Research Article Issue 7 | July 2009 | Vol. 117
Exposure to Traffic Pollution and Increased Risk of Rheumatoid Arthritis
Jaime E. Hart,1,2 Francine Laden,1,2,3 Robin C. Puett,4,5 Karen H. Costenbader,6 and Elizabeth W. Karlson6
Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease that affects approximately 1% of the adult population, and to date, genetic factors explain < 50% of the risk. Particulate air pollution, especially of traffic origin, has been linked to systemic inflammation in many studies.
We examined the association of distance to road, a marker of traffic pollution exposure, and incidence of RA in a prospective cohort study.
We studied 90,297 U.S. women in the Nurses’ Health Study. We used a geographic information system to determine distance to road at the residence in 2000 as a measure of traffic exposure. Using Cox proportional hazard models, we examined the association of distance to road and incident RA (1976–2004) with adjustment for a large number of potential confounders.
In models adjusted for age, calendar year, race, cigarette smoking, parity, lactation, menopausal status and hormone use, oral contraceptive use, body mass index, physical activity, and census-tract-level median income and house value, we observed an elevated risk of RA [hazard ratio (HR) = 1.31; 95% confidence interval (CI), 0.98–1.74] in women living within 50 m of a road, compared with those women living 200 m or farther away. We also observed this association in analyses among nonsmokers (HR = 1.62; 95% CI, 1.04–2.52), nonsmokers with rheumatoid factor (RF)-negative RA (HR = 1.77; 95% CI, 0.93–3.38), and nonsmokers with RF-positive RA (HR = 1.51; 95% CI, 0.82–2.77). We saw no elevations in risk in women living 50–200 m from the road.
The observed association between exposure to traffic pollution and RA suggests that pollution from traffic in adulthood may be a newly identified environmental risk factor for RA.
Citation: Hart JE, Laden F, Puett RC, Costenbader KH, Karlson EW. 2009. Exposure to Traffic Pollution and Increased Risk of Rheumatoid Arthritis. Environ Health Perspect 117:1065–1069; http://dx.doi.org/10.1289/ehp.0800503
Address correspondence to E.W. Karlson, 75 Francis St., Boston, MA 02115 USA. Telephone: (617) 732-5078. Fax: (617) 731-9032. E-mail: email@example.com
This work was supported by National Institutes of Health grants R01 AR49880, CA87969, P60 AR047782, K24 AR0524-01, and BIRCWH K12 HD051959 supported by the National Institute of Mental Health, National Institute of Allergy and Infectious Diseases, National Institute of Child Health and Human Development, and Office of the Director. K.H.C. is the recipient of an Arthritis Foundation/American College of Rheumatology Arthritis Investigator Award and a Katherine Swan Ginsburg Memorial Award.
The authors declare they have no competing financial interests.
Received: 18 December 2008
Accepted: 4 March 2009
Advance Publication: 4 March 2009
Final Publication: 1 July 2009
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Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease affecting approximately 1% of the adult population (Doran et al. 2002; Drosos et al. 1997; Gabriel et al. 1999). Genetic factors are thought to be responsible for < 50% of RA risk, suggesting that environmental factors could contribute to the development of RA in the genetically predisposed (Begovich et al. 2004; Gregersen et al. 1987; Kobayashi et al. 2005). Cigarette smoking is a strong environmental risk factor for the development of RA, with a clear dose–response relationship. Risk of RA rises after 10 pack-years of smoking and remains elevated up to 20 years after smoking discontinuation (Costenbader et al. 2006). Epidemiologic evidence has also suggested associations of RA with occupational exposures to silica and mineral oil and with environmental exposures such as cigarette smoke (Criswell et al. 2002; Hazes et al. 1990; Heliovaara et al. 1993; Hernandez Avila et al. 1990; Karlson et al. 1999; Krishnan et al. 2003; Padyukov et al. 2004; Raychaudhuri et al. 2008; Stolt et al. 2003, 2005; Sverdrup et al. 2005; Symmons et al. 1997; Uhlig et al. 1999; Vessey et al. 1987; Voigt et al. 1994), suggesting that respiratory exposures activating the immune system may lead to RA. We have recently examined the geographic variation of RA in a prospective cohort of U.S. women (Costenbader et al. 2008). We observed significantly higher RA risk in the Midwest and Northeast regions of the United States (compared with the West) in women who had lived in one region throughout most of their lives. These regions have historically had higher levels of air pollution, and our evolving understanding of RA pathogenesis suggests that inhaled particulate matter, similar to cigarette smoke, may induce local lung inflammation as well as systemic inflammation. Indirect support of this hypothesis comes from the observation that air pollution has been clearly linked with other diseases of local lung and systemic inflammation, including asthma and chronic bronchitis, cardiovascular disease, and lung and laryngeal cancers (Dockery et al. 1993; Karakatsani et al. 2003; Künzli et al. 2005; Laden et al. 2006; Nafstad et al. 2003; Penard-Morand et al. 2005; Pereira et al. 2005; Pope et al. 2002; Pope and Dockery 2006; Sunyer 2001; van Eeden et al. 2005). Associations with overall mortality have been shown most strongly with particles from traffic, coal, and residual oil combustion (Laden et al. 2000; Schwartz et al. 2002). Therefore, in this analysis we examine the association of incidence of RA and distance to the nearest road as a marker of traffic pollution in a cohort of U.S. women.
Materials and Methods
Study population. The Nurses’ Health Study (NHS) is a long-term prospective cohort study of U.S. female nurses. The NHS was initiated in 1976 when 121,700 U.S. registered female nurses, 30–55 years of age, completed a mailed questionnaire and provided informed consent. At the study inception they resided in 11 states throughout the United States (California, Connecticut, Florida, Massachusetts, Maryland, Michigan, New Jersey, New York, Ohio, Pennsylvania, and Texas). Although most of the nurses have not moved, they now reside in all 50 states. Follow-up questionnaires, with response rates > 90%, are mailed every 2 years to update information on risk factors and the occurrence of major illnesses. We included women in the present study if their 2000 residential address was successfully geocoded to the street segment level in the continental United States and they had no history of RA or cancer (other than nonmelanoma skin cancer) at baseline in 1976. A total of 90,297 members were available for analysis.
Assessment of outcome. We used a two-stage procedure to identify nurses with RA. All nurses reporting RA or other connective tissue disease on a biennial questionnaire (n = 11,674) received a follow-up screening questionnaire for connective tissue symptoms (Karlson et al. 1995). If the screening questionnaire was positive, we requested medical records, which underwent detailed examination for American College of Rheumatology diagnostic criteria for RA. Subjects who self-reported but later denied RA diagnosis, denied permission to obtain medical records, or who had a negative screening questionnaire were excluded (n = 8,877) (Karlson et al. 2004). In this analysis, we included a total of 687 incident cases (1976–2004), 390 (57%) of whom had rheumatoid factor (RF)-positive RA as determined by medical record review.
Exposure assessment. We studied distance to road in the year 2000 as a proxy for traffic pollution exposure. Distance to road (in meters) for all available nurses’ addresses was determined using geographic information system software (ArcGIS, version 9.2; ESRI, Redlands, CA). Road segments in the 2000 U.S. Census Topologically Integrated Geographic Encoding and Referencing system (TIGER) files (http://www.census.gov/geo/www/tiger/) were selected by U.S. Census feature class code to include A1 (primary roads, typically interstates, with limited access), A2 (primary major, noninterstate roads), or A3 (smaller, secondary roads, usually with more than two lanes) road segments. We calculated the shortest distance between each address and the closest road segment. We conducted analyses using the distance to the closest of all three road types, and the distance to the nearest primary road (A1, A2 only). For the main analyses, we used the distance to A1–A3 roads at the 2000 mailing address. In sensitivity analyses, we also assessed the associations with distance to road for all other available address years and to primary roads only. Based on the distribution of distance to road in this cohort and previous exposure studies showing exponential decay in exposures with increasing distance to road, we divided distance to road into the following categories (0–50, 50–200, ≥ 200 m) (Adar and Kaufman 2007; Lipfert et al. 2006; Lipfert and Wyzga 2008; Sahlodin et al. 2007; Zhu et al. 2002).
Additional covariates. Information on potential confounders and effect modifiers is updated every 2 years in the NHS, so we assigned each woman updated covariate values for each individual questionnaire cycle where appropriate. We examined possible confounding by age (in months), non-Caucasian race, age at menarche, parity, total months of lactation, current menopausal status, menopausal hormone use, oral contraceptive use, physical activity, and body mass index (BMI), many of which have been shown to be risk factors for RA (Costenbader et al. 2008; Karlson et al. 2004). To control for smoking, we used data from lifetime smoking history to calculate pack-years (number of packs/day multiplied by number of years of cigarette smoking) and current smoking status (current/former/never). Because smoking is a major risk factor for RA and residual confounding by smoking may obscure any traffic pollution effect, we also restricted models to never-smokers. To control for individual level socioeconomic status, we included several variables, including nurses’ educational level, occupation of both parents, marital status, and, if applicable, husband’s education. To control for area-level socioeconomic status, we included area-level information from the 2000 Census on tract level median income and house value.
Statistical analysis. Time-varying Cox proportional hazards models were used to assess the relationship of incident RA (1976–2004) with distance to road. These models were based on a biennial time scale and were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). Person-time accrued from 1 January 1976 until diagnosis of RA, date of death, or the end of follow-up (31 May 2004), whichever was first. All Cox models were stratified by age in months and calendar year. We also ran sensitivity analyses restricted to women who were nonsmokers at baseline and by RF status (positive/negative). All statistical analyses used SAS (version 9.1; SAS Institute Inc. 2006).
Table 1 presents the characteristics of the cohort at baseline (1976) by distance to road category. The average (± SD) age at baseline of women in NHS was 42.4 ± 7.1, and the average BMI was 23.7 ± 4.0. Only 31.4% of the women were current smokers, and 44.4% had never smoked cigarettes. Most of the cohort was premenopausal, and more than half of the postmenopausal women had never used postmenopausal hormones. Twenty percent of the women had < 3 metabolic equivalent hours per week of physical activity, and only 11.2% had more than 27. Most of the women had Registered Nurse degrees, were married, and had husbands with a high school education or greater. There was little difference in the distribution of RA risk factors by exposure level. As expected, members of the cohort living closer to roads did live in census tracts with lower median family income and home values than did those living farther away from roads.
In models adjusted for age and calendar year, individuals living within 50 m of an A1–A3 road had a 33% (95% CI, 0–77%) higher risk of incident RA compared with those living 200 m or farther away (Table 2). Women living 50–200 m from these roads had a non-statistically significant decreased risk (HR = 0.85; 95% CI, 0.66–1.09). Additional adjustment for race, cigarette smoking, parity/lactation, menopausal status and hormone use, oral contraceptive use, BMI, physical activity, and census-tract-level median income and house value did not change the results (0–50 m: HR = 1.31; 95% CI, 0.98–1.74; 50–200 m: HR = 0.84; 95% CI, 0.65–1.08). Among never-smokers, the association of living within 50 m and incident RA was slightly elevated compared with that in the full cohort, with an HR = 1.62 (95% CI, 1.04–2.52) in fully adjusted models. The results were similar in sensitivity analyses using a subsample of women who did not move between 1988–2004 [Supplemental Material, Table 1 (available online at http://www.ehpon-line.org/members/2009/0800503/suppl.pdf)], as well as analyses using distance to road in all other available address years (data not shown). This is reasonable given the residential stability in this cohort (58% of the cohort had only one address between 1988–2004, and among the participants who did move, the median number of moves was 1).
We also observed associations with distance to road with RF-positive RA (Table 3). In fully adjusted models, women living within 50 m of a road had a 44% higher risk (95% CI, 0–107%) of RF-positive RA than did those living 200 m or farther away. The association among never-smokers was similar but did not achieve statistical significance. Among RF-negative RA cases, women living within 50 m of a road had a non-statistically significant 15% increased risk (95% CI, –17% to 83%) in fully adjusted models. The association between distance to road and RF-negative RA among never-smokers was also elevated (HR = 1.77; 95% CI, 0.93–3.38).
In multivariable analyses restricted to primary (A1 and A2) roads (Table 4), women living within 50 m of a primary road had an HR of 1.63 (95% CI, 1.06–2.51), whereas those living 50–200 m away had an HR of 0.86 (95% CI, 0.60–1.23). Unlike models including A1–A3 roads, the HRs were not higher when the cohort was limited to nonsmokers. There were too few cases living within 50 m of a primary road to conduct analyses stratified by RF status.
In a prospective assessment of incident RA and distance to road, we found that women living within 50 m of an A1–A3 road are at a 31% increased risk of RA compared with women living more than 200 m away. This association was also observed in analyses among nonsmokers (especially among RF-negative cases) and in women with RF-positive RA. We found higher risks for those women living closer to primary roads (A1, A2). These results suggest that higher exposure to traffic pollution may be associated with RA risk. To the best of our knowledge, this is the first time an association had been demonstrated between RA incidence and residential distance to the closest road.
A large body of health effects literature has developed using distance to road as an indicator of traffic exposures (Adar and Kaufman 2007; Beelen et al. 2008; Brunekreef et al. 1997; Ciccone et al. 1998; Duhme et al. 1996; English et al. 1999; Finkelstein et al. 2004; Garshick et al. 2003; Guo et al. 1999; Hoek et al. 2002; Jerrett et al. 2005a, 2005b; Lipfert et al. 2006; Maheswaran and Elliott 2003; Nitta et al. 1993; Oosterlee et al. 1996; Tonne et al. 2007; Venn et al. 2000, 2001, 2005; Weiland et al. 1994; Wjst et al. 1993). Adverse health effects have been demonstrated with respiratory symptoms, asthma, lung function, and all cause and cardiopulmonary mortality in populations living near roads around the world. Because traffic is a major source of air pollution, these results are also consistent with the general air pollution health effect literature. Many studies have demonstrated the adverse effects of air pollution on mortality and morbidity (Downs et al. 2007; Pope and Dockery 2006; Schikowski et al. 2005; Sunyer et al. 2006), and specifically air pollution from traffic sources (Beelen et al. 2008; Laden et al. 2000; Schwartz et al. 2005). Our observed higher risks in nonsmokers are also consistent with results from the general air pollution literature. In an analysis of particulate matter exposures with all-cause mortality and coronary heart disease events in the NHS cohort, we found higher risks among women who were never-smokers, with no associations seen in current smokers (Puett et al. 2008). This suggests that the overall detrimental effects of smoking may mask the effects of traffic or air pollution. In these multivariable models, compared with never-smokers, the HR for being a current smoker was 2.12 (95% CI, 1.29–3.48) and for former smokers was 2.57 (95% CI, 1.62–4.09). Therefore, the 31% higher risk we observed for living within 50 m of an A1–A3 road, and the 63% higher risk for those near A1–A2 roads are much smaller than the risks from former/current smoking in this cohort.
Epidemiologic evidence has provided strong evidence that cigarette smoke is a risk factor for RA (Costenbader et al. 2006; Criswell et al. 2002; Hazes et al. 1990; Heliovaara et al. 1993; Hernandez Avila et al. 1990; Karlson et al. 1999; Krishnan et al. 2003; Padyukov et al. 2004; Stolt et al. 2003, 2005; Sverdrup et al. 2005; Symmons et al. 1997; Uhlig et al. 1999; Vessey et al. 1987; Voigt et al. 1994). Stronger effects have been seen in individuals with seropositive RA, similar to our findings with distance to road. Cigarette smoke contains hundreds of compounds, many of which have been shown to lead to elevated levels of inflammation (Bermudez and Ridker 2002; Tracy et al. 1997). Traffic exposures and cigarette smoking may act to increase risk of RA through similar mechanisms. Respiratory exposure to particulate matter (of which traffic is a major source) has similarly been associated with increased systemic inflammation (Jimenez et al. 2002; Peters et al. 1997; Seaton et al. 1995; van Eeden et al. 2005). Human exposure to high levels of ambient particles stimulates the production of inflammatory cytokines in the lung, which may stimulate the bone marrow to release neutrophils and monocytes into the circulation (Tan et al. 2000). In animals, respiratory exposure to particulate matter accelerates transit of neutrophils and monocytes in bone marrow and expands the leukocyte pool size (Mukae et al. 2001; Terashima et al. 1997). Studies in cellular and animal models suggest that reactive oxygen species are generated by respiratory exposure to particulate matter (Gonzalez-Flecha 2004). Reactive oxygen species and oxidative stress are generated indirectly by proinflammatory mediators released from stimulated macrophages, but there is also evidence of direct effects of particles on intracellular sources of reactive oxygen species. Many proinflammatory genes induced upon exposure to particulate matter are regulated by redox-sensitive transcription factors, such as nuclear factor κ B (NFκB) (Shukla et al. 2000). In vivo models of inhalation exposure to particulate matter demonstrate that NFκB- regulated genes, including interleukin-6, tumor necrosis factor-α, and γ-interferon, are up-regulated by exposure to particulate matter (Jimenez et al. 2000; Kennedy et al. 1998; Shukla et al. 2000). Oxidative stress, in turn, may be involved in the mechanism of RA initiation after respiratory exposure.
This analysis has several important limitations. We used distance to A1–A3 road as a proxy for exposure, so we did not have information on actual pollutant levels at the residential addresses over time. Additionally, we do not have information on the intensity of traffic, which could be used as an additional proxy for the exposures experienced at these residential locations. However, the results were slightly stronger when we considered only primary roads, presumably with higher traffic volume. We did not have power to break out the road categories individually. In our primary analyses, we focused on the distance to road in 2000, because that was the year the Census TIGER file of roads was created (U.S. Census Bureau 1992). In our sensitivity analyses using other available address years (1986–2004), the results were similar, suggesting that this is not likely to be an important limitation, potentially because most of the cohort had only one address during this time period and results in nonmovers were also similar. By using only one point in time, however, we are unable to determine potentially important time windows of exposure. All of these issues likely lead to exposure misclassification, which would bias our results toward the null and make associations harder to detect. Our conclusions are also weakened by the lack of a dose response. It is also possible that access to rheumatology specialists and differences in RA diagnostic proclivity may be an unmeasured confounder in this study. We examined differences in the RA cases at diagnosis according to distance to road category, and although the mean age at diagnosis did not vary with distance to road, the percentage of RF-positive cases increased at greater distances.
The observed association between exposure to traffic pollution and RA suggests that pollution from traffic in adulthood may be a newly identified environmental risk factor for RA. This association study should be followed by further research into whether fine particles or chemicals are associated with RA risk and to discern whether there are time windows of exposure that may be particularly important.
Beelen R, Hoek G, van den Brandt PA, Goldbohm RA, Fischer P, Schouten LJ, et al. 2008. Long-term effects of traffic-related air pollution on mortality in a Dutch cohort (NLCS-AIR study). Environ Health Perspect 116:196–202.
Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, Chokkalingam AP, Alexander HC, et al. 2004. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet 75(2):330–337.
Ciccone G, Forastiere F, Agabiti N, Biggeri A, Bisanti L, Chellini E, et al. 1998. Road traffic and adverse respiratory effects in children. SIDRIA Collaborative Group. Occup Environ Med 55(11):771–778.
Criswell LA, Merlino LA, Cerhan JR, Mikuls TR, Mudano AS, Burma M, et al. 2002. Cigarette smoking and the risk of rheumatoid arthritis among postmenopausal women: results from the Iowa Women’s Health Study. Am J Med 112(6):465–471.
Doran MF, Pond GR, Crowson CS, O’Fallon WM, Gabriel SE. 2002. Trends in incidence and mortality in rheumatoid arthritis in Rochester, Minnesota, over a forty-year period. Arthritis Rheum 46(3):625–631.
Duhme H, Weiland SK, Keil U, Kraemer B, Schmid M, Stender M, et al. 1996. The association between self-reported symptoms of asthma and allergic rhinitis and self-reported traffic density on street of residence in adolescents. Epidemiology 7(6):578–582.
English P, Neutra R, Scalf R, Sullivan M, Waller L, Zhu L. 1999. Examining associations between childhood asthma and traffic flow using a geographic information system. Environ Health Perspect 107:761–767.
Gregersen PK, Silver J, Winchester RJ. 1987. The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis. Arthritis Rheum 30(11):1205–1213.
Guo YL, Lin YC, Sung FC, Huang SL, Ko YC, Lai JS, et al. 1999. Climate, traffic-related air pollutants, and asthma prevalence in middle-school children in Taiwan. Environ Health Perspect 107:1001–1006.
Hoek G, Brunekreef B, Goldbohm S, Fischer P, van den Brandt PA. 2002. Association between mortality and indicators of traffic-related air pollution in the Netherlands: a cohort study. Lancet 360(9341):1203–1209.
Jerrett M, Arain A, Kanaroglou P, Beckerman B, Potoglou D, Sahsuvaroglu T, et al. 2005a. A review and evaluation of intraurban air pollution exposure models. J Expo Anal Environ Epidemiol 15(2):185–204.
Jimenez LA, Drost EM, Gilmour PS, Rahman I, Antonicelli F, Ritchie H, et al. 2002. PM(10)-exposed macrophages stimulate a proinflammatory response in lung epithelial cells via TNF-alpha. Am J Physiol Lung Cell Mol Physiol 282(2):L237–L248.
Jimenez LA, Thompson J, Brown DA, Rahman I, Antonicelli F, Duffin R, et al. 2000. Activation of NF-kappaB by PM(10) occurs via an iron-mediated mechanism in the absence of IkappaB degradation. Toxicol Appl Pharmacol 166(2):101–110.
Karakatsani A, Andreadaki S, Katsouyanni K, Dimitroulis I, Trichopoulos D, Benetou V, et al. 2003. Air pollution in relation to manifestations of chronic pulmonary disease: a nested case-control study in Athens, Greece. Eur J Epidemiol 18(1):45–53.
Karlson EW, Lee IM, Cook NR, Manson JE, Buring JE, Hennekens CH. 1999. A retrospective cohort study of cigarette smoking and risk of rheumatoid arthritis in female health professionals. Arthritis Rheum 42(5):910–917.
Karlson EW, Mandl LA, Hankinson SE, Grodstein F. 2004. Do breast-feeding and other reproductive factors influence future risk of rheumatoid arthritis? Results from the Nurses’ Health Study. Arthritis Rheum 50(11):3458–3467.
Kennedy T, Ghio AJ, Reed W, Samet J, Zagorski J, Quay J, et al. 1998. Copper-dependent inflammation and nuclear factor-kappaB activation by particulate air pollution. Am J Respir Cell Mol Biol 19(3):366–378.
Kobayashi M, Thomassen MJ, Rambasek T, Bonfield TL, Raychaudhuri B, Malur A, et al. 2005. An inverse relationship between peroxisome proliferator-activated receptor gamma and allergic airway inflammation in an allergen challenge model. Ann Allergy Asthma Immunol 95(5):468–473.
Laden F, Schwartz J, Speizer FE, Dockery DW. 2006. Reduction in fine particulate air pollution and mortality: extended follow-up of the Harvard Six Cities study. Am J Respir Crit Care Med 173(6):667–672.
Mukae H, Vincent R, Quinlan K, English D, Hards J, Hogg JC, et al. 2001. The effect of repeated exposure to particulate air pollution (PM10) on the bone marrow. Am J Respir Crit Care Med 163(1):201–209.
Nitta H, Sato T, Nakai S, Maeda K, Aoki S, Ono M. 1993. Respiratory health associated with exposure to automobile exhaust. I. Results of cross-sectional studies in 1979, 1982, and 1983. Arch Environ Health 48(1):53–58.
Padyukov L, Silva C, Stolt P, Alfredsson L, Klareskog L. 2004. A gene-environment interaction between smoking and shared epitope genes in HLA-DR provides a high risk of seropositive rheumatoid arthritis. Arthritis Rheum 50(10):3085–3092.
Penard-Morand C, Charpin D, Raherison C, Kopferschmitt C, Caillaud D, Lavaud F, et al. 2005. Long-term exposure to background air pollution related to respiratory and allergic health in schoolchildren. Clin Exp Allergy 35(10):1279–1287.
Puett RC, Schwartz J, Hart JE, Yanosky JD, Speizer FE, Suh H, et al. 2008. Chronic particulate exposure, mortality, and coronary heart disease in the Nurses’ Health Study. Am J Epidemiol 168:1161–1168.
Schikowski T, Sugiri D, Ranft U, Gehring U, Heinrich J, Wichmann HE, et al. 2005. Long-term air pollution exposure and living close to busy roads are associated with COPD in women. Respir Res 6:152.10.1186/1465-9921-6-152 [Online 22 December 2005].
Shukla A, Timblin C, BeruBe K, Gordon T, McKinney W, Driscoll K, et al. 2000. Inhaled particulate matter causes expression of nuclear factor (NF)-kappaB-related genes and oxidant-dependent NF-kappaB activation in vitro. Am J Respir Cell Mol Biol 23(2):182–187.
Stolt P, Bengtsson C, Nordmark B, Lindblad S, Lundberg I, Klareskog L, et al. 2003. Quantification of the influence of cigarette smoking on rheumatoid arthritis: results from a population based case-control study, using incident cases. Ann Rheum Dis 62(9):835–841.
Stolt P, Kallberg H, Lundberg I, Sjogren B, Klareskog L, Alfredsson L. 2005. Silica exposure is associated with increased risk of developing rheumatoid arthritis: results from the Swedish EIRA study. Ann Rheum Dis 64(4):582–586.
Sverdrup B, Kallberg H, Bengtsson C, Lundberg I, Padyukov L, Alfredsson L, et al. 2005. Association between occupational exposure to mineral oil and rheumatoid arthritis: results from the Swedish EIRA case-control study. Arthritis Res Ther 7(6):R1296–R1303.
Symmons DP, Bankhead CR, Harrison BJ, Brennan P, Barrett EM, Scott DG, et al. 1997. Blood transfusion, smoking, and obesity as risk factors for the development of rheumatoid arthritis: results from a primary care-based incident case-control study in Norfolk, England. Arthritis Rheum 40(11):1955–1961.
Tracy RP, Psaty BM, Macy E, Bovill EG, Cushman M, Cornell ES, et al. 1997. Lifetime smoking exposure affects the association of C-reactive protein with cardiovascular disease risk factors and subclinical disease in healthy elderly subjects. Arterioscler Thromb Vasc Biol 17(10):2167–2176.
U.S. Census Bureau. 1992. Tiger/Line Files Appendix E: Census Feature Class Codes (CFCC). Available: http://www.census.gov/geo/www/tiger/appendxe.asc [accessed 12 June 2005].
Venn A, Lewis S, Cooper M, Hubbard R, Hill I, Boddy R, et al. 2000. Local road traffic activity and the prevalence, severity, and persistence of wheeze in school children: combined cross sectional and longitudinal study. Occup Environ Med 57(3):152–158.
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