Advertisement Banner
Skip to content

EHP

Short-Term Effects of PM10 and NO2 on Respiratory Health among 
Children with Asthma or Asthma-like Symptoms: A Systematic Review 
and Meta-Analysis

Gudrun Weinmayr1, Elisa Romeo2, Manuela De Sario2, Stephan K. Weiland1, Francesco Forastiere2

1 Institute of Epidemiology, Ulm University, Ulm, Germany, 2 Department of Epidemiology, Local Health Authority Rome E, Rome, Italy



Environ Health Perspect 118:449-457 (2010). http://dx.doi.org/10.1289/ehp.0900844 [online 12 November 2009]

Review

Abstract

Objective: Our goal was to quantify the short-term effects of particulate matter with aerodynamic diameter ≤ 10 µm (PM10) and nitrogen dioxide (NO2) on respiratory health of asthmatic children from published panel studies, and to investigate the influence of study and population characteristics as effect modifiers.

Data extraction: After a systematic literature review, we extracted quantitative estimates of the association of PM10 and/or NO2 with respiratory symptoms and peak expiratory flow (PEF). Combined effect estimates for an increase of 10 µg/m3 were calculated by random effects meta-analysis for all studies and for different strata defined by study characteristics. The effect of publication bias was investigated with Egger’s and Begg’s tests and “trim-and-fill” analyses.

Data synthesis: We identified 36 studies; 14 were part of the European Pollution Effects on Asthmatic Children in Europe (PEACE) study. Adverse associations of PM10 with asthma symptoms were statistically significant [odds ratio (OR) = 1.028; 95% confidence interval (CI), 1.006–1.051]. There were also associations, although not statistically significant, of PM10 with cough (OR = 1.012; 95% CI, 0.997–1.026) and on PEF (decrease of –0.082 L/min; 95% CI, –0.214 to 0.050). NO2 had statistically significant associations with asthma symptoms in the overall analysis considering all possible lags (OR = 1.031; 95% CI, 1.001–1.062), but not when we evaluated only the 0–1 lag. We found no publication bias, although it appeared when excluding the PEACE studies. When we applied the trim-and-fill method to the data set without the PEACE studies, the results were similar to the overall estimates from all studies. There was an indication for stronger PM10 associations for studies conducted in summer, outside of Europe, with longer lags, and in locations with higher NO2 concentrations.

Conclusions: We found clear evidence of effects of PM10 on the occurrence of asthma symptom episodes, and to a lesser extent on cough and PEF. The results for NO2 are more difficult to interpret because they depend on the lag times examined. There was an indication of effect modification by several study conditions.

Key words: air pollution, asthma, children, NO2, PM, short-term effects

Address correspondence to G. Weinmayr, Institute of Epidemiology, Ulm University, Helmholtzstr. 22, D-89081 Ulm, Germany. Telephone: 49-731-50-31071. Fax: 49-731-50-31069. E-mail: gudrun.weinmayr@uni-ulm.de

The authors declare they have no competing financial interests.

We thank A. Kleiner for her help in statistical analyses and construction of the tables and M. Schmidt for preparing the graphs.

Received 27 March 2009; accepted 12 November 2009; online 12 November 2009.

S.K.W. is now deceased.

Particulate matter (PM) with an aerodynamic diameter ≤ 10 µm (PM10) and nitrogen dioxide (NO2) are important ambient air pollutants regulated by European and national legislations. Measurements of PM10 include PM of different aerodynamic diameter (coarse, fine, and ultrafine PM), and the size distribution is related to the emission source, with the coarse fraction mainly originating from soil and natural sources and fine and ultrafine PM mainly originating from combustion or being secondary aerosols from sources that can be far away (Williams 1999). Notwithstanding possible long-range transport, most of NO2 in the ambient air arises from oxidization of emitted NOx from combustion mainly from motor engines in urban areas (Williams 1999), and it is considered to be a good marker of traffic-related air pollution.

The health effects of PM10 and NO2 have been extensively reviewed, and air quality standards and guidelines have been proposed to protect public health [U.S. Environmental Protection Agency (EPA) 2005, 2008a; World Health Organization (WHO) Regional Office for Europe 2000, 2006]. Nevertheless, important clinical effects are currently detectable in real-life exposure to traffic-related pollutants among susceptible subgroups of the population, such as individuals with asthma. A recent study from London has clearly shown that asthmatic adults have a significant decrease in lung function after 2 hr of walking along a street in the center of London as opposed to walking in a nearby park (McCreanor et al. 2007). The effects were stronger in individuals with moderate asthma compared with individuals with mild asthma. Several studies have been conducted among children with asthma focusing on the short-term effects of air pollution, that is, its effects on daily symptoms and lung function. Most studies used air pollution measurements from central monitoring sites that provide daily data. Mostly PM10, NO2, and ozone (O3) have been evaluated; results for carbon monoxide, black smoke, and PM2.5 (PM with aerodynamic diamter ≤ 2.5 µm) have been less reported to date. Studies on long-term effects typically involve proximity of the residence to roads, but they do not provide information on short temporal scales.

Both PM10 and NO2 have been associated with increases in the frequency of asthma symptoms and with lung function decrements in children on a day-to-day scale (Gielen et al. 1997; Ostro et al. 2001; Pope and Dockery 1992; Roemer et al. 1993; Romieu et al. 1996; Schildcrout et al. 2006; van der Zee et al. 1999; Vedal et al. 1998). However, the results of the existing studies have not been consistent, and a comprehensive quantitative evaluation of the respiratory effect in children is still lacking.

Two meta-analyses on the short-term effects of PM10 on children’s respiratory health have previously been performed (Anderson et al. 2004; Ward and Ayres 2004). Anderson et al. (2004) reviewed the effects on cough and medication use in European panel studies, a large number of which were conducted within the multicenter PEACE (Pollution Effects on Asthmatic Children in Europe) study that provided 28 of the 34 effect estimates. In their review, they found no effect of PM10 on cough in children [odds ratio (OR) = 0.999 for 10-µg/m3 increase in PM10; 95% confidence interval (CI), 0.987–1.011]. Ward and Ayres (2004) performed a meta-analysis of worldwide panel studies published through 2002 that included asthmatic and healthy children. They found a significant effect of PM10 on cough (OR = 1.004 per unit µg/m3 increase PM10; 95% CI, 1.002–1.006), on lower respiratory symptoms (LRS) or wheeze (OR = 1.004 per 1 µg/m3 PM10; 95% CI, 1.002–1.005), and on peak expiratory flow (PEF) (a decrease of –0.033 L/min per 1 µg/m3 in PM10; 95% CI, –0.019 to –0.047). In both meta-analyses, the results of the large multicenter European PEACE study had a strong influence because of its primarily null results.

To our knowledge, no quantitative meta-analysis on the effects of NO2 among children with asthma has so far been performed. The available evidence is inconsistent, with some studies showing a detrimental effect of NO2 on symptoms or lung function and other investigations indicating no effect (Ackermann-Liebrich and Rapp 1999).

To provide a quantitative estimate of the acute effects of short-term exposure to PM10 and NO2 on respiratory symptoms and lung function in asthmatic children, we performed a meta-analysis on panel studies published through July 2008. We assessed the role of the PEACE study on the overall evaluation, and we paid specific attention to the influence of publication bias. Because study characteristics and pollution mixtures vary with space and time, some heterogeneity among the study results conducted at different locations is to be expected. We therefore investigated the influence of study and population characteristics on the outcomes.

Methods

We conducted a systematic search of the literature from 1990 through July 2008 that focused on the short-term effects of outdoor NO2 and PM10 on respiratory health outcomes as determined in panel studies. To focus our study, we did not consider exposure to O3 or studies on indoor exposure; the latter has been typically investigated for long-term effects. We investigated lung function as measured by PEF and symptoms of cough and asthma, the latter being reported as wheeze or LRS. A MEDLINE (National Library of Medicine 2008) search was carried out; the search strings consisted of “asthma OR wheeze OR cough OR bronchitis OR lung function,” “air AND pollut*,” and “PM10 OR PM(10)” and “NO2 OR “NO(2)” OR “nitrogen dioxide.” Limits were set to retrieve only children (“All Child 0–18 years”). The exact search history is available from the authors. These criteria were applied to maximize sensitivity and to not miss any relevant publication. The age range of children in the panel studies was 5–19 years. Wheezing among infants was not considered because the asthma phenotype differs in very young children and there are essentially no panel studies on infants.

The references were then selected by hand according to the following inclusion/exclusion criteria: exclusion of indoor and laboratory studies; inclusion of panel studies on asthmatic or symptomatic (see definition below) children that reported a quantitative effect (regression coefficients); inclusion of only one publication of the same study/database for each outcome. With regard to the statistical analysis, we included only studies that controlled for the effect of daily temperature and day of the week, because these are important confounders and should be adjusted for to detect short-term effects of air pollution.

For the definition of “asthmatics” or “symptomatic” children, we relied on the criteria reported in the individual publications. Generally, children with asthma confirmed by a physician or who were referred from clinics, school nurses, and so on, with an asthma diagnosis were classified as “asthmatics.” We considered “symptomatic” children who reported, mostly in a questionnaire, wheezing or cough apart from cold or an asthma diagnosis, or who took medication for asthma.

The evaluated outcomes were “asthma symptoms” and “cough,” and the definitions differed in various studies, as indicated in “Results.” For PEF, we included only studies that reported changes as liters per minute or that allowed us to calculate the changes in liters per minute from the given percentages and were therefore directly comparable. Other lung function parameters and exhaled nitrogen oxide were not considered, because these studies are relatively scarce.

For the meta-analysis, we used the coefficients derived from single-pollutant models. Where necessary, the coefficient estimates were recalculated to reflect a 10-µg/m3 increase in pollutant assuming a linear relationship over the considered range. When coefficients for different lag times were given, we used the one that resulted in a statistically significant effect or, when all estimates were either significant or not significant, the lag reflecting the highest effect size. The same criterion was applied if lung function measurements were performed in the morning and in the evening. These criteria were modified in a sensitivity analysis as indicated below.

Combined estimates of the natural logarithm of the OR for respiratory symptoms and the linear regression coefficients for PEF, respectively, were calculated for all studies with a fixed effects and a random effects meta-analysis model (DerSimonian and Laird 1986; Petitti 2001) using the meta command of STATA (releases 8 and 9.1; StataCorp., College Station, TX, USA). This command uses inverse-variance weighting to calculate combined estimates. Although a fixed-effects model assumes that the studies reflect the same underlying average effect, in a random-effects model the study effects are coming from a common underlying distribution of effects. The corresponding weights include an additional term that reflects the between-study heterogeneity due to unexplained sources. Heterogeneity was assessed by calculating the I2 of Higgins and Thompson, which reflects the proportion of total variation in the combined estimate that is due to heterogeneity between studies (Higgins and Thompson 2002).

We evaluated publication bias with both the Begg test and the Egger test (Begg and Mazumdar 1994; Egger et al. 1997). The Egger et al. regression asymmetry test tends to suggest the presence of publication bias more frequently than the Begg adjusted rank correlation test, which has a low power.

Where necessary, a trim-and-fill analysis was performed to take account of publication bias (Duval 2000). This procedure estimates the number and outcomes of theoretical missing studies and incorporates them into the meta-analysis. All the calculations were done using the metabias and metatrim commands in STATA.

To explore heterogeneity in meta-analysis 
estimates, we considered the influence of the following study characteristics on meta-analytical estimates: continent (Europe; other countries), season (summer only; any other cases), population [asthmatics (confirmed diagnosis); symptomatics], duration (≤ 2 or > 2 months), lag (≤ 2 or > 2 days), average PM10 levels (< 40 or ≥ 40 µg/m3), and average NO2 levels (< 40 or ≥ 40 µg/m3). The influence of study characteristics was investigated by calculating the combined effect for each stratum and evaluating the difference between strata-specific estimates. The null hypothesis that the difference between the estimates from the two strata equals 0 was tested (with Z-score), and the corresponding p-value is reported here. Statistical significance was defined as p < 0.05 for all analyses.

Because the choice of the lag was a critical step, we performed additional analyses using, for all the studies, the effect estimate at lag 0–1 (instead of the most significant lag). The following criteria were applied. The default was lag 1; if lag 1 was not available, lag 0 or lag 0–1 was considered instead. In addition, we calculated the combined effects for PEF using only the evening values.

Results

We retrieved a total of 77 references for PM10 and 324 for NO2. Applying the inclusion/exclusion criteria outlined in “Materials and Methods,” 36 studies on PM10 and 24 on NO2 remained to be included in the meta-analysis (Table 1). Some of the excluded studies were on indoor NO2, notably related with cooking and heating. Other studies were time-series analyses on hospital admissions, and a few studies were on pathologic mechanisms and exposure assessment. Of the total of 36 studies (on 51 populations), 14 were PEACE studies (28 populations). In this review, we refer to each population as a separate study and use the corresponding estimates. Peacock et al. (2003) studied a subgroup of wheezy children but did not give estimates for the coefficient for this group. Nevertheless, because the authors stated that there was no effect modification by wheeze, we took the estimate for all children instead.

Table 1: Study characteristics of the panel studies.

Table 1

Study characteristics of the panel studies.

Download larger image (TIF File)

Of the total of 51 populations studied, 36 were from Europe and 15 from elsewhere, mainly the United States. Thirty populations were from urban areas, and 20 studies were conducted in rural environments (one unspecified). Four studies were carried out in the summer only; the other studies were conducted mainly in winter or during most of the year. The mean 24-hr average for NO2 ranged from 8 to 77 µg/m3, and the mean 24-hr average for PM10 ranged from 11 to 167 µg/m3 (but only Mexico City had a value of 167 µg/m3; all the others had a value < 100 µg/m3).

The definition of the outcome regarding asthma symptoms varied among the studies: We included the estimates for wheeze from five studies (Jalaludin et al. 2004; Roemer et al. 1993; Romieu et al. 1996, 1997; Vedal et al. 1998); 35 studies used a variable “lower respiratory symptoms” or “asthma symptoms,” which in most studies (including PEACE studies) consisted of wheezing, shortness of breath, and asthma attacks (Gielen et al. 1997; Ostro et al. 2001; Pope and Dockery 1992; Roemer et al. 1998b; van der Zee et al. 1999). Other studies also included chest tightness (Delfino et al. 1998, 2002, 2003; Mortimer et al. 2002; Yu et al. 2000), sputum production (Delfino et al. 2002, 2003), or cough (Delfino et al. 1998, 2002, 2003; Mortimer et al. 2002; Ostro et al. 2001; Pope and Dockery 1992; Yu et al. 2000). In the latter studies, no separate effect estimate for cough was given except by Pope and Dockery (1992). Cough was not more precisely defined except for nocturnal cough (Just et al. 2002), cough during the day or the previous night (Peters et al. 1997), and wet and dry cough (Pope and Dockery 1992).

The effect estimates extracted from the individual studies are given in the Supplemental Material, Table 1 (doi:10.1289/ehp.0900844) and are illustrated in Figures 13, which also give the combined effects calculated in the meta-analysis. When we considered all the studies in the fixed-effects models, we found a significant increase of 2.3% in asthma symptoms, 1.4% for cough, and –0.117 min/L for PEF for a 10-µg/m3 increase in PM10 (Table 2). However, we observed a considerable degree of heterogeneity among the studies, with I2 ranging from 35% to 77%. Therefore, the estimates based on the random effects model are likely to represent the overall effect more accurately. For an increase of 10 µg/m3 of PM10, we found a significant increase of 2.8% in asthma symptoms, and an increase for cough (1.2%) and a decrease of PEF (–0.082 L/min) that were borderline significant. For an increase of 10 µg/m3 NO2, we found a significant increase in asthma symptoms of 3.1%. We found no clear association of NO2 with cough or PEF; only when we excluded the PEACE studies did we find evidence of effect for NO2 on cough.

Figure 1: ORs with 95% CIs for the association between a rise of 10         µg/m3 PM10 (A) or NO2 (B) and the         occurrence of asthma symptoms. Abbreviations: FE, fixed effects; R, rural; RE,         random effects; U, urban.

Figure 1

ORs with 95% CIs for the association between a rise of 10 µg/m3 PM10 (A) or NO2 (B) and the occurrence of asthma symptoms. Abbreviations: FE, fixed effects; R, rural; RE, random effects; U, urban.

Download larger image (TIF File)

Figure 2: ORs with 95% CIs for the association between a rise of 10         µg/m3 PM10 (A) or NO2 (B) and the         occurrence of cough episodes. Abbreviations: FE, fixed effects; R, rural; RE, random         effects; U, urban.

Figure 2

ORs with 95% CIs for the association between a rise of 10 µg/m3 PM10 (A) or NO2 (B) and the occurrence of cough episodes. Abbreviations: FE, fixed effects; R, rural; RE, random effects; U, urban.

Download larger image (TIF File)

Figure 3: Mean increase in PEF (L/min) with 95% CIs for a rise of 10         µg/m3 PM10 (A) or NO2 (B).         Abbreviations: FE, fixed effects; R, rural; RE, random effects; U,         urban.

Figure 3

Mean increase in PEF (L/min) with 95% CIs for a rise of 10 µg/m3 PM10 (A) or NO2 (B). Abbreviations: FE, fixed effects; R, rural; RE, random effects; U, urban.

Download larger image (TIF File)

Table 2: Association of PM10 and NO2         exposure with episodes of asthma symptoms, episodes of cough, and PEF in         children symptomatic for or diagnosed with asthma.

Table 2

Association of PM10 and NO2 exposure with episodes of asthma symptoms, episodes of cough, and PEF in children symptomatic for or diagnosed with asthma.

Download larger image (TIF File)

When we considered all the studies, we found no evidence of publication bias. When we excluded the PEACE studies, publication bias was present for asthma symptoms for PM10 and NO2; after applying the trim-and-fill procedure, the random-effects estimates decreased from 5.5% to 3.5% and from 3.9 to 3.2, respectively, and were therefore similar to the estimates for all studies. We also saw a tendency for a similar publication bias for cough (PM10 and NO2), with significant values for the Egger test but not for the Begg test. However, the resulting trim-and-fill estimates for cough were more similar to those of the non-PEACE studies than to that for all studies (Table 2).

We found an effect modification of the effect of PM10 on asthma symptoms by continent (stronger association outside Europe), season (stronger association in studies carried out in summer only), study population (stronger effect among asthmatic children), and PM10 level (stronger association at levels < 40 µg/m3) (Table 3). When we excluded the PEACE studies, only season remained near significance (p < 0.1). For the effect of PM10 on cough (Table 4), there were higher associations in studies conducted outside of Europe, with lag > 2 days, or with higher NO2 levels; these effect modifications remained when excluding the PEACE studies. For the effect of PM10 on PEF (Table 4), there was a tendency for a higher decrease in PEF in asthmatic than in symptomatic children. We found no consistent effect modification, and there was no evidence for effect modification of the association between NO2 and any of the investigated outcomes s (Table 3 for asthma; for cough and PEF, data not shown).

Table 3: Stratum-specific combined estimates of the         association of PM10 and NO2 exposure with episodes         of wheezing in children symptomatic for or diagnosed with asthma.

Table 3

Stratum-specific combined estimates of the association of PM10 and NO2 exposure with episodes of wheezing in children symptomatic for or diagnosed with asthma.

Download larger image (TIF File)

Table 4: Stratum-specific combined estimates of the         association of PM10 exposure with change in PEF (L/min) and         with cough episodes in children symptomatic for or diagnosed with         asthma.

Table 4

Stratum-specific combined estimates of the association of PM10 exposure with change in PEF (L/min) and with cough episodes in children symptomatic for or diagnosed with asthma.

Download larger image (TIF File)

The results of the sensitivity analyses based on the predefined lag 0–1 (i.e., lag 1 or 0 or 0–1) and on evening PEF showed mostly a similar pattern, especially for PM10, although the associations were generally weaker [see Supplemental Material, Table 3 (doi:10.1289/ehp.0900844)]. However, the associations of NO2 with asthma symptoms and cough were not significant in this analysis. We found effect modification even when we omitted the PEACE studies (see Supplemental Material, Tables 4 and 5), for the effect of NO2 on asthma symptoms, with higher associations for asthmatics and during the summer (the latter based on two studies in one stratum). Furthermore, the estimated effects of PM10 on asthma symptoms were higher at higher concentrations of NO2.

Discussion

Our meta-analysis shows effects of PM10 on both asthma symptoms and cough. We found no indication of publication bias when we considered all the evidence. For NO2, we found statistically significant associations with asthma symptoms in the overall analysis but not in the sensitivity analysis restricted to the 0–1 lags. The effects of air pollutants on PEF were limited to PM10, and we saw a stronger association when we excluded the PEACE studies from the analysis. We found an indication of effect modification of PM10, with higher associations with asthma symptoms during summer and with cough for studies conducted outside of Europe, for a lag > 2 days, and at higher ambient NO2 concentrations. When considering lags 0–1 only, the pattern of effect modification was different.

A previous meta-analysis considered panel studies in children and summarized the evidence for PM10 up through June 2002 (Ward and Ayres 2004). Our meta-analysis extends this work further up through July 2008, adding 11 studies. On the other hand, we did not include nine studies (two from Europe) included in the Ward and Ayres (2004) analysis because the panels evaluated asymptomatic children and we focused specifically on children with asthma. Our estimates of the PM10 effect on asthma symptoms and cough are similar to those of the previous meta-analysis [1.04 and 1.028 for asthma symptoms, 1.04 and 1.031 for cough in Ward and Ayres (2004) and in our analysis, respectively]. Our random effects estimate for PEF is weaker than that from Ward and Ayres (–0.082 vs. –0.33 L/min for a 10-µg/m3 increase), whereas the fixed effects estimates are similar (–0.117 vs. –0.12 L/min).

We found no publication bias when considering all studies. However, excluding the PEACE studies, which highly influenced the estimates from the meta-analyses, resulted in clear publication bias for asthma symptoms, but less so for cough. The PEACE studies reported, on average, no effects of air pollution, with very few individual centers showing an association with PM10 (Roemer et al. 1998a). It is, on the one hand, the only multicenter series of studies that has been conducted with a unified protocol and whose results are not biased by publication procedures. On the other hand, limitations of the PEACE study have to be considered (Roemer et al. 1998a, 2000). There is concern that the entire study series might have been influenced by an influenza epidemic during the study period. If the study period is relatively short (e.g., 2 months as in the PEACE study), such unexpected events might confound the results, and it is generally more difficult to adjust adequately for time trend. In our analyses, we found no significant difference between studies with durations longer or shorter than 2 months. Nevertheless, for asthma symptoms, the estimate from the studies with durations longer than 2 months was slightly higher and statistically significant. In the Netherlands, where the data was collected during three winters instead of just one, there were clear effects of air pollution in symptomatic children (Roemer et al. 2000; van der Zee et al. 1999). In addition, all PEACE studies were carried out in the winter, when the effect of respiratory infections will putatively be greater compared with summer. Furthermore, in our analysis, we have found statistically greater associations in summer for asthma symptoms.

To the best of our knowledge, this is the first meta-analysis for effects related to monitored outdoor NO2 on respiratory health in asthmatic children, although the main investigations on NO2 have been extensively reviewed (U.S. EPA 2008b; WHO Regional Office for Europe 2006). In vitro studies at comparatively low concentrations of NO2, but still notably higher than ambient levels (400 ppb or 760 µg/m3), have shown cell damage accompanied by release of cytokines, such as tumor necrosis factor-α and interleukin-8 (Devalia et al. 1993). In controlled human studies, the same concentration for 1 hr led to an increased early and late asthmatic response (measured by forced expiratory volume in 1 sec) after challenge with house dust mite allergen compared with ordinary air (Tunnicliffe et al. 1994). Similarly, a 30-min exposure to 500 µg/m3 NO2 increased the early-phase response to an otherwise nonsymptomatic allergen dose (Strand et al. 1998). Although such concentrations can be reached during some episodes, the usual ambient concentrations of NO2 are lower. On the other hand, several studies on hospital admissions and emergency department visits for asthma conducted in Europe and elsewhere [reviewed by U.S. EPA (2008b); WHO Regional Office for Europe (2006)] did find an independent effect of NO2. Therefore, the extent to which the observed associations are related to a direct effect of NO2 and/or reflect the fact that NO2 is a marker for the urban pollution mix, particularly for ultrafine particles PM (Seaton and Dennekamp 2003), remains to be investigated. The correlation between PM10 and NO2 varies across settings (Katsouyanni et al. 2001), with the pollution mix related to NO2 generally being more variable in space and time. Notwithstanding these differences, the estimated effect size for NO2 observed in this meta-analysis is similar to that of the PM10 component, except for PEF.

There may be a concern that bias might be introduced when selecting effects that were not for the same lag. Our additional analysis for lags 0–1 provided nonsignificant estimates for NO2 but significant associations with PM10. It remains to be shown whether such a short lag is the most adequate for measuring the effect, given that higher associations may be observed at longer lags, as we found in our analysis of effect modification. Unfortunately, longer lags are less consistently reported in the literature.

There are limitations of the panel studies we have considered. When evaluating symptoms, the possibility of a confounding role of medications should be considered. Medication use on polluted days may influence symptoms and lung function. Although the PEACE studies found no correlation between the number of children using asthma medication and air pollution levels (Roemer et al. 2000), this does not account for the possibility that asthmatic children increase the dose on such days. Information regarding this possibility is generally missing in the individual study reports. The evaluation of the effect on PEF is difficult because of the large between-individual variability of this indicator that is likely to be strongly influenced by medication use among diseased subjects. Finally, another difficulty is that the measured pollutants are only part of a more complex air pollution mixture, and the effects of “PM10” and “NO2” may vary among studies and may be a less or more adequate measure of the effects of air pollution. In a meta-analysis, it is not possible to adequately assess the problems related to these mixes. Multipollutant (mostly two-pollutant) models were calculated for only 10 of the study populations, and the combinations of the pollutants varied among studies. Only if the raw data were available for all studies could one attempt to tease out individual pollutant effects and also avoid overestimation of the individual effect. It will nonetheless be a daunting task, because in most cases criteria air pollutants are measured, which may be indicators of different unmeasured compounds in different areas. Delfino et al. (2003) reported, for example, that the effect of “PM10” was lower when, for example, organic carbon, benzene, or m,p-xylene was included in two-pollutant models. This may be a general finding, or it may be typical for the region investigated. The results presented here therefore are not to be strictly understood as the effect of PM10 only or NO2 only; the greater context must be borne in mind.

We observed a high degree of heterogeneity among the investigated studies. Stratifying by the identified effect modifiers reduced the heterogeneity only to some extent. We obtained the greatest reduction in heterogeneity when using the same lag for all studies. Sources of heterogeneity may be linked to various design aspects of the study, such as the inclusion criteria for the panel, duration of the study, and the analytical strategies. For the PEACE study with its standardized study protocol and common analytical strategy, we calculated an I2 ranging from 40% to 79% depending on the outcome/pollutant only for the analysis using different lags, whereas the analyses with the uniform shorter lag reduced the heterogeneity among PEACE studies for symptoms and PEF (data not shown). Although this may highlight the importance of a standardized study protocol, caution is needed until it is better known which lag is the most appropriate. Therefore, other potential sources of the observed heterogeneity, such as differences in the air pollution mix related to spatial or temporal variability, may still be of importance even in well-
standardized studies. Different baseline characteristics of the populations studied may also have their influence.

The estimated effect of PM10 on asthma was higher in studies that were conducted in the summer. The composition of the air pollution mix may also be the reason for higher observed effects of PM10 in studies that have been conducted in summer only. Summer pollution is qualitatively different from winter pollution: O3 levels are higher, and in general the air pollution mixture is more strongly influenced by photochemical reaction. Ward and Ayres (2004) observed in their analysis a higher estimated effect in studies conducted in periods of high O3 levels. A time-series analysis of Atkinson et al. (2001) observed effect modification by O3 for hospital admission for respiratory conditions in persons older than 65 years, although not for asthma admissions in children or adults. Alternative reasons could be that the PM10 effect is confounded by the effect of O3. However, independent effects have been found for PM2.5, and for PM2.5–10 concerning cough [for a more detailed discussion, see Ward and Ayres (2004)]. The higher estimated effect of PM10 in the summer could also be linked to more (active) time spent outside, which could act in several ways. First, it would reduce misclassification due to less exposure to indoor conditions. Second, it could increase the effect of PM10 through increased inhalation during the activities outside (e.g., exercise), which also could increase the effect of O3.

Consideration of longer lags did result in elevated associations of PM10 with cough. This seems plausible because air pollution may act not only as a short-term trigger but also as a priming event by inducing processes of enhanced airways inflammation (Kimber 1998) that will build up over a period of hours to days and result in subsequent bronchial hyperreactivity (Mortimer et al. 2002). Indeed, lengthy lag periods have been found in panel studies as well as time-series studies of emergency department visits (Halonen et al. 2008; Mortimer et al. 2002).

Continent modified the association of PM10 with cough; we found a significant combined effect only for the studies outside of Europe, whereas for the European studies the combined effect was null (OR = 0.998; 95% CI, 0.983–1.014). This estimate is similar to that reported by Anderson et al. (2004) for Europe (OR = 0.999; 95% CI, 0.987–1.011). At first glance, a similar effect modification was present for asthma symptoms, but this disappeared after exclusion of the PEACE studies. It therefore remains speculative whether this is really an effect for Europe or is attributable to some other characteristic that is specifically related to the PEACE study.

Nevertheless, a stronger association of PM10 with respiratory symptoms reported in the United States compared with Europe was also observed in an earlier meta-analysis, conducted before the PEACE study, that also included healthy children (Dockery and Pope 1994). One plausible explanation could be different pollutant mixes on the two continents. The extent to which these differences are systematic and will provide relevant information remains to be investigated, given that also within the United States and within Europe there are marked differences concerning the air pollution mix, which may result in differing health effects via effect modification or due to a different composition of PM10 (Katsouyanni et al. 2001; Levy et al. 2000).

In our analysis, we found the association of PM10 with cough to be stronger for higher ambient NO2 concentration. However, we did not see this effect in the analysis restricted to lags 0–1, but in this latter analysis we found higher associations at higher NO2 levels with asthma symptoms. Effect modification by NO2 has been found in time series studies on mortality in Europe (Katsouyanni et al. 2001), and to a lesser extent in the United States (Levy et al. 2000). It has been discussed that NO2 is a marker for a certain air pollution mixture, notably arising from traffic, which is more noxious for health.

Conclusion

Our meta-analysis provides strong evidence for an effect of PM10 as an aggravating factor of asthma in children. Although there is no firm toxicologic evidence of adverse health effects of NO2 at ambient levels to date, the epidemiologic results suggest an adverse effect of NO2 on respiratory health in children with asthma. However, caution is needed in the final conclusion for NO2 because the association with asthma attacks was not robust to lag specification. The finding may reflect the fact that NO2 is associated at extended lags, or it may be only an artifact due to our method of choosing the specific lag to be included in the meta-analysis. More consistent reporting of longer lags is needed in panel studies to better judge the effect of monitored outdoor NO2. The results of the study support the need to protect asthmatic children with strict air quality standards for PM10 and, considering the precautionary principle, also for NO2.

References

  1. Ackermann-Liebrich U, Rapp R. 1999. Epidemiological effects of oxides of nitrogen, especially NO2. In: Air pollution and Health (Holgate ST, Samet JM, Koren HS, Maynard RL, eds). London:Academic Press. pp. 559–584.
  2. Aekplakorn W, Loomis D, Vichit-Vadakan N, Shy C, Wongtim S, Vitayanon P.. 2003. Acute effect of sulphur dioxide from a power plant on pulmonary function of children, Thailand. Int J Epidemiol 32:854–861.
  3. Anderson HR, Atkinson RW, Peacock JL, Marston L, Konstantinou K. 2004. Copenhagen:World Health Organization, Regional Office for Europe. Meta-Analysis of Time-Series Studies and Panel Studies of Particulate Matter (PM) and Ozone (O3): Report of a WHO Task Group. Available: http://www.euro.who.int/document/e82792.​pdf [accessed 12 February 2009]
  4. Atkinson RW, Anderson HR, Sunyer J, Ayres J, Baccini M, Vonk JM, et al. 2001. Acute effects of particulate air pollution on respiratory admissions: results from APHEA 2 project. Air Pollution and Health: A European Approach. Am J Respir Crit Care Med 164:1860–1866.
  5. Baldini G, Gotti A, Pifferi M, Ciacchini G, Codiglione P, Viegi G, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Pisa, Italy. Eur Respir Rev 8:108–116.
  6. Begg CB, Mazumdar M. 1994. Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088–1101.
  7. Beyer U, Franke K, Cyrys J, Peters A, Heinrich J, Wichmann HE, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Hettstedt and Zerbst, Eastern Germany. Eur Respir Rev 8:61–69.
  8. Clench-Aas J, Bartonova A, Skjønsberg OH, Leegard J, Hagen LO, Giæver P, et al. 1998. Air pollution and respiratory health of children: the PEACE study in Oslo, Norway. Eur Respir Rev 8:36–43.
  9. Delfino RJ, Gong H Jr, Linn WS, Pellizzari ED, Hu Y. 2003. Asthma symptoms in Hispanic children and daily ambient exposures to toxic and criteria air pollutants. Environ Health Perspect 111:647–656.
  10. Delfino RJ, Zeiger RS, Seltzer JM, Street DH. 1998. Symptoms in pediatric asthmatics and air pollution: differences in effects by symptom severity, anti-inflammatory medication use and particulate averaging time. Environ Health Perspect 106:751–761.
  11. Delfino RJ, Zeiger RS, Seltzer JM, Street DH, McLaren CE. 2002. Association of asthma symptoms with peak particulate air pollution and effect modification by anti-inflammatory medication use. Environ Health Perspect 110:A607–A617.
  12. DerSimonian R, Laird N.. 1986. Meta-analysis in clinical trials. Control Clin Trials 7:177–188.
  13. Devalia JL, Campbell AM, Sapsford RJ, Rusznak C, Quint D, Godard P, et al. 1993. Effect of nitrogen dioxide on synthesis of inflammatory cytokines expressed by human bronchial epithelial cells in vitro. Am J Respir Cell Mol Biol 9:271–278.
  14. Dockery DW, Pope CA III. 1994. Acute respiratory effects of particulate air pollution. Annu Rev Public Health 15:107–132.
  15. Duval SJTRL. 2000. A non-parametric “trim and fill” method of assessing publication bias in meta-analysis. J Am Stat Assoc 95:89–98.
  16. Egger M, Davey SG, Schneider M, Minder C. 1997. Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629–634.
  17. Englert N, Babisch W, Hoek G.. 1998. Air pollution and respiratory health of children: the PEACE panel study in Berlin, Germany. Eur Respir Rev 8:53–60.
  18. Forsberg B, Segerstedt B, Stjernberg N, Roemer W.. 1998. Air pollution and respiratory health of children: the PEACE panel study in Umea, Sweden. Eur Respir Rev 8:12–19.
  19. Gielen MH, van der Zee SC, van Wijnen JH, van Steen CJ, Brunekreef B. 1997. Acute effects of summer air pollution on respiratory health of asthmatic children. Am J Respir Crit Care Med 155:2105–2108.
  20. Halonen JI, Lanki T, Yli-Tuomi T, Kulmala M, Tiittanen P, Pekkanen J. 2008. Urban air pollution, and asthma and COPD hospital emergency room visits. Thorax 63:635–641.
  21. Haluszka J, Pisiewicz K, Miczynski J, Roemer W. , Tomalak. 1998. Air pollution and respiratory health of children: the PEACE panel study in Krakow, Poland. Eur Respir Rev 8:94–100.
  22. Higgins JP, Thompson SG. 2002. Quantifying heterogeneity in a meta-analysis. Stat Med 21:1539–1558.
  23. Jalaludin BB, Chey T, O’Toole BI, Smith WT, Capon AG, Leeder SR. 2000. Acute effects of low levels of ambient ozone on peak expiratory flow rate in a cohort of Australian children. Int J Epidemiol 29:549–557.
  24. Jalaludin BB, O’Toole BI, Leeder SR. 2004. Acute effects of urban ambient air pollution on respiratory symptoms, asthma medication use, and doctor visits for asthma in a cohort of Australian children. Environ Res 95:32–42.
  25. Just J, Segala C, Sahraoui F, Priol G, Grimfeld A, Neukirch F.. 2002. Short-term health effects of particulate and photochemical air pollution in asthmatic children. Eur Respir J 20:899–906.
  26. Kalandidi A, Gratziou C, Katsouyanni K, Manalis N, Tzala L, Pantazopoulou A, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Athens, Greece. Eur Respir Rev 8:117–124.
  27. Katsouyanni K, Touloumi G, Samoli E, Gryparis A, Le Tertre A, Monopolis Y, et al. 2001. Confounding and effect modification in the short-term effects of ambient particles on total mortality: results from 29 European cities within the APHEA2 project. Epidemiology 12:521–531.
  28. Kimber I.. 1998. Allergy, asthma and the environment: an introduction. Toxicol Lett 102–103:301–306.
  29. Kotesovec F, Vitnerova N, Leixner M, Benes I, Skorkovsky J, Roemer W.. 1998. Air pollution and respiratory health of children: the PEACE panel study in Teplice, Czech Republic. Eur Respir Rev 8:70–77.
  30. Levy JI, Hammitt JK, Spengler JD. 2000. Estimating the mortality impacts of particulate matter: what can be learned from between-study variability? Environ Health Perspect 108:109–117.
  31. McCreanor J, Cullinan P, Nieuwenhuijsen MJ, Stewart-Evans J, Malliarou E, Jarup L, et al. 2007. Respiratory effects of exposure to diesel traffic in persons with asthma. N Engl J Med 357:2348–2358.
  32. Mortimer KM, Neas LM, Dockery DW, Redline S, Tager IB. 2002. The effect of air pollution on inner-city children with asthma. Eur Respir J 19:699–705.
  33. National Library of Medicine 2008. PubMed. Available: http://www.ncbi.nlm.nih.gov/pubmed/ [accessed 14 July 2008]
  34. Nielsen J, Welinder H, Bensryd I, Martensson M, Skerfving S, Hoek G.. 1998. Air pollution and respiratory health of children: the PEACE panel study in urban and rural locations in southern Sweden. Eur Respir Rev 8:20–26.
  35. Niepsuj G, Niepsuj K, Nieroda-Muller A, Rauer R, Krzywiecki A, Borowska M, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Katowice, Poland. Eur Respir Rev 8:86–93.
  36. Ostro B, Lipsett M, Mann J, Braxton-Owens H, White M.. 2001. Air pollution and exacerbation of asthma in African-American children in Los Angeles. Epidemiology 12:200–208.
  37. Peacock JL, Symonds P, Jackson P, Bremner SA, Scarlett JF, Strachan DP, et al. 2003. Acute effects of winter air pollution on respiratory function in schoolchildren in southern England. Occup Environ Med 60:82–89.
  38. Peters A, Dockery DW, Heinrich J, Wichmann HE. 1997. Short-term effects of particulate air pollution on respiratory morbidity in asthmatic children. Eur Respir J 10:872–879.
  39. Petitti DB. 2001. Approaches to heterogeneity in meta-analysis. Stat Med 20:3625–3633.
  40. Pope CA III, Dockery DW. 1992. Acute health effects of PM10 pollution on symptomatic and asymptomatic children. Am Rev Respir Dis 145:1123–1128.
  41. Roemer W, Hoek G, Brunekreef B.. 1993. Effect of ambient winter air pollution on respiratory health of children with chronic respiratory symptoms. Am Rev Respir Dis 147:118–124.
  42. Roemer W, Hoek G, Brunekreef B.. 2000. Pollution effects on asthmatic children in Europe, the PEACE study. Clin Exp Allergy 30:1067–1075.
  43. Roemer W, Hoek G, Brunekreef B, Haluszka J, Kalandidi A, Pekkanen J.. 1998. . Daily variations in air pollution and respiratory health in a multicentre study: the PEACE project. Pollution Effects on Asthmatic Children in Europe. Eur Respir J 12:1354–1361.
  44. Roemer W, Hoek G, Brunekreef B, Schouten JP, Baldini G, Clench-Aas J, et al. 1998. . Effect of short-term changes in urban air pollution on the respiratory health of children with chronic respiratory symptoms: the PEACE project: introduction. Eur Respir Rev 8:4–11.
  45. Romieu I, Meneses F, Ruiz S, Huerta J, Sienra JJ, White M, et al. 1997. Effects of intermittent ozone exposure on peak expiratory flow and respiratory symptoms among asthmatic children in Mexico City. Arch Environ Health 52:368–376.
  46. Romieu I, Meneses F, Ruiz S, Sienra JJ, Huerta J, White MC, et al. 1996. Effects of air pollution on the respiratory health of asthmatic children living in Mexico City. Am J Respir Crit Care Med 154:300–307.
  47. Rudnai P, Vaskövi E, Paldy A, Sarkany E, Varro M, Farkas I, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Hungary. Eur Respir Rev 8:101–107.
  48. Schildcrout JS, Sheppard L, Lumley T, Slaughter JC, Koenig JQ, Shapiro GG. 2006. Ambient air pollution and asthma exacerbations in children: an eight-city analysis. Am J Epidemiol 164:505–517.
  49. Seaton A, Dennekamp M.. 2003. Hypothesis: ill health associated with low concentrations of nitrogen dioxide—an effect of ultrafine particles? Thorax 58:1012–1015.
  50. Segala C, Fauroux B, Just J, Pascual L, Grimfeld A, Neukirch F.. 1998. Short-term effect of winter air pollution on respiratory health of asthmatic children in Paris. Eur Respir J 11:677–685.
  51. Strand V, Svartengren M, Rak S, Barck C, Bylin G.. 1998. Repeated exposure to an ambient level of NO2 enhances asthmatic response to a nonsymptomatic allergen dose. Eur Respir J 12:6–12.
  52. Tiittanen P, Timonen KL, Ruuskanen J, Mirme A, Pekkanen J. 1999. Fine particulate air pollution, resuspended road dust and respiratory health among symptomatic children. Eur Respir J 13:266–273.
  53. Timonen K, Pekkanen J, Salonen RO, Jantunen MJ, Reponen A, Hosiokangas J, et al. 1998. Air pollution and respiratory health of children: the PEACE panel study in Kuopio, Finland. Eur Respir Rev 8:27–35.
  54. Tunnicliffe WS, Burge PS, Ayres JG. 1994. Effect of domestic concentrations of nitrogen dioxide on airway responses to inhaled allergen in asthmatic patients. Lancet 344:1733–1736.
  55. U.S. EPA 2005. Research Triangle Park, NC:Office of Air Quality Planning and Standards, U.S. Environmental Protection Agency. Review of the National Ambient Air Quality Standards for Particulate Matter: Policy Assessment of Scientific and Technical Information. OAQPS Staff Paper. Available: http://www.epa.gov/ttn/naaqs/standards/p​m/data/pmstaffpaper_20051221.pdf [accessed 20 August 2009]
  56. U.S. EPA 2008a. Research Triangle Park, NC:Office of Air Quality Planning and Standards, U.S. Environmental Protection Agency. Risk and Exposure Assessment to Support the Review of the NO2 Primary National Ambient Air Quality Standard. Available: http://www.epa.gov/ttn/naaqs/standards/n​ox/data/20081121_NO2_REA_final.pdf [accessed 20 August 2009]
  57. U.S. EPA 2008b. Research Triangle Park, NC:National Center for Environmental Assessment, RTP Division, Office of Research and Development, U.S. Environmental Protection Agency. 2008 Integrated Science Assessment (ISA) for Oxides of Nitrogen Health Criteria (Final Report). Available: http://cfpub.epa.gov/ncea/cfm/recordispl​ay.cfm?deid=194645 [accessed 22 October 2009]
  58. van der Zee S, Hoek G, Boezen M, Schouten J, van Wijnen J, Brunekreef B.. 1998. Air pollution and respiratory health of children: the PEACE study in Amsterdam, the Netherlands. Eur Respir Rev 8:44–52.
  59. van der Zee S, Hoek G, Boezen HM, Schouten JP, van Wijnen JH, Brunekreef B. 1999. Acute effects of urban air pollution on respiratory health of children with and without chronic respiratory symptoms. Occup Environ Med 56:802–812.
  60. Vedal S, Petkau J, White R, Blair J.. 1998. Acute effects of ambient inhalable particles in asthmatic and nonasthmatic children. Am J Respir Crit Care Med 157:1034–1043.
  61. Vondra V, Branis M, Reisova M, Maly M, Hoek G.. 1998. Air pollution and respiratory health of children: the PEACE panel study in Prague, Czech Republic. Eur Respir Rev 8:78–85.
  62. Ward DJ, Ayres JG. 2004. Particulate air pollution and panel studies in children: a systematic review. Occup Environ Med 61:e13.
  63. WHO Regional Office for Europe 2000. Air Quality Guidelines for Europe, 2nd ed. WHO Regional Publications, European Series, No. 91. Copenhagen:World Health Organization.
  64. WHO Regional Office for Europe 2006. Copenhagen:World Health Organization. Air Quality Guidelines. Global Update 2005. Particulate Matter, Ozone, Nitrogen Dioxide and Sulfur Dioxide. WHO Regional Publications, European Series. Available: http://www.euro.who.int/Document/E90038.​pdf [accessed 15 January 2009]
  65. Williams ML. 1999. Patterns of air pollution in developed countries. In: Air pollution and Health (Holgate ST, Samet JM, Koren HS, Maynard RL, eds). London:Academic Press. pp. 83–104.
  66. Yu O, Sheppard L, Lumley T, Koenig JQ, Shapiro GG. 2000. Effects of ambient air pollution on symptoms of asthma in Seattle-area children enrolled in the CAMP study. Environ Health Perspect 108:1209–1214.

WP-Backgrounds Lite by InoPlugs Web Design and Juwelier Schönmann 1010 Wien