Searchable abstracts of presentations at key conferences in endocrinology

ea0090p714 | Reproductive and Developmental Endocrinology | ECE2023

Newly diagnosed diabetes in Turner syndrome: what is the role of incretins?

Cecchetti Carolina , Dionese Paola , Belardinelli Elisabetta , Rotolo Laura , Solmi: Beatrice , Fanelli Flaminia , Pagotto Uberto , Gambineri Alessandra

Introduction: Diabetes mellitus (DM) develops early in Turner syndrome (TS) and appears not related to common risk factors. The precise mechanism of its development is still a matter of debate: a defective insulin response seems to be involved, but the role of incretins is still undefined.Objective: To evaluate the implication of incretin release in the early stages of DM development in TS. Materials and Methods: 153 Turner patient...

ea0099ep253 | Reproductive and Developmental Endocrinology | ECE2024

Characterization of liver abnormalities in a population of adult turner women: results from an observational study

Cecchetti Carolina , Rotolo Laura , Dionese Paola , Belardinelli Elisabetta , Solmi Beatrice , Vestito Amanda , Dajti Elton , Colecchia Antonio , Pagotto Uberto , Gambineri Alessandra

Introduction: Liver function test abnormalities (LFA) are common in patients with Turner syndrome (TS). The etiopathogenesis of this complication remains unclear, probably being multifaceted. Metabolic syndrome, generalized vasculopathy, and autoimmunity have been proposed as possible causal mechanisms.Objectives: - To describe the prevalence and possible related factors of morpho-functional liver abnormalities in TS adult patients. - To evaluate the uti...

ea0090rc4.5 | Rapid Communications 4: Reproductive and Developmental Endocrinology | ECE2023

Women carrying CYP21A2 mutations display clinical findings and metabolic/hormonal profile analogous to women with non classical congenital adrenal hyperplasia and polycystic ovary syndrome

Livadas Sarantis , Goulis Dimitrios , eBelardinelli Elisabetta , Armeni Elena , Solmi Beatrice , Veneti Stavroula , Lambrinoudaki Irene , Cecchetti Carolina , Macut Djuro P. , Gambineri Alessandra

Heterozygotes carrying CYP21A2 gene mutations are found in 5-10% of the general population in Mediterranean countries. Accumulating data suggest a survival advantage of this population, despite the fact that carriers of two mutations suffer from either classical or non-classical congenital adrenal hyperplasia (NC-CAH), an entity with increased mortality. In an attempt to elaborate on this issue we evaluated females of reproductive age with CYP21A2 heterozygocity (HET). We have...

ea0099rc1.7 | Rapid Communications 1: Reproductive and Developmental Endocrinology | ECE2024

Characterisation of the daily rhythm of salivary androgens in healthy women and in women with polycystic ovary syndrome by liquid chromatography-tandem mass spectrometry

Rotolo Laura , Gambineri Alessandra , Bissi Valentina , Zauli Francesca , Galante Greta , Cecchetti Carolina , Dionese Paola , Belardinelli Elisabetta , Solmi Beatrice , Pagotto Uberto , Fanelli Flaminia

Background: PCOS is characterised by increased production of ovarian and adrenal androgens. Obesity is closely connected to excess androgens and to the disruption of hormone circadian rhythmicity. To date, it is not clear whether hyperandrogenism in PCOS, complicated or not by obesity, is associated with androgen rhythm dysregulation.Aim: To investigate androgen diurnal rhythmicity and overall daily androgen exposure by measuring testosterone(T), androst...