Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep910 | Thyroid cancer | ECE2015

Thyroid cancer in Ireland: a 10-year review of the National Cancer Registry

Lennon Paul , Deedy Sandra , Healy Marie-Louise , Kinsella John , Timon Conrad , O'Neill James Paul

Introduction: The increased incidence of thyroid cancer is driven mainly by a large increase in papillary thyroid cancer (PTC). The number of patients that succumb to the disease has remained stable. The aim of our study is to analyze the incidence and mortality of thyroid cancer in Ireland.Methods and design: A retrospective analysis of the National Cancer Registry was undertaken, between 1st of January 1998 and the 31st December 2007. The Kaplan–M...

ea0036oc3.5 | Oral Communications 3 | BSPED2014

Statistical prediction of HRpQCT microstructural trabecular parameters using 1.5T skeletal MRI

Dimitri Paul , Lekadir Karim , Whitby Elspeth , Armitage Paul , Hoogendoorn Corne , Franji Alejandro

Background: High resolution peripheral quantitative computed tomography (HRpQCT) can accurately determine three-dimensional in-vivo skeletal microstructure. However, HRpQCT is limited to the ultradistal radius and tibia (9 mm) imaging. MRI may be an alternative approach to cortical and trabecular bone analysis; to date there is limited information regarding the accurate quantification of trabecular bone.Method: Ninety-three 13–16 years-old ...

ea0013p201 | Endocrine tumours and neoplasia | SFEBES2007

Pheochromocytoma- an experience from a south indian referral center

Thomas Nihal , Seshadri Mandalam , Paul Thomas , Nair Aravindan , Mj Paul , Rajarathinam Simon , Prabu Suresh , Oommen Regi

Background: Pheochromocytomas are tumors arising from chromaffin cells diagnosed in <1% of patient evaluated for hypertension.Methodology: A retrospective analysis of case records of those patients with histopathologically confirmed pheochromocytoma in our hospital from 1993–2006 (14 years) was conducted.Result: A total of 94 patients were diagnosed to have pheochromocytoma during this period. The median age at presentatio...

ea0077p25 | Bone and Calcium | SFEBES2021

Seasonal variations in circulating vitamin D appear gender dependent and may highlight a novel health inequality

Laing Ian , Allcock Rebecca , Aitchison Michael , Perkins Karen , Wignall Paul

Vitamin D is a pleotropic hormone with important actions in a wide variety of cell types. Whilst its role in the endocrine control of calcium metabolism via the active circulating metabolite 1,25- dihydroxy cholecalciferol is widely appreciated, other actions in a range of cells and tissues depend on activation of circulating 25-hydroxy vitamin D by intracrine mechanisms and paracrine actions which may be locally controlled. Of particular interest are the roles of vitamin D pe...

ea0077p182 | Metabolism, Obesity and Diabetes | SFEBES2021

Rat primary hypothalamic, but not cortical, astrocytes increase use of glutamate to fuel metabolism after recurrent low glucose

Potter Paul Weightman , Randall Andy , Ellacott Kate , Beall Craig

Aims: A critical function of astrocytes is to recycle glutamate to neurons as glutamine to sustain glutamatergic neurotransmission. In the hypothalamus, this is required for effective counterregulatory hormone release in response to hypoglycaemia. However, after recurrent hypoglycaemia in vivo, this is attenuated. The aim of this study was to characterise how rat primary hypothalamic and cortical astrocytes adapt to recurrent low glucose (RLG) with repeated exposure t...

ea0077p222 | Neuroendocrinology and Pituitary | SFEBES2021

SDHD missense pathogenic variants: not always benign

Haboosh Sara , Carroll Paul , Izatt Louise , Quinn Mark , Velusamy Anand

Pathogenic variants in the SDHx genes are responsible for ~20% of familial Phaeochromocytoma/Paraganglioma (PPGL) tumours. Metastatic disease is lower in SDHD in comparison to SDHA, B and C mutations. Although the genotype-phenotype relationship is not well established it is considered that truncating SDHD pathogenic variants have a higher risk of causing disease in comparison to missense variants. We present two cases of metastatic paraganglioma in patients with heterozygous ...

ea0055wc2 | Workshop C: Disorders of the thyroid gland (I) | SFEEU2018

Toxic nodule: wait or treat?

Hafeez Saba , Kumar Rakshit , Velusamy Anand , Powrie Jake , Carroll Paul

68 years old female initially referred to endocrine clinic in November 2016 for assessment of fluctuating thyroid function. She had a history of long standing primary hypothyroidism, stable on treatment with 100 mcg Levothyroxine. In last one year, Levothyroxine was tapered and stopped due to persistent suppression of TSH and high normal Free T4. Last tests showed TSH of <0.01mIU/l and Free T4 of 27.1 pmol/l. She had ongoing complaints of feeling increasingly tired and gen...

ea0081p116 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Association of uric acid levels with diabetic retinopathy in filipino patients with type 2 diabetes mellitus at a tertiary government hospital: a cross-sectional analytic study

Bariuad-Garcia Irene Kei , Jimeno Cecilia , Siopongco Paul

Objectives: Diabetic retinopathy, is the most frequent cause of new cases of blindness among adults aged 20–74 years in developed countries. In 15 of the 23 studies in developing countries and in ethnic minority groups within developed countries, the prevalence of diabetic retinopathy was over 35%. In developed countries, only 2 of 16 studies reported a prevalence of 35% or over. Variation in neither population demographics nor method of retinopathy assessment appeared to...

ea0050oc6.3 | Bone, Calcium and Neoplasia | SFEBES2017

Generation of multiple endocrine neoplasia type 1 and death-domain-associated protein pluripotent stem cell lines to investigate mechanisms of pancreatic neuroendocrine tumourigenesis

Dissanayake Kumara , Davidson Lindsay , Poland Conor , Newey Paul

Background: Despite a wealth of gene-discovery studies identifying recurrently mutated genes in hereditary and sporadic endocrine tumours, the molecular mechanisms underpinning tumourigenesis frequently remain ill-defined, in part reflecting a lack of physiologically relevant model systems to investigate gene function. Here, using pancreatic neuroendocrine tumours as an example, we explored the utility of human induced pluripotent stem cell (iPSCs) and CRISPR/Cas9 gene-editing...

ea0050p261 | Neuroendocrinology and Pituitary | SFEBES2017

Morbidity and mortality in patients with hyperprolactinaemia: The prolactin epidemiology, audit, and research study (PROLEARS)

Soto-Pedre Enrique , Newey Paul , Bevan John , Leese Graham

Purpose: High serum prolactin concentrations have been associated with adverse health outcomes in some but not all studies. This study aimed to examine the morbidity and all-cause mortality associated with hyperprolactinaemia.Methods: A population-based matched cohort study in Tayside (Scotland, UK) from 1988 to 2014. Record-linkage technology (biochemistry, prescribing, hospital admissions, cancer registration, mat...