Searchable abstracts of presentations at key conferences in endocrinology

ea0037gp.19.10 | Pituitary–Acromegaly | ECE2015

A phase 2 study of antisense oligonucleotide therapy directed at the GH receptor demonstrates lowering of serum IGF1 in patients with acromegaly.

Trainer Peter , Newell-Price John , Ayuk John , Aylwin Simon , Rees Aled , Drake Will , Chanson Philippe , Brue Thierry , Webb Susan , Fajardo Carmen , Aller Javier , McCormack Ann , Torpy David , Tachas George , Atley Lynne , Bidlingmaier Martin

ATL1103 is a second generation antisense oligomer directed at the GH receptor. It is a 20mer with a phosphorothioate backbone and 2′-O-methoxyethyl modifications of the five nucleotides at either end intended to increase its plasma half-life and affinity for the target RNA to allow post-hybridization RNaseH degradation. We report a phase 2 randomised, open-label, parallel group study of subcutaneously administered ATL1103 in patients with active acromegaly. Appr...

ea0070aep44 | Adrenal and Cardiovascular Endocrinology | ECE2020

Etiology and extent of impaired quality of life, fatigue and affective, cognitive, and emotional dysfunction in patients with cushing’s syndrome – The IQFACE-CS study

de Vries Friso , Papakokkinou Eleni , Santos Alicia , van Haalen Femke , Valassi Elena , Biermasz Nienke , Johansson Birgitta , Gómez-Ansón Beatriz , Bauduin Stéphanie , Resmini Eugenia , van der Wee Nic , Pereira Alberto M , Webb Susan , Ragnarsson Oskar

Background: Patients with Cushing’s Syndrome (CS) suffer from a variety of neuropsychiatric and cognitive problems. Following remission, some, but not all of these symptoms resolve. Recent cross-sectional studies in patients with CS show persistent structural and functional brain abnormalities. However, longitudinal studies using magnetic resonance imaging, and a detailed neurocognitive assessment, performed before and after treatment, are not available.<p class="abs...

ea0070aep675 | Pituitary and Neuroendocrinology | ECE2020

Gender dimorphism of intramuscular fatty infiltration and related muscle dysfunction in patients with long-term control of acromegaly

Martel-Duguech Luciana , Alonso-Pérez Jorge , Bascuñana Helena , Diaz-Manera Jordi , Alonso-Jimenez Alicia , Llauger Jaume , Nuñez-Peralta Claudia , Montesinos Paula , Webb Susan M. , Valassi Elena

Background: Muscle weakness persists in patients with acromegaly (ACRO) even long-term after disease control. Mechanisms determining this sustained impairment are not known. We hypothesized that alteration of muscle architecture, due to intramuscular fatty infiltration, is associated with muscle dysfunction in these patients.Patients and Methods: Thirty-seven acromegalic patients [21 females and 16 males, mean (± s.d.)age, 53 ± 9 years...

ea0032p873 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Relationship between telomere length and dyslipidemia in patients with Cushing's syndrome

Aulinas Anna , Jose Ramirez Maria , Jose Barahona Maria , Mato Eugenia , Bell Olga , Valiente Cristian , Valassi Elena , Resmini Eugenia , Santos Alicia , Crespo Iris , Corcoy Rosa , Surralles Jordi , Webb Susan M.

Introduction: Cushing’s syndrome (CS) is associated with increased mortality and morbidities. Hypercortisolism is also present in chronic mood disorders (CMD) and stress, where telomere length (TL) has been found to be shorter than in matched controls. Since hypercortisolism is present in CS and CMD, we hypothesized that telomere shortening could also be present in CS. The aim of this study was to investigate TL in CS patients compared to matched controls.<p class="ab...

ea0030oc2.8 | Oral Communications 2 | BSPED2012

Genetic screening in a large cohort of patients with congenital hypopituitarism; current knowledge and future directions

Alatzoglou Kyriaki S , Turton James P G , Kelberman Daniel , McCabe Marc J , Gregory Louise C , Webb Emma A , McNay David E G , Woods Kathryn S , Mehta Ameeta , Dattani Mehul T

Background and aims: Congenital hypopituitarism (CH) encompasses a spectrum of phenotypes. Known genetic factors account for variable percentage of cases depending on the cohort screened. We analysed the results of genetic screening in a large cohort of patients with CH with the following aims: i) to clarify the genetic aetiology of CH ii) identify any phenotype genotype correlations and iii) propose a screening strategy.Patients and methods: Over 15 yea...

ea0026p20 | Adrenal cortex | ECE2011

Clinical presentation of Cushing’s syndrome in a large series from the European Registry on Cushing's syndrome (ERCUSYN)

Valassi Elena , Santos Alicia , Yaneva Maria , Toth Miklos , Strasburger Christian , Chanson Phillippe , Wass John , Chabre Olivier , Pfeifer Marija , Feelders Richard , Tsagarakis Stylianos , Trainer Peter , Franz Holger , Zopf Kathrin , Zacharieva Sabina , Lamberts Steven , Webb Susan

The European Registry on Cushing’s syndrome (ERCUSYN) is designed to collect prospective and follow-up data at EU level on patients with Cushing’s syndrome (CS). Baseline data on 481 CS patients (390 females, 91 males; mean age (±S.D.): 44±14 years) collected from 36 centres in 23 countries. This cohort included new patients since 2008 and retrospective cases since 2005. Patients were divided into four major etiologic groups: pituitary-depend...

ea0026p216 | Pituitary | ECE2011

Long-term treatment of acromegaly with pegvisomant (Somavert): cross-sectional observations from ACROSTUDY, a post-marketing, international, safety, surveillance study

van der Lely A J , Lundgren F , Biller B M K , Brue T , Cara J , Ghigo E , Hadavi J Hey , Rajicic N , Saller Bernhard , Sanocki John , Strasburger Christian , Webb Susan , Haggstrom Maria Koltowska

Introduction: Somavert is a GH receptor blocker, which inhibits hepatic production of IGF1. While it has been approved for the treatment of acromegaly since 2003 there are few data regarding its effects in everyday clinical practice.Methods/design: ACROSTUDY is an open-label, international, prospective, non-interventional, post-marketing surveillance study monitoring the long-term safety and efficacy of Somavert.Results: As of Dece...

ea0026p255 | Pituitary | ECE2011

Quality of life and cortisol diurnal rhythm after 3 months of medical treatment for Cushing’s disease

van der Pas R , de Bruin C , Pereira A , Romijn J , Netea R , Hermus A , Zelissen P , de Jong F , van der Lelij A , de Herder W , Webb S , Lamberts S , Hofland L , Feelders R

Introduction: Cushing’s disease (CD) is characterized by various symptoms, amongst which fatigue, muscle weakness and depression. The chronic state of hypercortisolism severely impairs quality of life (QoL). In addition, the physiological cortisol diurnal rhythm (CDR) is disturbed in CD. Transsphenoidal surgery is the primary treatment for CD, but long-term remission rates are disappointing. We performed a prospective trial in which stepwise medical treatment was applied ...

ea0022p621 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Decreased cortical thickness on MRI in patients with Cushing's syndrome: preliminary experience

Santos Alicia , Granell Esther , Resmini Eugenia , Ybarra Juan , Portella Maria J , Perez Victor , Barahona Maria J , Mourelo Olga Lopez , Vives Yolanda , De Juan Manuel , Pires Patricia , Gomez Anson Beatriz , Webb Susan

Introduction: Patients with Cushing’s syndrome might present a variety of brain alterations. There is however little evidence from MRI studies demonstrating atrophy of either frontal or medial temporal brain regions.Aims: To study cortical alterations (decreased cortical thickness) on MRI in patients with Cushing’s syndrome (CS), as compared to controls (C), and long-standing major depressive disorder (MDD).Material and m...

ea0019p241 | Pituitary | SFEBES2009

The acromegalic cardiovascular and respiratory outcomes with primary analogue therapy (A.C.R.O.P.A.T.) trial

Webb A , Gayton E , Annamalai A , Pilsworth S , Wallace S , Khan S , O'Toole S , Ariyaratnam S , Maki-Petaja K , Scoffings D , Antoun N , Wilkinson I , Dutka D , Shneerson J , Simpson H , Gurnell M

Seventeen newly-diagnosed acromegalic patients (8 female, 9 male: mean age 55 year, range 26–73 year) were recruited to the A.C.R.O.P.A.T. trial. Patients were assessed prior to, and following, 6 months of treatment with Somatuline Autogel® (SA).Growth hormone (GH) & insulin-like growth factor 1 (IGF1): Following treatment, GH and IGF1 levels fell significantly in all but one subject: median GH change −17.23 mU/l (interquar...