Searchable abstracts of presentations at key conferences in endocrinology

ea0056p183 | Bone ' Osteoporosis | ECE2018

Trabecular bone score in patients with active acromegaly

Tsoriev Timur , Belaya Zhanna , Sasonova Natalia , Chernova Tatiana , Melnichenko Galina , Dedov Ivan

Introduction: In previous studies, it was noted that increased serum growth hormone (GH) and insulin-like growth factor-1 (IGF-1) lead to the increased vertebral fractures risk in patients with acromegaly. This may be explained by the altered quality of bone rather than bone mineral density (BMD) loss. Trabecular bone score (TBS) is an easily available tool to obtain some surrogate information on bone microarchitecture from a routine DXA.Objective: To ev...

ea0056p767 | Neuroendocrinology | ECE2018

Female patients with acromegaly in Russian hypothalamic and pituitary tumors registry (OGGO)

Lutsenko Alexander , Vorotnikova Svetlana , Stanoevich Irina , Przhiyalkovskaya Elena , Pigarova Ekaterina , Rozhinskaya Liudmila , Belaya Zhanna

Aim: To assess the data of the registry concerning women with acromegaly.Materials and methods: Russian hypothalamic and pituitary tumors registry database, containing the information on 3968 acromegalic patients.Results: From all patients with acromegaly registered in the database, 2878 patients (72.5%) are women. We assessed the following data on gonadal status and reproductive function in this group: 512 patients have irregular ...

ea0056p833 | Pituitary - Clinical | ECE2018

Registry for central diabetes insipidus in Russia: prevalence and etiologies of the disease

Pigarova Ekaterina , Dzeranova Larisa , Belaya Zhanna , Rozhinskaya Liudmila , Lutsenko Alexander , Melnichenko Galina , Dedov Ivan , Consortium CDI The

Introduction: Epidemiological data for central diabetes insipidus (CDI) are quite sparse.Objectives: To provide an epidemiological data on CDI in different regions of Russia (20 from 83 Federal regions).Materials and methods: We used the Russian Registry for Central Diabetes Insipidus (RCDI) to study the epidemiological features of CDI.Results: A total of 2004 patients with CDI were recorded, 47% women and 59...

ea0073aep416 | General Endocrinology | ECE2021

A single-center observational study of patients with ectopic ACTH syndrome

Golounina Olga , Rozhinskaya Liudmila , Arapova Svetlana , Pikunov Michael , Khandaeva Patimat , Dzeranova Larisa , Marova Evgenia , Belaya Zhanna

BackgroundEctopic ACTH syndrome (EAS) is a rare cause of endogenous hypercortisolism.ObjectiveTo analyze clinical, biochemical features and treatment outcomes of patients with EAS.Materials and methodsRetrospective, observational study on 129 patients (79 women, 50 men) with EAS diagnosed between 1990 and 2020. Plasma levels of ACTH (reference range: morning 7.2&#...

ea0073aep501 | Pituitary and Neuroendocrinology | ECE2021

Clinical features, diagnostic criteria and treatment outcomes in 40 patients with thyrotropin-secreting pituitary tumors

Dimitrova Diana , Przhiyalkovskaya Elena , Grigoriev Andrey , Azizyan Vilen , Lapshina Anastasia , Belaya Zhanna , Melnichenko Galina

IntroductionThyrotropin-secreting pituitary adenomas (TSH-omas) are rare. For this reason each case of TSH-secreting pituitary tumor can help expand extensive clinical experience in world practice.Materials and methodsWe included 40 patients with TSH secreting pituitary adenomas. Hormonal profile: TSH (0.25-3.5 mIU/L), FT4 (9-20 pmol/l) FT3 (2.5-5.5 pmol/l) were measured by Architect i2000SR (Abbott Laborator...

ea0073aep566 | Pituitary and Neuroendocrinology | ECE2021

Functioning gonadotroph adenoma accompanied by erythrocytosis in an elderly man

Mamedova Elizaveta , Buryakina Svetlana , Selivanova Liliya , Azizyan Vilen , Grigoriev Andrey , Belaya Zhanna

IntroductionClinically functioning gonadotroph adenomas (FGA) are rare, especially in men. We present a case of a LH/FSH-secreting functioning gonadotroph macroadenoma in an elderly patient, which manifested with visual impairment and was accompanied by secondary erythrocytosis.Clinical caseA 62-y.o. male was admitted to our hospital with a 9-month history of visual impairment and a 5-year history of plethora...

ea0099p519 | Pituitary and Neuroendocrinology | ECE2024

Machine learning in differential diagnosis of ACTH-dependent hypercortisolism

Belaya Zhanna , Golounina Olga , Voronov Kirill , Solodovnikov Alexander , Rozhinskaya Liudmila , Melnichenko Galina , Mokrysheva Natalia , Dedov Ivan

Objective: To develop a non-invasive method of differential diagnosis for ACTH-dependent hypercortisolism using machine learning methods based on clinical data analysis.Materials and methods: This is a single-center study of a retrospective cohort to predict the probability of EAS among patients with ACTH-dependent hypercortisolism using artificial machine learning algorithms. Patients were randomly stratified into 2 samples: training (80%) and test (20%...

ea0099ep735 | Adrenal and Cardiovascular Endocrinology | ECE2024

Heart failure and its reversibility in patients with cushing’s syndrome

Kosharnaia Raisa , Belaya Zhanna , Mamedova Elizaveta , Przhiyalkovskaya Elena , Zuraeva Zamira , Michurova Marina , Kalashnikov Victor

Myopathy is a common complication of Cushing’s syndrome (CS), which predicts the possibility of heart muscle damage and may be a cause of heart failure. Goal of this study is to evaluate the prevalence of heart failure in patients with active CS and the probability of recovery after achieving a remission.Materials and methods: We enrolled patients with CS hospitalized in our clinic from October 2018 to December 2022. To confirm the diagnosis of CS w...

ea0081ep699 | Pituitary and Neuroendocrinology | ECE2022

Pituitary adenomas characteristics in patients with multiple endocrine neoplasia type 1, its phenocopies and sporadic acromegaly

Trukhina Diana , Mamedova Elizaveta , Lapshina Anastasia , Nikitin Alexey , Koshkin Philipp , Azizyan Vilen , Grigoriev Andrey , Belaya Zhanna , Melnichenko Galina

Multiple endocrine neoplasia type 1(MEN1) is a hereditary condition caused by mutations in the MEN1 gene, which encodes menin protein. The syndrome predisposes to the development of tumors in both endocrine and non-endocrine systems. In patients with MEN1, pituitary adenomas (PA) occur in approximately 40% of all cases. If patient has MEN1 phenotype with no mutations in MEN1 gene, the condition is regarded as a phenocopy. The reason of several endocrine MEN1-...

ea0090ep679 | Pituitary and Neuroendocrinology | ECE2023

Epidemiologic and clinical characteristics of acromegaly in Russian hypothalamic and pituitary tumor registry (OGGO)

Lutsenko Alexander , Vikulova Olga , Belaya Zhanna , Przhiyalkovskaya Elena , Pigarova Ekaterina , Dzeranova Larisa , Rozhinskaya Liudmila , Melnichenko Galina , Mokrysheva Natalia

Background: Pituitary disease registries are major instruments of epidemiological and clinical data collection used worldwide.Objective: To assess the epidemiological and clinical characteristics of acromegaly in Russia according to Russian hypothalamic and pituitary tumor registryMaterial and methods: Database of the Russian hypothalamic and pituitary tumor registry, which includes data from 84 regions of the country, was used for...