Searchable abstracts of presentations at key conferences in endocrinology

ea0022p451 | Endocrine tumours &amp; neoplasia (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Prokineticin 1 stimulates prostate epithelial cell migration and proliferation in vitro

Visonti Daniela , Bellastella Giuseppe , Rossi Valentina , Chieffi Paolo , Maione Luigi , Punzo Paola , Bellastella Antonio , Sinisi Antonio Agostino

Prokineticin 1 (Prok1), the product of EGVEGF/PROK 1 gene, acts through two G-coupled receptors (PKR1 and PKR2) and is involved in a wide spectrum of actions, including tumorigenesis. Increased Prok1 expression has been found in prostate hyperplasia and cancer, suggesting a role in prostate cancer and BPH. Aim of this study was to elucidate the role of Prok1 on prostate cell function and growth. We evaluated the effects of Prok1 on epithelial prostate cell (PC) migration and p...

ea0022p543 | Male reproduction | ECE2010

Serum INSL3 dynamics in young men with congenital hypogonadotropic hypogonadism treated with gonadotropins

Bellastella Giuseppe , Esposito Dario , Maione Luigi , Visconti Daniela , Palumbo Vincenzo , De Bellis Annamaria , Bellastella Antonio , Sinisi Antonio Agostino

Insulin-like factor 3 (INSL3) is produced by Leydig cells. In boys, the levels of INSL3 rise at pubertal stage P2 and further increase throughout puberty in close correlation with T and LH concentrations. In men with hypogonadotropic hypogonadism (HH) INSL3 levels have been found very low and increased after short-term hCG treatment. Whether FSH plays a role in regulating INSL3 secretion is questioned. Aim of this study was to evaluate serum INSL3 levels during long-term hCG a...

ea0016s30.1 | Clinical highlights | ECE2008

Reversible Kallmann syndrome associated with a novel homozygous mutation in the prokineticin receptor-2 gene

Asci Roberta , Bellastella Giuseppe , Maione Luigi , Quinto Maria Chiara , De Bellis Annamaria , Jolascon Achille , Bellastella Antonio , Agostino Sinisi Antonio

Reversible Kallmann syndrome (KS) is a rare variant of hypogonadotropic hypogonadism (HH) reported in men, in which gonadotropin, testosterone (T) and fertility recover spontaneously following treatment with gonadotropins or T. In a few cases mutations of FGFR1 and KAL1 genes have been found. In this report we describe a subject with a KS carrying a new homozygous mutation of PROK-R2 gene and displaying an apparent reversal of his reproductive condition. The proband, born from...

ea0016oc5.3 | Reproduction | ECE2008

Prokineticin-2 and prokineticin receptor-2 gene analysis in men with Kallmann syndrome or normosmic hypogonadotropic hypogonadism

Sinisi Antonio Agostino , Asci Roberta , Bellastella Giuseppe , Esposito Dario , Maione Luigi , Visconti Daniela , Bellastella Antonio , Jolascon Achille

Prokineticins (PK1 and PK2) are peptides regulating multiple biological processes through two G-protein coupled receptors, PK-R1 and PK-R2. PK2/PKR2 signalling is critical for neurogenesis of olfactory bulb and GnRH migration. Mutant mice lacking PKR2 have abnormal development of olfactory bulb and reproductive system atrophy, suggesting that these genes may be novel candidate for Kallmann syndrome (KS) in humans. Recently, mutations in PK2 and PKR2 genes have been found in ne...

ea0092op-10-03 | Oral Session 10: Novel diagnostics in Thyroid cancer | ETA2023

KI67 proliferative index, but not mitotic count and necrosis, is a prognostic factor in patients with medullary thyroid cancer: a single-center retrospective analysis according to the 2022 who pathological classification

Prinzi Antonio , Bosco Agata , Mirone Alessandro , Tumino Dario , Di Benedetto Guenda , Gambero Federica , Bartoloni Giovanni , Frasca Francesco , Belfiore Antonino , Malandrino Pasqualino

Background: The 2022 WHO Classification of Endocrine and Neuroendocrine Tumors has introduced, as other neuroendocrine neoplasms, new pathological features to classify medullary thyroid carcinoma (MTC) in low/high grade. However, whether it can be reliable in clinical practice should be confirm by further studies.Aim: To verify the predictive value of the 2022 WHO grading system in patients with MTC.Materials and Methods: Tumor tis...

ea0037gp.22.06 | Pituitary–Therapy of Cushing's disease | ECE2015

A specific nursing educational programme in patients with Cushing's syndrome

Martinez-Momblan M Antonia , Porta Nuria , Gomez Carmen , Esteve Julia , Santos Alicia , Ubeda Inmaculada , Halperin Irene , Campillo Beatriz , Guillaumet Montserrat , Webb Susan M , Resmini Eugenia

Context: Cushing’s syndrome (CS) is a rare endocrine disease, due to cortisol hypersecretion. CS patients have several comorbidities, often still present after biochemical cure. There are no specific nursing healthcare programs to address this disease and achieve improved health related quality of life (HRQoL). Thus, an educational nursing intervention in these patients, through the development and promotion of specific educational tools, appears to be justified.<p cl...

ea0050cmw5.6 | Workshop 5: How do I. . . (2) | SFEBES2017

How do I manage.... myxoedema coma

Brooke Antonia

Myxoedema coma is a rare endocrine emergency with reported high mortality. Exact incidence is hampered by no clear consensus on its definition and the huge variability in its presentation. Most patients are not comatose, and have a form of severe, decompensated hypothyroidism. The common clinical features, including poor mentation, hypothermia, haemodynamic instability and lethargy, correlate poorly to degree of biochemical hypothyroidism. Early detection and identifying commo...

ea0050cmw5.6 | Workshop 5: How do I. . . (2) | SFEBES2017

How do I manage.... myxoedema coma

Brooke Antonia

Myxoedema coma is a rare endocrine emergency with reported high mortality. Exact incidence is hampered by no clear consensus on its definition and the huge variability in its presentation. Most patients are not comatose, and have a form of severe, decompensated hypothyroidism. The common clinical features, including poor mentation, hypothermia, haemodynamic instability and lethargy, correlate poorly to degree of biochemical hypothyroidism. Early detection and identifying commo...

ea0065ns1.2 | NICE – T3 | SFEBES2019

Health care professional & patient consultation – informed decision making

Brooke Antonia

Shared, informed decision making is a key component to high quality care in the NHS. This can occasionally be challenging through lack of time, lack of high-quality trial evidence to support treatment choices and financial limitations to treatment. Informed decision making includes open discussion of the risks and potential adverser consequences of treatment and alternatives. People with endocrine disorders often have symptoms that encompass both their psychological and physic...

ea0059mte10.2 | Service Improvements | SFEBES2018

The Society for Endocrinology peer review scheme

Brooke Antonia

Society for Endocrinology peer review is in its 16th year. In 2018 the format has been updated and single centre reviews are now being carried out. The catchment area of hospitals reviewed has varied from 280 000 to 2.5 million. A review helps to highlight a centre’s strengths and help focus on areas for development. It is a qualitative deep dive into a service which includes benchmarking against other similar services. The review is conducted by a team of clinical endocr...