Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep226 | Calcium and Vitamin D metabolism | ECE2015

Pitfalls in the interpretation of bone turnover markers in liver transplantation

Krol Charlotte , Meiland Desi , Dekkers Olaf , Veer Eveline van der , Kroon Herman , Rabelink Ton , Hoek Bart van , Hamdy Neveen

Introduction: Osteoporosis and fractures are common in liver disease and fracture incidence increases after orthotopic liver transplantation (OLT). The value of bone turnover markers (BMTs) in the prediction of bone loss and fracture risk pre- and post-OLT is not known.Study design: The BMTs P1NP, osteocalcin, BALP and CTX were measured initially or in Biobank stored sera at screening and at 3, 6 and 12 months post-OLT in consecutive OLT recipients betwe...

ea0070aep215 | Bone and Calcium | ECE2020

Progression of vertebral fractures in long-term controlled acromegaly: A 9-year follow-up study

Pelsma Iris , Claessen Kim , Pereira Alberto , van Furth Wouter , Appelman-Dijkstra Natasha , Kloppenburg Margreet , Kroon Herman , Biermasz Nienke

Objective: Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) excess results in both reversible and irreversible damage to the skeleton, and includes increased vertebral fracture (VF) risk in the presence of normal BMD. The prevalence of VFs is approximately 60% in controlled acromegaly patients, and these VFs can progress during short-term follow-up. We aimed to identify the course of VFs and their associated risk factors in a cohort of acromegaly patients in long-t...

ea0020p545 | Neuroendocrinology, Pituitary and Behaviour | ECE2009

Pre-treatment IGF-I concentrations predict radiographic osteoarthritis in acromegalic patients with long-term cured disease

Biermasz Nienke R , Wassenaar Moniek J E , van der Klaauw Agatha A , Pereira Alberto M , Smit Johannes W A , Roelfsema Ferdinand , Wolterbeek Ron , Kroon Herman M , Kloppenburg Margreet , Romijn Johannes A

Objective: To identify factors influencing the development of osteoarthritis during long-term control of acromegaly, focusing on disease specific parameters, growth hormone (GH) and insulin-like growth factor I (IGF-I) concentrations and duration of disease, adjusted for the well-known determinants of primary osteoarthritis.Design: Follow-up study.Methods: We studied 67 patients, with adequate biochemical control of acromegaly for ...

ea0020p552 | Neuroendocrinology, Pituitary and Behaviour | ECE2009

The D3 GH receptor polymorphism is associated with osteoarthritis, especially of the hip, in patients with long-term cured acromegaly

Wassenaar Moniek JE , Biermasz Nienke R , van der Klaauw Agatha A , Smit Johannes WA , Pereira Alberto M , Roelfsema Ferdinand , van der Straaten Tahar , Kroon Herman M , Kloppenburg Margreet , Guchelaar HJ , Romijn Johannes A

Objective: To evaluate the impact of the genomic deletion of exon 3 in the growth hormone receptor (d3GHR) on co-morbidities of acromegaly in a well-characterized cohort of patients with long-term remission of acromegaly.Design: Cross sectional study.Methods: The presence of the d3GHR polymorphism was assessed in 86 acromegalic patients and related to clinical outcome, i.e. anthropometric parameters, osteoarthritis, and the metabol...

ea0050p269 | Neuroendocrinology and Pituitary | SFEBES2017

Male IGSF1 deficient humans and mice exhibit somatotroph neurosecretory hyperfunction

Joustra Sjoerd D , Roelfsema Ferdinand , Endert Erik , van Trotsenburg ASPaul , Fliers Eric , Schneider Harald J , Kosilek Robert P , Kroon Herman M , Logan John , Turgeon Marc-Olivier , Zhou Xiang , Toufaily Chirine , Koulouri Olympia , Gurnell Mark , Bassett JHDuncan , Williams Graham R , Oostdijk Wilma , Wit Jan-Maarten , Pereira Alberto M , Biermasz Nienke R , Bernard Dan J , Schoenmakers Nadia

X-linked IGSF1 (immunoglobulin superfamily, member 1) loss-of-function mutations in males are associated with central hypothyroidism, macroorchidism, and a variable spectrum of anterior pituitary dysfunction. Igsf1 deficient male mice also exhibit central hypothyroidism, however, the physiological and molecular function of IGSF1 in both species has not yet been elucidated. Although partial transient GH deficiency is a ra...

ea0050p269 | Neuroendocrinology and Pituitary | SFEBES2017

Male IGSF1 deficient humans and mice exhibit somatotroph neurosecretory hyperfunction

Joustra Sjoerd D , Roelfsema Ferdinand , Endert Erik , van Trotsenburg ASPaul , Fliers Eric , Schneider Harald J , Kosilek Robert P , Kroon Herman M , Logan John , Turgeon Marc-Olivier , Zhou Xiang , Toufaily Chirine , Koulouri Olympia , Gurnell Mark , Bassett JHDuncan , Williams Graham R , Oostdijk Wilma , Wit Jan-Maarten , Pereira Alberto M , Biermasz Nienke R , Bernard Dan J , Schoenmakers Nadia

X-linked IGSF1 (immunoglobulin superfamily, member 1) loss-of-function mutations in males are associated with central hypothyroidism, macroorchidism, and a variable spectrum of anterior pituitary dysfunction. Igsf1 deficient male mice also exhibit central hypothyroidism, however, the physiological and molecular function of IGSF1 in both species has not yet been elucidated. Although partial transient GH deficiency is a ra...