Jul 2026· International Journal of Hygiene and Environmental Health· Vol 277, pp. 114877 - 114877· 0 citations· 52 references
Medicine
TL;DR
Firefighters assigned to structure defense had significantly higher increases in PAH metabolites compared to those assigned to wildland firefighting tasks and maximum post-fire concentrations in firefighters also exceeded the BEI for 1-hydroxyprene and trans,trans-muconic acid.
Abstract
Firefighters suppressing wildland urban interface (WUI) fires may be exposed to smoke from burning vegetation as well as structures and vehicles. To better understand firefighters’ internal dose exposures in the WUI environment, 250 firefighters from Southern California were enrolled into the Fire Fighter Cancer Cohort Study (FFCCS) in 2019, providing urine samples at enrollment and post-fire. One-hundred and twenty-five post-fire samples were collected from 89 participants. Samples were analyzed for metal(loid)s and metabolites of polycyclic aromatic hydrocarbons (PAHs), volatile organic compounds (VOCs), and organophosphate esters (OPEs). We assessed the difference between creatinine-corrected urine concentrations for each chemical at enrollment compared with post-fire, controlling for the individual participant. We also compared these concentrations to the general U.S. population concentrations from the National Health and Nutrition Examination Survey (NHANES) and the American Conference of Governmental Industrial Hygienists Biological Exposure Indices (BEIs) when available. All seven PAH and 11 VOC metabolite concentrations increased significantly from enrollment to post-fire. Diphenyl phosphate, antimony, and cadmium also significantly increased from enrollment to post-fire. Maximum post-fire concentrations in firefighters also exceeded the BEI for 1-hydroxyprene and trans,trans-muconic acid (a metabolite of benzene). Firefighters assigned to structure defense had significantly higher increases in PAH metabolites compared to those assigned to wildland firefighting tasks. Personal protective equipment (PPE) usage was not evaluated in this study, but future studies could combine personal sampling with the collection of detailed PPE usage to develop effective practices and decontamination strategies during WUI fire responses.
The results of the total carcinogenic risk for children aged 7–12 years in all schools caused by the presence of PAHs compounds in outdoor environments was acceptable and in some indoor environments, the values at certain schools exceeded the standard threshold of 10− 6-10− 4, indicating potential health risks.
Mohamad Firdaus Ismail, M. F. Fadzil, Nur Atifah binti Mohd Naim et al.· Asian Journal of Atmospheric...· 0 citations
Per/polyfluoroalkyl substance (PFAS) exposure is a serious concern for firefighters, but the contribution of firefighting activities to overall PFAS body burden remains poorly understood. We hypothesized that overlooked novel PFASs may be elevated in firefighter serum after fire suppression activities. We analyzed paired “baseline” (annual checkup) and “postfire” (within 35 h of fire) serum from 33 members of the Tucson Fire Department using high-resolution mass spectrometry. We measured concentrations of 49 PFASs via targeted quantitation and detected 15 in >50% of samples. Concentrations of target analytes were not significantly different between baseline and postfire paired samples. However, branched PFOS isomers and linear PFHxS were significantly elevated compared to the general population. Suspect screening enabled the identification of 26 additional PFASs. Two tentatively identified phosphate-containing PFASs were significantly (p < 0.01) elevated postfire. These chemicals may be associated with exposure to fluorinated aryl phosphate flame retardants or their combustion transformation products during fire response. Several other novel PFASs were detected in baseline and postfire samples, including bis(trifluoromethylsulfonyl)imide (bis-FMeSI). The presence of novel PFASs in serum from firefighters highlights the need for more research into their occurrence in occupationally exposed groups and the general population, exposure sources, and toxicokinetics.
Yanan Chen, N. Perera, S. Beitel et al.· Environmental Science and Te...· 0 citations
Firefighters are routinely exposed to complex mixtures of toxicants during fire suppression, and growing evidence links these exposures to elevated cancer risk. Proteomic profiling provides a sensitive means to detect early molecular alterations associated with such occupational hazards. In this study, we performed a comparative label-free proteomic analysis of paired serum (n = 42) and urine (n = 50) samples collected from firefighters at baseline and within 24 h postfire suppression. We identified and quantified 330 protein groups in serum and 1085 in urine. PLS-DA of total protein abundance showed clear separation between pre- and postexposure samples in both biofluids, indicating exposure-related proteomic changes. Volcano plot analysis further revealed multiple significantly altered proteins in both biofluids, wherein the urine-proteome showed a broader range of differential expressions. Proteins altered in at least 70% of samples were subjected to pathway enrichment analysis, identifying associations with several diseases, including small-cell lung cancer. Protein–protein interaction analysis revealed highly interconnected cancer-related networks involving LAMA4, LAMC1, VWF, and B2M. These findings suggest urine is a sensitive matrix for detecting acute exposure effects, while serum provides complementary systemic information. Integrating both biofluids into NFPA 1582-guided surveillance may enhance occupational health monitoring and support early cancer detection and prevention in firefighters.
Jooyeon Hwang, Zongkai Peng, Amit Singh et al.· Environment & Health· 0 citations
Polycyclic aromatic hydrocarbons (PAHs) are persistent semi-volatile organic contaminants generated mainly during the incomplete combustion of organic materials and petroleum-derived fuels. This study assessed PAH levels in indoor and outdoor air and estimated the associated inhalation health risks in Akpajo, Alesa and Aleto communities of Eleme Local Government Area, Rivers State, Nigeria, an industrially and traffic-influenced area of the Niger Delta. Twelve 24-hour integrated air-sampling conditions were evaluated across three communities, two seasons (dry and wet) and two microenvironments (indoor and outdoor). Airborne particulate-bound PAHs were collected using a high-volume air-sampling approach, solvent-extracted with dichloromethane:n-hexane (1:1, v/v), concentrated and quantified by gas chromatography-mass spectrometry. Method quality control included internal-standard calibration, field and method blanks, duplicate checks, surrogate recovery assessment, blank correction, and limits of detection and quantification. Statistical analysis was based on descriptive statistics, including range, arithmetic mean, pooled congener totals, community means, seasonal means and indoor-outdoor means. Total PAH concentrations ranged from 7.40 µg/m³ in Alesa wet-season indoor air to 30.55 µg/m³ in Aleto dry-season outdoor air. The mean total PAH concentration was highest in Aleto (21.41 µg/m³), followed by Akpajo (11.80 µg/m³) and Alesa (10.39 µg/m³). Dry-season air had a higher mean total PAH concentration (18.18 µg/m³) than wet-season air (10.88 µg/m³), while outdoor air (15.75 µg/m³) exceeded indoor air (13.32 µg/m³). Anthracene, pyrene, benzo(k)fluoranthene, naphthalene, fluorene and phenanthrene were the dominant contributors to the pooled PAH burden. Non-detected high-molecular-weight PAHs were reported as below the method detection limit rather than as true zero values. Screening-level risk assessment showed that children had higher estimated lifetime average daily dose and incremental lifetime carcinogenic risk than adults under the same sampling conditions. The highest child ILCR occurred in Aleto dry-season outdoor air (4.12E-04), while several child-risk estimates exceeded 1.00E-04, indicating potential concern under the assumptions used. The findings indicate measurable PAH contamination, higher dry-season burden and greater screening-level risk estimates for children. Routine monitoring, emission reduction, dust control and targeted public-health communication are recommended.
O. N. Nwidaa, T. Ideriah, O. Bull et al.· Journal of applied chemical...· 0 citations
Prescribed fire releases a complex mixture of volatile and semivolatile organic compounds to the environment. Firefighters are directly exposed to these hazardous mixtures through occupational activities. This study investigated the volatile and semivolatile chemical contamination profile of firefighter protective gear and the effectiveness of laundering as a decontamination strategy. Our results revealed that firefighter gear accumulated a broad spectrum of combustion-derived contaminants, predominantly composed of polycyclic aromatic hydrocarbons and derivatives, phenolic compounds, and aromatic hydrocarbons. Representative compounds identified included toluene, biphenyl, naphthalene, 1-methynaphthalene, 2-methylnaphthalene, acenaphthene, phenol, alkylated phenols, and chlorinated phenols. Quantitative analysis revealed representative combustion-derived compounds at concentrations (mean ± standard deviation, SD) including toluene (0.958 ± 0.293 ng/g), biphenyl (0.015 ± 0.004 ng/g), naphthalene (0.053 ± 0.020 ng/g), 1-methynaphthalene (0.468 ± 0.132 ng/g), 2-methylnaphthalene (0.009 ± 0.002 ng/g), and acenaphthene (0.303 ± 0.001 ng/g). Multivariate analysis showed that although laundering substantially reduced contaminant levels, residues of several compounds remained significantly detectable in washed samples. These results demonstrate that firefighter personal protective equipment (PPE) serves as a reservoir for toxic compounds, underscoring the additional risk of secondary exposure to firefighters through dermal contact, handling, and off-gassing. Together, our findings emphasize the need for the safe transport of protective gear (e.g., in sealed bags), proper storage before laundering, and periodic replacement of these protective materials. This will help mitigate secondary exposure and adverse long-term health effects.
Patrica-Ivy Agorsor, Husam I. S. Kafeenah, Margaret D. Taiwo et al.· Environmental Science &...· 0 citations
Organophosphate flame retardants (OPFRs) are additive chemicals that migrate from indoor materials and accumulate in settled dust. This study retrospectively characterized eight OPFRs in floor dust collected in Shanghai during 2016 to establish a seasonally resolved historical reference. A total of 136 residential dust samples were obtained from a convenience panel of 26 homes sampled at approximately two-month intervals; five office and four dormitory composite samples were included only for exploratory microenvironmental comparisons. Sampling, extraction, and LC-MS/MS determination were all completed in 2016. OPFRs were detected in all samples. Median (mean) Σ8OPFR concentrations were 1.51 × 103 (4.35 × 103), 2.48 × 103 (3.36 × 103), and 673 (963) ng·g−1 in residential, office, and dormitory dust, respectively, and chlorinated OPFRs—particularly tris(2-chloroisopropyl) phosphate and tris(2-chloroethyl) phosphate—dominated. Mixed-effects models accounting for repeated sampling confirmed significant season effects for Σ8OPFRs and all frequently detected congeners, with autumn generally lower than spring or winter. Under the mean 2016 concentration scenario, uptake-adjusted total estimated daily intakes were 3.3 ng·kg−1·day−1 for infants and 0.65 ng·kg−1·day−1 for adults. Oral administered-dose screening values did not exceed the selected non-cancer or cancer benchmarks. These measurements do not represent current exposure but provide a historical benchmark for method-matched follow-up monitoring.
Jiajun Chang, Li Li, Bing-Hong Cheng et al.· Toxics· 0 citations
