Searchable abstracts of presentations at key conferences in endocrinology

ea0056p379 | Diabetes (to include epidemiology, pathophysiology) | ECE2018

Maternally inherited diabetes and deafness (MIDD): the many faces of the same disease in a Spanish family

Silva Carlos , Garcia Elena , Villa Gema , Martin Alba , Males David , Martinez Guillermo , Leon Miguel

Introduction: Maternally inherited diabetes and deafness (MIDD), is a rare entity. Most commonly, it is related to a point mutation in the mitochondrial DNA (mtDNA) at position 3243 (m.3243A>G) encoding the gene for tRNA. A high index of suspicion is required for the diagnosis due to a wide heterogeneity in its clinical presentation which reflects different levels of mutated mtDNA among mitochondria in a given tissue (heteroplasmy). Thyroid cancer risk has never been speci...

ea0099p242 | Adrenal and Cardiovascular Endocrinology | ECE2024

Congenital adrenal hyperplasia and myelolipomas: A case report

Ocando Ana Paola Leon , Rodriguez OliverQuintero , Fernandez Selena Rodriguez , Gorrin KevinDiaz , Ondono ItziarAznar , Fernandez JudithLopez

Introduction: Adrenal myelolipomas are benign and fatty tumors usually detected incidentally in imaging tests. Their prevalence increases in patients with CAH, probably because corticosteroid deficiency causes high ACTH levels that stimulate adrenal growth, although their effect on the growth of adrenal tumors is not yet well established.Clinical case: A 41-year-old man with classic 21 OH deficiency, losing salt since he was 10 months old,with stable dos...

ea0099p284 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Analysis of the use of integrated continuous subcutaneous insulin infusion systems in pregnant women with type 1 diabetes

Hami Gil Sara , Gallego Diaz Celia , Puzigaca Pavle , Romero Munoz Manuel , Victoria Cozar Leon Maria

Introduction and objective: Treatment with integrated continuous subcutaneous insulin infusion (CSII) and continuous glucose monitoring systems (CGM) helps to improve glycaemic control in people with type 1 diabetes mellitus (DM1). There is increasing use in pregnant women, but there are no protocols for its continuation during delivery. The aim of this work is to analyse glycaemic control during pregnancy, in addition to studying obstetric and neonatal outcomes.<p class="...

ea0099ep813 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Clinical characteristics and complications of gestational diabetes mellitus: a single center spanish experience

Paola Leon Ocando Ana , Quintero Rodriguez Oliver , Rodriguez Fernandez Selena , Diaz Gorrin Kevin , Aznar Ondono Itziar

Introduction: Pregnancy involves distinct metabolic stages, initially characterized by maternal anabolism, followed by a catabolic phase driven by placental lactogen and various cytokines, leading to varying degrees of insulin resistance. DM is the most common metabolic disorder linked to pregnancy.Objective: The study aimed to detail the clinical characteristics, obstetric complications, and neonatal outcomes of patients with GDM and their children....

ea0099ep1069 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Bone mineral density in women with type 2 diabetes mellitus and postmenopause: a single center spanish experience

Paola Leon Ocando Ana , Quintero Rodriguez Oliver , Rodriguez Fernandez Selena , Diaz Gorrin Kevin , Aznar Ondono Itziar

Introduction: T2DM is associated with an increased risk of fractures. This heightened risk is attributed to factors such as prolonged disease duration and chronic glycemic control. Interestingly, despite this increased fracture risk, patients with T2DM often exhibit normal or even elevated BMD compared to non-diabetic individuals. This phenomenon is thought to be a result of reduced bone remodeling, coupled with changes in bone microarchitecture.Objectiv...

ea0099ep565 | Pituitary and Neuroendocrinology | ECE2024

Hyperprolactinaemia as a reason for referral to specialist consultation

Alvaro Romero Porcel Jose , Gallego Diaz Celia , Hami Gil Sara , Puzigaca Pavle , Victoria Cozar Leon Maria

Objective: Analysis of referrals from Primary Care to the Endocrinology Department for analytical findings of elevated prolactin levels and their subsequent management after initial assessment.Material and methods: Retrospective descriptive study of 118 patients who were referred to the Endocrinology and Nutrition department of the Dos Hermanas Peripheral Specialities Centre between October 2020 and December 2022. Patients already diagnosed with hyperpro...

ea0081p704 | Reproductive and Developmental Endocrinology | ECE2022

Intracranial idiopathic hypertension in a maletranssexual patient after testosterone overdosing

Javier Martinez Martin Francisco , Hernandez-Lazaro Alba , de Leon-Durango Ricardo , Kuzior Agnieszka , Gonzalez-Diaz Paula , Perdomo-Herrera Esperanza , Lucia Tocino-Hernandez Alba , Arnas-Leon Claudia , Acosta-Calero Carmen , del Pino Perez-Garcia Maria

Introduction: Intracranial Idiopathic Hypertension (IIH) is a rare complication of testosterone therapy. It is usually benign, but may result and permanent blindness. Its diagnosis is based on a high CSF (> 25 cm H2O) pressure, in the absence of specific causes. The androgen receptor is expressed in the human choroid plexus, and may enhance the activity of Na+/K+-ATPase, and therefore CSF secretion.Methods: Review of the patientÂ’s cli...

ea0081p705 | Reproductive and Developmental Endocrinology | ECE2022

Lessons from a patient with the 48XXXY karyotype: Not just another case of Klinefelter’s syndrome

Kuzior Agnieszka , Hernandez-Lazaro Alba , de Leon-Durango Ricardo , Rios-Gomez Carlos , Arnas-Leon Claudia , Acosta-Calero Carmen , Maria Fernandez-Trujillo-Comenge Paula , Delia Santana-Suarez Ana , Gonzalez-Diaz Paula , Javier Martinez Martin Francisco

Introduction: The 48XXXY karyotype is an infrequent (incidence about 1/50000 male births) sporadic aneuploidy of the sex chromosomes, classically considered as a variant of the Klinefelter syndrome (47XXY). Although many of their characteristics are shared, patients with the 48XXXY karyotype suffer from additional endocrinological and neuropsychological disturbances which are not part of the classic Klinefelter syndrome. Hereby we present a clinical case.<p class="abstext"...

ea0081p506 | Late-Breaking | ECE2022

Initial results and patient satisfaction with the new oral formulation of semaglutide

Martinez Martin Francisco Javier , Kuzior Agnieszka , Arnas-Leon Claudia , Fernandez-Trujillo-Comenge Paula , Quintana-Arroyo Sara , Acosta-Calero Carmen , Delia Santana-Suarez Ana , Gonzalez-Diaz Paula , Hernandez-Lazaro Alba , de Leon-Durango Ricardo

Introduction: Oral semaglutide has been available in the Spanish market since November 2021. This new formulation has broken the self-injection barrier, and may enhance patient satisfaction.Methods: Retrospective review of the patients′ records and presential or telephonic interviews. All patients expressed their consent for the anonymous processing of their data. Numeric data are given as mean + s.d; paired t-test was used for comparison. Satisfac...

ea0081ep194 | Calcium and Bone | ECE2022

Vitamin D deficiency in the type 2 diabetic population of Northern Gran Canaria Island: Still highly prevalent but supplementation is on the rise

Hernandez-Lazaro Alba , de Leon-Durango Ricardo , Kuzior Agnieszka , Acosta-Calero Carmen , Arnas-Leon Claudia , del Sol Sanchez-Bacaicoa Maria , Garcia-Alamo Debora , Martin-Perez Marta , Gonzalez-Diaz Paula , Martin Francisco Javier Martinez

Introduction: Vitamin D deficiency is associated with higher risk of severe COVID-19, and type 2 diabetic patients are a vulnerable group. We described an alarming rate of vitamin D deficiency (around 80.0% with plasma calcifediol <30 ng/ml) in unsupplemented type 2 diabetes patients during the 2020 spring lockdown and the following winter in Northern Gran Canaria. There is an increasing awareness of this problem, both in family physicians and the general population, and t...