Background Approximately half of all patients who underwent a lung transplantation suffer from bronchiolitis obliterans syndrome (BOS), the clinical correlate of chronic rejection, within 5 years after transplantation. This prevalence is much higher than for other solid organ transplantations, possibly due to the lung's direct contact with the environment. The authors assessed the association between proximity of the home to major roads and BOS and mortality in a cohort of patients after lung transplantation.
Methods The authors calculated hazard ratios for BOS and mortality in relation to proximity of the home to major roads, adjusting for relevant covariables, in 288 patients after lung transplantation at the Leuven University Hospital between 1997 and 2009 and with follow-up until August 2009. Inflammatory parameters in plasma and bronchoalveolar lavage were assessed in 207 patients.
Results During follow-up, 117 (41%) patients developed BOS and 61 (21%) died. Patients who lived within 171 m of a major road (lowest tertile) were 2.06 (95% CI 1.39 to −3.05) times more likely to develop BOS and 2.20 (1.25 to −3.86) times more likely to die than patients living farther away. The adjusted hazard ratios of BOS and mortality were 0.57 and 0.72 for each 10-fold increase in distance from major roads. Proximity to a major road was inversely associated with plasma C-reactive protein levels, neutrophil percentage and interleukin-6 concentration in bronchoalveolar lavage.
Conclusion Traffic-related air pollution appears to constitute a serious risk of BOS and mortality after lung transplantation.
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Lung transplantation is an accepted treatment option for patients with end-stage lung disease. The long-term survival of patients after lung transplantation (median of 5 years) is much lower than for other solid organ transplantation.1 This is mainly because half the patients develop bronchiolitis obliterans syndrome (BOS)—the clinical correlate of chronic rejection—within 5 years of transplantation. BOS is the most important cause of late mortality (25–35%).2
BOS is triggered by alloimmune and non-alloimmune risk factors, such as HLA mismatch, acute rejection, receptor/donor age, cytomegalovirus (CMV) and other viral infections.2 Recently, airway colonisation by Pseudomonas, lymphocytic bronchitis/bronchiolitis and gastro-oesophageal reflux have been added as risk factors.3–7 These risk factors act via neutrophilic airway inflammation, suggesting that activation of the innate immune system is a trigger of BOS. Many inhaled air pollutants also give rise to activation of the innate immune system.8 9 Moreover, air pollution exposure exerts adverse health effects, especially in patients with cardiopulmonary diseases,10–12 and can aggravate chronic inflammatory lung disorders.13 14 A substantial proportion of ambient air pollution results from the combustion of fossil fuels by vehicle traffic.15
As the lung is in direct contact with the environment, the authors hypothesised that air pollution may be a risk factor for BOS and mortality after lung transplantation. The incidence of BOS and mortality was assessed in a large cohort of well characterised and closely monitored patients after lung transplantation in relation to their exposure to (traffic-related) air pollution, as measured by the proximity of their home to a major road.
This study considered patients who had had a lung transplant between 1 January 1997 and 31 December 2008 with long-term follow-up at UZ Leuven. Of these 403 transplantations, the authors excluded 22 patients living outside Belgium, 24 patients who died within 3 months after transplantation, 29 patients in whom BOS could not be diagnosed according to international criteria (suture stenosis n=15, cancer n=6, post-transplant lymphoproliferative disease n=3, neurological problems n=1, pneumonectomy n=1, insufficient follow-up data n=3) and 40 patients of the active group in a randomised placebo-controlled trial with azithromycin (inclusion from July 2005 to November 2007).16 These 40 patients were excluded because azithromycin was started 1 month after transplantation and reduced neutrophilia and C-reactive protein (CRP), and so abolished the effect of pollution. In seven patients the first and second transplantation were included as two separate transplantations. The study therefore examined 288 lung transplantations in 281 patients whose characteristics are summarised in table 1. The authors gathered information on gender, donor/receptor age at transplantation, place of residence, socioeconomic status (SES), lifestyle, smoking habits, reason for transplantation, type of transplantation, CMV mismatch, primary graft dysfunction, and baseline therapy at about 90 days after transplantation. We coded SES according to the UK Office of Population Censuses and Surveys (1980) and scored it using a scale ranging from 1 to 3.17 Smoking habits (not in all patients) were assessed by questionnaire, urinary cotinine and exhaled carbon monoxide.18 Relevant clinical information was collected up to 31 August 2009, including BOS and death (main outcomes); bronchoscopic procedures with transbronchial biopsies and bronchoalveolar lavage (BAL); incidences of histopathologically diagnosed acute rejections; treated CMV infections and treated non-CMV infections; Pseudomonas aeruginosa airway colonisation; gastro-oesophageal reflux (gastroscopy or pH impedance measurement). The Ethical Review Board of the Leuven University Medical Faculty approved the study. All participants gave informed consent at recruitment.
BOS diagnosis, BOS therapy and airway or systemic inflammation
BOS was detected and diagnosed according to guidelines of the International Society for Heart and Lung Transplantation.19 BOS was detected by routine lung function testing. BOS was defined as the occurrence of a sustained (3 weeks or more) decrease in forced expiratory volume in the first second (FEV1) by at least 20% from the patient's mean of the two best postoperative FEV1 measurements taken at least 3 weeks apart, in the absence of other causes, which were generally established by bronchoscopy.
All patients received conventional postoperative immunosuppressive and prophylactic treatment, consisting of triple-drug immunosuppressive therapy with methylprednisolone, cyclosporine A or tacrolimus, and azathioprine or mycophenolate mofetil. If BOS was diagnosed, doses were increased or alternative immunosuppressive agents (tacrolimus or mycophenolate mofetil) were given. Total lymph node irradiation or retransplantation was needed in rare instances. From 2002, BOS was treated with azithromycin (250 mg/day for 5 days followed by 250 mg every other day). Other complications, such as acute rejection, infections and gastro-oesophageal reflux disease, were treated according to the International Society for Heart and Lung Transplantation guidelines and our local experience, as previously described.4
Since 2001, routine follow-up after lung transplantation included clinical examination, biochemical, radiological, lung functional and bronchoscopic examinations at fixed time points (3, 9, 12, 18, 24 and 36 months post transplant). These procedures were repeated whenever complications were suspected. Bronchoscopy always included BAL for microbiological assessment, quantification of cell differentials, and protein levels (interleukin-6 (IL-6), IL-8); transbronchial biopsies were routinely taken at 90 days post transplant and when indicated.4 20
To characterise exposure to traffic-related air pollution, a residence-based approach was adopted, as previously described.21 Home addresses at baseline were geocoded with a geographic information system. Using official digitised maps, distances between homes and major roads (defined as 1, 2 or 3—highways, national roads or large local roads respectively) were calculated with a precision of at least 5 m.21 The minimal proximity to a major road was set at 10 m. An indicator variable was constructed for street canyons.
To assess background air pollution, daily mean values were calculated for particulate matter with a diameter less than 10 μm (PM10) and NO2 for the year 2002 (midpoint of the baseline examination, as done by Miller et al)12 at each participant's home address, using a validated model22 that provides interpolated values for PM10 and NO2 in 4 by 4 km grids based on the Belgian telemetric air quality network. The interpolation is based on a detrended Kriging interpolation method using landcover data obtained from satellite images (Corine landcover dataset). The model has shown a good agreement between the daily model-derived values and the measured air pollution.22 Besides using 2002 as the reference year, sensitivity analysis was also performed for 2000 and the mean of 2000–2006.
For database management and statistical analyses, SAS software version 9.1 was used. Means were compared using the standardised normal z test, medians using the Mann–Whitney test, and proportions using the χ2 test. Log-transformed variables were described by their geometric mean and the 5th–95th percentiles. All statistical tests were two sided.
Survival or incidence curves were constructed by Kaplan–Meier survival function estimates and the log-rank test. Cox regression was applied to model the relation between failure time (ie, occurrence of BOS or death) and distance from major roads, with and without adjusting for other potential explanatory variables including sex, age, SES, type of transplantation (single or double lung transplantation), cumulative rates of CMV and non-CMV infections, cumulative rates of acute rejection, and year of transplantation. Distance from major roads was log-transformed because this parameter had a skewed distribution and also because traffic-related pollutants decay exponentially with increasing distance from roads.23 Non-proportionality was tested by the Kolmogorov-type supremum test, as implemented in the PROC PHREG procedure of the SAS package, and by testing the interaction terms between follow-up duration and the log of distance to major roads. For the model of both BOS and death the result of the Kolmogorov-type supremum test was not significant for log distance (all p>0.21). Therefore, the ‘proportional hazards assumption’ was not violated. The study also investigated associations using a cut-off point of 171 m, based on the lowest tertile of distances between home and the nearest major road. The shape of the association was studied by using fractional polynomials (see online supplement). Based on the best model, the hazard ratio (HR) was calculated with 1000 m as reference.
Attributable and population-attributable fractions were calculated using standard formulas to estimate the number of events of BOS or deaths that would not have occurred at defined distances from major roads.24 Finally, while adjusting for time after transplantation, we regressed inflammatory parameters (cell count, neutrophilia, IL-6, and IL-8 in BAL and plasma CRP) and distance to major roads at different time points after transplantation, using mixed models to account for intra-individual variation.
The studied cohort included 288 lung transplantations (in 281 patients) and accrued 939 person-years, with a median follow-up of 2.7 years (range 0.2–10.8) from January 1997 to August 2009. During this period, there were 117 (41%) events of BOS and 61 (21%) patients died. The characteristics of the 96 patients who had had a lung transplant (lowest tertile) and lived close (within 171 m) to a major road did not differ from those (n=192) who lived further than 171 m (table 1).
The crude rate of BOS was higher (p<0.001) in patients living close (≤171 m) to major roads (19.3 per 100 person-years) compared with those living farther away (9.9 per 100 person-years; figure 1). The corresponding figures for mortality during follow-up were 7.6 per 100 person-years in patients living close to major roads and 3.9 deaths per 100 person-years in those living more than 171 m away (p<0.001; figure 1).
The risk of BOS was not associated with gender (p=0.49), age (p=0.26) or non-CMV infections (p=0.59). However, recipients of double lung transplantations had a lower risk (HR 0.56, 95% CI 0.35 to 0.92, p=0.021) of developing BOS. BOS was also associated with the number of acute rejections (HR 1.77, 95% CI 1.33 to 2.36, p<0.001 if more than two acute rejections compared with none) and with CMV infection during follow-up (HR 1.45, 95% CI 0.90 to 2.36, p=0.13 compared with no CMV infection), and was lower in those with a higher SES (HR 0.31, 95% CI 0.12 to 0.77, p=0.01).
The risk of death was not associated with gender (p=0.17), age (p=0.32) or type of transplantation (p=0.11). However, mortality was associated with the number of acute rejections (HR 2.35, 95% CI 1.59 to 3.46, p<0.0001 if more than two acute rejections compared with none), with CMV infections (HR 1.83, 95% CI 0.99 to 3.38, p=0.05 compared with no infections), and with non-CMV infection (HR 2.78, 95% CI 1.44 to 5.36, p=0.002 if more than two infections compared with none).
Patients with BOS during follow-up had a near twofold increased risk of dying (HR 2.05, 95% CI 1.21 to 3.46, p=0.008) compared with those who were BOS free. Patients receiving azithromycin for BOS had a 46% lower risk of dying (HR 0.24, 95% CI 0.12 to 0.50, p<0.0001).
The risks of BOS and death increased with proximity to major roads. In unadjusted analyses, living within 171 m of a major road was associated with HRs of 2.06 (95% CI 1.39 to 3.05) for developing BOS and 2.20 (95% CI 1.25 to 3.86) for dying compared with living farther away (table 2), yielding population attributable fractions of 25% and 28% respectively. These HRs increased after adjustment for gender, age, single or double lung transplantation, acute rejection rate, CMV or non-CMV infection rates, SES, and additional adjustments for the average background levels of PM10 in the area of residence (table 2). Figure 2 provides the HRs and attributable fractions for distances from 50 m to 800 m (compared with 1000 m or more) for BOS and mortality. The estimated local PM10 background level was not significantly associated with either BOS or death: a 10 μg/m3 increase in average background PM10 level gave HRs of 1.15 (95% CI 0.79 to 1.66, p=0.47) for BOS and 0.79 (95% CI 0.43 to 1.42, p=0.43) for mortality.
After correction for having developed BOS during follow-up and macrolide treatment, the risk of dying after lung transplantation decreased by 31% (HR 0.69, 95% CI 0.43 to 1.12, p=0.14) for each 10-fold increase in distance between home and a major road.
A subanalysis of the cohort with reliable data on smoking status (172 patients; 70% of the total population) demonstrated similar results as in the entire group (see online supplement).
In further sensitivity analyses, the authors evaluated a potential interaction between major road distance and an indicator variable for residence in street canyons (n=12), but this interaction was not significant (p for interaction=0.93). Models in which the interpolated PM10 (table 2) was replaced by interpolated NO2 did not alter the reported associations.
In 207 lung transplant patients, followed from day 50 until 3.5 years after transplantation, there were 943 BALs and 929 plasma samples.
For analysing inflammatory parameters with respect to distance (log), multivariate linear mixed-effect models were used to take the clustering pattern into account (table 3). The proportions of BAL neutrophils, BAL IL-6 and plasma CRP were inversely associated with distance of the home to the nearest major road (table 3).
For all previous reported analyses, the sensitivity analyses, in which seven retransplantations were excluded, confirmed the study's findings.
Traffic-related air pollution, as estimated by the proximity of the home to a major road, is a major risk factor for BOS and mortality after lung transplantation. The risk was present in either a dichotomous or a continuous analysis, and was not affected by adjustments for relevant covariables. Indicators of pulmonary (BAL neutrophils, IL-6) and systemic (plasma CRP) inflammation, which are probably involved in the onset of BOS, were also associated with proximity to traffic.
The strengths of our study include the relatively large lung transplant population from a single centre and the statistically robust associations. The statistical significance of our observations follows in part from the high incidence of BOS and mortality. The robustness of the associations is apparent from the fact that inclusion of relevant potential confounders, ranging from SES, transplantation-related characteristics to active smoking, tended to increase the risk estimates.18
Many other authors have estimated exposure to traffic-related air pollution by using the geocoded distance between the home and the nearest major road.25–28 However, true exposure may differ from the estimated exposure. First, this method does not consider time spent elsewhere than at home, but this limitation may be less relevant in the case of our patient group who presumably were more housebound than other groups. Second, specific traffic counts or diesel-powered vehicle counts were not available. A major road was defined based on an independent, official classification of roads as highways or major local roads, which generally have the heaviest through traffic. It is more likely that some major roads actually had little traffic and that minor roads had a lot of traffic. Therefore the authors believe the (unavoidable) imprecision of the exposure variable probably tended to reduce associations towards the null, rather than to exaggerate them. Finally, only proximity to the nearest major road was evaluated and not the effect of living close to multiple roads (eg, near road junctions), but only a few patients had more than one major road within 200 m of their home.
In view of the epidemiological evidence about the cardiopulmonary effects of particulate air pollution,26 27 29 the lack of effect of PM10 was unexpected. However, traffic-related air pollution by ultrafine particles is probably not well captured by (modelled or actual) levels of PM10 or NO2, which are dominated by large-scale geographical and weather-dependent factors. Moreover, Belgium is a small country (approximately 33 000 km2) with a high population density (357 people/km2). Therefore the relatively high overall PM10 background pollution with little spatial variation and with few areas of low pollution30 could explain why estimates of local PM10 had no effect in our analysis. A multicentre study with patients from areas with high and low PM10 levels might resolve this issue.
A higher SES was associated with a lower risk of BOS (though not of mortality), but there was no doubting the association between SES and proximity to traffic.
Our findings are also biologically robust because they are consistent with a large body of data on the adverse effects of air pollutants on the lung and cardiovascular system.11 13 21 31 The steep decline in the hazard ratios (figure 2) until about 400 m and little or no additional risk decline beyond about 600 m are compatible with the known logarithmic decrease in the concentration of vehicle-emitted pollutants with increasing distance from the road.23 Ultrafine particles represent a toxicologically important fraction of vehicle emissions, although they hardly affect the mass concentrations of particulates (PM10 or PM2.5). Combustion-generated ultrafine particles produced by diesel engines are believed to be, at least partly, responsible for the cardiopulmonary effects of outdoor urban air pollution, possibly through proinflammatory effects.32 33
Biological plausibility is supported by our observations in over 700 BAL and plasma samples, which revealed inverse associations between distance from major roads and markers of inflammation in BAL and plasma. Neutrophils in particular are known to be involved in the onset of BOS.34 Moreover, the study demonstrated that both airway neutrophilia and systemic CRP are prognostic factors for BOS and BOS-related mortality.20 35 The association of CRP with distance from a major road is compatible with the notion that inhaled particulates exert systemic inflammatory effects outside the respiratory tract.11
After organ transplantation, the 5-year survival is 45% for lung, 72% for heart or liver and 90% for kidney transplantation.36 It is tempting to attribute the higher failure rate of lung transplantation to air pollution. The observed systemic effect could indicate an adverse affect for traffic-related air pollution in other solid organ transplantations, especially the heart.
The observed HRs found in this study allow the authors to estimate that in the lung transplant population, 25% of the BOS events and 28% of the deaths could be attributed to living close to a major road (171 m). These population-attributable fractions are significant not only in terms of patient suffering but also in terms of healthcare costs. The yearly mean cost after lung transplantation is €46 100 for a stable patient and €79 100 for a patient with BOS.37 38
In conclusion, the study found that exposure to traffic-related air pollution independently increased the risk of BOS and mortality in lung transplant patients and was associated with lung and systemic inflammation. The observed impact of traffic-related air pollution is not insignificant and, if confirmed by other studies, has substantial clinical and public health implications.
Review history and Supplementary material
Funding GMV is holder of the GSK (Belgium) chair in respiratory pharmacology at the KULeuven, and is supported by the Research Foundation Flanders (FWO): G.0643.08 and G.0723.10 and 'Onderzoeksfonds K.U.Leuven (OT/10/050). RV is a research fellow and BMV, DEVR and LJD are senior research fellows of the FWO. The environmental health research at Hasselt University is supported by the FWO (1.5.158.09.N.00) and Internal UHasselt University grants (Bijzonder Onderzoekdsfonds, BOF).
Competing interests None.
Patient consent Obtained.
Ethics approval This study was conducted with the approval of the Ethical Review Board of the Leuven University Medical Faculty.
Provenance and peer review Not commissioned; externally peer reviewed.
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