Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep916 | Thyroid | ECE2020

Subclinical hypothyroidism and non-alcoholic fatty liver disease: A systematic review and meta-analysis

Guzman-Prado Yuli , Samson Ondrej

Introduction: Hypothyroidism has been reported as an important factor in the pathogenesis of non-alcoholic fatty liver disease (NAFLD) but studies about the relation between subclinical hypothyroidism and NAFLD have shown contradictory findings. The aim of this study was to conduct a systematic review and meta-analysis exploring the association between subclinical hypothyroidism and NAFLD.Methods: MEDLINE, EMBASE, Cochrane Library and sources for grey li...

ea0041ep775 | Nuclear receptors and Signal transduction | ECE2016

The impact of mycophenolate mofetil on androgen receptor activity in prostate cancer cells 22Rv1

Zenata Ondrej , Dvorak Zdenek , Vrzal Radim

Mycophenolate mofetil (MYC) is widely used in transplant medicine as an immunosuppressant drug to prevent rejection in organ transplantation. In this work we investigated the effect of MYC on the activity of androgen receptor (AR) by employing gene reporter assay (GRA) and PCR in prostate cancer cell line 22Rv1.Slight but significant activation of AR was observed for cells treated with MYC in stably transfected 22Rv1 cells (AIZ-AR). Moreover, significant...

ea0086p206 | Metabolism, Obesity and Diabetes | SFEBES2022

Circulating levels of adipose-derived lipokines correlate positively with fasting insulin in states of increased insulin insensitivity in humans

Gamwell Jonathan , Riecan Martin , Pinnick Katherine , Kuda Ondrej , Hodson Leanne

Introduction: Palmitoleate, a proposed adipose tissue (AT)-derived lipokine, has been suggested to contribute to glucose homeostasis. However, data relating to the association between circulating palmitoleate and markers of insulin sensitivity in humans are equivocal. Recently, AT-derived fatty acid-hydroxy fatty acids (FAHFAs) have also been suggested to play a role in glucose homeostasis by increasing glucose uptake in AT. Again, data is conflicting for the association betwe...

ea0090p44 | Calcium and Bone | ECE2023

CYP24A1 mutation - a rare cause of hypercalcemia and nephrocalcinosis in adulthood

Brunerova Ludmila , Reeš Ondrej , Zoubkova Veronika , Votypka Pavel

Background: CYP24A1 gene encodes the enzyme vitamin D 24-hydroxylase, which converts active vitamin D to inactive metabolites. More than 20 currently described, usually biallelic pathogenic variants of this gene are responsible for idiopathic infantile hypercalcemia manifested typically in childhood (often in newborns) with hypercalcemia, hypercalciuria and nephrocalcinosis. However, a few patients (mostly with monoallelic heterozygous pathogenic variant) can develop mild symp...

ea0043oc20 | Design a Clinical Program for Success | WCTD2016

Selected adipokines in patients with type 2 diabetes: relationship to markers of vascular damage

Karasek David , Gajdova Jaromira , Kubickova Veronika , Cibickova Lubica , Krystynik Ondrej , Vaverkova Helena

Introduction: Adiponectin, adipocyte fatty acid-binding protein (A-FABP), fibroblast growth factor 21 (FGF-21), C1q/TNF-related protein 9 (CTRP9) and allograft inflammatory factor-1 (AIF-1) belong to the proteins produced by adipocyte tissue, which differently contribute to oxidative stress, chronic inflammation, insulin resistance and endothelial damage. The aim of this pilot study was to compare their levels in patients with diabetes and in healthy individuals and determine ...

ea0037ep751 | Pituitary: clinical | ECE2015

Endonasal endoscopic pituitary adenoma resection

Masopust Vaclav , Netuka David , Benes Vladimir , Bradac Ondrej , Marek Josef , Hana Vaclav , Krsek Michal

Introduction: In the past 10 years, endoscopic resection of pituitary adenomas has become an alternative to microsurgical resection with the additional advantage of increasing the patient’s postoperative comfort. This analysis explored whether endoscopic resection can reduce the risk of postoperative neurohypophyseal dysfunction.Material and methods: We rated and compared the need to administer desmopressin during the first four postoperative days a...

ea0022oc1.3 | Diabetes and obesity | ECE2010

NME7: a new candidate gene for T2DM

Vcelak Josef , Seda Ondrej , Vankova Marketa , Lukasova Petra , Vrbikova Jana , Tremblay Johanne , Bendlova Bela , Hamet Pavel

The identification of genomic determinants responsible for common multifactorial diseases like type 2 diabetes mellitus (T2DM) is facilitated in large families from relatively genetically-isolated populations and can extend results from GWS based on a case–control cohort to detect rare alleles with strong effects. In order to search for sequence variants conferring risk of T2DM we previously conducted a genome-wide linkage study in 108 French–Canadian families from t...

ea0063p896 | Diabetes, Obesity and Metabolism 3 | ECE2019

NME7 gene is associated with the shape of glucose curves during oral glucose tolerance test

Bendlova Běla , Vejražkova Daniela , Šedova Lucie , Šeda Ondrej , Včelak Josef , Vaňkova Marketa

Introduction: The shape of the glucose curve during oral glucose tolerance test (OGTT) reflects the dynamic of the glucose stimulus-response, and it can be considered as predictor of the impaired glucose tolerance and Type 2 Diabetes (T2D). Nucleoside diphosphate kinase 7, non-metastatic cells 7 (NME7) is an acknowledged member of ciliome and is involved in the biogenesis or function of cilia. Due to the fact that obesity and T2D are common in several ciliopathies, we enrolled...

ea0035p931 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Population-based cohort study: PROP1 gene mutations are the most prevalent cause of congenital multiple pituitary hormone deficiency in Lithuania

Navardauskaite Ruta , Dusatkova Petra , Obermannova Barbora , Pfaeffle Roland W , Blum Werner F , Adukauskiene Dalia , Smetanina Natalija , Cinek Ondrej , Verkauskiene Rasa , Lebl Jan

Introduction: Congenital multiple pituitary hormone deficiency (MPHD) may result from defects of transcription factors that govern the early pituitary development. The most prevalent are two mutation of PROP1 gene: the c.296delGA and c.150delA.Methods: Seventy-five Lithuanian MPHD patients were tested for PROP1 defects. Perinatal and postnatal data were obtained from medical records. Hormonal investigations, pituitary imaging and GH the...