- Open Access
The effects of facemasks on airway inflammation and endothelial dysfunction in healthy young adults: a double-blind, randomized, controlled crossover study
Particle and Fibre Toxicology volume 15, Article number: 30 (2018)
Facemasks are increasingly worn during air pollution episodes in China, but their protective effects are poorly understood. We aimed to evaluate the filtration efficiencies of N95 facemasks and the cardiopulmonary benefits associated with wearing facemasks during episodes of pollution.
We measured the filtration efficiencies of particles in ambient air of six types of N95 facemasks with a manikin headform. The most effective one was used in a double-blind, randomized, controlled crossover study, involving 15 healthy young adults, conducted during 2 days of severe pollution in Beijing, China. Subjects were asked to walk along a busy-traffic road for 2 h wearing authentic or sham N95 facemasks. Clinical tests were performed four times to determine changes in the levels of biomarkers of airway inflammation, endothelial dysfunction, and oxidative stress within 24 h after exposure.
The facemasks removed 48–75% of number concentrations of ambient air particles between 5.6 and 560 nm in diameter. After adjustments for multiple comparison, the exhaled nitric oxide level and the levels of interleukin-1α, interleukin-1β, and interleukin-6 in exhaled breath condensate increased significantly in all subjects; however, the increases in those wearing authentic facemasks were statistically significantly lower than in the sham group. No significant between-group difference was evident in the urinary creatinine-corrected malondialdehyde level. In arterial stiffness indicators, the ejection duration of subjects wearing authentic facemasks was higher after exposure compared to the sham group; no significant between-group difference was found in augmentation pressure or the augmentation index.
In young healthy adults, N95 facemasks partially reduced acute particle-associated airway inflammation, but neither systemic oxidative stress nor endothelial dysfunction improved significantly. The clinical significance of these findings long-term remains to be determined.
The trial registration number (TRN) for this study is ChiCTR1800016099, which was retrospectively registered on May 11, 2018.
Exposure to particulate matter (PM) of aerodynamic diameter less than 2.5 μm (PM2.5) is the fourth leading health risk factor in China and is linked to more than 1.3 million premature deaths annually [1,2,3]. PM air pollution is associated with substantial increases in respiratory and cardiovascular morbidity and mortality, and has aroused great public concern in China, especially in highly polluted areas such as Beijing [4,5,6]. To reduce individual exposure, the use of facemasks, especially those trapping PM2.5, has become very popular, particularly since many cities experienced severe episodes of air pollution in 2011. N95 facemasks, which are generally recommended by health researchers, are the most widely used [7, 8].
The U.S. Food and Drug Administration (FDA) has explained that the N95 descriptor means that, on careful testing, the filter blocks at least 95% of very small (0.3-μm diameter) test particles. The facemasks are used to protect those occupationally exposed to, or at increased risk of, severe illness caused by influenza or other respiratory diseases [9,10,11,12]. Although the filters have been suggested to trap airborne particles very efficiently, filtration efficiencies have not been tested in real-world environments and may not be as high as suggested when trapping small particles in ambient air [13, 14].
Although N95 facemasks are commonly used, reports on their protective effects are limited. To the best of our knowledge, only three single-blind studies have been conducted, which reported that use of a typical N95 facemask reduced blood pressure and heart rate variability in healthy volunteers and patients with coronary heart disease, respectively [15,16,17]. A chamber study using N95 facemasks to control PM2.5 exposure indicated that, in the absence of filtration, PM exposure impaired vasomotor function and increased heart rate variability in overweight middle-aged and elderly adults . More field experiments are required to measure the actual protective effects of facemasks. We hypothesize that changes in levels of subclinical biomarkers caused by exposure to PM in ambient particles can be influenced by wearing a N95 facemask. Therefore, we conducted a double-blind, randomized controlled trial to investigate the effects of N95 facemasks on human respiratory inflammation, endothelial dysfunction, and oxidative stress on days of severe air pollution.
We calculated that a sample size of 14 was required to detect the minimal expected changes in urinary creatinine-corrected malondialdehyde levels before and after exposure of subjects wearing authentic and sham facemasks to air pollution (See Additional file 1 for more details). Hence, we recruited 15 healthy volunteers from Peking University (PKU); their characteristics are listed in Table 1. All were nonsmokers who were not on regular medication, had no history of coronary or respiratory disease, and no symptoms of upper airway infection commencing 4 weeks prior to study initiation until all measurements had been completed. Groups of four (or, in one instance, three) lived in the same dormitories, and the groups were required to spend the days immediately preceding the experimental days, and the experimental days, together, maintaining the same time schedules, activities, and diets. The study was approved by the Institutional Review Board of the PKU Health Science Center (approval no. 13073), and written informed consent was obtained from all participants before enrollment.
The double-blind, randomized, controlled crossover study design
We performed a double-blind, randomized, controlled crossover study on two days associated with severe air pollution in Beijing, China (daily average PM2.5 concentration = 246.1 μg/m3 and 258.0 μg/m3, respectively) from November 2013 to February 2014. On the first clinical visit, each subject underwent tests including biomarker measurements and collection of samples for further biomarker analyses, according to the timetable shown in Fig. 1. These tests were performed in the basement of the PKU hospital, where the average PM2.5 concentration was 30.6 ± 3.1 μg/m3 over the entire study period (an air filtration system was operative). Next, each participant was randomized to wear a reusable facemask with or without a high-efficiency filter. Wearing the facemasks, the subjects were asked to walk together along a defined (off-campus) route with busy traffic for 2 h. When they returned to the hospital, they were immediately told to remove the facemasks and have a rest, and the second and third tests were performed after 15 min and 6 h of rest. The fourth test was performed at 11 a.m. on the next day, 24 h after the 2 h walk. After a 1-month washout interval, the subjects who wore real and sham facemasks exchanged roles and the entire procedure was repeated. All the subjects were required to complete the two visits at the same time.
Air pollution monitoring
During the two clinical visits, the levels of air pollution and meteorological parameters were collected from the Peking University Urban Atmosphere Environment Monitoring Station (PKUERS), which located on the roof of a six-story building (~ 20 m above the ground). The station has been used for monitoring ambient pollutants in numerous studies [19,20,21] and can represent the air pollutants at a relative large scale including the walking route in our study. The station provided 1-min PM2.5 (Model 1400 TEOM; Thermo), sulfur dioxide (SO2) (Model 43i-TL; Thermo), nitrogen oxides (NOx) (Model 42i-TL; Thermo), ozone (O3) (Model 49i; Thermo), carbon monoxide (CO) (Model 48i-TLE; Thermo), temperature and relative humidity (Met One Instruments Inc., Grants Pass, OR, USA). Especially, to better assess the PM exposure during the two 2-h walks, real-time PM2.5 concentrations were measured at 1-min intervals using a Grimm optical particle counter (model 1.108; Grimm, Germany), carried in the backpack of a subject (data shown in Table 2).
Facemask filtration efficiencies
We tested the filtration efficiencies of the six most popular types of N95 facemasks available from the two largest Chinese e-commerce websites (Taobao.com and Tmall.com), which were visited by approximately 25% of all Chinese shoppers in 2013 . All facemasks were certified by the National Institute for Occupational Safety and Health (NIOSH) under regulation 42 CFR 84 , and their filtration efficiencies were evaluated using identical NIOSH procedures by Beijing Municipal Institute of Labor Protection, China (See details in the Additional file 1).
A manikin headform based on standard Asian faces was used to test the filtration efficiencies of particles in ambient air . Compared with a human participant, the headform was more representative and could avoid interference of exhaled breath. A Fast Mobility Particle Sizer (model 3091; TSI Inc., USA) was used to measure the number concentrations of particles of diameter 5.6–560 nm in 32 size channels at a flow rate of 10 L/min. The experimental setup is presented in Fig. 2. The most effective type of the six facemasks (Respirator 3200 with Particulate Filter 3701CN; 3 M, USA) were used in the study. All the filtration efficiencies in this study were evaluated based on particle number concentration.
To ensure that the study was double-blinded, we used reusable facemasks without filters (Respirator 3200; 3 M, USA) as sham devices, which could not remove any particles, to control for potential placebo effects. Before the visits, all the participants were trained on how to wear and remove the facemasks correctly. Subjects still encountered respiration resistance even when the facemasks contained no filters; they could not tell whether they were wearing real or sham facemasks, which was confirmed in every participant.
Exhaled nitric oxide (eNO) and the levels of six pro-inflammatory cytokines (interleukin [IL]-1α, IL-1β, IL-2, IL-6, IL-8, and tumor necrosis factor [TNF]-α) in exhaled breath condensate (EBC) were measured to evaluate airway inflammation [25,26,27]; urinary creatinine-corrected malondialdehyde (MDA) levels were measured to quantify systemic oxidative stress [28, 29]; and pulse wave analysis (PWA) (including assessment of augmentation pressure [AP], the augmentation index [AIx], and ejection duration [ED]) was performed to evaluate arterial stiffness (a measure of endothelial dysfunction) [30,31,32]. The eNO and cytokine levels were measured, and PWA performed, at every test, but MDA measurements were obtained at only the pre-exposure (first) and the 24-h post-exposure (fourth) tests associated with each experiment.
Exhaled nitric oxide (eNO)
Exhaled air samples were collected following the instruction of ATS/ERS 2005 . Before sampling, subjects must gargle for 3 times and wear a nose clip. Then they were asked to inhale deeply, and then exhale to wash the “dead space” from the device for 3 times. Subjects were instructed to inhale to tidal capacity and then exhale into a 4-L Teflon bag with a flow of 150 L/h and a pressure of 13 cm H2O (to close the soft palate and prevent nasal exhalation). A tube filled with activated carbon was used to filter out NO from the ambient air and was shown to remove up to 99.6% of NO in a laboratory simulation of the protocol used in the field. The device was equipped with a flow meter as a flow restrictor and a pressure indicator. Concentration levels of eNO in the samples were determined with a NO–NO2–NOx analyzer (model 42i; Thermo, USA). We recorded 10 readings after the concentration showed in the instrument is stable and used their average as the final result. This method has been used in our previous studies [25, 34, 35].
Cytokines in exhaled breath condensate (EBC)
Exhaled breath condensate (EBC) was collected by EcoScreen (Jaeger, Germany), and the procedure of collection and storage followed the recommended instruction . Before collection, subjects were required to rest for at least 5 min, gargle for 3 times and wear a nose clip, sequentially. For collection, the subjects breathed normally for 5 min, and the samples collected were stored in − 80 °C.
The BD™ Cytometric Bead Array (CBA) method was performed to determine the cytokine concentrations in EBC with a multiplex fluorescent bead immunoassay (Cytometric Bead Array, BD-Biosciences, San Jose, CA, USA). Cytokines in test samples and recombinant standards as bound to capture beads were detected by PE-conjugated detection antibodies and measured by flow cytometry (FACS Calibur, BD-Biosciences, San Jose, CA, USA; ). Following acquisition of sample data, the sample results were generated in graphical and tabular format using the CBA analysis software (BD-Biosciences, San Jose, CA, USA). The broad dynamic range of fluorescence detection via flow cytometry and the efficient capturing of multiple analytes via suspended particles enable the CBA system to obtain the concentration of an unknown in substantially less time and using fewer sample dilutions compared to the conventional ELISA methodology, and the CBA method has been widely used in serum cytokine detection [38,39,40]. To avoid the potential influence from pH in EBC (pH = 5.6–6.8), 10 μl phosphate buffer saline (PBS) was added into every 40 μl EBC to modify the pH of the samples to 7.4. Detection limits of the six proinflammatory cytokines (IL-1α, IL-1β, IL-2, IL-6, IL-8, TNF-α) are 2.0, 2.4, 2.6, 2.4, 2.4, 3.8 pg/mL, respectively.
Urinary malondialdehyde and creatinine
As the product of lipid oxidation, urinary creatinine-corrected-malondialdehyde presents the systemic oxidative stress in a relatively long term. We thus only determined it at pre-exposure (baseline) and 24-h post- exposure, and morning urine samples were required for collection. Malondialdehyde, released from its bound form(s) in urine by acid treatment, was measured as thiobarbituric acid derivative, using HPLC-UV (Model e2695, Waters, USA) according to . Briefly, 150 μL urine, 450 μL thiobarbituric acid (TBA) solutions (Sigma-Aldrich, St. Louis, USA), and 900 μL 0.5 mol/L phosphorous acid were added into 1.5 mL plastic centrifuge tube. The mixtures were incubated at 95 °C for 1 h, cooled in ice water for 5 min, followed by 5-min centrifugation (5000 g/min). HPLC with chromatographic column X-Terra RP18 C18 (X-Terra, USA) was used to detect maloniadehyde concentration in the mixtures at the wavelength of 532 nm by Photodiode Array (PDA) detector (Waters 2998, USA) with the flow rate of 0.8 mL/min. The mobile phase was phosphate buffer (pH = 6.8) and methanol (60:40, V/V).
In our study, concentrations of maloniadehyde were corrected by creatinine due to its highly potential influence by metabolism. Urinary creatinine levels were analyzed by a commercial ELISA kit (Jiancheng Bioengineering Institute, Nanjing, China), based on the Jaffe reaction and spectrophotometry .
Pulse wave analysis (PWA)
Pulse wave analysis was performed using micromanometer applanation tonometry (Millar Instruments, Texas, USA) of the radial artery at the wrist. The pulse wave data was directly collected into a portable computer and an averaged waveform was generated by the SphygmoCor™ system (AtCor Medical, Sydney, Australia) in accordance with the manufacturer’s recommendations. Briefly, pulse wave analysis derives an aortic pulse pressure waveform from the radial artery wave via a mathematical transfer function. The arterial pressure waveform is a composite of the forward pressure wave created by ventricular contraction and a reflected wave generated by peripheral vascular resistance. The systolic part of central arterial waveform is characterized by two pressure peaks. The first peak is caused by left ventricular ejection, whereas the second peak is a result of wave reflection. The difference between both pressure peaks reflects the degree to which central arterial pressure is augmented by wave reflection. Augmentation pressure (mm Hg), is the difference between the second and first systolic peaks. Augmentation index (%) is defined as the percentage of the central pulse pressure which is attributed to the reflected pulse wave and, therefore, reflects the degree to which central arterial pressure is augmented by wave reflection. Ejection Duration (second) is defined as the sum of time to wave reflection (Tr) and systolic duration of reflection wave (SDR) [43,44,45].
All biomarker levels were subjected to analysis of skewness and kurtosis to explore whether they exhibited Gaussian distributions (α = 0.05). The paired Student’s t-test was used to compare biomarker levels before and after the experiments. To control the family-wise type I error rate at a 0.05 level, a Bonferroni correction was applied; with 11 biomarkers measured in this study, each individual 2-sided test was considered statistically significant relative to a 0.005 significance level. All analyses were performed with the aid of R statistical software (version 2.15.3, R Core Team 2013).
In tests following the NIOSH guidelines, we found that all six types of facemask met the standard N95 requirements with efficiencies of 97.2–99.4% (detailed data shown in Additional file 1). However, the performance of the facemasks in terms of filtration of ambient PM 5.6–560 nm in diameter was less impressive. The most effective facemask removed only 75% of the particles and the least effective one 48% (Fig. 3). Although filtration efficiency varied greatly at different particle diameters, particles removed most efficiently by all the six facemasks was in the range of 69.8–93.1 nm in diameter.
Pollution descriptive statistics
Additional file 1: Table S1 lists the average air pollutant concentrations during the 2-h walks of the two experiments; the PM2.5 concentrations were above 101 μg/m3 (average, 204 μg/m3), consistent with those of typical winter air pollution episodes in Beijing [6, 46].
Biomarker descriptive statistics
Figure 4 shows the biomarker levels of the four tests. The levels of all six cytokines (IL-1α, IL-1β, IL-2, IL-6, IL-8, and TNF-α) in EBC were above the analytical detection limits (compared with negative controls). In the first test (before the walk), no significant difference in any biomarker level was evident between the groups wearing real and sham facemasks during the walk.
Effects of facemasks on airway inflammation
After the 2-h walk, the levels of all biomarkers changed (Fig. 5). At 15 min post-exposure, the concentration of eNO in both groups increased significantly (p < 0.005), but the increase in the group wearing real facemasks was 38.3% less than the sham group (p < 0.005). At 6 and 24 h post-exposure, the eNO concentrations returned to relatively low levels, and did not differ significantly between the groups who had worn real and sham facemasks (p > 0.05).
In terms of cytokine levels in EBC, we found no significant change at 15 min, 6 h, or 24 h post-exposure in the group that had worn real facemasks (p > 0.05) (Fig. 5). In the sham group, the levels of IL-1α, IL-1β, and IL-6 in EBC were significantly elevated at 6 h post-exposure (all p < 0.005). Compared to the group wearing real facemasks, the IL-1α and IL-1β levels in EBC at 6 h post-exposure were significantly higher (82.4 and 91.4%, respectively) in the sham group (both p < 0.005). Similarly, the TNF-α level at 24 h post-exposure was significantly higher in the sham group (by 112.5%) After adjustments for multiple comparisons, changes in the other outcomes were not statistically significant (Fig. 5).
Effects of facemasks on oxidative stress and endothelial dysfunction
As shown in Fig. 5, at 24 h post-exposure, the urinary creatinine-corrected MDA concentrations were higher (compared with baseline) in both groups, but did not differ significantly between the groups (p > 0.05). Of the endothelial dysfunction biomarkers, only the ED increased significantly (compared with baseline) in the group wearing real facemasks, at 15 min post-exposure (p < 0.005). The level was 40.0% higher than that of the sham group, but the difference was not significant (p > 0.05).
Using a robust, double-blind, randomized, controlled crossover design, we assessed the effects of wearing N95 facemasks on days of severe air pollution in Beijing, China. We measured changes in the levels of biomarkers reflecting airway inflammation, oxidative stress, and endothelial function four times within 24 h after a 2-h exposure to ambient air (walking along a busy road). We evaluated six of the most popular types of N95 facemasks in terms of ambient air filtration efficiency during typical episodes of Beijing pollution . Our study recruited young healthy adults and observed the biomarkers changes linking interventions in air pollution, which might be particularly important because they are less sensitive to air pollution exposure than other subpopulations . To minimize subjective differences, the characteristics of all volunteers were similar; and they maintained identical time schedules and dietary habits before and during the study days, reducing exposure differences and minimizing individual bias. Moreover, we gave facemasks without filters to the sham group, to reduce any possible subjective bias and maintain the double-blind design. Previous studies did not feature sham facemasks, and the outcomes may thus have been influenced by anxiety [15,16,17].
To the best of our knowledge, this is the first study to describe the real-world PM filtration capacities of available facemasks in terms of particle size fractions between 5.6 and 560 nm in diameter (Fig. 3). Previous laboratory studies on filtration performance suggested that such facemasks were very efficient. However, these experiments used particles of specific composition (e.g., sodium chloride) [48,49,50]. Only one study  reported the filtration efficiency of diesel exhaust, but did not distinguish between the different size fractions. The reduced facemask filtration efficiencies of ambient air may be explained by the fact that N95 facemasks were initially designed and are commonly used for occupational protection in industrial and healthcare settings . The filtration efficiencies of specific particles cannot be generalized to ambient particles, first because chemical species vary greatly in penetration, and, second, because ambient PM is a very complicated mixture exhibiting large spatial and temporal variations [13, 52]. Previous laboratory studies indicated that the filtration efficiencies were influenced by multiple factors, including particle sizes, particle compositions, aerosol concentrations, etc. [53,54,55,56]. Evaluation of facemask filtration efficiencies in terms of different PM size fractions is important. It has been suggested that the association between health effects and number concentration of fine particulates depended on particle size, and ultrafine particles are primarily responsible for the adverse health effects [27, 38,39,40,41]. Smaller particles would have greater toxicity than larger particles due to their larger active surface area absorbing more toxic chemicals and higher deposition efficiency in the respiratory tract [35, 57,58,59,60]; besides, number concentration of ultrafine particles is much higher, which constitutes over 90% of aerosol fine particles in China . Fibrous facemask filters are least effective when removing particles ranging from 0.1 to 0.4 μm in diameter [54, 61]. Thus, N95 facemasks might not exhibit filtration efficiencies as impressive as expected.
Many studies have confirmed that inflammation is one of the most critical biological pathways affected by PM [62, 63]. The eNO level is an acute clinical surrogate of airway inflammation, and increases following exposure to PM [25, 27, 64, 65]. We found a significant acute increase in the eNO concentration following high-level exposure to PM in subjects wearing real or sham facemasks, but the increase in the group wearing real facemasks was substantially less than that in the sham group. This suggests that N95 facemasks may reduce, but not eliminate, respiratory inflammation induced by high-level PM exposure. Given the features of facemask efficiency described above, the fact that the eNO level increased in the group wearing real facemasks implies that smaller particles contributed significantly to inflammation. However, the possibility that high-level gaseous pollutants (e.g., nitrogen oxides and sulfur dioxide) were responsible for the elevation in eNO [66, 67] cannot be excluded. Additional research is required.
Many reports have shown that short-term exposure to PM increased the levels of inflammatory cytokines including IL-6, IL-1β, TNF-α, IL-γ, and IL-8, in bronchial fluid, EBC, and sometimes blood [68,69,70,71,72,73]. Although the sources of cytokines and the extent of their involvement in the systemic inflammatory response following PM exposure remain unclear, pulmonary inflammation may be attributable to both innate immune cells (neutrophils and macrophages) and adaptive immune cells such as T cells . Previous studies suggested that PM inhalation induced inflammatory cytokine release by neutrophils and macrophages 6–24 h later [74,75,76,77]. We found that the levels of TNF-α and IL-6 in EBC in the group wearing sham facemasks increased significantly 6 and 24 h after exposure, respectively. However, PM-induced T cells have been suggested to contribute to the observed increases in IL-1, IL-4, IL-6, and IL-10 . We found that IL-1α, IL-1β, and IL-6 levels in EBC increased significantly 6 h after exposure in the group wearing sham facemasks. In contrast, cytokine levels in EBC did not change significantly following PM exposure in the group wearing real facemasks. Indeed, the IL-1α and IL-1β levels in EBC 6 h after exposure were significantly lower than in the sham group. Changes in the cytokine levels paralleled those of eNO, suggesting that, upon exposure to PM, the increase in pulmonary inflammation induced by either immune cells or T cells was effectively prevented with the use of a facemask.
Applanation tonometry of the radial artery and PWA are typically used to measure arterial stiffness and central aortic blood pressure. Controlled experiments have shown that short-term exposure to ambient PM may trigger acute vasoconstriction, vascular endothelial dysfunction, and increases in blood pressure and arterial stiffness, which may in turn explain the observed increase in associated cardiovascular events . PWA accurately records peripheral pressure waveforms, and generates the corresponding central waveform, from which the AIx, AP, and ED can be derived . However, the effects of air pollution on PWA outcomes have received little attention. It has been reported that exposure to wood and tobacco smoke, as well as diesel exhaust, increased arterial stiffness [32, 71, 79]. We found no significant change in the AIx or AP following PM exposure. The ED was significantly increased in the group wearing real facemasks 15 min after exposure, suggesting that acute PM exposure increased arterial stiffness in those wearing facemasks. The increase was not significant in the sham group. ED is a complex surrogate of cardiovascular effects, and may become elevated when the heart rate changes . Although the volunteers tolerated the facemasks well, the masks increased respiration resistance, perhaps raising the heart rate [12, 15, 81] and thus the ED. Another possibility is that the wearing of a facemask may trigger deeper breathing, increasing the inhalation flow rate. Thus, finer particles may deposit in deeper sections of the respiratory system, causing more severe cardiovascular injury. This hypothesis could also explain the decreases in AP and AIx, and the increase in MDA, in the group wearing real facemasks, although the changes did not differ significantly from those in the sham group. The mild changes in AP and AIx are possibly attributable to the fact that we studied young healthy volunteers, whose cardiovascular systems were less vulnerable to PM exposure. N95 facemasks exhibit respiration resistance that may stimulate the cardiovascular system, and the U.S. FDA does not recommend their use by children, older subjects, or those with chronic respiratory or cardiac conditions, unless their healthcare providers indicate that the masks are appropriate . Additionally, we found no significant difference in the urinary MDA level (a surrogate marker of systemic oxidative stress) before and after exposure, possibly because the MDA concentration typically peaks 40–70 h after exposure , or because our volunteers were not susceptible to such stress. Further work is required.
We measured biomarker levels three times following PM exposure to increase our understanding of the mechanisms and timing of the respiratory, pulmonary, and systemic inflammatory responses to sustained exposure, particularly PM2.5, in healthy subjects. Moreover, our findings have significant implications for public health. First, the fact that the filtration efficiency of ultrafine ambient particles was low indicates that facemasks that filter smaller particles better are required. Second, exposure to ambient air pollution was associated with direct, measurable adverse effects even in young healthy adults habitually exposed to such pollution. Third, N95 facemasks appeared to effectively reduce short-term PM-induced respiratory inflammation, but are unlikely to completely eliminate inflammation. Fourth, we did not observe significant cardiovascular benefits produced by N95 facemasks. Although more work is needed to confirm or refute, healthcare providers should be cautious when recommending N95 facemasks to susceptible subjects.
Our study had certain limitations. First, our sample size was small, which may have masked the significance of changes in the levels of some biomarkers. Additional tests with larger numbers of subjects are necessary. Second, our experimental days featured not only high-level PM, but also gaseous pollutants, which may have influenced our findings. Third, although the two air pollution episodes studied were similar, the specific concentrations of various pollutants may have varied, affecting our results and conclusions. Fourth, we did not consider potential face-seal leaks of the facemasks, which can be a penetration pathway for aerosol particles. Fifth, we recruited young healthy adults rather than subjects more susceptible to air pollution, and the changes in some biomarker levels might thus have been minimal in our volunteers. Although it is likely that our findings will be relevant in other populations, further studies are required.
In summary, acute respiratory inflammation in healthy young adults caused by air pollution was partially reduced by N95 facemasks, but systemic oxidative stress and endothelial dysfunction may not have been alleviated. Although the clinical significance of these findings long-term remains to be determined, this study provides quasi-experimental, mechanistic data for the potential cardiopulmonary effects associated with wearing facemasks during episodes of pollution.
Cytometric Bead Array
exhaled breath condensate
enzyme-linked immunosorbent assay
Exhaled nitric oxide
Food and Drug Administration
National Institute for Occupational Safety and Health
Peking University Urban Atmosphere Environment Monitoring Station
- PM2.5 :
particulate matter of aerodynamic diameter less than 2.5 μm
pulse wave analysis
tumor necrosis factor
Yang G, Wang Y, Zeng Y, et al. Rapid health transition in China, 1990–2010: findings from the global burden of disease study 2010. Lancet. 2013;381(9882):1987–2015.
Liu J, Han Y, Tang X, et al. Estimating adult mortality attributable to PM2.5 exposure in China with assimilated PM2.5 concentrations based on a ground monitoring network. Sci Total Environ. 2016;568:1253–62.
Giannadaki D, Lelieveld J, Pozzer A. Implementing the US air quality standard for PM2.5 worldwide can prevent millions of premature deaths per year. Environ Health. 2016;15(1):88.
Hu W, Hu M, Hu W, et al. Chemical composition, sources, and aging process of submicron aerosols in Beijing: contrast between summer and winter. Journal of Geophysical Research Atmospheres. 2016;121(4):1955–77.
Liu J, Mauzerall DL, Chen Q, et al. Air pollutant emissions from Chinese households: a major and underappreciated ambient pollution source. Proc Natl Acad Sci U S A. 2016;113(28):7756–61.
Zheng G, Duan F, Su H, et al. Exploring the severe winter haze in Beijing: the impact of synoptic weather, regional transport and heterogeneous reactions. Atmospheric Chemistry & Physics. 2015;15(6):2969–83.
Gold DR, Samet JM. Air pollution, climate, and heart disease. Circulation. 2013;128(21):e411–4.
Cai DP, He YM. Daily lifestyles in the fog and haze weather. Journal of Thoracic Disease. 2016;8(1):E75.
Brienen NCJ, Timen A, Wallinga J, et al. The effect of mask use on the spread of influenza during a pandemic. Risk Anal. 2010;30(8):1210–8.
Cowling BJ, Zhou Y, Ip DKM, et al. Face masks to prevent transmission of influenza virus: a systematic review. Epidemiol Infect. 2010;138(04):449–56.
Simmerman JM, Suntarattiwong P, Levy J, et al. Findings from a household randomized controlled trial of hand washing and face masks to reduce influenza transmission in Bangkok, Thailand. Influenza Other Respir Viruses. 2011;5(4):256–67.
Fadnis M, Agarkhedkar S, Sahasrabudhe T. Case control study to assess the prevalence of obstructive airway disease in flour mill workers. Eur Respir J. 2012;40(Suppl 56):P1028.
Bałazy A, Toivola M, Adhikari A, et al. Do N95 facemasks provide 95% protection level against airborne viruses, and how adequate are surgical masks? Am J Infect Control. 2006;34(2):51–7.
Han Y, Zhu T. Health effects of fine particles (PM2.5) in ambient air. Science China. Life Sci. 2015;58(6):1–3.
Langrish JP, Mills NL, Chan JKK, et al. Beneficial cardiovascular effects of reducing exposure to particulate air pollution with a simple facemask. Part Fibre Toxicol. 2009;6(1):1.
Langrish JP, Bosson J, Unosson J, et al. Cardiovascular effects of particulate air pollution exposure: time course and underlying mechanisms. J Intern Med. 2012;272(3):224–39.
Shi J, Lin Z, Chen R, et al. Cardiovascular benefits of wearing particulate-filtering respirators: a randomized crossover trial. Environ Health Perspect. 2016;125(2):175–80.
Hemmingsen JG, Rissler J, Lykkesfeldt J, et al. Controlled exposure to particulate matter from urban street air is associated with decreased vasodilation and heart rate variability in overweight and older adults. Particle and fibre toxicology. 2015;12(1):1.
Wu Z, Hu M, Liu S, et al. New particle formation in Beijing, China: Statistical analysis of a 1-year data set. J Geophys Res: Atmospheres (1984–2012). 2007;112:D09209.
Yue D, Hu M, Zhang R, et al. Potential contribution of new particle formation to cloud condensation nuclei in Beijing. Atmos Environ. 2011;45(33):6070–7.
Guan T, Yao M, Wang J, et al. Airborne endotoxin in fine particulate matter in Beijing. Atmos Environ. 2014;97:35–42.
Chen MC, Wu PJ, Xiong WH. Explicating the trends of China’s logistics Services for Electronic Commerce. Industrial Engineering, Management Science and Applications 2015. Springer Berlin Heidelberg. 2015;349:871–80.
National Institute for Occupational Safety and Health (NIOSH). Respiratory Protective Devices; Final Rules and Notice. Washington, D.C.: U.S. Government Printing Office, Office of the Federal Register; 1995. Federal Register 60(110):3033630398.
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China and Standardization Administration of the People's Republic of China. Respiratory protective equipment: Non-powered air-purifying particle respirator. GB2626–2006. 2006.
Lin W, Huang W, Zhu T, et al. Acute respiratory inflammation in children and black carbon in ambient air before and during the 2008 Beijing Olympics. Environ Health Perspect. 2011;119(10):1507.
Vossoughi M, Schikowski T, Vierkötter A, et al. Air pollution and subclinical airway inflammation in the SALIA cohort study. Immun Ageing. 2014;11(1):1.
Mirowsky J, Gordon T. Noninvasive effects measurements for air pollution human studies: methods, analysis, and implications. Journal of Exposure Science and Environmental Epidemiology. 2015;25(4):354–80.
Gong J, Zhu T, Kipen H, et al. Malondialdehyde in exhaled breath condensate and urine as a biomarker of air pollution induced oxidative stress. Journal of Exposure Science and Environmental Epidemiology. 2013;23(3):322–7.
Lin W, Zhu T, Xue T, et al. Association between changes in exposure to air pollution and biomarkers of oxidative stress in children before and during the Beijing Olympics. Am J Epidemiol. 2015;181(8):575–83.
Hoffmann B, Luttmann-Gibson H, Cohen A, et al. Opposing effects of particle pollution, ozone, and ambient temperature on arterial blood pressure. Environ Health Perspect. 2012;120(2):241.
Mehta AJ, Zanobetti A, Koutrakis P, et al. Associations between short-term changes in air pollution and correlates of arterial stiffness: the veterans affairs normative aging study, 2007–2011. Am J Epidemiol. 2013;179(2):192–9.
Unosson J, Blomberg A, Sandström T, et al. Exposure to wood smoke increases arterial stiffness and decreases heart rate variability in humans. Particle and fibre toxicology. 2013;10(1):1.
Dweik RA, Boggs PB, Erzurum SC, et al. An official ATS clinical practice guideline: interpretation of exhaled nitric oxide levels (FENO) for clinical applications. Am J Respir Crit Care Med. 2012;184(5):602-15.
Gong JC, Zhu T, Zhang JF, Hu M, Wu ZJ. Measurement of nitric oxide in human exhaled air as a biomarker of the health effects of ultrafine particles [in Chinese]. Environ Chem. 2006;25(6):768–71.
Han Y, Zhu T, Guan T, et al. Association between size-segregated particles in ambient air and acute respiratory inflammation. Sci Total Environ. 2016;565:412–9.
Horvath I, Hunt J, Barnes PJ. Exhaled breath condensate: methodological recommendations and unresolved questions. Eur Respir J. 2005;26(3):523–48.
de Jager W, Rijkers GT. Solid-phase and bead-based cytokine immunoassay: a comparison. Methods. 2006;38(4):294–303.
Dabitao D, Margolick JB, Lopez J, et al. Multiplex measurement of proinflammatory cytokines in human serum: comparison of the Meso scale discovery electrochemiluminescence assay and the cytometric bead Array. J Immunol Methods. 2011;372(1):71–7.
Wyns H, Croubels S, Demeyere K, et al. Development of a cytometric bead array screening tool for the simultaneous detection of pro-inflammatory cytokines in porcine plasma. Vet Immunol Immunopathol. 2013;151(1):28–36.
da Cunha NB, Vianna GR, da Almeida Lima T, et al. Molecular farming of human cytokines and blood products from plants: challenges in biosynthesis and detection of plant-produced recombinant proteins. Biotechnol J. 2014;9(1):39–50.
Lee K, Bartsch H, Nair J, et al. Effect of short-term fasting on urinary excretion of primary lipid peroxidation products and on markers of oxidative DNA damage in healthy women. Carcinogenesis. 2006;27(7):1398–403.
Slot C. Plasma creatinine determination. A new and specific Jaffe reaction method. Scand J Clin Lab Investig. 1965;17(4):381.
Nürnberger J, Keflioglu-Scheiber A, Saez AMO, et al. Augmentation index is associated with cardiovascular risk. J Hypertens. 2002;20(12):2407–14.
Mills NL, Miller JJ, Anand A, et al. Increased arterial stiffness in patients with chronic obstructive pulmonary disease: a mechanism for increased cardiovascular risk. Thorax. 2008;63(4):306–11.
Denardo J, Nandyala R, Freeman GL, et al. Pulse wave analysis of the aortic pressure waveform in severe left ventricular systolic dysfunction. Circulation: Heart Failure. 2010;3(1):149–56.
Zhao XJ, Zhao S, Xu J, et al. Analysis of a winter regional haze event and its formation mechanism in the North China Plain. Atmos Chem Phys. 2013;13(11):5685–96.
Guan T, Xue T, Liu Y, et al. Differential susceptibility in ambient particle-related first-ever stroke onset risk: findings from a national case-crossover study. Am J Epidemiol. 2018. https://doi.org/10.1093/aje/kwy007.
Rengasamy S, Miller A, Eimer BC. Evaluation of the filtration performance of NIOSH-approved N95 filtering facepiece facemasks by photometric and number-based test methods. J Occup Environ Hyg. 2011;8(1):23–30.
Bałazy A, Toivola M, Reponen T, et al. Manikin-based performance evaluation of N95 filtering-Facepiece facemasks challenged with nanoparticles. Ann Occup Hyg. 2006;50(3):259–69.
Grinshpun SA, Haruta H, Eninger RM, et al. Performance of an N95 filtering facepiece particulate respirator and a surgical mask during human breathing: two pathways for particle penetration. J Occup Environ Hyg. 2009;6(10):593–603.
Roberge RJ, Kim JH, Powell JB. N95 respirator use during advanced pregnancy. Am J Infect Control. 2014;42(10):1097–100.
Qian Y, Willeke K, Grinshpun SA, et al. Performance of N95 facemasks: filtration efficiency for airborne microbial and inert particles. American Industrial Hygiene Association. 1998;59(2):128–32.
Rengasamy S, Shaffer R, Williams B, et al. A comparison of facemask and respirator filtration test methods. Journal of Occupational & Environmental Hygiene. 2016;14(2):92–103.
Rengasamy S, Eimer BC, Shaffer RE. Comparison of nanoparticle filtration performance of NIOSH-approved and CE-marked particulate filtering facepiece respirators. Ann Occup Hyg. 2009;53(2):117–28.
Rengasamy S, Eimer BC. Nanoparticle filtration performance of NIOSH-certified particulate air-purifying filtering facepiece respirators: evaluation by light scattering photometric and particle number-based test methods. Journal of Occupational & Environmental Hygiene. 2012;9(2):99–109.
Chen H, Zhang Z, Zhang Z, et al. Enhancement of filtration efficiency by electrical charges on nebulized particles. Particuology. 2017;37:81–90.
Meng X, Ma Y, Chen R, et al. Size-fractionated particle number concentrations and daily mortality in a Chinese city. Environ Health Perspect. 2013;121(10):1174.
Zanobetti A, Schwartz J, Gold D. Are there sensitive subgroups for the effects of airborne particles? Environ Health Perspect. 2000;108(9):841.
Kan H, London SJ, Chen G, et al. Differentiating the effects of fine and coarse particles on daily mortality in shanghai, China. Environ Int. 2007;33(3):376–84.
Franck U, Odeh S, Wiedensohler A, et al. The effect of particle size on cardiovascular disorders—the smaller the worse. Sci Total Environ. 2011;409(20):4217–21.
TSI Incorporated. Mechanisms of filtration for high efficiency fibrous filters. 2012. Available: http://www.tsi.com/uploadedFiles/_Site_Root/Products/Literature/Application_Notes/ITI-041.pdf [Accessed: 21 September, 2016].
Schwarze PE, Øvrevik J, Låg M, et al. Particulate matter properties and health effects: consistency of epidemiological and toxicological studies. Human & experimental toxicology. 2006;25(10):559–79.
Swiston JR, Davidson W, Attridge S, et al. Wood smoke exposure induces a pulmonary and systemic inflammatory response in firefighters. Eur Respir J. 2008;32(1):129–38.
Reddel HK, Taylor DR, Bateman ED, et al. An official American Thoracic Society/European Respiratory Society statement: asthma control and exacerbations: standardizing endpoints for clinical asthma trials and clinical practice. Am J Respir Crit Care Med. 2009;180(1):59–99.
Sarnat SE, Raysoni AU, Li WW, et al. Air pollution and acute respiratory response in a panel of asthmatic children along the US-Mexico border. Environ Health Perspect. 2012;120(3):437.
Strak M, Janssen NA, Godri KJ, et al. Respiratory health effects of airborne particulate matter: the role of particle size, composition, and oxidative potential-the RAPTES project. Environ Health Perspect. 2012;120(8):1183.
La Grutta S, Ferrante G, Malizia V, et al. Environmental effects on fractional exhaled nitric oxide in allergic children. J Allergy. 2012;2012:6. Article ID 916926.
Mills NL, Robinson SD, Fokkens PHB, et al. Exposure to concentrated ambient particles does not affect vascular function in patients with coronary heart disease. Environ Health Perspect. 2008;116(6):709.
Patel MM, Miller RL. Air pollution and childhood asthma: recent advances and future directions. Curr Opin Pediatr. 2009;21(2):235.
Corradi M, Gergelova P, Mutti A. Use of exhaled breath condensate to investigate occupational lung diseases. Curr Opin Allergy Clin Immunol. 2010;10(2):93–8.
Brook RD, Rajagopalan S, Pope CA, et al. Particulate matter air pollution and cardiovascular disease an update to the scientific statement from the American Heart Association. Circulation. 2010;121(21):2331–78.
Lucking AJ, Lundbäck M, Barath SL, et al. Particle traps prevent adverse vascular and Prothrombotic effects of diesel engine exhaust inhalation in MenClinical perspective. Circulation. 2011;123(16):1721–8.
Xu Y, Barregard L, Nielsen J, et al. Effects of diesel exposure on lung function and inflammation biomarkers from airway and peripheral blood of healthy volunteers in a chamber study. Part Fibre Toxicol. 2013;10(1):1.
Lohmann-Matthes ML, Steinmuller C, Franke-Ullmann G. Pulmonary macrophages. Eur Respir J. 1994;7(9):1678–89.
van EEDENSF, Tan WC, Suwa T, et al. Cytokines involved in the systemic inflammatory response induced by exposure to particulate matter air pollutants (PM10). Am J Respir Crit Care Med. 2001;164(5):826–30.
Törnqvist H, Mills NL, Gonzalez M, et al. Persistent endothelial dysfunction in humans after diesel exhaust inhalation. Am J Respir Crit Care Med. 2007;176(4):395–400.
Barath S, Mills NL, Lundbäck M, et al. Impaired vascular function after exposure to diesel exhaust generated at urban transient running conditions. Part Fibre Toxicol. 2010;7(1):1.
Denardo SJ, Nandyala R, Freeman GL, et al. Pulse wave analysis of the aortic pressure waveform in severe left ventricular systolic dysfunction. Circulation: Heart Failure. 2010;3(1):149–56.
Lundback M, Mills NL, Lucking A, et al. Experimental exposure to diesel exhaust increases arterial stiffness in man. Part Fibre Toxicol. 2009;6(7):928.
Wilkinson IB, MacCallum H, Flint L, et al. The influence of heart rate on augmentation index and central arterial pressure in humans. J Physiol. 2000;525(1):263–70.
Li Y, Tokura H, Guo YP, et al. Effects of wearing N95 and surgical facemasks on heart rate, thermal stress and subjective sensations. Int Arch Occup Environ Health. 2005;78(6):501–9.
U.S. Food & Drug Administration. 2015. Available: http://www.fda.gov/medicaldevices/productsandmedicalprocedures/generalhospitaldevicesandsupplies/personalprotectiveequipment/ucm055977.htm [Accessed: 21 September, 2016].
The study was supported by Natural Science Foundation of China (grant no. 21190051, 41421064, 41121004, 21507166), the Ministry of Science and Technology project (grant no. 2015CB553401), and the Collaborative Innovation Center for Regional Environmental Quality, for data collection and data analysis.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study was approved by the Institutional Review Board of the Peking University Health Science Center (approval no. 13073), and written informed consent was obtained from all participants before enrollment.
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The authors declare that they have no competing interests
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Guan, T., Hu, S., Han, Y. et al. The effects of facemasks on airway inflammation and endothelial dysfunction in healthy young adults: a double-blind, randomized, controlled crossover study. Part Fibre Toxicol 15, 30 (2018). https://doi.org/10.1186/s12989-018-0266-0
- N95 facemask
- Filtration efficiency
- Ambient particulate matter
- Airway inflammation
- Endothelial dysfunction
- Oxidative stress