Associations between life course exposure to ambient air pollution with cognition and later-life brain structure: a population-based study of the 1946 British Birth Cohort.

IF 13.4 Q1 GERIATRICS & GERONTOLOGY
Thomas Canning, Jorge Arias-de la Torre, Helen L Fisher, John Gulliver, Anna L Hansell, Rebecca Hardy, Stephani L Hatch, Ian S Mudway, Amy Ronaldson, Molly Cartlidge, Sarah-Naomi James, Sarah E Keuss, Jonathan M Schott, Marcus Richards, Ioannis Bakolis
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引用次数: 0

Abstract

Background: Previous research has linked higher exposure to air pollution to increased cognitive impairment at older ages. We aimed to extend the existing evidence in this area by incorporating exposures across the life course in addition to measures of cognition and brain structural imaging in participants at midlife to older age.

Methods: For this population-based study, we used data from the Medical Research Council National Survey of Health and Development (NSHD; also known as the 1946 British Birth Cohort) and a neuroimaging substudy of the NSHD known as Insight 46. Participants were recruited after birth in a single week during March, 1946. Our objectives were to assess whether exposure to air pollutants in midlife (age 45-64 years) was associated with poorer processing speed and poorer verbal memory between the ages of 43 years and 69 years, and whether exposures were associated with poorer cognitive state and brain structure outcomes at age 69-71 years. Air pollution exposure data were available for nitrogen dioxide (NO2; ages 45-64 years); particulate matter with diameter less than 10 μm (PM10; ages 55-64 years); and nitrogen oxides (NOx) and particulate matter with diameters less than 2·5 μm (PM2·5) and between 2·5 μm and less than 10 μm (PMcoarse) and particulate matter absorbance (PM2·5abs) as a measure of black carbon absorption (ages 60-64 years), with adjustments for early-life exposures to black smoke and sulphur dioxide. Verbal memory was tested with a 15-item recall task and processing speed with a visual search task at ages 43, 53, 60-64, and 69 years. The Addenbrooke's Cognitive Examination III (ACE-III), a measure of cognitive state, was conducted at age 69 years. Whole-brain, ventricular, hippocampal, and white matter hyperintensity volumes were assessed by MRI at age 69-71 years. Generalised linear models and generalised mixed linear models were used to explore associations between pollution exposure, cognitive measures, and brain structural outcomes, adjusted for sociodemographic factors including smoking status and neighbourhood deprivation.

Findings: Between the ages of 43 years and 69 years, we included 1534 NSHD participants in the verbal memory and processing speed analysis. Of 2148 participants who underwent testing during the wave of follow-up in 2015-16, at age 69 years, 1761 were included in the ACE-III analysis. Of the 502 NSHD participants recruited into the Insight 46 substudy, 453 were included in the analysis. Higher exposure to NO2 and PM10 was associated with slower processing speed between the ages of 43 years and 69 years (NO2 β -8·121 [95% CI -10·338 to -5·905 per IQR increase in exposure]; PM10 β -4·518 [-6·680 to -2·357]). Higher exposure to all tested pollutants was associated with lower ACE-III score at age 69 years (eg, NO2 β -0·589 [-0·921 to -0·257]). Higher exposure to NOx was associated with smaller hippocampal volume (β -0·088 [-0·172 to -0·004]) and higher exposure to NO2 and PM10 was associated with larger ventricular volume (NO2 β 2·259 [0·457 to 4·061]; PM10 β 1·841 [0·013 to 3·669]) at age 69-71 years.

Interpretation: Acknowledging the probable effects of exposure early in life, higher exposure to nitrogen dioxide, nitrogen oxides, and coarse particulate matter in midlife to older age was associated with poorer cognition, processing speed, and brain structural outcomes, strengthening evidence for the adverse effects of air pollution on brain function in older age.

Funding: The National Institute for Health and Care Research, the Medical Research Council (MRC), Alzheimer's Research UK, the Alzheimer's Association, MRC Dementias Platform UK, and Brain Research UK.

生命过程中暴露于环境空气污染与认知和晚年大脑结构之间的关系:一项基于1946年英国出生队列的人口研究。
背景:之前的研究表明,暴露在空气污染中的时间越长,老年人的认知障碍就越严重。我们的目标是扩展这一领域的现有证据,除了对中年至老年参与者的认知和脑结构成像测量外,还纳入了整个生命过程中的暴露。方法:在这项基于人群的研究中,我们使用了医学研究委员会国家健康与发展调查(NSHD;也被称为1946年英国出生队列)和NSHD的神经影像学亚研究,被称为洞察46。参与者在1946年3月出生后的一个星期内被招募。我们的目的是评估中年(45-64岁)暴露于空气污染物是否与43岁至69岁期间较差的处理速度和较差的言语记忆有关,以及暴露于空气污染物是否与69-71岁时较差的认知状态和大脑结构结果有关。二氧化氮(NO2)的空气污染暴露数据;年龄45-64岁);直径小于10 μm的颗粒物(PM10);年龄55-64岁);氮氧化物(NOx)和直径小于2.5 μm的颗粒物(pmm2·5)和直径在2.5 μm至小于10 μm之间的颗粒物(pm粗)以及颗粒物吸光度(pmm2·5abs)作为黑碳吸收(60-64岁)的指标,并根据早期暴露于黑烟和二氧化硫进行调整。在43岁、53岁、60-64岁和69岁的人群中,通过15项回忆任务和视觉搜索任务的处理速度测试了言语记忆。阿登布鲁克认知测验III (ACE-III),一种认知状态的测量,在69岁时进行。在69-71岁时,通过MRI评估全脑、心室、海马和白质高强度体积。使用广义线性模型和广义混合线性模型来探索污染暴露、认知测量和大脑结构结果之间的关系,并根据吸烟状况和邻里剥夺等社会人口因素进行了调整。结果:在43岁至69岁之间,我们纳入了1534名NSHD参与者进行言语记忆和处理速度分析。在2015-16年随访期间接受检测的2148名参与者中,年龄为69岁,其中1761人被纳入ACE-III分析。在Insight 46子研究中招募的502名NSHD参与者中,有453人被纳入分析。较高的NO2和PM10暴露与43岁至69岁之间的加工速度较慢相关(NO2 β -8·121 [95% CI -10·338至-5·905 / IQR暴露增加);PM10 β - 4,518[- 6,680至- 2,357])。在69岁时,暴露于所有测试污染物的水平越高,ACE-III评分越低(例如,NO2 β - 0.589[- 0.921至- 0.257])。较高的NOx暴露与较小的海马体积相关(β - 0.088[- 0.172至- 0.004]),较高的NO2和PM10暴露与较大的心室体积相关(NO2 β 2.259[0.457至4.061];PM10 β为1·841[0·013 ~ 3·669],年龄为69 ~ 71岁。解释:考虑到生命早期接触二氧化氮、氮氧化物和粗颗粒物质的可能影响,中年到老年接触高浓度二氧化氮、氮氧化物和粗颗粒物质与较差的认知能力、处理速度和大脑结构结果相关,这加强了空气污染对老年大脑功能不利影响的证据。资助:国家健康与护理研究所、医学研究委员会(MRC)、英国阿尔茨海默氏症研究所、阿尔茨海默氏症协会、英国MRC痴呆症平台和英国大脑研究所。
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来源期刊
Lancet Healthy Longevity
Lancet Healthy Longevity GERIATRICS & GERONTOLOGY-
CiteScore
16.30
自引率
2.30%
发文量
192
审稿时长
12 weeks
期刊介绍: The Lancet Healthy Longevity, a gold open-access journal, focuses on clinically-relevant longevity and healthy aging research. It covers early-stage clinical research on aging mechanisms, epidemiological studies, and societal research on changing populations. The journal includes clinical trials across disciplines, particularly in gerontology and age-specific clinical guidelines. In line with the Lancet family tradition, it advocates for the rights of all to healthy lives, emphasizing original research likely to impact clinical practice or thinking. Clinical and policy reviews also contribute to shaping the discourse in this rapidly growing discipline.
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