Searchable abstracts of presentations at key conferences in endocrinology

ea0063oc1.5 | Calcium and Bone | ECE2019

Renal function in 711 patients with hypoparathyroidism during more than 4 years of therapy

Siggelkow Heide , Stamm Bettina , Stamm Niklas , Blaschke Martina , Gruszendorf Martin

Patients (pts) with hypoparathyroidism (HypoPT) are at risk to develop renal failure possibly caused by hypercalciuria and nephrocalcinosis. We retrospectively evaluated the data of 711 Patients with HypoPT in 3 endocrine centres in Germany.Methods: Records of 711 pts with HypoPT were reviewed. Patients were predominantly female (n=592, male: n=119; age 50.9±14.1 years, range 12 – 99 years). The following parameters were docum...

ea0090p484 | Thyroid | ECE2023

Normative Values for the Hypoparathyroidism Patient Questionnaire (HPQ28) in the General German Population

Blaschke Martina , Wilde Deborah , Schulz Maxi , Herrmann-Lingen Christoph , Siggelkow Heide

Introduction: Patients with hypoparathyroidism (hypoPT) suffer from a number of complaints and reduced quality of life (QoL) besides having serum values for disease-specific parameters in the target range. To be able to quantify symptoms in hypoPT patients we lately developed a disease-specific questionnaire, the Hypoparathyroidism patient questionnaire with 28 items (HPQ28). The aim of this study was to present normative values for the HPQ28.Methods: A ...

ea0063p1044 | Interdisciplinary Endocrinology 2 | ECE2019

Current medical care in women with Turner syndrome-retrospective data from five different specialist endocrinology centers in Germany

Kahlert Elin , Blaschke Martina , Janssen Onno E , Stahnke Nikolaus , Strik Dominika , Merkel Martin , Mann Alexander , Liesenkoetter Klaus-Peter , Siggelkow Heide

Introduction: Turner syndrome (TS) is characterized by the complete or partial loss of one X chromosome and associated with a wide range of clinical manifestations. The clinical appearance depends on the specific karyotype, which may include different mosaic forms. Main features of almost all the karyotypes are short stature and delayed or absent puberty. Adult women in particular are at high risk of developing cardiac complications, metabolic syndrome, increased liver enzyme ...

ea0049ep353 | Steroid metabolism + action | ECE2017

Genetic variations in the HSD11B1 gene in patients treated with glucocorticoids show associations with bone mineral density

Siggelkow Heide , Blaschke Martina , Armbrecht Gabriele , Thomasius Friederike , Bock Oliver , Tzvetkov Mladen , Gluer Claus-C , Felsenberg Dieter

Introduction: Physiological glucocorticoids play an essential role in bone formation but can cause osteoporosis if present in excess. The key enzyme converting inactive cortisone into the active cortisol and vice versa is 11-beta-hydroxy-steroid-dehydrogenase (11β-HSD1). We have reported that genetic variations in the HSD11B1 gene correlate with increased cortisol levels in dexamethasone suppression and with changes in bone mineral density (BMD) suggesting indivi...

ea0070aep148 | Bone and Calcium | ECE2020

Successful quantification of symptom load by a disease-specific questionnaire HPQ 40/28 and analysis of influencing biochemical parameters in patients with postsurgical hypoparathyroidism

Wilde Deborah , Wilken Lara , Stamm Bettina , Heppner Christina , Leha Andreas , Blaschke Martina , Herrmann-Lingen Christoph , Siggelkow Heide

In hypoparathyroidism (HypoPT), patients suffer severely from reduced quality of life. The complexity of HypoPT demands a disease-specific control instrument to characterize symptom load. We employed a newly developed disease-specifichypoparathyroid patient questionnaire (the HPQ 40/28) to investigate and quantify HypoPT patients’ complaints and contributing factors. In this cross-sectional, two-center study, patients with postsurgical HypoPT (n = 49) were m...