Williams Victoria J, Trane Ralph, Sicinski Kamil, Herd Pamela, Engelman Michal, Asthana Sanjay
Division of Geriatrics and Gerontology, Department of Medicine, University of Wisconsin at Madison, School of Medicine and Public Health, Madison, Wisconsin, USA.
Wisconsin Alzheimer's Disease Research Center, University of Wisconsin at Madison, School of Medicine and Public Health, Madison, Wisconsin, USA.
Alzheimers Dement. 2024 Dec;20(12):8263-8278. doi: 10.1002/alz.14216. Epub 2024 Nov 22.
Late-life air pollution exposure is associated with an increased risk for dementia, with this effect exacerbated among apolipoprotein E-4 (ApoE-4) carriers. However, whether midlife occupational exposures likewise influence dementia outcomes, and varies as a function of ApoE-4 status is unknown.
Using data from 3814 participants in the Wisconsin Longitudinal Study (WLS), we employed weighted logistic regression to evaluate associations between midlife occupational respiratory exposures and late-life air pollution on all-cause dementia risk, stratified by ApoE-4 status.
Midlife occupational exposure was associated with increased odds of all-cause dementia preferentially among ApoE-4 noncarriers (odds ratio [OR] = 1.59, p = 0.01), whereas higher late-life urban air pollution exposure was associated with increased dementia risk among ApoE-4 carriers (OR = 1.258, p = 0.029).
Associations between environmental exposures and dementia risk vary based on the timing of exposure and ApoE-4 status. While late-life environmental exposures are associated with dementia among ApoE-4 carriers, for noncarriers midlife environmental exposure confers the greatest risk.
The effect of adult environmental respiratory exposures on subsequent dementia risk varies as a function of both ApoE-4 carrier status and exposure timing. Midlife occupational exposure to respiratory hazards is preferentially associated with increased dementia odds among ApoE-4 noncarriers. Late-life exposure to ambient air pollution is associated with dementia risk, but only among ApoE-4 carriers. While higher exposure to PM increases the risk for dementia, higher exposure to ozone was associated with reduced risk for dementia among ApoE-4 carriers.
晚年暴露于空气污染中与患痴呆症的风险增加有关,这种影响在载脂蛋白E-4(ApoE-4)携带者中更为严重。然而,中年职业暴露是否同样会影响痴呆症的发病结果,以及是否因ApoE-4状态而异尚不清楚。
利用威斯康星纵向研究(WLS)中3814名参与者的数据,我们采用加权逻辑回归来评估中年职业性呼吸道暴露和晚年空气污染与全因痴呆风险之间的关联,并按ApoE-4状态进行分层。
中年职业暴露在ApoE-4非携带者中与全因痴呆症几率增加相关(优势比[OR]=1.59,p=0.01),而晚年城市空气污染暴露较高与ApoE-4携带者患痴呆症风险增加相关(OR=1.258,p=0.029)。
环境暴露与痴呆症风险之间的关联因暴露时间和ApoE-4状态而异。虽然晚年环境暴露与ApoE-4携带者的痴呆症有关,但对于非携带者来说,中年环境暴露带来的风险最大。
成人环境呼吸道暴露对后续痴呆症风险的影响因ApoE-4携带者状态和暴露时间而异。中年职业性接触呼吸道危害物质在ApoE-4非携带者中优先与痴呆症几率增加相关。晚年暴露于环境空气污染与痴呆症风险有关,但仅在ApoE-4携带者中如此。虽然较高的细颗粒物暴露会增加患痴呆症的风险,但较高的臭氧暴露与ApoE-4携带者患痴呆症的风险降低有关。