|
|
||||||||
1 Unit of Environmental Epidemiology, National Public Health Institute, 70701, Kuopio, 2 Institute of Environmental Physics, University of Tartu, Ülikooli street 18, EE2400, Tartu, Estonia and 3 Dept of Environmental Sciences, University of Kuopio, 70211, Kuopio, Finland
CORRESPONDENCE: J. Pekkanen, Unit of Environmental Epidemiology, National Public Health Institute, 70701, Kuopio, Finland. Fax: 35817201265
Keywords: air pollution, asthma, particles, particle size, peak expiratory flow rate, respiratory symptoms
Received: January 27, 2000
Accepted May 28, 2000
This
study was supported by the EU ENVIRONMENT and CLIMATE Research Programme Contracts
ENV4-CT96-0205 and ENV4-CT97-0568 and the Academy of Finland.
P. Penttinen was supported financially by the North-Savo Cultural Foundation.
| Abstract |
|---|
|
|
|---|
To test the hypothesis adult asthmatics were followed with daily peak expiratory flow (PEF) measurements and symptom and medication diaries for six months, while simultaneously monitoring particulate pollution in ambient air. The associations between daily health endpoints of 57 asthmatics and indicators of air pollution were examined by multivariate regression models.
Daily mean number concentration of particles, but not particle mass (PM10 (particle mass <10 µm), PM2.510, PM2.5, PM1), was negatively associated with daily PEF deviations. The strongest effects were seen for particles in the ultrafine range. However, the effect of ultrafine particles could not definitely be separated from other traffic generated pollutants, namely nitric oxide, nitrogen dioxide and carbon monoxide. No associations were observed with respiratory symptoms or medication use.
Particle mass measurements can be strongly influenced by mechanically produced, soil-derived particles, which may not be associated with adverse health effects. Therefore, air quality monitoring should include particle number concentrations, which mainly reflect ultrafine particles.
A number of studies have shown that urban particulate air pollution is associated with declines in peak expiratory flow and increased respiratory symptoms, hospital admissions and mortality from cardiorespiratory causes 16. However, the biological mechanism of these effects is unclear. It has been suggested that the high number of particles below 0.1 µm in diameter (ultrafine particles) may be responsible for the adverse health effects of particulate air pollution 79. To test this hypothesis the authors conducted a half-year follow-up study with daily peak expiratory flow (PEF) measurements on a group of 57 adult asthmatics. Simultaneously with the health study, an extensive ambient air monitoring campaign was conducted in a central monitoring site.
Existing air quality standards in the European Union use a gravimetric measure of particulate matter <10 µm in aerodynamic diameter PM10, as a basis for standard setting. However, in the subarctic climatic conditions of Finland, high levels of PM10 are frequently caused by resuspended road dust in autumn and spring. A secondary objective of the study was to determine whether the health effects of PM10 measurements (including resuspended road dust) differ from air quality indicators reflecting traffic exhaust.
| Material and methods |
|---|
|
|
|---|
The study group consisted of 78 adult asthmatic persons from urban Helsinki. The group was recruited with newspaper announcements, direct mail, and through the local association of pulmonary disabled. Only adult, non-smoking asthmatics were admitted to the group. Asthma diagnosis was confirmed from the sickness insurance card supplied by the Social Insurance Institution of Finland. The entire study group resided within 2 km of the air quality monitoring site to ensure that the point measurement of pollutants reflects the pollutant exposure of the study subjects as well as possible.
The results of 57 subjects out of 78 (73%) were used for the study. A total of 125 (60% of possible days) participation days was required for a person to be included in the analysis and this was the reason for exclusion of 20 subjects, most of whom dropped out during the first week. One subject was excluded because of unreliable reporting and one subject because asthma diagnosis could not be confirmed.
The respiratory health of the subjects was monitored daily with PEF measurements and a symptom and medication diary. In addition, the subjects visited the study clinic biweekly to perform a spirometric lung function test. The symptom diary included a numerical (scale 03) estimate on the severity of the following symptoms: cough, phlegm, a runny/stuffed nose, awakened by breathlessness, breathlessness, wheezing, attack involving breathlessness and wheezing, and fever. The names, dosages and daily doses of respiratory medication were also recorded in the diary. Finally, the diary included numerical estimates of time spent outdoors, time spent in locations with tobacco smoke, and time spent outside of urban Helsinki. The study subjects measured PEF values every day in standing position immediately after getting up (06:0012:00), after work (14:0018:00) and before going to sleep (18:0000:00) with a mini-Wright peak flow meter (Airmed; Clement Clarke International, Essex, UK). Each measurement included three blows, and all of them were recorded in the diary. The subjects were advised to do the measurements before taking any medication or having a meal. In addition, a supervised PEF-manoeuvre was done at each biweekly clinic visit to verify correct performance of the measurement. The subjects were also characterised with a standard methacholine challenge test and a skin-prick test with the 13 most common local allergens.
Air pollutants were monitored on a fixed site in central urban Helsinki. Daily variation of particle number concentrations measured at this fixed site reflects well those measured in other sites in urban Helsinki 10. Particulate air pollution was monitored with five methods. Number concentration of particles in the size range 0.0110 µm were measured continuously with an Electric Aerosol Spectrometer (EAS; University of Tartu, Tartu, Estonia) in 12 size ranges, all of which were added up to get the total particle number concentration (PNC). The first 4 size ranges were added up for NC0.010.1 and the next 4 were added up for NC0.11. EAS has been shown to be comparable to other aerosol spectrometers for particle numbers in the submicrometer range, but may overestimate the number of larger particles 11. For quality control purposes, particle counts were also monitored continuously with a Condensation Nuclear Counter (CNC; TSI Inc, St. Paul, MN, U.S.A.). The correlation coefficient between PNC and particle counts measured by CNC was 0.98. Twenty-four hour particle mass concentrations were monitored with single-stage Harvard impactors (Air diagnostics and engineering, Naples, ME, USA) for particles <10 µm (PM10), <2.5 µm (PM2.5) and <l µm (PM1) in diameter. Coarse particle mass (PM2.510) was calculated by subtracting the value of PM2.5 from the value of PM10. The particle monitors were located approximately 50 m away from major traffic sources in a residential neighbourhood. Gaseous pollutants were measured with continuously recording monitors at the same site. Carbon monoxide (CO) was measured with a CO10M (Environment, Poissy, France), nitric oxide (NO) and nitrogen dioxide (NO2) with an AC30M (Environment), sulphur dioxide (SO2) with Thermo Environmental model 43 (Thermo Environmental Instruments Inc., Franklin, MA, U.S.A) and O3 with Thermo Environmental model 49 (Thermo Environmental Instruments Inc.). The data for gaseous pollutants and meteorological parameters (wind speed, wind direction, relative humidity, minimum temperature) were provided by the Helsinki Metropolitan Area Council (YTV).
Twenty-four hour mean values of pollutants (from noon to noon) were used in the analyses. Lag0 was defined as the 24 h period ending on the noon of the day when the PEF was measured. Five-day average was defined as a mean of lag0lag4.
To ensure the reliability of the reported PEF data, the following procedures were used. The highest of the three consecutive PEF-values was accepted for the analysis only if it was within 10% of the next highest value. If the difference was greater than 10%, the median value was chosen. The first four days of data for PEF of each participant were omitted to control for a possible "learning effect" in the manoeuvre.
Daily mean peak flow deviation (PEF deviation, separately for morning, afternoon and evening), daily symptom prevalence and daily mean use of bronchodilators were used as dependent variables in the analyses. For PEF analysis, the individual means were first calculated separately for morning, afternoon and evening PEF. Then individual means were subtracted from the individual daily values of PEF to get an individual daily deviation. Finally, a daily group mean (PEF deviation) for these individual deviations was calculated. For symptom analysis, a daily binary variable (symptoms/no symptoms) for each individual and each symptom was derived. A subject was coded to have an asthmatic symptom if any of the following symptoms were present on a given day: woken by breathlessness, breathlessness, wheezing, or an attack involving breathlessness and wheezing. Daily prevalences were calculated by dividing the sum of subjects with symptoms by the number of subjects answering that day.
Data were obtained on influenza activity from the Helsinki City Health Authorities and pollen counts from the Finnish Aerobiology Group 12 to control for potential confounding. Influenza activity was reported to be increased during the end of January and beginning of February. However, no serious epidemics were reported. Fever reporting was not increased during that period in the study group. Pollen counts were negligible during the whole study period and were not considered as confounders.
Preliminary analysis was done using a linear regression with only individual pollutants or meteorological variables and their lags up to three days as independent variables. Linearity was examined from scatter plots of PEF deviation versus variables. The preliminary analysis and visualisation of data were done with S-Plus 4.0 (Mathsoft Inc., Cambridge, MA, U.S.A.).
The final regression model was determined by including all the covariates associated with PEF deviation that changed the estimate of the pollutant in the model. The time trend used in the final model was the most parsimonious trend that did not leave any visually observable trend in the residual plot.
Final analyses were done using a first order autoregressive linear model to model for each PEF deviation and symptom score individually. The model for PEF deviation included a continuous variable of temperature and relative humidity, a day of study variable, day of study squared and a binary dummy variable to adjust for weekends. The model for symptom prevalence and bronchodilator use was adjusted for day of study, day of study squared, minimum temperature, minimum temperature squared, relative humidity, relative humidity squared and weekends. The models were weighted with daily numbers of participants to account for the differences in the number of participants between different days. Residual plots for the individual pollutants were examined for potential outliers and heteroscedasticity. The final analyses were done with Statistical Analysis Software (SAS) (SAS Institute Inc., Cary, NC, U.S.A.).
The study was approved by the ethics committees of the Skin and Allergy Hospital at Helsinki and the National Public Health Institute. Written informed consent was obtained from all of the participants. The procedures used in the study were in accordance with the Helsinki Declaration.
| Results |
|---|
|
|
|---|
|
|
|
|
|
|
|
|
|
| Discussion |
|---|
|
|
|---|
In a previous study, both PNC and particle mass were negatively associated with PEF in a group of asthmatic children 14. This previous study was done in Kuopio, Finland during mid-winter, when resuspended road dust did not have any significant effect on the particle mass measurements. Therefore, the findings of this paper and the previous study 14 are both consistent with an adverse effect on PEF by combustion particles, but less of an effect by resuspended particles.
Several toxicological studies have shown that particles cause inflammatory reaction in vitro and in vivo. Particles collected from the environment cause inflammatory reactions in rat lungs, rat cell lines and human cell lines 1517. Free radical activity or oxidative capacity of particulate matter might be essential for provoking these inflammatory responses. There is also evidence suggesting that the bulk of free radical activity is caused by the ultrafine fraction of urban ambient particles 18. Animal studies have also shown that ultrafine titanium and polytetrafluoroethylene (Teflon) particles can cause inflammatory responses in rat lungs 19, 20.
The oxidative capacity of particulate matter could be mediated by the substances attached to fine and ultrafine carbon particles. Carbon particles derived from combustion processes are the most numerous particles in the ultrafine range. Carbon particles aggregate easily into clusters containing substances like iron, other transition metals, volatile organic compounds and polycyclic aromatic hydrocarbons, which all have been associated with the inflamnmatory reaction caused by particles 1822. It has also been suggested that the inflammatory properties of ultrafine particles are mediated by their large numbers, small size and high penetration rate into the interstitium, independently of their chemical composition 23.
In the present data, mass measurements of particulate matter (PM10, PM2.510, PM2.5, and PM1)
were strongly influenced by road dust. The road dust phenomenon is typical
for subarctic weather conditions where the roads are sanded in the winter
for traffic safety and the use of studded tyres is common 24. Highest PM10 levels due to resuspended
road dust are observed in late fall and early spring, when snow cover does
not prevent resuspension. A large amount of evidence exists on the negative
health effects of particulate matter mass measured by impactors 1, 14, 21. However, this
study was not able to show any significant negative associations of PM10, PM2.510, PM2.5 or PM1 with
PEF deviations. In the linear regression models PM10, PM2.510 and PM2.5 were positively associated with PEF deviation,
but the residuals of the models did not have constant variance and the models
were somewhat sensitive to adjustments for time trend. This may be due to
the seasonal differences in the composition of particulate matter observed
in the present study, or it may reflect the relatively low levels and low
variation of particulate mass in the present study. Only very limited conclusions
can therefore be drawn from the linear regression models of PM10
or PM2.510 in table 3
.
In previous studies, mass measurements of particulate matter may have been surrogates for total number concentration, as the correlation between PM10 and number concentrations are, in general, relatively strong 7, 8. In contrast, in the present study, the correlation coefficients for mass measurements and PNC were 0.40 (PM1), 0.30 (PM2.5) and 0.30 (PM10). This low correlation is probably explained by the road dust phenomenon i.e. in the present study, variation in coarse particle concentrations was dominated by resuspended dust, not combustion sources.
In the present study, PNC was correlated with traffic generated gaseous pollutants. These pollutants were also associated with decreases in PEF rates although the associations tended to be less significant than those of PNC and also, except for the 5-day average of CO, smaller in magnitude. Due to the intercorrelation of the pollutants, it is difficult to distinguish the respiratory effects of PNC from that of CO or NOx. Two-pollutant models including either CO, NO or NO2 and PNC generally decreased the effect estimates and increased the standard errors for both pollutants included in the model.
The present results show that particle number concentrations in ambient air, especially in the ultrafine range, are negatively associated with the respiratory health of adult asthmatics. The effects of ultrafine particles could not be definitely separated from the effects of other traffic generated pollutants, namely oxides of nitrogen and carbon monoxide. In this study, no negative effect of particle mass was seen, probably because variation in particle mass <10 µm concentration was dominated by soil-derived, coarse particles. Current findings suggest that possibly particle number concentrations, in addition to mass measurements with impactors, should be used in air quality monitoring. These results also suggest that high levels of coarse, soil-derived particles observed in subarctic climates in the spring are not associated with as severe health effects as traffic generated particles.
| Acknowledgements |
|---|
|
|
|---|
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
Z J Andersen, S Loft, M Ketzel, M Stage, T Scheike, M N Hermansen, and H Bisgaard Ambient air pollution triggers wheezing symptoms in infants Thorax, August 1, 2008; 63(8): 710 - 716. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z J Andersen, P Wahlin, O Raaschou-Nielsen, M Ketzel, T Scheike, and S Loft Size distribution and total number concentration of ultrafine and accumulation mode particles and hospital admissions in children and the elderly in Copenhagen, Denmark Occup. Environ. Med., July 1, 2008; 65(7): 458 - 466. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Holder, D. Lucas, R. Goth-Goldstein, and C. P. Koshland Cellular Response to Diesel Exhaust Particles Strongly Depends on the Exposure Method Toxicol. Sci., May 1, 2008; 103(1): 108 - 115. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. T. Stern and S. E. McNeil Nanotechnology Safety Concerns Revisited Toxicol. Sci., January 1, 2008; 101(1): 4 - 21. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. McCreanor, P. Cullinan, M. J. Nieuwenhuijsen, J. Stewart-Evans, E. Malliarou, L. Jarup, R. Harrington, M. Svartengren, I.-K. Han, P. Ohman-Strickland, et al. Respiratory Effects of Exposure to Diesel Traffic in Persons with Asthma N. Engl. J. Med., December 6, 2007; 357(23): 2348 - 2358. [Abstract] [Full Text] [PDF] |
||||
![]() |
P E Schwarze, J Ovrevik, M Lag, M Refsnes, P Nafstad, R B Hetland, and E Dybing Particulate matter properties and health effects: consistency of epidemiological and toxicological studies Human and Experimental Toxicology, October 1, 2006; 25(10): 559 - 579. [Abstract] [PDF] |
||||
![]() |
B. Brunekreef and B. Forsberg Epidemiological evidence of effects of coarse airborne particles on health Eur. Respir. J., August 1, 2005; 26(2): 309 - 318. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-M. Kim, W. Reed, A. G. Lenz, I. Jaspers, R. Silbajoris, H. S. Nick, and J. M. Samet Ultrafine carbon particles induce interleukin-8 gene transcription and p38 MAPK activation in normal human bronchial epithelial cells Am J Physiol Lung Cell Mol Physiol, March 1, 2005; 288(3): L432 - L441. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. C. Nygaard, M. Samuelsen, A. Aase, and M. Lovik The Capacity of Particles to Increase Allergic Sensitization Is Predicted by Particle Number and Surface Area, Not by Particle Mass Toxicol. Sci., December 1, 2004; 82(2): 515 - 524. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Katsouyanni Ambient air pollution and health Br. Med. Bull., December 1, 2003; 68(1): 143 - 156. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. J. de Hartog, G. Hoek, A. Peters, K. L. Timonen, A. Ibald-Mulli, B. Brunekreef, J. Heinrich, P. Tiittanen, J. H. van Wijnen, W. Kreyling, et al. Effects of Fine and Ultrafine Particles on Cardiorespiratory Symptoms in Elderly Subjects with Coronary Heart Disease: The ULTRA Study Am. J. Epidemiol., April 1, 2003; 157(7): 613 - 623. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. v. Klot, G. Wolke, T. Tuch, J. Heinrich, D.W. Dockery, J. Schwartz, W.G. Kreyling, H.E. Wichmann, and A. Peters Increased asthma medication use in association with ambient fine and ultrafine particles Eur. Respir. J., September 1, 2002; 20(3): 691 - 702. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Pekkanen, A. Peters, G. Hoek, P. Tiittanen, B. Brunekreef, J. de Hartog, J. Heinrich, A. Ibald-Mulli, W. G. Kreyling, T. Lanki, et al. Particulate Air Pollution and Risk of ST-Segment Depression During Repeated Submaximal Exercise Tests Among Subjects With Coronary Heart Disease: The Exposure and Risk Assessment for Fine and Ultrafine Particles in Ambient Air (ULTRA) Study Circulation, August 20, 2002; 106(8): 933 - 938. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Granum and M. Lovik The Effect of Particles on Allergic Immune Responses Toxicol. Sci., January 1, 2002; 65(1): 7 - 17. [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |