Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep662 | Environmental Endocrinology | ECE2023

Early Dinner instead of Late Night reduce the risk of endocrine as well as genetic disruption

Naz Qulsoom , Usman Siddiqui Kausar , Verma Narsingh , Anjum B , Ali Mahdi Abbas

Background: Our bodies function optimally when we align our eating & sleeping patterns with our circadian rhythms, the innate 24-hour cycles that tell our bodies when to wake up, when to eat and when to fall asleep. Chronically disrupting this rhythm by eating late night meals & sleep could be a recipe for Hypertension, CVD, and metabolic trouble.Aim and objective: The aim of this study is to investigate whether there was a relationship between m...

ea0090ep663 | Environmental Endocrinology | ECE2023

Eating as well as sleeping later or modification of lifestyle can promote a negative profile of endocrine hormones & inflammatory markers

Usman Kauser , Naz Qulsoom

Background: Our bodies function optimally when we align our eating & sleeping patterns with our circadian rhythms, the innate 24-hour cycles that tell our bodies when to wake up, when to eat and when to fall asleep. Chronically disrupting this rhythm by eating late night meals & sleep could be a recipe for Diabetes, CVD, and metabolic trouble.Aim and objective: The aim of this study is to investigate whether there was a relationship between morni...

ea0094p224 | Metabolism, Obesity and Diabetes | SFEBES2023

Metabolic profiles of children of mothers with and without gestational diabetes at age of 5 years

Thakkar Simran , Mohammed Usman Khwaja , Asim Siddiqui Mohammad , Kumar Wangnoo Subash

Aims: Epidemiological studies have demonstrated that Indian babies born to mothers with gestational diabetes mellitus (GDM) have adverse metabolic profiles. The anthropometric and metabolic profiles in children of women with and without GDM were compared at age 5 years.Methods: Children born to mothers with GDM (CGDM) and without GDM (WGDM) were included in this prospective study. We examined maternal gestational BMI, GD...

ea0065p308 | Neuroendocrinology | SFEBES2019

Making best use of clinical genetic testing in the diagnosis of Neurohypophysial Diabetes Insipidus with significant family history – a case for early access

Siddiqui Shehla , Filipas Emanuela

Background: Familial Diabetes Insipidus is a very rare entity and can have either neurohypophyseal (FNDI) or nephrogenic forms with different transmission patterns. FNDI accounts for less than 5% of the 1:25 000 cases of DI diagnosed in UK. It is usually an autosomal dominant disorder caused by mutations in AVP (arginine vasopressin) gene, which regulates the vasopressin hormone synthesis; its signs and symptoms of polyuria & polydipsia usually become apparent in childhood...

ea0028p219 | Obesity, diabetes, metabolism and cardiovascular | SFEBES2012

Metabolic profile of Type 2 diabetes Indian Patients Undergoing Coronary Artery Bypass Surgery – a Tertiary Care Centre experience

Siddiqui Mohammad , Wangnoo Subhash

With increasing prevalence of type 2 diabetes in India, macrovascular complications are also on the rise. We undertook a retrospective study to evaluate the metabolic profile of type 2 diabetes patients undergoing coronary artery bypass grafting (CABG) at our centre. Clinical data on 672 consecutive patients undergoing elective CABG was included from the hospital data base after informed consent and ethics committee approval. Mean age of the patients was 49.7±9.5 years; 5...

ea0062wc10 | Workshop C: Disorders of the thyroid gland | EU2019

A case of thyroid hormone resistance due to mutation in THRβ gene

Shah Usman , Hanson Philippa

A 25 year old gentleman was referred to the endocrine clinic for evaluation of abnormal thyroid function tests. He reported symptoms of diffuse abdominal pain associated with loose stool up to six times a day with urgency, frequency and tenesmus. These symptoms had been present since childhood, becoming increasingly troublesome over the preceding two years. He also reported symptoms of tiredness, palpitations and sweating episodes. Thyroid function tests were abnormal. TSH was...

ea0077p67 | Metabolism, Obesity and Diabetes | SFEBES2021

Association of Vitamin D and Adiposity in Children and Adolescents with type 1 diabetes: a case-control study

Majeed Maria , Siddiqui Mohsin , Lessan Nader

Background: Vitamin D (25(OH)D) deficiency is a global public health issue. An association with obesity and diabetes has been described in adult and paediatric populations. This study investigates the prevalence of 25(OH)D deficiency and its correlates in population of Emirati children and adolescents attending a large diabetes centre in the United Arab Emirates.Methods: Participants aged 4-19 years were selected based on diabetes status [type 1 diabetes...

ea0021p165 | Diabetes and metabolism | SFEBES2009

Metabolic phenotype in brothers' of women with polycystic ovarian syndrome

Siddiqui Mohammad , Gupta Mukul , Wangnoo Subhash

Women with polycystic ovary syndrome (PCOS) have twice the risk for metabolic syndrome (MetS) compared to women from the general population. Mothers and sisters of affected women also have an increased prevalence of MetS. We undertook this study to evaluate whether these abnormalities are also present in brothers’ of affected women.Design and setting: A total of 59 brothers (age ≥18 and ≤40 years) of women with PCOS and 59 healthy men (o...

ea0086p234 | Metabolism, Obesity and Diabetes | SFEBES2022

Hyperglycaemia in patients with Acute Coronary syndromes (ACS): Retrospective audit data from Barnsley Hospital NHS Foundation Trust

Shankaran Vani , Chaudhry Shiza , Usman Mohammed

Hyperglycaemia is common in patients (~65%) when they are admitted to hospital with ACS. It is recognised to be one of the important prognostic indicators for all-cause mortality in patients who present with ACS, regardless of pre-existing diabetes1. NICE guidelines recommend to keep blood glucose (BG) levels below 11 mmol/l2 and offer all people with hyperglycaemia after ACS (without known diabetes) for HbA1c 3 check before discharge. We were interested to see whether we foll...

ea0062we2 | Workshop E: Disorders of the gonads | EU2019

Unexplained anaemia in men: Remember to screen for hypogonadism

Al-Sharefi Ahmed , Javaid Usman , Quinton Richard

Introduction: Hypogonadism is linked to anaemia, sarcopenia and osteoporosis in men. Whereas secondary hypogonadism (SH) is biochemically indistinguishable from nongonadal illness, primary hypogonadism (PH) can be easily diagnosable by the identification of raised gonadotropins.Case Presentation: A 66-years old male with a background history of type 2 diabetes mellitus, arthritis, and hypertension was referred to the haematology services to investigate h...