Searchable abstracts of presentations at key conferences in endocrinology

ea0022p825 | Thyroid | ECE2010

Effects of hyperthyroidism, hypothyroidism and thyroid autoimmunity on female sexual function

Franceschi Elisa , Oppo Alessandro , Atzeni Francesca , Taberlet Alessandro , Mariotti Stefano

Introduction: Thyroid hormones affect male and female sexual and reproductive function, but few studies have been performed on sexual dysfunctions in hyper- and hypothyroid women.Aim of the study: To evaluate female sexual function in untreated and treated hyper- and hypothyroidism and in euthyroid Hashimoto’s thyroiditis (HT).Patients and methods: Fifty consecutive women (38.5±8.2 years, range 18–53 years), 22 with ...

ea0021p86 | Clinical practice/governance and case reports | SFEBES2009

Cushing's syndrome: a rare cause of hypertension in pregnancy

Venu Maya , Stanley Katherine , Burgess Neil , Swords Francesca

A 34-year-old primi gravida, 11 weeks into pregnancy, presented with hypertension (blood pressure 170/110 mmHg) proteinuria and hypokalaemia. She gave a 6-week history of tiredness, weight gain, and easy bruising. On examination, there was marked facial puffiness, non pitting oedema, thin skin with multiple bruises, marked proximal myopathy and no pigmented striae. Pregnancy associated Cushing’s was suspected.Investigations: Hypokalaemia (K+</s...

ea0019p312 | Steroids | SFEBES2009

A biphasic rhythm of testosterone secretion: evidence for regulation by glucocorticoids

Waite Eleanor , Kershaw Yvonne , Spiga Francesca , Lightman Stafford

Two-way interactions between the hypothalamo–pituitary–adrenal (HPA) axis and the hypothalamo–pituitary–testicular (HPT) axis are well recognised. For example, in rats disruption of the HPT axis alters the circadian secretion of corticosterone. Conversely, stress conditions have varying effects on the level of testosterone secretion in both rats and humans. In contrast to humans, where several pulses of testosterone secretion can be detected across the 24 h...

ea0016p148 | Clinical cases | ECE2008

A case of hungry bone syndrome during therapy with methimazole for hyperthyroidism

Sanguin Francesca , Camozzi Valentina , Mantero Franco , Luisetto Giovanni

We describe a case of severe hypocalcemia after methimazole treatment for Graves disease, which closely resembles classic hungry bone syndrome.A 41-year-old woman with a history of Graves disease presented to our Internal Medicine ward with tachyarrythmia. Laboratory data showed a severe hyperthyroidism, an ecocardigraphy demonstrated a dilated cardiomyopathy. The patient was given beta-blockers, low molecular weight heparin, and methimazole (30 mg/day)....

ea0016p618 | Reproduction | ECE2008

Catecholestogens inhibit endothelial cell growth in an angiogenesis bioassay

Basini Giuseppina , Bussolati Simona , Santini Sujen Eleonora , Grasselli Francesca

Little is known about the negative regulation of angiogenesis in the ovary. Recent evidence has revealed that estradiol 17β and its metabolites may play an important role in this fine tuning1. In a previous work2, we set up an assay to quantify 2-hydroxyestradiol (2-OHE) and 4-hydroxyestradiol (4-OHE) in follicular fuids. In order to get an insight on the angiogenic effect of 4-OHE and 2-OHE, the objective of this research was to study their possible...

ea0094oc3.3 | Neuroendocrinology and Pituitary | SFEBES2023

A mutagenesis-based approach to stabilise D2 dopamine G protein-coupled receptor homomers

Sharrocks Katie , Fanelli Francesca , Byrne Bernadette , Hanyalolgu Aylin

The D2 dopamine receptor (D2R) is a G protein-coupled receptor (GPCR) known to have key roles in neurotransmission, hypothalamic-pituitary hormone release and glucose homeostasis. Thus, this receptor is a therapeutic target in schizophrenia, neurodegenerative disorders, endocrine tumours and even diabetes. As for many GPCRs, D2R can associate with itself as homodimers or heterodimers with distinct receptors. The balance between monomers, homodimers and heterodimers of D2R has ...

ea0063p60 | Adrenal and Neuroendocrine Tumours 1 | ECE2019

Adrenal morphology in a large cohort of adult subjects with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Oriolo Claudia , Gasparini Daniela Ibarra , Altieri Paola , Ruffilli Francesca , Corzani Francesca , Dalmazi Guido Di , Vicennati Valentina , Pagotto Uberto , Gambineri Alessandra

Introduction: The adrenal morphology in congenital adrenal hyperplasia (CAH) is poorly described in the literature, so that adrenal radiological evaluation is not recommended in patients with CAH. The aim of this study was to evaluate the adrenal morphology in a large cohort of adult patients with CAH due to 21-hydroxylase deficiency and its correlation with the subtype of CAH (non-classical-NCAH, simple virilizing-SV, or salt wasting-SW), the hormonal status and the treatment...

ea0063p597 | Diabetes, Obesity and Metabolism 2 | ECE2019

A new neurocognitive phenotype in Alstrom sindrome

Lorusso Riccardina , Dassie Francesca , Benavides-Varela Silvia , Milan Gabriella , Favaretto Francesca , Vettor Roberto , Semenza Carlo , Maffei Pietro

Background: Alstrom syndrome (AS; OMIM#203800) is a rare (<1:100.000) autosomal recessive monogenic ciliopathy and it is caused by mutations in ALMS1 (chromosome 2p13), which function is still unknown. AS is characterized by multisystemic fibrosis, cone-rod retinal dystrophy leading to blindness, hearing loss, obesity, type 2 diabetes mellitus (T2DM), dilated cardiomyopathy, and progressive hepatic and renal failure. Most patients present neurological issue on developmenta...

ea0020p516 | Paediatric Endocrinology | ECE2009

Short stature in pediatric Cushing's syndrome: effectiveness of hypercortisolism cure

Paragliola Rosa Maria , Lovicu Rosa Maria , Ingraudo Francesca , Ianni Francesca , Locantore Pietro , Rota Carlo Antonio , Pontecorvi Alfredo , Corsello Salvatore Maria

Cushing’s disease (CD) is the most common cause of endogenous Cushing’s syndrome in children and adolescents and represents a rare cause of short stature. A 14-year-old boy came to our attention for progressive weight gain and short stature. Birth length and weight were normal; clinical history was negative for use of glucocorticoids. At examination, height was 140 cm (3th centile), weight was 37.7 kg (10th centile). Tanner stage was: G2, PH 3, testis 3 ml. Hypothyro...

ea0016p449 | Neuroendocrinology | ECE2008

Prevalence of metabolic syndrome in adult hypopituitaric patients with GH deficiency (GHD)

Di Somma Carolina , Rota Francesca , Tufano Antonella , Rota Francesca , Di Minno Dario Nicola , D'Andrea Marianna , Lombardi Gaetano

The prevalence of the metabolic syndrome is increasing worldwide. The untreated metabolic syndrome places individuals at risk both for diabetes and cardiovascular disease. Adult GH deficiency syndrome present some of the 5 features of the metabolic syndrome, abdominal obesity, high triglycerides, low HDL-cholesterol, elevations of blood glucose, hypertension and a 2-fold higher risk of death for CD compared with controls. The aim of this study was to determine the prevalence o...