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胰岛自身免疫的环境决定因素(ENDIA):一项针对1型糖尿病高危儿童从孕期到生命早期的队列研究

Environmental determinants of islet autoimmunity (ENDIA): a pregnancy to early life cohort study in children at-risk of type 1 diabetes.

作者信息

Penno Megan A S, Couper Jennifer J, Craig Maria E, Colman Peter G, Rawlinson William D, Cotterill Andrew M, Jones Timothy W, Harrison Leonard C

出版信息

BMC Pediatr. 2013 Aug 14;13:124. doi: 10.1186/1471-2431-13-124.

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.

摘要

背景

1型糖尿病的发病率在全球范围内呈上升趋势,尤其是在年幼儿童以及遗传易感性较低的人群中。这些观察结果表明,现代环境中的某些因素会促进胰岛自身免疫以及胰岛素生成β细胞的破坏。胰岛自身免疫环境决定因素(ENDIA)研究正在调查可能导致胰岛自身免疫和1型糖尿病发生的候选环境暴露因素以及基因-环境相互作用。

方法/设计:ENDIA是南半球唯一一项针对高危儿童1型糖尿病决定因素的前瞻性妊娠/出生队列研究。该研究将在澳大利亚的五个州招募1400名未出生婴儿或6个月以下的婴儿,这些婴儿的一级亲属(即母亲、父亲或兄弟姐妹)患有1型糖尿病。从怀孕早期到儿童期,对怀孕的母亲/婴儿进行前瞻性跟踪,以研究基因型、胰岛自身免疫(以及随后的1型糖尿病)的发展与产前和产后环境因素之间的关系。ENDIA将评估微生物组、营养、体重/组成、代谢组-脂质组、胰岛素抵抗、先天性和适应性免疫功能以及病毒感染。将采用系统生物学方法整合这些数据。调查将在母亲怀孕期间每3个月进行一次评估,然后在孩子24个月大之前每3个月进行一次评估,此后每6个月进行一次评估。主要结局指标是持续性胰岛自身免疫,定义为连续检测中存在针对一种或多种胰岛自身抗原的自身抗体。

讨论

确定在生命早期启动和/或促进胰岛素生成β细胞破坏的基因-环境相互作用,将为1型糖尿病的一级预防方法提供依据。ENDIA的优势在于从怀孕早期到幼儿期进行前瞻性、全面且频繁的全系统分析,以捕捉可能影响胰岛自身免疫发展的动态环境暴露因素。

试验注册

澳大利亚新西兰临床试验注册中心ACTRN12613000794707。

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