Fine Particulate Matter and Markers of Alzheimer's Disease Neuropathology at Autopsy in a Community-Based Cohort

被引:16
作者
Shaffer, Rachel M. [1 ]
Li, Ge [2 ,3 ,4 ]
Adar, Sara D. [5 ]
Keene, C. Dirk [6 ]
Latimer, Caitlin S. [6 ]
Crane, Paul K. [7 ]
Larson, Eric B. [7 ,8 ]
Kaufman, Joel D. [1 ,9 ]
Carone, Marco [10 ]
Sheppard, Lianne [1 ,10 ]
机构
[1] Univ Washington, Dept Environm & Occupat Hlth Sci, Sch Publ Hlth, Seattle, WA USA
[2] VA Puget Sound Hlth Care Syst, VA Northwest Network Mental Illness Res Educ & Cl, Seattle, WA USA
[3] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[4] VA Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA
[5] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[6] Univ Washington, Dept Lab Med & Pathol, Div Neuropathol, Seattle, WA USA
[7] Univ Washington, Sch Med, Seattle, WA USA
[8] Kaiser Permanente Washington Hlth Res Inst, Seattle, WA USA
[9] Univ Washington, Dept Med, Sch Publ Hlth, Seattle, WA USA
[10] Univ Washington, Dept Biostat, Sch Publ Hlth, Seattle, WA USA
关键词
Air pollution; Alzheimer's disease; autopsy; dementia; neuropathology; particulate matter; BODY-MASS INDEX; AMBIENT AIR-POLLUTION; NATIONAL INSTITUTE; AMYLOID-BETA; ASSOCIATION GUIDELINES; PATHOLOGICAL PROCESS; COGNITIVE FUNCTION; NEURITIC PLAQUES; SELECTION BIAS; BLOOD-PRESSURE;
D O I
10.3233/JAD-201005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Evidence links fine particulate matter (PM2.5) to Alzheimer's disease (AD), but no community-based prospective cohort studies in older adults have evaluated the association between long-term exposure to PM2.5 and markers of AD neuropathology at autopsy. Objective: Using a well-established autopsy cohort and new spatiotemporal predictions of air pollution, we evaluated associations of 10-year PM2.5 exposure prior to death with Braak stage, Consortium to Establish a Registry for AD (CERAD) score, and combined AD neuropathologic change (ABC score). Methods: We used autopsy specimens (N = 832) from the Adult Changes in Thought (ACT) study, with enrollment ongoing since 1994. We assigned long-term exposure at residential address based on two-week average concentrations from a newly developed spatiotemporal model. To account for potential selection bias, we conducted inverse probability weighting. Adjusting for covariates with tiered models, we performed ordinal regression for Braak and CERAD and logistic regression for dichotomized ABC score. Results: 10-year average (SD) PM2.5 from death across the autopsy cohort was 8.2 (1.9) mu g/m(3). Average age (SD) at death was 89 (7) years. Each 1 mu g/m(3) increase in 10-year average PM2.5 prior to death was associated with a suggestive increase in the odds of worse neuropathology as indicated by CERAD score (OR: 1.35 (0.90, 1.90)) but a suggestive decreased odds of neuropathology as defined by the ABC score (OR: 0.79 (0.49, 1.19)). There was no association with Braak stage (OR: 0.99 (0.64, 1.47)). Conclusion: We report inconclusive associations between PM2.5 and AD neuropathology at autopsy among a cohort where 94% of individuals experienced 10-year exposures below the current EPA standard. Prior studies of AD risk factors and AD neuropathology are similarly inconclusive, suggesting alternative mechanistic pathways for disease or residual confounding.
引用
收藏
页码:1761 / 1773
页数:13
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