Searchable abstracts of presentations at key conferences in endocrinology

ea0014p51 | (1) | ECE2007

Comparison of plasma homocysteine concentrations (HYC) in patients with acute coronary syndrome (ACS) and newly or previously diagnosed type 2 diabetes

Kurowska Maria , Tarach Jerzy S , Gernand Wojciech , Kudlicki Janusz , Tarkowski Adam , Nowakowski Andrzej , Czekajska Teresa , Solski Janusz

Introduction: The patients with ACS and scheduled for an elective coronary angiography have high frequency of both newly and previously diagnosed diabetes. The diabetic patients with acute myocardial infarction have an increased risk of death. Elevated blood HYC is strongly related to an increased risk for atherosclerosis and cardiovascular disease. This association is particularly evident in patients with diabetes.Aim of the study: An attempt to evaluat...

ea0014p633 | (1) | ECE2007

Three months exercise training improves cardiopulmonary functional capacity in polycystic ovary syndrome

Orio Francesco , Giallauria Francesco , Palomba Stefano , Cascella Teresa , Vuolo Laura , Tafuri Domenico , Manguso Francesco , Lombardi Gaetano , Colao Annamaria , Vigorito Carlo

Introduction and Aim: Polycystic Ovary Syndrome (PCOS) is an endocrine disease closely related to several risk factors for cardiovascular disease. Previous study demonstrated an impaired cardiopulmonary functional capacity in PCOS women. The present study was performed to evaluate the effects of 3-months exercise training (ET) programme on cardiopulmonary functional capacity in young women with PCOS.Patients and Methods: The study was conducted according...

ea0056gp163 | Paediatrics, Developmental ' Female Reproduction | ECE2018

Global DNA methylation since early infancy to adulthood in the offspring of women with polycystic ovary syndrome (PCOS)

Sir-Petermann Teresa , Echiburu Barbara , Maliqueo Manuel , Perez-Bravo Francisco , Crisosto Nicolas , Flores Cristian , Sandoval Daniel , Recabarren Sergio E

DNA methylation is an epigenetic mechanism of gene regulation that can be modified during intrauterine and postnatal life. Pregnant women with polycystic ovary syndrome (PCOS) present elevated androgen and insulin levels, which can affect the DNA methylation pattern of their offspring. Then, we studied the global DNA methylation pattern (GDNAm) in daughters and sons born to PCOS women compared to controls. Daughters (99 born to PCOS and 87 born to control women) and sons (74 b...

ea0056p273 | Clinical case reports - Thyroid/Others | ECE2018

Hypercalcemia not mediated by PTH: a case report

Zambrano-Huerta Yolanda , Gregorio Oliva-Garcia Jose , Teresa Herrera-Arranz Maria , Olvera-Marquez Pilar , Marquez-Mesa Elena , Lorenzo-Gonzalez Cristina

Introduction: Hypercalcemia is a frequent hydroelectrolytic disorder, and primary hyperparathyroidism is the most common cause in oupatients. It is important to make an early diagnosis and adequate treatment in order to avoid possible complications such as nephrolithiasis, osteoporosis or the deterioration of glomerular filtration rate.Clinical case: A 63-year-old female patient referred for hypercalcemia. Past medical history included stage IV chronic r...

ea0056p288 | Bone & Osteoporosis | ECE2018

Fragility index in type 2 diabetes for identification of patients with risk of osteoporotic fracture or prevalent fracture

Garcia-Martin Antonia , Dolores Aviles-Perez Maria , Garcia-Fontana Beatriz , Marquez-Herandez Maria Teresa , Hayon Maria , Munoz-Torres Manuel

Introduction: Diabetes mellitus is associated with an increased risk of osteoporotic fractures, which leads to an increased risk of disability and frailty.Aims: To assess the prevalence of frailty in type 2 diabetes and to analyze the relationship with bone mineral density (BMD) and Trabecular Bone Score (TBS), fracture risk and prevalent fractures.Methods: We carried out a cross-sectional study of 75 diabetic patients (65±7 y...

ea0056p698 | Clinical case reports - Pituitary/Adrenal | ECE2018

Diabetes insipidus as first clinical manifestation of pineal tumor

Gonzalez Cristina Lorenzo , Mesa Elena Marquez , Huerta Yolanda Zambrano , Marquez Maria Pilar Olvera , Arranz Maria Teresa Herrera , Abizanda Enrique Palacio

Introduction: Central diabetes insipidus is a disorder characterized by polyuria and polydipsia due to vasopressin deficiency caused by a lesion at the hypothalamo-hypophyseal axis. Frequently, central diabetes insipidus is wrongly considered idiopathic if not associated with other neurological signs and symptoms. Herein we present the report of a case that illustrates the difficulties in the diagnosis of this condition.Case report: A 17 year-old male wa...

ea0056p719 | Clinical case reports - Pituitary/Adrenal | ECE2018

From adrenal incidentalomas to Cushing’s disease

Alves Pereira Teresa , Ferreira Lia , Furtado Ines , Lopes Ana , Fonseca Liliana , Amaral Claudia , Palma Isabel , Cardoso Helena

Introduction: Adrenal incidentalomas are asymptomatic adrenal masses found accidentally during routine examination, not intended for adrenal pathology evaluation. The functionality of these lesions must be further investigated. Rarely, bilateral adrenal nodular hyperplasia can be detected in a patient with Cushing’s disease. The authors present the case of a patient with possible autonomous cortisol secretion of adrenal origin that eventually emerged as Cushing’s dis...

ea0056p945 | Female Reproduction | ECE2018

Current situation of adult patients with Turner syndrome in Tenerife (Spain)Current situation of adult patients with Turner syndrome in Tenerife (Spain)

Mesa Elena Marquez , Garcia Jose Gregorio Oliva , Rodriguez Jose Manuel Rial , Marquez Pilar Olvera , Arranz Maria Teresa Herrera

Introduction/ objectives: Turner syndrome (TS) comprises a group of sex chromosomal abnormalities of heterogeneous clinical presentation. During the infant period, the pediatric endocrinologist coordinates their follow-up and it is important to ensure its continuation during the adult stage. The objective of this study is to know the current clinical situation, occupational, educational, social and medical monitoring of patients affected TS in Tenerife.M...

ea0056p1106 | Thyroid (non-cancer) | ECE2018

Analysis of association of vitamin D receptor gene Cdx2 (rs11568820) polymorphism with autoimmune thyroid diseases

Maciejewski Adam , Kowalczyk Michal J , Gasinska Teresa , Herman Waldemar , Szeliga Anna , Dorszewska Jolanta , Zaba Ryszard , Lecka Katarzyna

Introduction: Vitamin D is postulated to play a significant role in the immune system modulation and its deficiency has been reported in some autoimmune disorders. Polymorphisms of different vitamin D-related genes, among them vitamin D receptor gene (VDR), could either be a risk factor for autoimmune diseases. Therefore the aim of the study was to assess the association between VDR Cdx2 (rs11568820) polymorphism and autoimmune thyroid disease (AITD) among th...

ea0073oc10.3 | Oral Communications 10: Thyroid | ECE2021

Predictive factors for recurrent non-diagnostic fine-needle aspiration biopsy in thyroid nodules

Benido Silva Vânia , Maria Teresa Vânia , Carvalho André , Freitas Cláudia

IntroductionThe most cost-effective, minimally invasive and accurate tool to discriminate benign from malignant thyroid nodules is a fine-needle aspiration biopsy (FNAB). However, 2%–24% of FNABs provide non-diagnostic results, which are a clinical challenge, particularly when this result is recurrent.AimTo determine the predictive factors for recurrent non-diagnostic FNAB in thyroid nodules.<p class...