Searchable abstracts of presentations at key conferences in endocrinology

ea0005p266 | Thyroid | BES2003

Psychological well-being in patients on 'adequate' doses of L-Thyroxine

Saravanan P , Chau F , Roberts N , Vedhara K , Greenwood R , Dayan C

Objective: Many patients receiving thyroid hormone replacement therapy complain of persistent lethargy and related symptoms even with normal TSH levels. However, it remains unclear whether this is related to thyroxine replacement or coincidental psychological morbidity.Design: Using general practice computer records, 961 patients on thyroxine (minimum of 4 months) and their age- and sex-matched controls were identified and sent a two-page questionnaire, comprising the shor...

ea0003p200 | Neuroendocrinology | BES2002

Disease activity in acromegaly may be assessed four weeks after discontinuation of pegvisomant

Drake W , Loureiro R , Parkinson C , Roberts M , Akker S , Monson J , Besser G , Trainer P

Patients with acromegaly treated with medical therapy intermittently discontinue therapy to allow assessment of underlying disease activity. This is particularly so in patients treated with pituitary irradiation. Typical 'washout' times include 5 weeks for bromocriptine and 2 weeks for short-acting sc octreotide; longer periods are required for cabergoline and slow-release somatostatin analogues. Pegvisomant is a novel medical therapy for acromegaly that functions as a GH rece...

ea0099rc7.2 | Rapid Communications 7: Endocrine-related Cancer | ECE2024

The presence of abortive changes in thyroid tumors serves as a strong indicator of underlying DICER1 mutations

Condello Vincenzo , Roberts James , Stenman Adam , Larsson Catharina , Viswanathan Kartik , Juhlin Christofer

Background: Somatic and bi-allelic DICER1 mutations have been reported in subsets of sporadic thyroid tumors, affirming a clear involvement of this gene in the development of thyroid tumors. As a recent study has highlighted associations between DICER1 mutations and macrofollicular patterns, abortive changes, and papillary structures, we aimed to investigate these observations in a bi-institutional cohort.Methods: A total of 61 thyroid lesions (...

ea0099rc12.3 | Rapid Communications 12: Diabetes, Obesity, Metabolism and Nutrition | Part II | ECE2024

Adipose tissue analysis toolkit (ATAT) for automated analysis of adipocyte size and extracellular matrix in white adipose tissue

Robino Jacob , Plekhanov Alexander , Zhu Qingzhang , Jensen Michael , Scherer Philipp , Roberts Charles , Varlamov Oleg

The pathological expansion of white adipose tissue (WAT) in obesity involves adipocyte hypertrophy accompanied by expansion of collagen-rich pericellular extracellular matrix (ECM) and the development of crown-like structures (CLS). Traditionally, WAT morphology is assessed through immunohistochemical analysis of WAT sections. However, manual analysis of large histological sections is time-consuming, and available digital tools for analyzing adipocyte size and pericellular ECM...

ea0099p446 | Calcium and Bone | ECE2024

Investigating the etiology of non-surgical hypoparathyroidism: insights from a sponsored genetic testing program

Mannstadt Michael , Marelli Claudio , Sridhar Ananth , Smith Lyndsay , Roberts Mary Scott , Adler Scott , Mathew Arun

Hypoparathyroidism is a rare endocrine disorder characterized by inadequate production of parathyroid hormone to maintain normal blood calcium levels. Hypoparathyroidism is most frequently caused by damage to or removal of the parathyroid glands but can also be associated with genetic etiologies. Genetic forms of hypoparathyroidism can present as isolated or as part of a syndrome and include disorders of parathyroid gland formation, parathyroid hormone secretion, and damage to...

ea0077ec1.4 | Clinical Endocrinology Trust Best Abstract Basic | SFEBES2021

The vagal Calcium Sensing Receptor mediates the effect of protein ingestion on insulin release and regulates macronutrient metabolism

Norton Mariana , Roberts Anna , Alonso Aldara Martin , Cao Ye , Gribble Fiona , Reimann Frank , Chang Wenhan , Salem Victoria , Murphy Kevin G

Protein stimulates insulin release and improves post-prandial glycaemic excursions. The underlying mechanism has previously been attributed to gastric emptying, incretin release and direct pancreatic stimulation. However, our studies suggest the calcium sensing receptor (CaSR) in the vagus nerve plays an important role. The CaSR has a well characterised role in calcium homeostasis, but also acts as a protein metabolite sensor. In response to the amino acid products of protein ...

ea0077oc3.5 | Metabolism, Obesity and Diabetes | SFEBES2021

Microbial tryptophan metabolites modulate L-cell induced GLP-1 secretion to improve glucose homeostasis

Phuah Phyllis , Cheng Sijing , Norton Mariana , Roberts Anna , Otsubo Emile , Gribble Fiona , Reimann Frank , Hanyaloglu Aylin , Owen Bryn , Murphy Kevin

Growing evidence implicates gut microbiota-derived metabolites in metabolic homeostasis. Gut microbial dysbiosis occurs in obesity, while high-fibre and high-protein diets, which improve glucose tolerance and induce weight loss, are associated with the generation of microbial metabolites. Understanding how the gut responds to microbial metabolites may identify mechanisms that induce satiety and improve glucoregulation, revealing novel therapeutic targets. Indole is generated f...

ea0077p180 | Metabolism, Obesity and Diabetes | SFEBES2021

Neurotensin improves glucose tolerance via activation of peripheral NTSR1-expressing neurons

Roberts Anna , Norton Mariana , Martin Alonso Aldara , Phuah Phyllis , Cheng Sijing , Smitherman-Cairns Tobias , Hanyaloglu Aylin , Murphy Kevin

Neurotensin is a 13-amino acid peptide expressed in both the brain and the gastrointestinal tract where it acts as a neuropeptide and gut hormone, respectively. Centrally, neurotensin plays a role in appetite, analgesia and thermoregulation, whereas peripheral neurotensin regulates lipid absorption, gastric emptying and exocrine pancreatic secretion. The role of neurotensin in the control of glucose homeostasis currently remains unclear. We found peripheral administration of n...

ea0090rc8.4 | Rapid Communications 8: Calcium and Bone | ECE2023

Encaleret (CLTX-305) normalized mineral homeostasis parameters in patients with autosomal dominant hypocalcemia type 1: Results over 12 months in a phase 2 study (NCT04581629)

Collins Michael , Hartley Iris , Roszko Kelly , Nemeth Edward , Pozo Karen , Boykin Winsome , Mathew Arun , Roberts Mary Scott , Adler Scott

Autosomal dominant hypocalcemia type 1 (ADH1), caused by gain-of-function calcium-sensing receptor gene (CASR) variants, is characterized by low parathyroid hormone (PTH) levels, hypocalcemia, hypercalciuria, hyperphosphatemia and hypomagnesemia. Conventional therapy (calcium and active vitamin D) worsens hypercalciuria, which may result in renal complications. Calcilytics, such as encaleret, are negative allosteric modulators of the calcium-sensing receptor (CaSR). T...