4.7 Article

Acute effects of personal exposure to fine particulate matter on salivary and urinary biomarkers of inflammation and oxidative stress in healthy adults

期刊

CHEMOSPHERE
卷 272, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.129906

关键词

Fine particulate matter; Biomarker; Saliva; Urine; Inflammation; Oxidative stress

资金

  1. National Key Research and Development Program of China [2016YFC0206202, 2018YFC1313600]
  2. National Natural Science Foundation of China [91543114, 91843302, 91643205]

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By conducting a longitudinal study among 40 healthy adults in Shanghai, China, this research found robust associations of salivary inflammatory markers (e.g., CRP, TNF-alpha) and urinary oxidative stress markers (e.g., 8-iso-PGF(2 alpha)) with short-term PM2.5 exposure. The study identified sub-daily (6-12 hours) and daily (similar to 24 hours) periods as sensitive time windows to detect the responses of salivary and urinary biomarkers, respectively.
Non-invasive bio-samples, such as saliva and urine, are promising tools for assessment of inflammation and oxidative stress biomarkers. Few studies have investigated potential responses of those biomarkers towards short-term PM2.5 exposure. We conducted a longitudinal study with 4 repeated examinations among 40 healthy, nonsmoking adults in Shanghai, China. Personal samplings were performed for PM2.5 exposure assessment. Then, five biomarkers, including C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-alpha), alpha-1 antitrypsin (A1AT) in saliva and 8-Iso-Prostaglanding F-2 alpha (8-iso-PGF(2 alpha)), total antioxidant capacity (TAC) in urine, were measured. We fitted linear mixed-effect models to evaluate short-term effect of personal PM2.5 exposure on salivary and urinary biomarkers, adjusting for potential confounders of meteorology, sociodemographic characteristics and biomarker detection. We also explored sensitive time windows of exposure for different biomarkers. We found robust associations of salivary CRP, TNF-alpha, and urinary 8-iso-PGF(2 alpha) with PM2.5 exposure, and responses of salivary inflammatory markers occurred more acutely than urinary oxidative stress markers. For instance, a 10 mg/m(3) increase in PM2.5 was associated with an elevation of 5.49% (95% CI: 1.17%, 9.99%) in CRP and 7.05% (95% CI: 1.29%, 13.13%) in TNF-alpha both at lag 12 h, and 6.97% (95% CI: 1.33%, 12.92%) in 8-iso-PGF(2 alpha) at lag 01 d. Based on non-invasive samples, this study provided evidence on effect of PM2.5 exposure on responses of systematic inflammation and oxidative stress. Sub-daily (6-12 h) and daily (similar to 24 h) period after PM2.5 exposure might be sensitive time window to detect the responses of salivary (i.e. CRP, TNF) and urinary biomarkers (i.e. 8-iso-PGF(2 alpha)), respectively. (C) 2021 Elsevier Ltd. All rights reserved.

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