The aim of this study was to investigate the association between fine particulate matter 2.5 (PM2.5) and oral cancer among Taiwanese men. Four linked data sources including the Taiwan Cancer Registry, Adult Preventive Medical Services Database, National Health Insurance Research Database, and Air Quality Monitoring Database were used. Concentrations of sulfur dioxide, carbon monoxide, ozone, NOx (nitrogen monoxide and nitrogen dioxide), coarse particulate matter (PM10-2.5) and PM2.5 in 2009 were assessed in quartiles. A total of 482 659 men aged 40 years and above were included in the analysis. Logistic regression was used to examine the association between PM2.5 and oral cancer diagnosed from 2012 to 2013. After adjusting for potential confounders, the ORs of oral cancer were 0.91 (95% CI 0.75 to 1.11) for 26.74≤PM2.5<32.37, 1.01 (95% CI 0.84 to 1.20) for 32.37≤PM2.5<40.37 µg/m3 and 1.43 (95% CI 1.17 to 1.74) for PM2.5≥40.37 µg/m3 compared with PM2.5<26.74 µg/m3. In this study, there was an increased risk of oral cancer among Taiwanese men who were exposed to higher concentrations of PM2.5.
- medical research
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Significance of this study
What is already known about this subject?
Exposure to particulate matter 2.5 (PM2.5) is associated with an increased risk of cardiovascular diseases and lung cancer.
The oral cavity is one of the routes by which PM2.5 gains access into the lungs and alveoli.
The incidence of oral cancer among Taiwanese men is increasing.
Some of the known risk factors for oral cancer are betel quid chewing, smoking, and drinking.
What are the new findings?
When compared with PM2.5<26.74 μg/m3, PM2.5≥40.37 μg/m3 was significantly associated with an increased risk of oral cancer.
Ozone (28.69≤O3<30.97 ppb) was significantly associated with an increased risk of oral cancer.
Smoking and frequent betel quid chewing were significantly associated with an increased risk of oral cancer.
How might these results change the focus of research or clinical practice?
These results have increased knowledge regarding fine particulate pollution as a risk factor for oral cancer.
This study indicates the need for further research to investigate the association between oral cancer and PM2.5, including lower exposure levels.
Oral cancer is a serious and growing problem in many parts of the world.1 In 2012, the global incidence and deaths resulting from oral cancer were estimated at 300 000 and 145 000, respectively.2 A study reported an increase in the incidence of oral cancer among Taiwanese men.3 Betel quid chewing, smoking, drinking, and human papillomavirus (HPV) have been associated with an increased risk of oral cancer.4–7
Exposure to heavy metals like arsenic, nickel, and chromium especially at higher concentrations, as well as emissions from petroleum and chemical plants have been shown to increase the risk of oral cancer.8–10 Particulate matter less than or equal to 2.5 microns in diameter (PM2.5) is harmful to human health, contributing to respiratory and cardiovascular diseases.11–13 This risk is partly because PM2.5 can be inhaled into the lungs and bronchi, owing to its small size.14 Long-term and short-term exposures to PM2.5 have also been linked to increased hospital admissions and cardiovascular mortality.12 15 However, few studies have been conducted to investigate the relationship between PM2.5 and oral cancer. The aim of this study was to investigate the association between PM2.5 and oral cancer among Taiwanese men.
Materials and methods
Four data sources which included the Taiwan Cancer Registry (TCR), Adult Preventive Medical Services Database (APMSD), National Health Insurance Research Database (NHIRD), and the Air Quality Monitoring Database (AQMD) were used in this study. The data sets were linked using personal identification numbers of the participants which were protected for privacy reasons.
Air pollution data were retrieved from the AQMD which had been set up by the Environmental Protection Administration of the Executive Yuan. This database contains daily concentrations of pollutants collected from fully automated air quality monitoring stations. The data are available from 1998 through 2011. Nonetheless, data on PM2.5 are available only from 2006. The air pollution data used in this study were collected from 66 air quality monitoring stations located in 64 different municipalities. Two municipalities had two monitoring stations each, while the other 62 had only one station each.
The annual average concentrations of sulfur dioxide (SO2), carbon monoxide (CO), ozone (O3), NOx (nitrogen monoxide (NO), nitrogen dioxide (NO2)), PM10, PM2.5, and PM10−2.5 in 2009 were determined. The PM10−2.5 concentration was determined by subtracting the concentration of PM2.5 from that of PM10. The pollution levels in 2009 were selected, because this year marked the midpoint of the available PM2.5 pollution data. To draw inferences regarding pre-2006 PM2.5 exposure trends, we examined the correlation between PM10 and PM2.5 in the years that data on both pollutants were available.
Study participants and measures
Since 1996, adults in Taiwan have enjoyed free preventive medical services. Valid electronic records of persons who use the services were established only in 2012. These records are maintained by the Health Promotion Administration of the Ministry of Health and Welfare.
The study participants included men aged 40 years and older who lived in the 64 different municipalities. Birthdate and gender were retrieved from the NHIRD. Age was determined by subtracting the birthdate found in the NHIRD from the enrollment date found in the 2012–2013 APMSD. Air pollution exposure was assigned based on the participants’ household registration municipality in the NHIRD. Data on smoking and betel chewing were only available from 2012 and 2013. Hence, the study participants (both cases and controls) were restricted to those who attended the adult preventive medical services in 2012 or 2013 and provided information on smoking and betel chewing. This information was obtained by asking participants whether they have ever chewed betel quid or smoked cigarettes. Those whose response was ‘no’ were considered as never chewers/smokers. For those whose response was ‘yes’, they were further asked how often they chewed betel quid or smoked cigarettes. Those whose response was ‘almost every day’ were defined as frequent chewers/smokers, while those whose response was ‘sometimes or on social occasions’ were defined as occasional chewers/smokers.
Oral cancer data diagnosed from 2012 to 2013 were collected from the TCR. The International Classification of Diseases Oncology, third version codes used included C00–C06, C09–C10, and C12–C14. Persons with incomplete personal information were excluded from the study. A total of 482 659 participants were included in the final analysis.
Data were analyzed using SAS V.9.4. Pearson correlation was used to assess the correlation among air pollutants (CO, NOx, O3, PM10, PM10−2.5, PM2.5, and SO2), while Spearman’s correlation was used to assess the PM2.5 correlation from 2006 to 2011. The collinearity of the air pollutants with PM2.5 was determined and the variance influence factors >10 were deleted from the regression analysis. Logistic regression analysis was used to assess the relationship between PM2.5 and oral cancer. Concentrations of air pollutants were stratified into quartiles. PM2.5<26.74 µg/m3 (Q1) was set as the reference. The ORs and 95% CI were determined and p<0.05 was considered statistically significant. Adjustments were made for PM10−2.5, SO2, O3, age, betel quid chewing, and smoking.
The concentrations of the air pollutants are shown in table 1. For PM2.5, Q1, median and Q3 were 26.74, 32.37, and 40.37 µg/m3, respectively. The correlation among the air pollutants is shown in table 2. After checking for collinearity of the other air pollutants with PM2.5, the variance influence factors for CO and NOx were >10 (table not shown) and they were therefore deleted from the regression analysis. The descriptive data of the participants are shown in table 3. There were 1617 oral cancer cases (mean age=60.69±10.89 years) and 481 042 non-oral cancer cases (mean age=61.2±12.77 years). The mean ages of cases and non-cases were not significantly different.
Table 4 presents the association of oral cancer with PM2.5 after multivariable adjustments. The ORs of oral cancer were 0.91 (95% CI 0.75 to 1.10) for 26.74≤PM2.5<32.37, 1.00 (95% CI 0.84 to 1.20) for 32.37≤PM2.5<40.37 µg/m3 and 1.42 (95% CI 1.17 to 1.73) for PM2.5≥40.37 µg/m3 after adjusting for PM10−2.5, SO2, O3, age, and betel quid chewing (table 4, Model 1). After a further adjustment including smoking (table 4, Model 2), the effect of PM2.5 on oral cancer risk did not change. In both models, PM10−2.5 and SO2 had no significant association with oral cancer regardless of their concentrations. However, O3, frequent betel quid chewing, occasional, as well as frequent smoking were significantly associated with oral cancer (table 4, Models 1 and 2). Spearman’s analysis showed that PM2.5 concentrations were highly correlated from 2006 to 2011 (table 5).
This study, with a large sample size, is the first to associate oral cancer with PM2.5 using the aforementioned databases. After adjusting for the potential confounders, higher concentrations of PM2.5 (≥40.37 µg/m3) were significantly associated with oral cancer in Taiwanese men. These findings add to the growing evidence on the adverse effects of PM2.5 on human health.11–13 The adverse health effects of PM2.5 could be linked to its relatively smaller diameter, yet a larger surface area which may potentially facilitate the adsorption and condensation of higher concentration of toxic substances and other pollutants.16 17 Some of the components of PM2.5 including metals like lead, cadmium, arsenic, chromium, and nickel, as well as organic compounds like polycyclic aromatic hydrocarbons (PAHs), among others17–19 are carcinogenic. For instance, exposure to heavy metal pollutants like arsenic, nickel, and chromium has been associated with oral cancer risk.8 9 Moreover, exposure to asbestos and PAHs adsorbed on PM2.5 is reported to have increased the risk of oral cancer.20 The carcinogenicity of PM2.5 has been linked to oxidative DNA damage, metabolism of organic compounds as well as inflammatory injury.16 18 21 22 Undetoxified carcinogenic substances and unrepaired damaged DNA, as well as replication of damaged DNA can aggravate carcinogenicity.23 24
In the current study, O3 was significantly associated with an increased risk of oral cancer. The deleterious effects of ozone on the respiratory tract are well known.25 Nonetheless, ozone was inversely associated with oral cancer risk though not statistically significant.26 Besides O3, smoking and betel quid chewing were associated with an increased risk of oral cancer in this study. Similar results have been previously reported.4 5
This study is not without limitations. First, the concentration of PM2.5 that is delivered to mouth is not known. Second, there were no PM2.5 exposure data before 2006. Nevertheless, those for PM10 were available from 1998 to 2011. The concentrations of PM2.5 from 2006 to 2011 were highly correlated. In addition, the concentrations of PM10 from 1998 to 2011 were highly correlated. Furthermore, there were high correlations between PM2.5 and PM10 from 2006 to 2011. These indicate that the participants might have been previously exposed to PM2.5 for quite some time. Therefore, we believe that high correlations could have also existed if there were historical data on PM2.5 exposure before 2006. The concentrations of PM2.5 and PM10 (μg/m3) between 2006 and 2011 are shown in the online Supplementary tables 1 and 2, respectively.
In conclusion, higher concentrations of PM2.5 may be associated with increased risk of oral cancer in Taiwanese men. The mechanism through which this occurs is not clearly understood, hence further investigations are required.
Contributors Y-HC, S-WK, P-CK, S-JL and Y-PL designed the study and analyzed the data. Y-HC and DMT reviewed the manuscript. All the authors interpreted the data, drafted the manuscript and approved the final version of the manuscript.
Funding This research was funded by the Ministry of Science and Technology (MOST), Taiwan (MOST 105-2627-M-040-002, MOST 106-2627-M-040-002 and MOST 106-EPA-F-016-001).
Competing interests None declared.
Patient consent Not required.
Ethics approval Institutional Review Board of Chung Shan Medical University Hospital.
Provenance and peer review Not commissioned; externally peer reviewed.
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