Joint International Research Laboratory of Environment and Health, Ministry of Education, Department of Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.
Department of Geriatric Medicine, Union Shenzhen Hospital of Huazhong University of Science and Technology, Shenzhen, China.
J Hazard Mater. 2024 Dec 5;480:136498. doi: 10.1016/j.jhazmat.2024.136498. Epub 2024 Nov 13.
Exposure to air pollution has been associated with increased dementia. However, it remains unknown what specific metabolic mechanisms play a role in this relationship. We included 192,300 dementia-free participants from the UK Biobank cohort study. Annual concentrations of air pollution were assessed based on the residential address. Elastic net regression was performed to identify air pollution-related metabolites, and metabolic score was constructed. Cox regression models and covariate balancing generalized propensity scores (CBGPS) regression models were conducted to explore the longitudinal associations between air pollution/metabolic signatures and dementia risk. The underlying mechanisms between air pollution and dementia driven by metabolic signature or specific metabolites were also investigated. A total of 2592 incident dementia cases were documented. We identified the metabolite profiles in response to air pollution exposure, including 87 metabolites for PM, 65 metabolites for PM, 76 metabolites for NO, and 71 metabolites for NO. The air pollution-related metabolic signatures were associated with increased risk of dementia, with hazard ratios (HR) of 1.17 (95 % CI: 1.12, 1.22), 1.06 (95 % CI: 1.02, 1.11), 1.16 (95 % CI: 1.10, 1.21), and 1.17 (95 % CI: 1.12, 1.22) for PM, PM, NO and NO, respectively. The associations persisted using causal models. Metabolic signatures mediated the associations between air pollution exposure and dementia risk, with mediation proportions ranging from 6.57 % to 12.71 %. Additionally, we observed that a metabolite known as free cholesterol in medium VLDL (M-VLDL-FC) played a crucial mediating role. Our study provides novel insights into the metabolic mechanisms linking air pollution exposure to dementia risk.
暴露于空气污染与痴呆症的增加有关。然而,目前尚不清楚哪些特定的代谢机制在这种关系中发挥作用。我们纳入了英国生物库队列研究中的 192300 名无痴呆症的参与者。根据居住地址评估了每年的空气污染浓度。采用弹性网络回归识别与空气污染相关的代谢物,并构建代谢评分。采用 Cox 回归模型和协变量平衡广义倾向评分(CBGPS)回归模型探讨了空气污染/代谢特征与痴呆风险的纵向关联。还研究了代谢特征或特定代谢物驱动的空气污染与痴呆之间的潜在机制。共记录了 2592 例新发痴呆病例。我们确定了对空气污染暴露有反应的代谢物谱,包括 PM 相关的 87 种代谢物、PM 相关的 65 种代谢物、NO 相关的 76 种代谢物和 NO 相关的 71 种代谢物。与空气污染相关的代谢特征与痴呆风险增加相关,PM 的危害比(HR)为 1.17(95%CI:1.12,1.22)、PM 为 1.06(95%CI:1.02,1.11)、NO 为 1.16(95%CI:1.10,1.21)和 NO 为 1.17(95%CI:1.12,1.22)。使用因果模型,这些关联仍然存在。代谢特征介导了空气污染暴露与痴呆风险之间的关联,中介比例范围为 6.57%至 12.71%。此外,我们观察到一种称为中密度脂蛋白(M-VLDL-FC)中的游离胆固醇的代谢物起着至关重要的中介作用。我们的研究为空气污染暴露与痴呆风险之间的代谢机制提供了新的见解。