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
BMC Pediatr. 2013 Aug 14;13:124. doi: 10.1186/1471-2431-13-124.
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.
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.
Australia New Zealand Clinical Trials Registry ACTRN12613000794707.
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。
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。
澳大利亚新西兰临床试验注册中心ACTRN12613000794707。