英国生物数据库中以核磁共振成像测量的脑容量为中介的空气污染与痴呆症发病率之间的纵向联系

IF 10.3 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Rhiannon Thompson, Xinning Tong, Xueyi Shen, Jinjun Ran, Shengzhi Sun, Xiaoxin Iris Yao, Chen Shen
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引用次数: 0

摘要

背景虽然越来越多的证据表明环境暴露与神经退行性疾病的风险有关,但评估人类潜在介质的机理证据仍然有限。方法英国生物数据库是一项大型长期研究,从 2006 年到 2010 年共招募了 50 万名 40-69 岁的成年人。通过健康记录链接确定了截至 2022 年的痴呆病例 ICD-10 分类报告(阿尔茨海默病、血管性痴呆、其他分类疾病中的痴呆和未指定痴呆)。住宅空气污染、交通噪音和绿地暴露的估计值已被模拟出来。在 2014 年至 2022 年期间进行了脑结构磁共振成像,事先确定了与痴呆症相关的脑容量。使用线性回归和逻辑回归检验了环境暴露、脑容量和痴呆症病例(核磁共振成像后诊断)之间的关联,并对年龄、性别、家庭收入、种族、教育、吸烟和地区贫困程度进行了调整。使用准贝叶斯蒙特卡洛法(N = 34,817-39,772 例)模拟了可信脑容量(与环境暴露和痴呆症结果均相关的脑容量)对暴露-结果关联的中介作用。结果观察到,PM2.5abs暴露与痴呆症风险之间存在微小但显著的中介效应(2%-8%的中介关系)。在提供脑成像数据的队列子集中,绿地和噪声与痴呆症结果无关。我们的研究结果提供了新的证据,证明脑容量的差异可能是这些关系的中介。未来的研究需要证明这一机制,并确定暴露于空气污染可能增加痴呆症风险的其他机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Longitudinal associations between air pollution and incident dementia as mediated by MRI-measured brain volumes in the UK Biobank

Longitudinal associations between air pollution and incident dementia as mediated by MRI-measured brain volumes in the UK Biobank

Background

Although there is increasing evidence that environmental exposures are associated with the risk of neurodegenerative conditions, there is still limited mechanistic evidence evaluating potential mediators in human populations.

Methods

UK Biobank is a large long-term study of 500,000 adults enrolled from 2006 to 2010 age 40–69 years. ICD-10 classified reports of dementia cases up to 2022 (Alzheimer’s disease, vascular dementia, dementia in other classified diseases, and unspecified dementia) were identified from health record linkage. Estimates of residential air pollution, traffic noise, and greenspace exposure have been modelled. Structural brain MRI was conducted from 2014 to 2022, with brain volumes relevant to dementia identified a priori. Associations between environmental exposures, brain volumes, and dementia cases (diagnosed post-MRI) were tested using linear and logistic regression and adjusted for age, sex, household income, ethnicity, education, smoking, and area-level deprivation. Mediation of exposure-outcome associations by plausible brain volumes (those associated with both environmental exposure and dementia outcomes) were modelled using the quasi-Bayesian Monte Carlo method (N = 34,817–39,772).

Results

Small but significant mediating effects (2%-8% of relationships mediated) were observed between PM2.5abs exposure and dementia risk by reduced total brain volume, NOx and Alzheimer’s disease risk by reduced peripheral cortical grey matter, PM2.5abs and vascular dementia risk by reduced peripheral cortical grey matter, PM2.5abs and other dementia risk by reduced total grey matter, and PM10 and other dementia risk by reduced total grey matter. Greenspace and noise were not associated with dementia outcomes in the subset of the cohort providing brain imaging data.

Conclusions

This study adds to existing evidence of associations between environmental exposures and dementia outcomes. Our findings provide novel evidence that differences in brain volume may mediate these relationships. Future research is required to prove this mechanism and establish the other mechanisms through which exposure to air pollution might increase dementia risk.
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来源期刊
Environment International
Environment International 环境科学-环境科学
CiteScore
21.90
自引率
3.40%
发文量
734
审稿时长
2.8 months
期刊介绍: Environmental Health publishes manuscripts focusing on critical aspects of environmental and occupational medicine, including studies in toxicology and epidemiology, to illuminate the human health implications of exposure to environmental hazards. The journal adopts an open-access model and practices open peer review. It caters to scientists and practitioners across all environmental science domains, directly or indirectly impacting human health and well-being. With a commitment to enhancing the prevention of environmentally-related health risks, Environmental Health serves as a public health journal for the community and scientists engaged in matters of public health significance concerning the environment.
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