Smog, sugar, and synapses: Unraveling the PM2.5-insulin resistance-Alzheimer’s disease axis

Chronic exposure to fine particulate matter (PM2.5) and insulin resistance (IR) are each linked to Alzheimer's disease (AD), but IR has not been systematically positioned as a mechanistic conduit through which PM2.5 heightens AD vulnerability. Drawing on epidemiological, animal, and cellular studies, this review outlines converging pathways along a PM2.5-IR-AD axis: chronic neuroinflammation, oxidative stress and mitochondrial dysfunction, blood-brain barrier disruption, and impaired amyloid-β (Aβ) clearance. Across sections, study-specific limitations are comprehensively discussed. Positioning IR as a central node linking PM2.5 exposure to AD reframes air pollution as a modifiable metabolic-neurologic risk. Potential therapeutic and preventive avenues are also highlighted. Future work could prioritize longitudinal and interventional studies that directly interrogate the PM2.5-IR-AD triad and refine biomarkers to guide precision prevention.

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Publication Details

Journal
Redox Biology
Published
2026-01-14
DOI
https://doi.org/10.1016/j.redox.2026.104031
Citations
1
Primary Topic
Air Quality and Health Impacts
Type
article
Field-Weighted Citation Impact
31.09
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article

Smog, sugar, and synapses: Unraveling the PM2.5-insulin resistance-Alzheimer’s disease axis

Lai Chih-Ho, Chia-Lin Wu, Hsuan-Yu Huang, Yu-Yin Huang et al.
1 citations
Redox Biology
Air Quality and Health Impacts
31.09
article

Smog, sugar, and synapses: Unraveling the PM2.5-insulin resistance-Alzheimer’s disease axis

Lai Chih-Ho, Chia-Lin Wu, Hsuan-Yu Huang, Yu-Yin Huang, Wei-Chien Huang
article en
1 citations

Abstract

Chronic exposure to fine particulate matter (PM2.5) and insulin resistance (IR) are each linked to Alzheimer's disease (AD), but IR has not been systematically positioned as a mechanistic conduit through which PM2.5 heightens AD vulnerability. Drawing on epidemiological, animal, and cellular studies, this review outlines converging pathways along a PM2.5-IR-AD axis: chronic neuroinflammation, oxidative stress and mitochondrial dysfunction, blood-brain barrier disruption, and impaired amyloid-β (Aβ) clearance. Across sections, study-specific limitations are comprehensively discussed. Positioning IR as a central node linking PM2.5 exposure to AD reframes air pollution as a modifiable metabolic-neurologic risk. Potential therapeutic and preventive avenues are also highlighted. Future work could prioritize longitudinal and interventional studies that directly interrogate the PM2.5-IR-AD triad and refine biomarkers to guide precision prevention.

Redox BiologyVol. 90
Chang Gung University (TW), China Medical University (TW), Chang Gung Memorial Hospital (TW), China Medical University Hospital (TW)
Good health and well-being
Openalex Percentile: Top 2%
Air Quality and Health Impacts
31.09
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