Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep18 | Adrenal and Cardiovascular Endocrinology | ECE2020

Aetiology, clinical presentation and mortality of Addison’s disease in India: A retrospective follow-up study over 14 years

Bhatia Eesh , Sri Harsha Gunna , Marak Rungmei SK , Pandey Rakesh , Yu Liping

Background: Autoimmune destruction is the most common aetiology of primary adrenal insufficiency (PAI) in Europe and north America. In contrast, tuberculosis is a common cause of PAI in developing countries. More recently, adrenal histoplasmosis (AH) is being increasingly reported from IndiaAims: To study the aetiology, clinical presentation and mortality in adults with PAI who were diagnosed between 2006-2019 and to determine the changes in aetiology si...

ea0035p40 | Adrenal cortex | ECE2014

21-hydroxylase autoantibody positivity is influenced by HLA genotype in South African patients with Addison's disease

Ross Ian , Babu Sunanda , Yu Liping , Armstrong Taylor , Zhang Li , Schatz Desmond , Pugliese Alberto , Eisenbarth George , Baker Peter

Background: Data examining HLA associations in Addison’s disease (AD) from South Africa (SA) are limited. We wished to determine the HLA in South African AD patients either positive or negative for 21 hydroxylase autoantibodies (21 OH-AA) and matched healthy controls, hypothesising that certain HLA alleles could predominate, but there may be differences from Western countries.Methods: SA patients (n=73) were enrolled as part of a nationwide...

ea0037gp.01.08 | Adrenal | ECE2015

Autoimmune polyendocrine syndrome in India: clinical aspects, AIRE mutations, and functional analysis

Bhatia Eesh , Zaidi Ghazala , Sarangi Aditya , Bhatia Vijayalakshmi , Bharani Nisha , Sachan Alok , Zhang Li , Yu Liping , Jain Vandana , Sahu Saroj , Srivastava Rashmi , Bharti Niharika , Aggarwal Rakesh , Aggarwal Amita

Introduction: Autoimmune polyendocrine syndrome 1 (APS1) is an uncommon, serious autosomal recessive disorder, due to AIRE gene mutations which result in impaired central tolerance. India has a complex genetic structure and also communities with high prevalence of consanguinity, which may result in varied clinical manifestations and genetic mutations.Aims: To study clinical features, interferon-α antibodies (IFNA), AIRE mutations, ...