Canning Thomas, Arias-de la Torre Jorge, Fisher Helen L, Gulliver John, Hansell Anna L, Hardy Rebecca, Hatch Stephani L, Mudway Ian S, Ronaldson Amy, Cartlidge Molly, James Sarah-Naomi, Keuss Sarah E, Schott Jonathan M, Richards Marcus, Bakolis Ioannis
Department of Biostatistics and Health Informatics, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; Health Service and Population Research Department, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Health Service and Population Research Department, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; CIBER Epidemiology and Public Health, Madrid, Spain; Institute of Biomedicine, University of Leon, Leon, Spain; Care in Long Term Conditions Research Division, Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King's College London, London, UK.
Lancet Healthy Longev. 2025 Jul 16:100724. doi: 10.1016/j.lanhl.2025.100724.
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.
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 (NO; ages 45-64 years); particulate matter with diameter less than 10 μm (PM; ages 55-64 years); and nitrogen oxides (NO) and particulate matter with diameters less than 2·5 μm (PM) and between 2·5 μm and less than 10 μm (PM) and particulate matter absorbance (PMabs) 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.
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 NO and PM was associated with slower processing speed between the ages of 43 years and 69 years (NO β -8·121 [95% CI -10·338 to -5·905 per IQR increase in exposure]; PM 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, NO β -0·589 [-0·921 to -0·257]). Higher exposure to NO was associated with smaller hippocampal volume (β -0·088 [-0·172 to -0·004]) and higher exposure to NO and PM was associated with larger ventricular volume (NO β 2·259 [0·457 to 4·061]; PM β 1·841 [0·013 to 3·669]) at age 69-71 years.
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.
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.
以往研究表明,老年人接触空气污染程度越高,认知障碍风险越高。我们旨在通过纳入整个生命历程中的暴露情况,以及对中年至老年参与者的认知和脑结构成像测量,来扩展该领域的现有证据。
在这项基于人群的研究中,我们使用了医学研究理事会全国健康与发展调查(NSHD,也称为1946年英国出生队列)的数据,以及NSHD的一项神经影像学子研究Insight 46的数据。参与者于1946年3月的单一周内出生后招募。我们的目标是评估中年(45 - 64岁)接触空气污染物是否与43岁至69岁之间较差的处理速度和较差的言语记忆有关,以及接触是否与69 - 71岁时较差的认知状态和脑结构结果有关。空气污染暴露数据包括二氧化氮(NO;45 - 64岁);直径小于10μm的颗粒物(PM;55 - 64岁);氮氧化物(NO)和直径小于2.5μm的颗粒物(PM)以及直径在2.5μm至小于10μm之间的颗粒物(PM)和颗粒物吸光度(PMabs)作为黑碳吸收的指标(60 - 64岁),并对早年接触黑烟和二氧化硫进行了调整。在43、53、60 - 64和69岁时,通过15项回忆任务测试言语记忆,通过视觉搜索任务测试处理速度。在69岁时进行Addenbrooke认知检查III(ACE - III)以测量认知状态。在69 - 71岁时通过MRI评估全脑、脑室、海马和白质高信号体积。使用广义线性模型和广义混合线性模型来探索污染暴露、认知测量和脑结构结果之间的关联,并对包括吸烟状况和邻里贫困在内的社会人口学因素进行了调整。
在43岁至69岁之间,我们将1534名NSHD参与者纳入言语记忆和处理速度分析。在2015 - 16年随访期间接受测试的2148名参与者中,69岁时,1761名被纳入ACE - III分析。在招募到Insight 46子研究中的502名NSHD参与者中,453名被纳入分析。在43岁至69岁之间,较高的NO和PM暴露与较慢的处理速度相关(NO β -8.121 [95% CI -10.338至 -5.905,暴露每增加一个四分位数间距];PM β -4.518 [-6.680至 -2.357])。在69岁时,所有测试污染物的较高暴露与较低的ACE - III得分相关(例如,NO β -0.589 [-0.921至 -0.257])。在69 - 71岁时,较高的NO暴露与较小的海马体积相关(β -0.088 [-0.172至 -0.004]),较高的NO和PM暴露与较大的脑室体积相关(NO β 2.259 [0.457至4.061];PM β 1.841 [0.013至3.669])。
认识到早年暴露可能产生的影响,中年至老年期间较高的二氧化氮、氮氧化物和粗颗粒物暴露与较差的认知、处理速度和脑结构结果相关,这进一步证明了空气污染对老年人脑功能的不利影响。
国家健康与照护研究机构、医学研究理事会(MRC)、英国阿尔茨海默病研究协会、阿尔茨海默病协会、MRC英国痴呆症平台以及英国脑研究协会。