青少年早期的空气污染暴露、前额叶连通性与情绪行为

Air Pollution Exposure, Prefrontal Connectivity, and Emotional Behavior in Early Adolescence.

作者信息

Herting M M, Burnor E, Ahmadi H, Eckel S P, Gauderman W, Schwartz J, Berhane K, McConnell R, Chen J-C

机构信息

University of Southern California, Los Angeles, California, USA.

Harvard University, Cambridge, Massachusetts, USA.

出版信息

Res Rep Health Eff Inst. 2025 Mar(225):1-56.

DOI:
Abstract

INTRODUCTION

Emerging evidence suggests that ambient air pollution may affect the developing brain and contribute to an increased risk of mental health problems. However, most studies have focused on prenatal or early postnatal periods of exposure, with less attention given to the dynamic neurodevelopment period of early adolescence. Moving forward, it is necessary to consider additional periods of exposure, such as adolescence, and the biological mechanisms that may drive potential neurotoxicological effects. This project aimed to investigate whether 1-year exposure to ambient fine particulate matter (PM) and nitrogen dioxide (NO) at 9-10 years of age was associated with (1) concurrent prefrontal white matter connectivity at ages 9-10 years and (2) emotional health problems at ages 9-10 years as well as 1 year later. Lastly, we hypothesized that poor prefrontal white matter connectivity might be an intermediate marker (i.e., mediator) for the association between 1-year ambient exposure and mental health outcomes.

METHODS

We leveraged data from the multisite, nationwide Adolescent Brain Cognitive Development Study (ABCD Study; N = 11,880), with cross-sectional data on diffusion-weighted imaging at 9-10 years (baseline visit) and longitudinal emotional health outcomes at 9-10 (baseline visit) and 10-11 years (1-year follow-up). Based on residential addresses at ages 9-10 years, novel hybrid spatiotemporal exposure models were applied to estimate 1-year average ambient exposure to PM and NO. Diffusion tensor imaging (DTI) was used to measure white matter microstructure in tracts that innervate the prefrontal cortex. Emotional behavioral problems were measured based on caregiver reports using the Child Behavioral Checklist (CBCL). Mixed-effect two-pollutant models were fit using both PM and NO and adjusted for the study site, several potential sociodemographic and lifestyle characteristics, and magnetic resonance imaging (MRI) precision variables when necessary. For emotional health outcomes, longitudinal models included interaction terms for pollutant-by-time for both pollutants. Sensitivity analyses were conducted that also accounted for the number of years the child resided at the residential address, as well as adjusting for prenatal PM and NO exposures.

RESULTS

The final analytic sample included 7,546 participants with DTI data and 9,334 participants with emotional behavior data. The annual exposures to PM and NO across 21 study sites were 7.66 μg/m [1.72-15.90 μg/m] and 18.61 ppb [0.73-37.94 ppb], respectively. Annual exposure to PM was found to be significantly related to prefrontal structural connectivity, including fractional anisotropy (FA) in the right superior longitudinal fasciculus and widespread differences in mean diffusivity (MD) in the corpus callosum, bilateral uncinate fasciculus, left cingulum-hippocampal region, left anterior thalamic radiation, and left superior longitudinal fasciculus. The observed associations between PM and MD were negative and nonlinear, with greater decreases in MD seen at higher exposure levels. Annual exposure to NO was found to have significant, negative linear associations with FA in the right anterior thalamic radiation, left uncinate fasciculus, and corpus callosum. In terms of emotional behavior, 1-year PM annual exposure was related to slightly less internalizing, anxiety/depression, and aggression problems at the 1-year follow-up. Similarly, 1-year NO annual exposure was related to slightly less internalizing and total problems at the 1-year follow-up. Although some of these associations were statistically significant, small parameter estimates suggest these noted effects on emotional outcomes may not be of clinical importance. Given the later findings, the required conditions to test mediation formally were not met.

CONCLUSIONS

Our analyses indicate that white matter microstructure is uniquely associated with annual exposure to PM and NO at ages 9-10 years. Against our hypotheses, annual exposure was not related to more emotional problems at ages 9-10 years or after a 1-year follow-up period. These findings suggest air pollution exposure levels below US national ambient air quality standards may have important implications for child white matter development and add to the literature suggesting neurotoxicity at low exposure levels of air pollution may be critical to include in the continuing review and risk assessment for the National Ambient Air Quality Standard.

摘要

引言

新出现的证据表明,环境空气污染可能会影响发育中的大脑,并增加心理健康问题的风险。然而,大多数研究都集中在产前或产后早期暴露阶段,而对青春期早期这一动态神经发育阶段的关注较少。展望未来,有必要考虑其他暴露阶段,如青春期,以及可能驱动潜在神经毒理学效应的生物学机制。本项目旨在研究9至10岁儿童暴露于环境细颗粒物(PM)和二氧化氮(NO)1年是否与以下因素相关:(1)9至10岁时的前额叶白质连接性;(2)9至10岁以及1年后的情绪健康问题。最后,我们假设前额叶白质连接性差可能是1年环境暴露与心理健康结果之间关联的一个中间标志物(即中介物)。

方法

我们利用了多地点、全国性的青少年大脑认知发展研究(ABCD研究;N = 11,880)的数据,该研究包含9至10岁(基线访视)的扩散加权成像横断面数据以及9至10岁(基线访视)和10至11岁(1年随访)的纵向情绪健康结果数据。根据9至10岁时的居住地址,应用新型混合时空暴露模型来估计1年的PM和NO环境平均暴露量。扩散张量成像(DTI)用于测量支配前额叶皮质的神经束中的白质微观结构。情绪行为问题基于照顾者使用儿童行为清单(CBCL)的报告进行测量。使用PM和NO拟合混合效应双污染物模型,并在必要时针对研究地点、一些潜在的社会人口统计学和生活方式特征以及磁共振成像(MRI)精度变量进行调整。对于情绪健康结果,纵向模型包括两种污染物的污染物-时间交互项。进行了敏感性分析,该分析还考虑了儿童在居住地址居住的年数,并对产前PM和NO暴露进行了调整。

结果

最终分析样本包括7546名有DTI数据的参与者和9334名有情绪行为数据的参与者。21个研究地点的PM和NO年暴露量分别为7.66 μg/m [1.72 - 15.90 μg/m]和18.61 ppb [0.73 - 37.94 ppb]。发现PM年暴露量与前额叶结构连接性显著相关,包括右上纵束中的分数各向异性(FA)以及胼胝体、双侧钩束、左扣带回-海马区、左丘脑前辐射和左上纵束中平均扩散率(MD)的广泛差异。观察到的PM与MD之间的关联为负且呈非线性,在较高暴露水平下MD的下降幅度更大。发现NO年暴露量与右丘脑前辐射、左钩束和胼胝体中的FA存在显著的负线性关联。在情绪行为方面,1年的PM年暴露量与1年随访时内化、焦虑/抑郁和攻击问题略少相关。同样,1年的NO年暴露量与1年随访时内化和总问题略少相关。尽管其中一些关联具有统计学意义,但小参数估计表明这些对情绪结果的显著影响可能不具有临床重要性。鉴于后续发现,未满足正式检验中介作用的必要条件。

结论

我们的分析表明,白质微观结构与9至10岁儿童每年暴露于PM和NO存在独特关联。与我们的假设相反,每年的暴露与9至10岁或1年随访后的更多情绪问题无关。这些发现表明,低于美国国家环境空气质量标准的空气污染暴露水平可能对儿童白质发育具有重要影响,并补充了相关文献,表明低水平空气污染的神经毒性可能对国家环境空气质量标准的持续审查和风险评估至关重要。

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