Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep279 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Prediction of post-COVID syndrome development in type 2 diabetes: retrospective analysis based on national survey in Ukraine

Matviichuk Anton , Gurianov Vitalii , Yerokhovych Viktoriia , Livkutnyk Oleksandr , Falalyeyeva Tetyana , Komisarenko Iuliia , Sulaieva Oksana , Kobyliak Nazarii

Background: Post-COVID-19 condition (long COVID-19, post-acute COVID-19, long-term effects of COVID-19) is an emerging health problem in people recovering from COVID-19 infection within the past 4-6 months. Patients with type 2 diabetes (T2D) are in the risk group for a more severe course of COVID-19 and the development of its complications. Aim: to define the prevalence and prediction of post-COVID-syndrome development in patients with T2D according to ...

ea0081ep369 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Development of THE allele-specific PCR method for studying insulin gene rs689 polymorphism

Saatov Talat , Ibragimov Zafar , Alimov Timur , Ibragimova Elvira , Ishankhodjaev Tokhir , Shamansurova Zulaykho , Karimov Kha , Azimova Shakhnoza , Boboev Kodirjon , Makhnyov Anton

Background: Insulin gene (INS) is known to be responsible for production of insulin by the pancreatic β-cells. It includes variable number of tandem repeats (VNTR) of oligonucleotide consequence (ACAGGGGT (G/C) (T/C) GGGG) in the promoter region (Bell et al, 1981,1982); being the gene involved in the susceptibility to various pathologies. The allele-specific PCR allows direct diagnosis of some genetically determined disorders is rather simple and precise. However, by toda...

ea0086op6.2 | Endocrine Cancer and Late Effects | SFEBES2022

Investigating the utility of microRNA signatures as a tumour biomarker in patients with succinate dehydrogenase deficient phaeochromocytoma, paraganglioma and GIST

Enright Anton , Rodgers Faye , Karcanias Alexandra , Giger Olivier , ten Hoopen Rogier , Challis Ben , Bulusu Venkata , Maher Eamonn , Casey Ruth

Background: International consensus supports interval biochemical and imaging surveillance for all asymptomatic carriers of succinate dehydrogenase (SDHx) gene mutations and patients with a history of SDH deficient tumours. There is growing awareness that the life time penetrance of the SDHx genes is much lower than that originally estimated and that long term radiological surveillance carries a significant risk including ionizing radiation exposure and incidental findings. Th...

ea0063p356 | Thyroid 1 | ECE2019

Relationship among T- and B-lymphocytes of the peripheral blood and thyroid tissue in patients with Graves’ disease

Dudina Margarita A , Savchenko Andrey A , Dogadin Sergey A , Borisov Alexandr G , Kudryavcev Igor V , Moshev Anton V , Man'kovsky Vladimir A

The exact pathogenesis and causative interaction between T- and B-lymphocytes in peripheral blood and thyroid gland immune-mediated mechanisms of Graves disease (GD) are still unknown. Detailed knowledge about lymphocyte subpopulation composition in peripheral blood and thyroid tissue will therefore enhance our understanding of the pathogenesis of GD and might support the development of new immunomodulatory treatment approaches. Aim: to study the relationship between helper- (...

ea0049ep1010 | Pituitary - Clinical | ECE2017

Hypertension, acromegaly and pegvisomant treatment: Experience from ACROSTUDY

Vila Greisa , Jan vanderLely Arrt , Neggers Sebastian , Luger Anton , Webb Susan , Biller Beverly , Jonsson Peter , Hey-Hadavi Judith

Introduction: Hypertension (HTN) is a major cardiovascular (CV) risk factor and independent predictor of the increased mortality in patients with acromegaly. Surgical cure of acromegaly is associated with improvement in blood pressure (BP) levels, however little is known on the effect of pegvisomant (PEGV) treatment on HTN.Methods/design: ACROSTUDY is an open-label, international, prospective, non-interventional study monitoring the long-term safety of P...

ea0049ep1176 | Male Reproduction | ECE2017

Methylation of the CPG islands from MTHFR promoter in male infertility

Vladoiu Suzana , Botezatu Anca , Dinu Draganescu Daniela , Manda Dana , Oros Sabina , Paun Diana , Rosca Roxana , Badiu Corin , Anton Gabriela

: A large number of studies are now focused on the causes of male infertility. Among these are epigenetic modifications, which are important contributors to reproductive pathology in the male by providing dynamic changes of the phenotype according to the environmental and metabolic factors. The most known epigenetic modification is DNA methylation and alterations in this pattern in several genes could induce male infertility. Alterations in DNA methylation patterns in several ...

ea0049ep1180 | Male Reproduction | ECE2017

Study of CDX-2 VDR gene polymorphisms in male infertility

Vladoiu Suzana , Draganescu Daniela Dinu , Botezatu Anca , Manda Dana , Oros Sabina , Rosca Roxana , Anton Gabriela , Paun Diana , Badiu Corin

The CDX2 VDR polymorphism (rs11568820) is located in the promoter region of exon 1 in the 5′-untranslated region of the VDR gene.Objective: The current investigation examines the association between CDX2 VDR polymorphism and male infertility.Subjects and methods: The study was conducted on 69 infertile men, aged between 20 and 50 years, divided into three groups, based on spermatic parameters: group with azoospermia (19 subje...

ea0041gp51 | Cardiovascular endocrinology | ECE2016

Pericardial rather than intramyocardial fat is independently associated with systolic and diastolic left ventricular heart function in metabolically healthy humans

Wolf Peter , Winhofer Yvonne , Smajis Sabina , Jankovic Drazenka , Anderwald Christian-Heinz , Trattnig Siegfried , Luger Anton , Krebs Michael , Krssak Martin

Background: Obesity is a major risk factor to develop heart failure, in part due to possible lipotoxic effects of increased intramyocardial (MYCL) and/or pericardial (PERI) lipid accumulation. Recent evidence suggests that MYCL is highly dynamic and might rather be a surrogate marker for disturbed energy metabolism than the underlying cause of cardiac dysfunction. On the other hand, PERI might contribute directly by mechanic and paracrine effects. Therefore, we hypothesized th...

ea0041ep323 | Clinical case reports - Pituitary/Adrenal | ECE2016

Pituitary and legg calvé perthes syndrome – is there a connexion?

Puiu Mirela , Belceanu Alina , Crumpei Iulia , Bursuc Anamaria , Armasu Ioana , Zmau George-Sebastian , Anton Mihaela , Gavrilescu Simona , Vulpoi Carmen

Introduction: Legg calvé perthes (LCP) is a disease characterized by idiopathic avascular necrosis of the proximal femoral epiphysis caused by decreased blood flow. More frequently in boys between 2 and 12 years of age. LCPD is of unknown etiology.We present two male patients of LCP associated with pituitary disorders.Case presentation: Case 1: g.i.c., 8 years 8 month, was first addressed to the endocrinology department for in...

ea0041ep703 | Growth hormone IGF axis - basic | ECE2016

High normal TSH – risk factor for subclinical hypothyroidism in GH treatement for pituitary dwarfism?

Belceanu Alina Daniela , Bursuc Anamaria , Armasu Ioana , Constantinescu Georgiana Andreea , Crumpei Iulia , Leustean Letitia , Anton Mihaela , Vulpoi Carmen

Background: Normal thyroid function is necessary for the optimal effect of recombinant growth hormone (rhGH) on growth rate. GH therapy in children with GH deficiency (GHD) has yielded conflicting results concerning its impact on thyroid function. Data about patients developing subclinical hypothyroidism (SH) are scanty, but it is thought to be associated with impairment of metabolic profile and lower growth response.Objective: To evaluate the effect of ...