Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/81247
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Type: Journal article
Title: Environmental determinants of islet autoimmunity (ENDIA): a pregnancy to early life cohort study in children at-risk of type 1 diabetes
Author: Penno, M.
Couper, J.
Craig, M.
Colman, P.
Rawlinson, W.
Cotterill, A.
Jones, T.
Harrison, L.
Baghurst, P.
Barry, S.
Cameron, F.
Dodd, J.
Duran, C.
Forbes, J.
Makrides, M.
Morahan, G.
Nelson, K.
Nankervis, A.
Sinnott, R.
Wentworth, J.
Citation: BMC Pediatrics, 2013; 13(1):1-15
Publisher: BioMed Central Ltd.
Issue Date: 2013
ISSN: 1471-2431
1471-2431
Contributor: Baghurst, Peter Adrian
Barry, Simon Charles
Dodd, Jodie Michele
Makrides, Maria
Statement of
Responsibility: 
Megan AS Penno, Jennifer J Couper, Maria E Craig, Peter G Colman, William D Rawlinson, Andrew M Cotterill, Timothy W Jones, Leonard C Harrison and ENDIA Study Group
Abstract: BACKGROUND The incidence of type 1 diabetes has increased worldwide, particularly in younger children and those with lower genetic susceptibility. These observations suggest factors in the modern environment promote pancreatic islet autoimmunity and destruction of insulin-producing beta cells. The Environmental Determinants of Islet Autoimmunity (ENDIA) Study is investigating candidate environmental exposures and gene-environment interactions that may contribute to the development of islet autoimmunity and type 1 diabetes. METHODS/DESIGN ENDIA is the only prospective pregnancy/birth cohort study in the Southern Hemisphere investigating the determinants of type 1 diabetes in at-risk children. The study will recruit 1,400 unborn infants or infants less than six months of age with a first-degree relative (i.e. mother, father or sibling) with type 1 diabetes, across five Australian states. Pregnant mothers/infants will be followed prospectively from early pregnancy through childhood to investigate relationships between genotype, the development of islet autoimmunity (and subsequently type 1 diabetes), and prenatal and postnatal environmental factors. ENDIA will evaluate the microbiome, nutrition, bodyweight/composition, metabolome-lipidome, insulin resistance, innate and adaptive immune function and viral infections. A systems biology approach will be used to integrate these data. Investigation will be by 3-monthly assessments of the mother during pregnancy, then 3-monthly assessments of the child until 24 months of age and 6-monthly thereafter. The primary outcome measure is persistent islet autoimmunity, defined as the presence of autoantibodies to one or more islet autoantigens on consecutive tests. DISCUSSION Defining gene-environment interactions that initiate and/or promote destruction of the insulin-producing beta cells in early life will inform approaches to primary prevention of type 1 diabetes. The strength of ENDIA is the prospective, comprehensive and frequent systems-wide profiling from early pregnancy through to early childhood, to capture dynamic environmental exposures that may shape the development of islet autoimmunity. TRIAL REGISTRATION Australia New Zealand Clinical Trials Registry ACTRN12613000794707.
Keywords: Type 1 diabetes
Islet autoimmunity
Beta cell
Pregnancy
Infancy
Microbiome
Insulin resistance
Immunity
Virus
Systems biology
Description: Members of ENDIA Study Group: Peter Baghurst, Simon Barry, Jodie Dodd, Maria Makrides for the University of Adelaide.
Rights: © 2013 Penno et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
DOI: 10.1186/1471-2431-13-124
Published version: http://dx.doi.org/10.1186/1471-2431-13-124
Appears in Collections:Aurora harvest 4
Paediatrics publications

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