Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; Better Outcomes Registry & Network (BORN) Ontario, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada; School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Environ Res. 2024 Nov 15;261:119706. doi: 10.1016/j.envres.2024.119706. Epub 2024 Jul 30.
The direction and magnitude of association between maternal exposure to ambient air pollutants across gestational windows and offspring risk of autism spectrum disorders (ASD) remains unclear. We sought to evaluate the time-varying effects of prenatal air pollutant exposure on ASD. We conducted a matched case-control study of singleton term children born in Ontario, Canada from 1-Apr-2012 to 31-Dec-2016. Provincial birth registry data were linked with applied behavioural analysis services and ambient air pollutant datasets to ascertain prenatal exposure to nitrogen dioxide (NO), ground-level ozone (O), fine particulate matter (PM), and ASD diagnoses. Covariate balance between cases and controls was established using coarsened exact matching. Conditional logistic regression was used to assess the association between prenatal air pollutant exposure and ASD. Distributed lag non-linear models (DLNM) were used to examine the effects of single-pollutant exposure by prenatal week. Sensitivity analyses were conducted to assess the impact of exposure period on the observed findings. The final sample included 1589 ASD cases and 7563 controls. Compared to controls, cases were more likely to be born to mothers living in urban areas, delivered by Caesarean section, and assigned male sex at birth. NO was a consistent and significant contributor to ASD risk after accounting for co-exposure to O, PM and covariates. The odds ratio per interquartile range increase was 2.1 (95%CI 1.8-2.3) pre-conception, 2.2 (2.0-2.5) for the 1st trimester, 2.2 (1.9-2.5) for the 2nd trimester, and 2.1 (1.9-2.4) for the 3rd trimester. In contrast, findings for O and PM with ASD were inconsistent. Findings from DLNM and sensitivity analyses were similar. Exposure to NO before and during pregnancy was significantly associated with ASD in offspring. The relationship between prenatal O and PM exposure and ASD remains unclear. Further investigation into the combined effects of multi-pollutant exposure on child neurodevelopment is warranted.
母亲在妊娠期暴露于环境空气污染物与后代自闭症谱系障碍(ASD)风险之间的关联方向和程度尚不清楚。我们试图评估产前空气污染物暴露对 ASD 的时变影响。我们对 2012 年 4 月 1 日至 2016 年 12 月 31 日期间在加拿大安大略省出生的单胎足月儿童进行了一项匹配病例对照研究。省级出生登记处的数据与应用行为分析服务和环境空气污染物数据集相链接,以确定产前接触二氧化氮(NO)、地面臭氧(O)、细颗粒物(PM)和 ASD 诊断。通过粗化精确匹配来建立病例和对照之间的协变量平衡。使用条件逻辑回归评估产前空气污染物暴露与 ASD 之间的关联。分布式滞后非线性模型(DLNM)用于检查产前周单一污染物暴露的影响。进行敏感性分析以评估暴露期对观察到的结果的影响。最终样本包括 1589 例 ASD 病例和 7563 例对照。与对照组相比,病例组的母亲更有可能居住在城市地区、剖腹产分娩和出生时为男性。在考虑到与 O、PM 和协变量的共同暴露后,NO 是 ASD 风险的一个一致且显著的因素。每个四分位距增加的比值比为 2.1(95%CI 1.8-2.3)在受孕前,第 1 孕期为 2.2(2.0-2.5),第 2 孕期为 2.2(1.9-2.5),第 3 孕期为 2.1(1.9-2.4)。相比之下,O 和 PM 与 ASD 的相关性不一致。DLNM 和敏感性分析的结果相似。妊娠前和妊娠期间接触 NO 与后代 ASD 显著相关。产前 O 和 PM 暴露与 ASD 之间的关系尚不清楚。需要进一步研究多污染物暴露对儿童神经发育的综合影响。