Searchable abstracts of presentations at key conferences in endocrinology

ea0029p293 | Cardiovascular Endocrinology and Lipid Metabolism | ICEECE2012

Chemerin/CMKLR1 and adiponectin/T-cadherin expression in human aortic wall and periaortic adipose tissue in correlation with atherosclerosis

Kostopoulos C. , Karamouzis I. , Spiroglou S. , Papadaki H.

Introduction: Periadventitial adipose tissue has been implicated in vascular physiology and pathology, including atherosclerosis, through paracrine and endocrine mechanisms, mainly adipokine production. We investigated the expression of adipokines chemerin and adiponectin and their receptors CMKLR1 and T-cadherin, respectively, in human aortic arterial wall and periaortic fat as well as their correlation with aortic atherosclerosis.Methods: Paraffin embe...

ea0007p192 | Reproduction | BES2004

Intramuscular testosterone (T) undecanoate for the treatment of male hypogonadism: a parallel-group randomised open-label pharmacokinetic study

Hay C , Wu F

Objective: To identify the optimal regime for physiological replacement in hypogonadism. We assessed the pharmacokinetics of 3 different dose-intervals for i.m. administration of the new parenteral formulation of testosterone undecanoate in castor oil (Schering AG Berlin).Methods: Ten hypogonadal subjects (primary n equals 4 or secondary n equals 6) with a baseline T at diagnosis of less than 7 nanomols per litre were recruited and randomly allocated int...

ea0092ps1-10-08 | Basic Thyroid Gland, Iodine & Autoimmunity Basic | ETA2023

Thyroid-Resident memory T-cells specific for SARS-COV-2 are enriched in patients with thyroid disorders related to covid-19

Carelli Elena , Silvestri Ylenia , Clemente Francesca , Moschetti Giorgia , Maioli Sara , Espadas de Aris Alejandro , Torelli Rosanna , Longhi Elena , De Feo Tullia , Salvi Mario , Mantovani Giovanna , Arosio Maura , Bombaci Mauro , Pesce Elisa , Grifantini Renata , Abrignani Sergio , Geginat Jens , Muller Ilaria

Objectives: SARS CoV-2 infections have been associated with the onset of classic subacute thyroiditis (SAT) or atypical SAT, observed in 10-15% of patients hospitalized for severe COVID19 disease (COV-A-SAT) and characterized by absence of neck pain, mild thyrotoxicosis associated with non-thyroidal illness syndrome and thyroiditis-like areas which may persist in the thyroid gland up to 12 months following SARS-CoV-2 infection, despite normalization of thyroid function. Little...

ea0022p347 | Diabetes | ECE2010

Quantitative and qualitative changes in T regulatory lymphocytes (Tregs) in newly-diagnosed patients with type 1 diabetes

Paschou Stavroula , Vartholomatos George , Kolaitis Nikolaos , Papadopoulos George , Tsatsoulis Agathocles

Introduction: T regulatory lymphocytes (Tregs) are defined as CD4+CD25high T lymphocytes and are thought to regulate immune tolerance. The Foxp3 protein level in Tregs is proportional to CD25 protein surface expression and regulatory function, but inversely proportional to IL-7R (CD127) level, the receptor for the growth and survival of T cells. We investigated possible differences in Tregs between newly diagnosed type 1 diabetes (DM1) patients and contro...

ea0073aep399 | Endocrine-Related Cancer | ECE2021

Heterogeneity of the clinical presentation of the MEN1 LRG_509t1 c.781C > T (p.Leu261Phe) variant within a three-generation family

Gilis-Januszewska Aleksandra , Anna Boguslawska , Godlewska Magdalena , Hasse-Lazar Kornelia , Jurecka-Lubieniecka Beata , Jarzab Barbara , Sowa-Staszczak Anna , Skalniak Anna , Hubalewska-Dydejczyk Alicja

BackgroundMultiple neuroendocrine neoplasia type 1 is a rare, heterogeneous genetic disorder with an autosomal dominant inheritance, predisposing to benign and malignant tumors. The phenotype of MEN1 syndrome varies between patients in terms of tumor localisation, age of onset and clinical aggressiveness, even between affected members of the same family. We report a heterogenic phenotype of the MEN1 variant c.[781C > T] (LRG_509t1) previously reporte...

ea0084op-11-53 | Oral Session 11: Young Investigators / Basic | ETA2022

CD3+CD8+CD20+ T cells as a marker of the inflammatory phase in thyroid autoimmune and related polyautoimmune disorders: a pilot study

Stramazzo Ilaria , Virili Camilla , Capriello Silvia , Brusca Nunzia , Flavia Bagaglini Maria , Romeo Giovanna , Mangino Giorgio , Centanni Marco

Objectives: Human CD3+CD20+ T cells represents 3-5% of circulating T cells and may be detected in all lymphatic organs and in the cerebrospinal fluid. In healthy individuals CD3+CD20+ T cells have been shown to produce higher levels of IL-17A and/or IFN-γ than those of CD3+CD20- T cells. Some reports described the role of CD3+CD20+ T cells in autoimmune disorders such as multiple scler...

ea0081ep784 | Pituitary and Neuroendocrinology | ECE2022

A novel population of activated cytotoxic T cells infiltrate pituitary neuroendocrine tumour subytpes

Mazzitelli Oriana , Ebejer Jean Paul , Pace Nikolai Paul , Gruppetta Mark , Vassallo Josanne , Saliba David

Non-functional pituitary adenomas (NFPA) are non-hormone secreting pituitary tumours while growth hormone-secreting pituitary adenomas (GHPA) are active pituitary tumours causing acromegaly. Since immunotherapy is becoming the preferred therapeutic strategy in cancers, understanding the diversity of immune cells infiltrating the tumour microenvironment is warranted. However, little is known about the immune landscape of pituitary tumours. We validated an acoustic-assisted hydr...

ea0037ep1031 | Thyroid (non-cancer) | ECE2015

Role of regulatory T cell and CTLA-4 gene as risk factor relapse in Graves' disease

Eliana Fatimah , Suwondo Pradana

Introduction: Graves’ disease (GD) management in Indonesia are generally preceded by administration of antithyroid drugs. Antithyroid drug delivery requires a long time to achieve remission, even more than 50% of patients who had remission can recur after antithyroid medication is stopped. The purpose of this study was to determine the role of CTLA-4 gene and regulatory T cells against recurrence in patients GD in Indonesia.Methods: The study was co...

ea0070aep227 | Bone and Calcium | ECE2020

Osteogenesis imperfecta type V due to a rare mutation c.119C> T in the IFITM5: A case report

Grebennikova Tatiana , Gavrilova Alina , Tiulpakov Anatoly , Tarbaeva Natalia , Melnichenko Galina , Belaya Zhanna

Osteogenesis imperfecta (OI) is a heritable skeletal disorder caused by defective bone formation. OI type V (MIM#:614757) develops due to mutation in the IFITM. Mutation c.-14C >T in the IFITM5 is more common whereas only five reported patientshave a c.119C >T mutation. Patients with IFITM5:c.119C >T mutation usually have low-traumatic fractures in the prenatal period of development, severe limb and chest deformities, short height, verteb...

ea0056p164 | Bone ' Osteoporosis | ECE2018

Influence of the levels of vitamin D on T-score in HIP measured by DXA of colombian postmenopausal women

Buendia Richard , Cardenas Santiago , Zambrano Monica , Buendia Andres , Varon Maria De Los Angeles , Mier Heidy Carolina , Morales Alejandra , Alejo Adriana , Sanchez Diego

Introduction: The 25hydroxyvitamin(OH)D deficiency has been linked to the risk of postmenopausal fractures and osteoporosis. In Colombia,the prevalence of 25(OH)vitaminD deficiency is high, reaching more than 53% of the total population. It can be stated that hip fracture is one of its most feared complications, with a high risk of mortality and morbidity,which can affect even osteopenic patients. The objective of this study is to assess modifications in hip T-score (using dua...