Searchable abstracts of presentations at key conferences in endocrinology

ea0050ep050 | Clinical Biochemistry | SFEBES2017

Starvation ketoacidosis – a rare but significant metabolic condition

Nardeosingh Siddarth , Savage Amy , Banerjee Moulinath

Diabetic ketoacidosis and pregnancy related ketoacidosis are the most common forms of ketoacidosis seen in acute medical units. We describe here two rare cases of starvation ketoacidosis.Case 1: 63 years old gentleman with no history of diabetes, presented with persistent vomiting for 48 hours. His admission bloods revealed Serum Bicarbonate of 8, pH 7.19, pCO2 2.7, base excess of -17.8, plasma glucose 5.2 mmol/l and serum alc...

ea0050ep050 | Clinical Biochemistry | SFEBES2017

Starvation ketoacidosis – a rare but significant metabolic condition

Nardeosingh Siddarth , Savage Amy , Banerjee Moulinath

Diabetic ketoacidosis and pregnancy related ketoacidosis are the most common forms of ketoacidosis seen in acute medical units. We describe here two rare cases of starvation ketoacidosis.Case 1: 63 years old gentleman with no history of diabetes, presented with persistent vomiting for 48 hours. His admission bloods revealed Serum Bicarbonate of 8, pH 7.19, pCO2 2.7, base excess of -17.8, plasma glucose 5.2 mmol/l and serum alc...

ea0081p260 | Adrenal and Cardiovascular Endocrinology | ECE2022

Menopause and muscle mass of humans and increase in fat mass

Kumar Naween , Singh Siddharth , Prakash A S

Background: Menopause has been related to a deficiency of bulk and an increment in fat mass. Testosterone treatment is being considered to further develop body organization in menopausal women. Notwithstanding, the portion reaction connections among testosterone and the progressions in body structure and muscle strength in women have not been set up. To decide the portion subordinate impacts of reviewed dosages of testosterone on body arrangement and muscle strength in precise...

ea0081ep1032 | Thyroid | ECE2022

Efficacy of ethanol injection in cystic thyroid nodules

Kumar Naween , Ranjan Rajeev , Singh Siddharth

Introduction: Thyroid cystic nodules (TCN) are generally due to degenerative changes within colloid nodules or adenomas. True thyroid cysts are uncommon. But the prevalence of malignancy among TCN is controversial since some authors consider it to be low risk while some others consider it to have the same risks as malignancy as the solid lesions of the thyroid. Percutaneous ethanol injection (PEI) is utilised for treating benign cystic thyroid nodules. It is a protected option...

ea0081p361 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Comparison of glycemic variability in type 2 diabetes mellitus patients on oral anti diabetic drugs (OAD) with and without insulin using ambulatory glucose profile (AGP)

S Sidharth , Aggarwal Ramesh , Prakash Anupam , Ghotekar L H , Aggarwal Meenakshi

Introduction: Assessment of diabetes with daily blood glucose fluctuations including peaks and nadirs forms the crux of the modern management. Use of glycemic variability (GV) as a parameter to assess these fluctuations is emerging. Diabetes mellitus patients follow different clinical trajectories which can be traced by the ambulatory glucose profile (AGP) obtained from flash glucose monitoring system (FGMS).Methodology: This comparative observational st...

ea0020p358 | Diabetes and Cardiovascular | ECE2009

Biphasic insulin aspart 30/70 improves glycaemic control in patients with type 2 diabetes: clinical practice experience from Indian subgroup of the IMPROVE study™

Unnikrishnan AG , Shah Siddharth , Asirvatham Arthur , Chakkarwar Praful , Moharana Ashok , Kapoor Dheeraj

Aims & objectives: IMPROVE™ is a 6-month, multi-national, prospective, observational study, assessing the safety and efficacy of biphasic insulin aspart 30/70 (BiAsp 30) in patients with type 2 diabetes.Methods: We present the efficacy data from the Indian cohort of IMPROVE study. A total of 17 995 subjects entered the study and 16 942 subjects completed the study. BiAsp 30 was initiated and dose was adjusted at the physician’s discretion, ...

ea0095p131 | Miscellaneous/other 2 | BSPED2023

Hypernetwork analysis: A novel approach for epigenome analysis, with Kabuki syndrome as an exemplar

Martirosian Evgenii , Cuvertino Sara , Garner Terence , Walusimbi Bridgious , Kimber Susan , Banka Siddharth , Stevens Adam

Background/objectives: Kabuki Syndrome 1 (KS1) is a neurodevelopmental disorder caused by loss-of-function of histone 3 lysine 4 mono-methyltransferase KMT2D. In addition, to neurodevelopmental features, some Kabuki Syndrome patients also exhibit endocrine-related phenotypes, such as hypoglycaemia. KMT2D is involved in global gene regulation, therefore, it is important to have a systems-based approach to understand pathomechanisms of KS1.<p class="abstext"...

ea0090oc5.4 | Oral Communications 5: Adrenal and Cardiovascular Endocrinology 1 | ECE2023

Adrenal Insufficiency Associated with Biallelic Mutations in Porphyria Genes

Smith Chris , Jackson Adam , Al-Salihi Ahmed , Janecke Andreas , Steichen Elisabeth , Darby Denise , Griffin Liezel , Banka Siddharth , Elsayed Solaf , Chan Li , Metherell Louise

Adrenal insufficiency (AI) is life-threatening and can present alone or in combination with other co-morbidities. Here we describe families with a novel association of AI with porphyria caused by biallelic mutations in protoporphyrinogen oxidase (PPOX) or coproporphyrinogen oxidase (CPOX). The porphyrias are a group of disorders caused by defects in one of eight enzymes within the haem biosynthetic pathway, divided into acute porphyrias, resulting in mainly n...

ea0034oc4.6 | Thyroid and bone | SFEBES2014

An ENU-induced Tyr265Stop mutation in Polg2 is associated with renal calcification in RCALC2 mice

Gorvin Caroline , Piret Sian , Ahmad Bushra , Stechman Michael , Loh Nellie , Hough Tertius , Leo Paul , Marshall Mhairi , Sethi Siddharth , Bentley Liz , Reed Anita , Christie Paul , Simon Michelle , Mallon Ann-Marie , Brown Matthew , Cox Roger , Brown Steve , Thakker Rajesh

Renal calcification (nephrocalcinosis), which has a multi-factorial etiology involving environmental and genetic determinants, affects ~8% of adults by 70 years. Nephrocalcinosis may occur as a familial disorder in ~65% of patients, and in 70% of patients, nephrocalcinosis may be associated with endocrine and metabolic disorders that include primary hyperparathyroidism, renal tubular acidosis, hypercalciuria, cystinuria, and hyperoxaluria. Investigations of families with hered...

ea0094op5.3 | Adrenal and Cardiovascular | SFEBES2023

Adrenal insufficiency can be associated with biallelic mutations in porphyria genes

Smith Chris , Al-Salihi Ahmed , Janecke Andreas , Steichen Elisabeth , Banka Siddharth , Jackson Adam , Darby Denise , Griffin Liezel , Stewart Sarah , Elsayed Solaf , Talbi Neila , Gouya Laurent , Chan Li , Metherell Louise

Adrenal insufficiency (AI) is life-threatening and can present alone or in combination with other co-morbidities. Acute porphyria attacks can also be serious, resulting in permanent disability or death and symptoms can be similar to AI. Previous literature describing hormonal perturbations in porphyria suggest an association between the two conditions. We were referred a family with 4 individuals with porphyria and AI, the clinical picture included global developmental delay, ...