werther (Melbourne, Australia)
Auditorium
14:00S3.1Differential Diagnosis of Monogenic Diabetes
14:30S3.2New Genes, New Mechanisms, New Phenotypes
15:00S3.3Epidemiology of Monogenic Diabetes
14:00-15:30Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Chair(s): Jan -Maarten Wit (Leiden, The Netherlands) & Filippo De Luca (Messina, Italy)
Liffey A
14:00S4.1Management of Central Hypothyroidism
14:30S4.2Novel role(s) for immunoglobulin superfamily, member 1 (IGSF1) in the hypothalamic-pituitary-thyroid axis
15:00S4.3Novel Insights into Thyroid Hormone Resistence
15:30-16:00Coffee Break
16:00-17:00Meet the Expert Parallel Sessions
16:00 - 17:00MTE1.1Management of a Child with Cryptorchidism
16:00 - 17:00MTE2.1The challenges of extreme obesity
16:00 - 17:00MTE3.1Evaluation of Precocious Pubarche
16:00 - 17:00MTE4.1Management and prevention of complications in adolescents with Diabetes
16:00-17:00Yearbook of Paediatric Endocrinology
Chair(s): Gary Butler (London, UK) & Peter Bang (Linköping, Sweden)
Auditorium
16:00-17:00New Technological Aids in Clinical Paediatric Endocrinology 1
Liffey Hall 2
16:00NTA1.1The BoneXpert methods for fully automated assessment of skeletal maturity ('bone age') and adult height prediction
16:30NTA1.2Growth monitor platform: New application to predict growth and synchronize data between devices
17:15-18:45Industry-sponsored Satellite Symposium 2
Liffey A
19:00-Welcome Reception
CCD

19 September 2014

07:00-Registration Opens
07:30-08:30Meet the Expert Parallel Sessions
07:30 - 08:30MTE5.1Management of childhood fractures
07:30 - 08:30MTE6.1Assessment of Thyroid Nodules
07:30 - 08:30MTE7.1Clinical Management of Cystic Fibrosis Related Diabetes (CFRD) in Childhood
07:30 - 08:30MTE8.1Evaluation and the Management of Tall Stature
07:30-08:30New Technological Aids in Clinical Paediatric Endocrinology 2
Liffey Hall 2
07:30NTA2.1Two girls with precocious puberty; application of the www.espe-elearning.org portal for interactive classroom teaching on your personal mobile device.
08:30-08:45Coffee Break
08:45-09:45Free Communication 1 - Adrenal
Chair(s): Evangelia Charmandari (Athens, Greece) & Anna Lauber Biason (Fribourg, Switzerland)
Liffey Hall 2
08:45FC1.1Molecular Mechanisms of Nongenomic Glucocorticoid Actions: The Role of Human Glucocorticoid Receptor S-Palmitoylation.
08:55FC1.2Clinical phenotype of patients with MCM4 mutation suggests pubertal delay in males in addition to adrenal failure, absent adrenarche and short stature in boys and girls
09:05FC1.3Genetic engineering using TALENs to study the redox regulation of steroidogenesis in vivo
09:15FC1.4A novel non-invasive Short Synacthen Test
09:25FC1.5Antenatal glucocorticoid treatment and polymorphisms in glucocorticoid and mineralocorticoid receptor genes are associated with long-term
09:35FC1.6Molecular Characterization of Testicular Adrenal Rest Tumours (TART) in Congenital Adrenal Hyperplasia (CAH); Lesions with both Adrenocortical and Leydig Cell Features
08:45-09:45Free Communication 2- Bone & Mineral
Chair(s): Nick Shaw (Birmingham, UK) & Ciara McDonnell (Dublin, Ireland)
Liffey Hall 1
08:45FC2.1Asfotase Alfa: Sustained Improved Growth and Function with Extended Treatment in Children with Hypophosphatasia
08:55FC2.2Hypophosphatasia: Gross motor function and height improvement in infants and young children treated with asfotase alfa for up to 3 years
09:05FC2.3Calcium Homeostasis in Adolescents with Beta-Thalassemia Major: Effect of Intramuscular Injection of a Megadose of Cholecalciferol
09:15FC2.4Fractures in children with chronic inflammatory and/or disabling conditions: the SNAP study
09:25FC2.5Pharmacokinetics (PK) and Pharmacodynamics (PD) of a Human Monoclonal Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) Following Four Month Intra-Dose Escalation in Adults with X-linked Hypophosphatemia (XLH)
09:35FC2.6Efficacy and Safety Following Four Monthly Subcutaneous (SC) Doses of a Human Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) in Adults with X-Linked Hypophosphatemia (XLH)
08:45-09:45Free Communication 3 - Diabetes
Chair(s): John Gregory (Cardiff, UK) & Nuala Murphy (Dublin, Ireland)
Liffey A
08:45FC3.1HIGH MOBILITY GROUP BOX-1(HMGB-1) SERUM CONCENTRATIONS INCREASE AT ONSET OF DIABETES IN CYSTIC FIBROSIS (CF) PATIENTS
08:55FC3.2HbA1c level as a predictive marker of progression to clinical diabetes
09:05FC3.3Improved hepatic insulin sensitivity in children randomized to CSII treatment from onset of type 1 diabetes
09:15FC3.4Genetics of pediatric type 2 diabetes: ABCC8 mutation in obesity-associated insulin secretion defects
09:25FC3.5Pancreatic N-Methyl-D-Aspartate receptors as novel drug targets for the treatment of diabetes mellitus
09:35FC3.6ALPHA-LIPOIC ACID AND ANTI-OXIDANT DIET HELPS TO IMPROVE ENDOTHELIAL DYSFUNCTION IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES.
08:45-09:45Free Communication 4- Growth
Chair(s): Veronica Mericq (Santiago, Chile) & Stefano Cianfarani (Rome, Italy)
Wicklow Hall 2
08:45FC4.1HETEROZYGOUS IGF1R MUTATIONS REPRESENT A FREQUENT FINDING IN PATIENTS WITH PRE- AND/OR POSTNATAL PROPORTIONAL UNDERGROWTH AND LOW, NORMAL OR SUPRANORMAL IGF1
08:55FC4.2The effect of GRB10-deficiency in Zebrafish: a translational animal model to study human growth
09:05FC4.3Oscillations in gene expression profiles across childhood highlight the relation of growth and specific metabolic functions in both sexes
09:15FC4.4Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations
09:25FC4.5Fetal and postnatal growth in Turner Syndrome and their associations with the dosage effects of the X-linked gene: a cross-sectional data base analysis of the French national rare disease network
09:35FC4.6LONGITUDINAL GROWTH OF FINNISH CHILDREN WITH GESTATIONAL DIABETES IN MOTHERS
08:45-09:45Free Communication 5- Neuroendocrinology
Chair(s): Nicholas de Roux (Paris, France) & Taneli Raivio (Helsinki, Finland)
Wicklow Hall 1
08:45FC5.1Derivation of GnRH neuron-like cells from human embryonic stem cell-derived neural crest progenitors
08:55FC5.2Mutations in the maternally imprinted gene MKRN3 are a frequent cause of familial central precocious puberty
09:05FC5.3Loss of Function Mutations in PNPLA6 Cause Hypogonadotropic Hypogonadism due to Impaired LH Release from Pituitary Gonadotropes
09:15FC5.4Reference values for urinary gonadotropins in preterm and full-term infants in “minipuberty”
09:25FC5.5Characterization of IGF-I receptor expression and localization in paediatric gliomas upon diagnosis according to WHO 2007 grading
09:35FC5.6The diencephalic syndrome (DS) of emaciation in infantile hypothalamochiasmatic low-grade gliomas (HCLGGs): a retrospective case-control study of diagnostic parameters and long-term outcomes over 30 years of follow-up
08:45-09:45New Perspectives 1
Chair(s): Mohamad Maghnie (Liguria, Italy) & Martin Wabitsch (Ulm, Germany)
Micro-RNAs in Health and Diseases
Liffey B
08:45NP1.1Non Coding RNA's: Introduction to Non-Coding RNAs and the Role of MicroRNAs in GnRH Neurons
09:15NP1.2The Role of MicroRNAs in Diabetes
08:45-09:45Yearbook of Paediatric Endocrinology
Chair(s): Franco Chiarelli (Chieti, Italy) & Angela Webber (Dresden, Germany)
Auditorium
09:45-10:15Coffee Break
10:15-10:45Plenary Session 3
Chair(s): Laura Audi (Barcelona, Spain) & Peter Clayton (Manchester, UK)
Auditorium
10:15PL3Sex, Stem Cells and Decision of Cell Fate
10:45-11:45ESPE Award and Activities
Auditorium
11:45-12:15Plenary Session 4
Chair(s): Laura Audi (Barcelona, Spain) & Peter Clayton (Manchester, UK)
Auditorium
11:45PL4Gene therapy in cerebral form of X-linked adrenoleukodystrophy
12:30-13:30Lunch
Visit to the Posters and Exhibition
13:00-14:00Industry-sponsored Satellite Symposium
Liffey B
14:15-15:45Symposium 5 - Novel Insights into Hypoadrenalism
Chair(s): Tsutomu Ogata (Hamamatsu, Japan) & Christa Fluck (Bern, Switzerland)
Auditorium
14:15S5.1Aetiology of Congenital Hypoadrenalism
14:45S5.2Adrenarche: Coming of age in the era of genomics and metabolomics
15:15S5.3CAH: Health Status in Adults (CaHASE)
14:15-15:45Symposium 6 - New Concepts in the Gonadotropic Axis
Chair(s): Jean-Claude Carel (Paris, France) & Nelly Pitteloud (Lausanne, Switzerland)
Liffey A
14:15S6.1Role of The Hypothalamic MicroRNA in Puberty Regulations
14:45S6.2New Syndromes Resulting in Secretory Pathway and Gonadotropic Axis Regulation Defects
15:15S6.3Genetic Dissection of Puberty in Mice
14:15-15:45Symposium 7 - Controversies in the Surgical Management of DSD
Chair(s): Peter Lee (Pennsylvania, USA) & Olaf Hiort (Lubeck, Germany)
Liffey B
14:15S7.1Evolution of Feminising Genitoplasty
14:30S7.2Pros and Cons of Early or Late Feminising Genitoplasty
15:00S7.3Masculinising Genitoplasty
14:15-15:45ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Chair(s): Jacquie Lyons & Sinead Moloney
Wicklow Hall 1
14.15 WG7.1Quality of life and anxiety in adolescents with differentiated thyroid cancer
14:35WG7.2Evolving Growth Hormone Therapy (GHT) Patient Training in a Digital World
14:55WG7.3Endocrine Nursing, social media and research: results of an international study
15:15Open discussion
14:15-15:45Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Chair(s): Dr Raul Calzada & Dr Asmahane Ladjouze
Liffey Hall 1
14:15 - 14:25WG8.1Word from GPED’s President
14:25 - 14:35WG8.2Inequities of treatment options in developing countries: Inequities in treatment options type 1 diabetes in Sudan
14:35 - 14:45WG8.3Inequities of treatment options in developing countries: Osteogenesis imperfecta in Indonesia
14:45 - 14:55WG8.4Inequities of treatment options in developing countries: Congenital Adrenal Hyperplasia
14:55 - 15:05Q & A
15:05 - 15:15WG8.5Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Costa Rica)
15:15 - 15:25WG8.6Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Ghana)
15:25 - 15:35WG8.7Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Nigeria)
15:35 - 15:45Q & A
15:45-16:15Coffee Break
16:15-17:45Industry-sponsored Satellite Symposium 4
Auditorium
16:15-17:45Industry-sponsored Satellite Symposium 5
Liffey B
16:15-17:45Industry-sponsored Satellite Symposium 6
Liffey A
18:00-19:30ESPE Business Meeting
Liffey A
19:30-Free Evening

20 September 2014

07:00-Registration Opens
07:30-08:30Meet the Expert Parallel Sessions
07:30 - 08:30MTE1.2Management of a Child with Cryptorchidism
07:30 - 08:30MTE2.2The challenges of extreme obesity
07:30 - 08:30MTE3.2Evaluation of Precocious Pubarche
07:30 - 08:30MTE4.2Management and Prevention of Complications in Adolescents with Diabetes
07:30 - 08:30MTE5.2Management of Childhood Fractures
08:45-09:45Free Communication 6 - Gonads & DSD
Chair(s): Abdulla Bereket (Istanbul, Turkey) & Faisal Ahmed (Glasgow, UK)
Wicklow Hall 2
08:45FC6.1Search for genetic defects in the transcription factor genes FOXL2, FOXE1, BMP15, NOBOX and GDF9 in children, adolescents and young adults with premature ovarian insufficiency (POI).
08:55FC6.2Next generation sequencing of the androgen receptor (AR) gene in patients with androgen insensitivity syndrome (AIS) and controls
09:05FC6.3LRH-1 rescues SF-1 deficiency for steroidogenesis in vitro but cannot explain the broad phenotype of SF-1 deficiency in men
09:15FC6.4FAMILIAL 46,XY COMPLETE FEMALE EXTERNAL SEX DEVELOPMENT AND PRIMARY AMENORRHEA ALONG WITH HIDDEN GONADAL TUMORS, SECONDARY TO A NOVEL p.MET64VAL SRY GENE MUTATION
09:25FC6.5Serum levels of AMH reflect ovarian morphology by MRI in 109 healthy peripubertal girls
09:35FC6.6Effects of exposure to the endocrine disruptor di(n-butyl) phthalate on testicular dysgenesis and fetal germ cell development in the rat and human fetal testis.
08:45-09:45Free Communication 7 - Growth Promoting Therapies
Chair(s): Leo Dunkel (London, UK) & Fayza Darendelier (Istanbul, Turkey)
Liffey A
08:45FC7.1Genetic markers of insulin resistance are associated with growth hormone response in short SGA children – the North European SGA Study (NESGAS)
08:55FC7.2The rs1024531 GRB10 promoter polymorphism is associated with response to growth hormone (GH) therapy in patients with GH deficiency (GHD): validation by in vitro functional analysis
09:05FC7.3Gene expression networks associated with changes in serum markers of metabolism and growth in growth hormone (GH)-treated children with GH deficiency (GHD)
09:15FC7.4A decade of clinical experience in a Swedish university centre using prediction models to optimize growth hormone (GH) treatment in prepubertal children
09:25FC7.5Impact of Growth Hormone on Adult Bone Quality in Turner Syndrome – A High Resolution Peripheral Quantitative Computed Tomography Study
09:35FC7.6Topicon™ ThermoMatrix™-Mediated Passive Transdermal Delivery of Human Growth Hormone (hGH) Across EpidermFT™ Full-Thickness Human Skin Equivalent (HSE): Towards an Extended-Wear hGH Patch
08:45-09:45Free Communication 8 - Fat Metabolism
Chair(s): Abei Lopez Bermejo (Girona, Spain) & Saraf Farooqi (Cambridge, UK)
Wicklow Hall 1
08:45FC8.1Activation of the ER stress response in cultured human umbilical vein endothelial cells (HUVECs) by plasma obtained from prepubertal obese children.
08:55FC8.2MicroRNA-152 promotes hepatic steatosis by suppressing the Wnt signaling pathway
09:05FC8.3Identification of death ligand TRAIL (TNF-related apoptosis-inducing ligand) as a potent mitogen in human preadipocytes
09:15FC8.4CREB-REGULATED TRANSCRIPTION COACTIVATOR 3 (CRTC3): A NEW ADIPOKINE RELATED TO CHILDHOOD OBESITY
09:25FC8.5Putative gain-of-function in rats carrying the Ghsr Q343X mutation
09:35FC8.6A Novel Missense Variant in the Insulin Receptor Gene in 3 unrelated Irish families with severe Insulin Resistance Syndrome - Evidence for an Irish Founder Effect.
08:45-09:45Free Communication 9 - Beta Calls
Chair(s): Renata Lorini (Genova, Italy) & Carlo Acerini (Cambridge, UK)
Liffey Hall 2
08:45FC9.1Inappropriately High Rates of Cell Proliferation in Diffuse Congenital Hyperinsulinism are Linked to Nuclear Expression of CDK6
08:55FC9.2Characterising the immunohistochemical expression of dipeptidyl peptidase-4 in pancreatic tissue from patients with diffuse and focal congential hyperinsulinism.
09:05FC9.3In search for new monogenic diabetes genes: PCBD1
09:15FC9.4Clinical characteristics and molecular genetics analysis of 20 patients with neonatal diabetes mellitus from a single centre of the South-Eastern region of Turkey
09:25FC9.5TRANSIENT NEONATAL DIABETES IN ADULTHOOD: METABOLIC AND NEURODEVELOPMENTAL OUTCOMES
09:35FC9.6Sulfonylurea therapy corrects hypotonia, attention deficits, improves complex neuropsychological functions and motricity in patients with neonatal diabetes secondary to mutation in potassium channel subunits, through a central nervous system effect.
08:45-09:45New Perspectives 2
Chair(s): Tim O'Brien (Galway, Ireland) & José C. Moreno (Madrid, Spain)
Regenerative Endocrinology
Liffey B
08:45NP2.1Pancreatic Beta Cell Development: from rodent to human
09:15NP2.2Formation of a Thyroid Gland from Embryonic Stem Cells
08:45-09:45Free Communications - Late Breaking
Chair(s): Irene Netchine (Paris, France) & Susan O'Connell (Cork, Ireland)
Liffey Hall 1
08:45FC-LB-1Top Line Results of Once-Weekly, CTP-Modified Human Growth Hormone (MOD-4023): Phase 2 Dose Finding Study in Children with Growth Hormone Deficiency (GHD)
08:55FC-LB-2Sonic Hedgehog is required for cell specification of Rathke’s pouch progenitors during normal development and is over-expressed in adamantinomatous craniopharyngioma
09:05FC-LB-3Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche
09:15FC-LB-4Does Severity of Hypothyroidism at Birth Contribute to Abnormal Cortical Development among Children with Congenital Hypothyroidism (CH)?
09:25FC-LB-5CB2 polymorphism could modulate the relationship between childhood obesity and age at menarche
09:35FC-LB-6Global Consensus Recommendations on Prevention and Management of Nutritional Rickets
10:15-10:45Plenary Session 5
Chair(s): Jan Lebl (Prague, Czech Republic) & Reiko Horikawa (Tokyo, Japan)
Auditorium
10:15PL5Obesity: Novel Treatments and the Imperative for Prevention
10:45-11:45ESPE Award Session and Activities 2
Auditorium
12:00-13:00Free Communication 10 - Programming & Early
Chair(s): Ken Ong (Cambridge, UK) & Colm Costigan (Crumlin, Ireland)
Liffey Hall 1
12:00FC10.1A role for Delta-like homologue 1 (DLK1) in a secretory placental population and implications for foetal growth
12:10FC10.2STK11 EXPRESSION IN ADIPOSE TISSUE FOLLOWING FETAL GROWTH RESTRICTION: RELATION TO CATCH-UP GROWTH AND VISCERAL FAT MASS.
12:20FC10.3Genetic and epigenetic defects at the GNAS locus lead to opposite patterns of fetal and postnatal growth
12:30FC10.4Influence of newborn and maternal factors on neonatal body composition
12:40FC10.5Contrasting associations of maternal smoking and alcohol intake in late pregnancy and offspring body composition in childhood
12:50FC10.6The PremAldo Study: Impaired Aldosterone Signaling Worsens Renal Sodium Loss in Preterm Infants
12:00-13:00Free Communication 11 - Pituitary
Chair(s): Ivo Arnhold (Sao Paulo, Brazil) & Juliane Leger (Paris, France)
Liffey A
12:00FC11.1ABNORMAL SONIC HEDGEHOG SIGNALING IN ADAMANTINOMATOUS CRANIOPHARYNGIOMAS AND ITS ASSOCIATION WITH CTNNB1/BETA-CATENIN MUTATIONS
12:10FC11.2Novel SOX2 mutation: identification of new molecular mechanisms of SOX2 action and interactions.
12:20FC11.3Early-Onset Central Diabetes Insipidus is associated with De novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 gene mutations
12:30FC11.4Management of hyperhydration in a child with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) using a selective vasopresin receptor agonist.
12:40FC11.5ENDOCRINE FEATURES OF A LARGE COHORT OF CHILDREN WITH SEPTO-OPTIC DYSPLASIA AND CONGENITAL MULTIPLE PITUITARY HORMONAL DEFICIENCIES
12:50FC11.6Clinical and neuroradiological characteristics in children and adolescents with Septo-Optic Dysplasia, Multiple Pituitary Hormone Deficiencies and Optic Nerve Hypoplasia: Experience from a single tertiary centre.
12:00-13:00Free Communication 12 - Obesity
Chair(s): Jean-Pierre Chanoine (Vancouver, Canada) & Judith Meehan (Dublin, Ireland)
Wicklow Hall 2
12:00FC12.1High-fat diet rapidly triggers circadian de-synchronization of clock genes, neuropeptides and inflammation mediators in the hypothalamus of C57BL mice
12:10FC12.2Obesity in childhood and adolescence is associated with shorter leucocyte telomere length
12:20FC12.3Increased resting energy expenditure in girls with Turner syndrome
12:30FC12.4Pediatric reference values for insulin from oGTT and prevalence of hyperinsulinemia in obese children
12:40FC12.5Low Circulating Levels of DKK-1 Protein in Obese Children Indicate Suppression of Canonical Wnt Signaling
12:50FC12.6Resveratrol inhibits inflammation-induced production of cytokines in human adipocytes
12:00-13:00Free Communication 13 - Thyroid
Chair(s): Marek Niedziela (Poznan, Poland) & Heiko Krude (Berlin, Germany)
Liffey Hall 2
12:00FC13.1Massive sequencing of thyroidal genes reveals unexpected polygenic defects in dyshormonogenic hypothyroidism.
12:10FC13.2Thyroid agenesis and severe thyroid hypoplasia caused by a new inactivating TSH receptor mutation Ala579Val
12:20FC13.3Overexpression of supressor tumoral PTEN, but not DREAM, was detected in multinodular goiter in humans.
12:30FC13.4The prevalence of congenital malformations in infants with TSH elevation on newborn screening – the importance of distinguishing between true and transient congenital hypothyroidism
12:40FC13.5THE ULTRASTRUCTURAL CHANGES IN THYROID CELLS IN THE COURSE OF DAMAGE IN HASHIMOTO’S THYROIDITIS
12:50FC13.6ABNORMAL THYROID HORMONE METABOLISM IN PATIENTS WITH THRA MUTATIONS DUE TO IMPAIRED EXPRESSION OF THE TYPE 3 DEIODINASE
12:00-13:00Free Communication 14 - Puberty
Chair(s): Margaret Zacharin (Melbourne, Austrailia) & Clodagh O'Gorman (Limerick, Ireland)
Liffey B
12:00FC14.1Brain structure and function in gender dysphoric adolescents
12:10FC14.2Infancy growth rate predicts timing of puberty both in girls and boys
12:20FC14.3Novel genetic variants in a cohort of paediatric and adolescent patients with Hypogonadotrophic Hypogonadism and Kallmann syndrome
12:30FC14.4Development of pubertal gynaecomastia - A longitudinal cohort study
12:40FC14.5Fertility of women treated during childhood for precocious puberty with triptorelin: PREFER retrospective study
12:50FC14.6QUALITY OF LIFE IN PATIENTS WITH CONGENITAL HYPOGONADOTROPIC HYPOGONADISM (CHH)
12:00-13:00Yearbook of Paediatric Endocrinology
Chair(s): Wieland Kiess (Leipzig, Germany) & Ze'ev Hochberg (Haifa, Israel)
Auditorium
13:00-13:30Lunch
Visit to the Posters and Exhibition
15:00-16:30Symposium 8 - Novel Therapies in Paediatric Endocrinology
Chair(s): Nils Krone (Birmingham, UK) & Alan Rogol (Virginia, USA)
Liffey B
15:00S8.1Hyperinsulinaemia
15:30S8.2Treatment of Hypophosphatasia
16:00S8.3Congenital Adrenal Hyperplasia
15:00-16:30Symposium 9 - Novel Insights into Pituitary Development and Function
Chair(s): Roland Pfaeffle (Leipzig, Germany) & Ron Rosenfeld (USA)
Wicklow Hall 2
15:00S9.1Paracrine Regulation in the Pituitary
15:30S9.2Sox2+ve cells in the adult murine pituitary are stem cells with tumour-inducing potential
16:00S9.3Pax7 dictates alternate pituitary cell fates during development
15:00-16:30Symposium 10 - Childhood Obesity: Challenges in Management
Chair(s): Phil Zeitler (Colorado, USA) & Ewa Malecka-Tendera (Katowice, Poland)
Liffey A
15:00S10.1The Metabolically Healthy Obese Child
15:30S10.2Childhood and Adolescent Obesity - Can Treatment Response be Predicted?
16:00S10.3Natural Course of Impaired Glucose Tolerance in Obese Children
15:00-16:00Meet the Expert Parallel Sessions
15:00 - 16:00MTE6.2Assessment of Thyroid Nodules
15:00 - 16:00MTE7.2Clinical Management of Cystic Firbrosis Related Diabetes (CRFD) in Childhood
15:00 - 16:00MTE8.2Evaluation and the Management of Tall Stature
16:30-17:00Coffee Break
17:00-17:30Plenary 6
Chair(s): Mehul Dattani (London, UK) & Cheri Deal (Montréal, Canada)
Auditorium
17:00PL6Genetics of Obesity
17:30-17:45President Poster Award
Auditorium
17:45-18:00Closing Ceremony
Auditorium
19:00-ESPE Evening