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A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability

BACKGROUND: For many individuals, daily commuting activities on roadways account for a substantial proportion of total exposure, as well as peak-level exposures, to traffic-related air pollutants (TRAPS) including ultrafine particles, but the health impacts of these exposures are not well-understood...

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Autores principales: Laumbach, Robert J, Kipen, Howard M, Ko, Susan, Kelly-McNeil, Kathie, Cepeda, Clarimel, Pettit, Ashley, Ohman-Strickland, Pamela, Zhang, Lin, Zhang, Junfeng, Gong, Jicheng, Veleeparambil, Manoj, Gow, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236446/
https://www.ncbi.nlm.nih.gov/pubmed/25361615
http://dx.doi.org/10.1186/s12989-014-0045-5
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author Laumbach, Robert J
Kipen, Howard M
Ko, Susan
Kelly-McNeil, Kathie
Cepeda, Clarimel
Pettit, Ashley
Ohman-Strickland, Pamela
Zhang, Lin
Zhang, Junfeng
Gong, Jicheng
Veleeparambil, Manoj
Gow, Andrew J
author_facet Laumbach, Robert J
Kipen, Howard M
Ko, Susan
Kelly-McNeil, Kathie
Cepeda, Clarimel
Pettit, Ashley
Ohman-Strickland, Pamela
Zhang, Lin
Zhang, Junfeng
Gong, Jicheng
Veleeparambil, Manoj
Gow, Andrew J
author_sort Laumbach, Robert J
collection PubMed
description BACKGROUND: For many individuals, daily commuting activities on roadways account for a substantial proportion of total exposure, as well as peak-level exposures, to traffic-related air pollutants (TRAPS) including ultrafine particles, but the health impacts of these exposures are not well-understood. We sought to determine if exposure to TRAPs particles during commuting causes acute oxidative stress in the respiratory tract or changes in heart rate variability (HRV), a measure of autonomic activity. METHODS: We conducted a randomized, cross-over trial in which twenty-one young adults took two 1.5-hr rides in a passenger vehicle in morning rush-hour traffic. The subjects wore a powered-air-purifying respirator, and were blinded to high-efficiency particulate air (HEPA) filtration during one of the rides. At time points before and after the rides, we measured HRV and markers of oxidative stress in exhaled breath condensate (EBC) including nitrite, the sum of nitrite and nitrate, malondialdehyde, and 8-isoprostane. We used mixed linear models to evaluate the effect of exposure on EBC and HRV outcomes, adjusting for pre-exposure response levels. We used linear models to examine the effects of particle concentrations on EBC outcomes at post-exposure time points. RESULTS: Mean EBC nitrite and the sum of nitrite and nitrate were increased from baseline at immediately post-exposure comparing unfiltered to filtered rides (2.11 μM vs 1.70 μM, p = 0.02 and 19.1 μM vs 10.0 μM, p = 0.02, respectively). Mean EBC malondialdehyde (MDA) concentrations were about 10% greater following the unfiltered vs. filtered exposures, although this result was not statistically significant. We found no significant associations between exposure to traffic particles and HRV outcomes at any of the time points. At immediately post-exposure, an interquartile range increase in particle number concentration was associated with statistically significant increases in nitrite (99.4%, 95% CI 32.1% to 166.7%) and nitrite + nitrate (75.7%, 95% CI 21.5% to 130.0%). CONCLUSIONS: Increases in markers of oxidative stress in EBC may represent early biological responses to widespread exposures to TRAPs particles that affect passengers in vehicles on heavily trafficked roadways.
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spelling pubmed-42364462014-11-19 A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability Laumbach, Robert J Kipen, Howard M Ko, Susan Kelly-McNeil, Kathie Cepeda, Clarimel Pettit, Ashley Ohman-Strickland, Pamela Zhang, Lin Zhang, Junfeng Gong, Jicheng Veleeparambil, Manoj Gow, Andrew J Part Fibre Toxicol Research BACKGROUND: For many individuals, daily commuting activities on roadways account for a substantial proportion of total exposure, as well as peak-level exposures, to traffic-related air pollutants (TRAPS) including ultrafine particles, but the health impacts of these exposures are not well-understood. We sought to determine if exposure to TRAPs particles during commuting causes acute oxidative stress in the respiratory tract or changes in heart rate variability (HRV), a measure of autonomic activity. METHODS: We conducted a randomized, cross-over trial in which twenty-one young adults took two 1.5-hr rides in a passenger vehicle in morning rush-hour traffic. The subjects wore a powered-air-purifying respirator, and were blinded to high-efficiency particulate air (HEPA) filtration during one of the rides. At time points before and after the rides, we measured HRV and markers of oxidative stress in exhaled breath condensate (EBC) including nitrite, the sum of nitrite and nitrate, malondialdehyde, and 8-isoprostane. We used mixed linear models to evaluate the effect of exposure on EBC and HRV outcomes, adjusting for pre-exposure response levels. We used linear models to examine the effects of particle concentrations on EBC outcomes at post-exposure time points. RESULTS: Mean EBC nitrite and the sum of nitrite and nitrate were increased from baseline at immediately post-exposure comparing unfiltered to filtered rides (2.11 μM vs 1.70 μM, p = 0.02 and 19.1 μM vs 10.0 μM, p = 0.02, respectively). Mean EBC malondialdehyde (MDA) concentrations were about 10% greater following the unfiltered vs. filtered exposures, although this result was not statistically significant. We found no significant associations between exposure to traffic particles and HRV outcomes at any of the time points. At immediately post-exposure, an interquartile range increase in particle number concentration was associated with statistically significant increases in nitrite (99.4%, 95% CI 32.1% to 166.7%) and nitrite + nitrate (75.7%, 95% CI 21.5% to 130.0%). CONCLUSIONS: Increases in markers of oxidative stress in EBC may represent early biological responses to widespread exposures to TRAPs particles that affect passengers in vehicles on heavily trafficked roadways. BioMed Central 2014-11-01 /pmc/articles/PMC4236446/ /pubmed/25361615 http://dx.doi.org/10.1186/s12989-014-0045-5 Text en © Laumbach et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Laumbach, Robert J
Kipen, Howard M
Ko, Susan
Kelly-McNeil, Kathie
Cepeda, Clarimel
Pettit, Ashley
Ohman-Strickland, Pamela
Zhang, Lin
Zhang, Junfeng
Gong, Jicheng
Veleeparambil, Manoj
Gow, Andrew J
A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title_full A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title_fullStr A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title_full_unstemmed A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title_short A controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
title_sort controlled trial of acute effects of human exposure to traffic particles on pulmonary oxidative stress and heart rate variability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236446/
https://www.ncbi.nlm.nih.gov/pubmed/25361615
http://dx.doi.org/10.1186/s12989-014-0045-5
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