Ram Sharan, Corbin Marine, 't Mannetje Andrea, Eng Amanda, Kvalsvig Amanda, Baker Michael G, Douwes Jeroen
Centre for Public Health Research, Massey University, Wellington, New Zealand.
Department of Public Health, University of Otago, Wellington, New Zealand.
JMIR Res Protoc. 2025 Feb 28;14:e66184. doi: 10.2196/66184.
The incidence of many common chronic childhood conditions has increased globally in the past few decades, which has been suggested to be potentially attributed to antibiotic overuse leading to dysbiosis in the gut microbiome.
This linkage study will assess the role of antibiotic use in utero and in early life in the development of type 1 diabetes (T1D), attention-deficit/hyperactive disorder (ADHD), and inflammatory bowel disease.
The study design involves several retrospective cohort studies using linked administrative health and social data from Statistics New Zealand's Integrated Data Infrastructure. It uses data from all children who were born in New Zealand between October 2005 and December 2010 (N=334,204) and their mothers. Children's antibiotic use is identified for 4 time periods (at pregnancy, at ≤1 year, at ≤2 years, and at ≤5 years), and the development of T1D, ADHD, and inflammatory bowel disease is measured from the end of the antibiotic use periods until death, emigration, or the end of the follow-up period (2021), whichever came first. Children who emigrated or died before the end of the antibiotic use period are excluded. Cox proportional hazards regression models are used while adjusting for a range of potential confounders.
As of September 2024, data linkage has been completed, involving the integration of antibiotic exposure and outcome variables for 315,789 children. Preliminary analyses show that both prenatal and early life antibiotic consumption is associated with T1D. Full analyses for all 3 outcomes will be completed by the end of 2025.
This series of linked cohort studies using detailed, complete, and systematically collected antibiotic prescription data will provide critical new knowledge regarding the role of antibiotics in the development of common chronic childhood conditions. Thus, this study has the potential to contribute to the development of primary prevention strategies through, for example, targeted changes in antibiotic use.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/66184.
在过去几十年中,全球许多常见儿童慢性病的发病率有所上升,这可能归因于抗生素的过度使用导致肠道微生物群失调。
这项关联研究将评估子宫内及生命早期使用抗生素在1型糖尿病(T1D)、注意力缺陷多动障碍(ADHD)和炎症性肠病发展中的作用。
该研究设计包括多项回顾性队列研究,使用来自新西兰统计局综合数据基础设施的关联行政健康和社会数据。它使用了2005年10月至2010年12月在新西兰出生的所有儿童(N = 334,204)及其母亲的数据。确定儿童在4个时间段(孕期、≤1岁、≤2岁和≤5岁)的抗生素使用情况,并测量从抗生素使用期结束到死亡、移民或随访期结束(2021年)(以先到者为准)期间T1D、ADHD和炎症性肠病的发生情况。在抗生素使用期结束前移民或死亡的儿童被排除。使用Cox比例风险回归模型,同时对一系列潜在混杂因素进行调整。
截至2024年9月,数据关联已完成,涉及315,789名儿童的抗生素暴露和结局变量整合。初步分析表明,产前和生命早期使用抗生素均与T1D有关。所有3项结局的全面分析将于2025年底完成。
这一系列使用详细、完整且系统收集的抗生素处方数据的关联队列研究,将提供有关抗生素在常见儿童慢性病发展中作用的关键新知识。因此,本研究有可能通过例如针对性地改变抗生素使用等方式,为一级预防策略的制定做出贡献。
国际注册报告识别码(IRRID):DERR1-10.2196/66184