TY - JOUR
T1 - The hidden infectious disease-related sepsis risk of wildfire-specific PM2.5
AU - Mahendran, Rahini
AU - Xu, Rongbin
AU - Zhang, Lei
AU - Ye, Tingting
AU - Zhang, Yiwen
AU - Xu, Zhihu
AU - Huang, Wenzhong
AU - Yang, Zhengyu
AU - Abramson, Michael J.
AU - Johnston, Fay H.
AU - Knibbs, Luke
AU - Hales, Simon
AU - Lavigne, Eric
AU - Yu, Pei
AU - Liu, Yanming
AU - Coelho, Micheline SZS
AU - Saldiva, Paulo HN
AU - Matus, Patricia
AU - Wen, Bo
AU - Wu, Yao
AU - Tantrakarnapa, Kraichat
AU - Kliengchuay, Wissanupong
AU - Marks, Guy
AU - Morawska, Lidia
AU - Yu, Wenhua
AU - Ju, Ke
AU - Zhou, Shuang
AU - Chen, Gongbo
AU - Heyworth, Jane
AU - Morgan, Geoffrey
AU - Guo, Yue Leon
AU - Li, Shanshan
AU - Guo, Yuming
N1 - Publisher Copyright:
© 2026 The Authors
PY - 2026/9/15
Y1 - 2026/9/15
N2 - Wildfire smoke is a major source of fine particulate matter (PM2.5) and may increase vulnerability to severe infectious outcomes such as sepsis, a condition responsible for an estimated 49 million cases and 11 million deaths annually. Despite this global burden, to our knowledge, no prior epidemiological study has specifically examined the association between wildfire-specific PM2.5 exposure and infectious disease-related sepsis. We conducted a multi-country time-series analysis across 1024 communities in seven countries/territories (2000–2019). Daily hospitalizations for infectious disease-related sepsis were identified using ICD-10 codes, restricted to explicit sepsis diagnoses. Wildfire-specific PM2.5 was estimated using the GEOS-Chem chemical transport model combined with machine learning calibration and linked to hospitalization data. Associations between wildfire-specific PM2.5 and sepsis hospitalizations were estimated using quasi-Poisson regression with distributed lag non-linear models over lag 0–7 days. Community-specific estimates were pooled using random-effects meta-analysis. Across all communities, we identified 2.3 million infectious disease-related sepsis hospitalizations, with the highest burden among older adults and in Brazil. Each 10 μg/m3 increase in wildfire-specific PM2.5 was associated with a 1.5% increase in sepsis hospitalizations (Relative Risk [RR]: 1.015, 95% Confidence Interval [CI]: 1.007–1.024), nearly double the effect of non-wildfire PM2.5 (0.8%). Strongest associations were found among children aged <5 years (RR: 1.063, 95%CI: 1.029–1.097) and those aged 5–19 years (1.093, 1.050–1.138), in moderately populated communities, and in New Zealand and Brazil. Sensitivity analyses confirmed the robustness of the findings. Short-term exposure to wildfire-specific PM2.5 was associated with increased risk of hospitalization for infectious disease-related sepsis, particularly greater risks in adolescents and young children. These findings underscore the need of further research to clarify underlying mechanisms and long-term impacts.
AB - Wildfire smoke is a major source of fine particulate matter (PM2.5) and may increase vulnerability to severe infectious outcomes such as sepsis, a condition responsible for an estimated 49 million cases and 11 million deaths annually. Despite this global burden, to our knowledge, no prior epidemiological study has specifically examined the association between wildfire-specific PM2.5 exposure and infectious disease-related sepsis. We conducted a multi-country time-series analysis across 1024 communities in seven countries/territories (2000–2019). Daily hospitalizations for infectious disease-related sepsis were identified using ICD-10 codes, restricted to explicit sepsis diagnoses. Wildfire-specific PM2.5 was estimated using the GEOS-Chem chemical transport model combined with machine learning calibration and linked to hospitalization data. Associations between wildfire-specific PM2.5 and sepsis hospitalizations were estimated using quasi-Poisson regression with distributed lag non-linear models over lag 0–7 days. Community-specific estimates were pooled using random-effects meta-analysis. Across all communities, we identified 2.3 million infectious disease-related sepsis hospitalizations, with the highest burden among older adults and in Brazil. Each 10 μg/m3 increase in wildfire-specific PM2.5 was associated with a 1.5% increase in sepsis hospitalizations (Relative Risk [RR]: 1.015, 95% Confidence Interval [CI]: 1.007–1.024), nearly double the effect of non-wildfire PM2.5 (0.8%). Strongest associations were found among children aged <5 years (RR: 1.063, 95%CI: 1.029–1.097) and those aged 5–19 years (1.093, 1.050–1.138), in moderately populated communities, and in New Zealand and Brazil. Sensitivity analyses confirmed the robustness of the findings. Short-term exposure to wildfire-specific PM2.5 was associated with increased risk of hospitalization for infectious disease-related sepsis, particularly greater risks in adolescents and young children. These findings underscore the need of further research to clarify underlying mechanisms and long-term impacts.
KW - Hospitalization
KW - Infectious disease
KW - Particulate matter
KW - Sepsis
KW - Wildfire air pollution
UR - https://www.scopus.com/pages/publications/105044403420
UR - https://www.mendeley.com/catalogue/20f247fe-cfa0-3c1d-bae5-19b454a44b5c/
U2 - 10.1016/j.envres.2026.125212
DO - 10.1016/j.envres.2026.125212
M3 - Article
AN - SCOPUS:105044403420
SN - 0013-9351
VL - 306
JO - Environmental Research
JF - Environmental Research
M1 - 125212
ER -