Skip to main content

ORIGINAL RESEARCH article

Front. Public Health, 05 September 2023
Sec. Environmental Health and Exposome
This article is part of the Research Topic Urban Environment and Public Health View all 27 articles

Short-term effects of high-resolution (1-km) ambient PM2.5 and PM10 on hospital admission for pulmonary tuberculosis: a case-crossover study in Hainan, China

Pan-Pan Zhu&#x;Pan-Pan Zhu1Yi Gao,&#x;Yi Gao2,3Gui-Zhong Zhou&#x;Gui-Zhong Zhou4Rui LiuRui Liu4Xiao-Bo LiXiao-Bo Li5Xian-Xian FuXian-Xian Fu6Jian FuJian Fu3Feng LinFeng Lin3Yuan-Ping Zhou,
Yuan-Ping Zhou2,7*Li Li
Li Li1*
  • 1State Key Laboratory of Organ Failure Research, Department of Biostatistics, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China
  • 2Department of Infectious Disease and Hepatology Unit, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China
  • 3Department of Infectious Disease, Hainan General Hospital, Hainan Medical University, Haikou, Hainan, China
  • 4Department of Infectious Disease, The Second Affiliated Hospital, Hainan Medical University, Haikou, Hainan, China
  • 5Department of Neurosurgery, Haikou Municipal People’s Hospital and Central South University Xiangya Medical College Affiliated Hospital, Haikou, Hainan, China
  • 6Clinical Lab, Haikou Municipal People’s Hospital and Central South University Xiangya Medical College Affiliated Hospital, Haikou, Hainan, China
  • 7Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China

Introduction: There is limited evidence regarding particulate matter (PM)’s short-term effects on pulmonary tuberculosis (PTB) hospital admission. Our study aimed to determine the short-term associations of the exposure to ambient PM with aerodynamic diameters <2.5 μm (PM2.5) and < 10 μm (PM10) with hospital admission for PTB in Hainan, a tropical province in China.

Methods: We collected individual data on patients hospitalized with PTB, PM2.5, PM10, and meteorological data from 2016 to 2019 in Hainan Province, China. Conditional logistic regression models with a time-stratified case-crossover design were used to assess the short-term effects of PM2.5 and PM10 on hospital admission for PTB at a spatial resolution of 1 km  ×  1 km. Stratified analyses were performed according to age at admission, sex, marital status, administrative division, and season of admission.

Results: Each interquartile range (IQR) increases in the concentrations of PM2.5 and PM10 were associated with 1.155 (95% confidence interval [CI]: 1.041–1.282) and 1.142 (95% CI: 1.033–1.263) hospital admission risks for PTB at lag 0–8 days, respectively. The stratified analyses showed that the effects of PM2.5 and PM10 were statistically significant for patients aged ≥65 years, males, married, and those residing in prefecture-level cities. Regarding seasonal differences, the associations between PM and hospital admission for PTB were statistically significant in the warm season but not in the cold season. The effect of PM2.5 was consistently stronger than that of PM10 in most subgroups.

Conclusion: Short-term exposure to PM increases the risk of hospital admission for PTB. The potential impact of PM with smaller aerodynamic diameter is more detrimental. Our findings highlight the importance of reducing ambient PM level to alleviate the burden of PTB.

Introduction

Tuberculosis (TB) is a contagious infection caused by Mycobacterium tuberculosis (1). Transmission of TB occurs when an infected person passes microbial aerosols into the alveoli of a new host through coughing. Drainage from any site of active TB can be a source of infection (2). TB poses a significant threat to public health worldwide (3). In 2019, there were 10 million TB case notifications and TB was one of the top ten causes of death, resulting in 1.4 million deaths worldwide. The fourth Sustainable Development Goal is to end the TB epidemic by 2030. However, TB incidence declined by only 9% from 2015 to 2019 (i.e., from 142 to 130 per 100,000 individuals) (4). Global TB targets are off track with the incidence increasing from 127 to 134 per 100,000 individuals between 2020 and 2021 (5).

TB is a disease of poverty (6). There is an apparent socio-economic gradient in TB burden across different locations, with the poorest being at the highest risk (7). Common risk factors for TB include human immunodeficiency virus (HIV) infection, smoking, diabetes, alcohol abuse, undernutrition, and indoor air pollution (8). Outdoor air pollution may also affect TB infection and/or disease progression (9). Particulate matter (PM) with aerodynamic diameters <2.5 μm (PM2.5) and < 10 μm (PM10) are the two main ambient air pollutants. PM10 can be deposited in the bronchi and PM2.5 can further reach the alveoli. The adverse impacts of the PM exposure on human health have been comprehensively discussed in epidemiological, experimental, and mechanism studies (1013). As for the impact of outdoor exposure to PM on TB, a few studies have suggested that short-term exposure to ambient PM2.5 is positively associated with TB incidence (1416), while others have reported a statistically non-significant association (17, 18). Similarly, the short-term association between exposure to PM10 and TB incidence has also been inconclusive (1921). TB is a chronic infectious disease. Patients with relatively severe TB symptoms must be hospitalized. However, previous studies have seldom explored the association between PM exposure and hospital admission for TB (22).

China has a high TB burden, ranking third following India and Indonesia in 2019. In that year, 833,000 individuals (i.e., 58.3 per 100,000 individuals) developed TB in China, accounting for 8.4% of the global population (4). Of these, 775,764 had pulmonary tuberculosis (PTB), representing 93.1% of the total number of patients with TB in China (23). Hainan Province is a relatively less developed province in China. From 2016 to 2019, the PTB case notification rate in Hainan Province increased from 76.5 to 90.3 per 100,000 individuals, with an average annual increase of >4.0% (24). Further, Hainan Province had China’s fifth-highest notification rate of PTB cases in 2019. Probing the association between PM exposure and hospital admission for PTB in Hainan Province would enrich our knowledge of the impact of PM on population health in tropical areas, shed light on targeted intervention measures, and help reduce the PTB burden more effectively. Herein, we aimed to determine the associations of hospital admission for PTB with PM2.5 and PM10, and further identify the potentially vulnerable populations in Hainan Province, China from 2016 to 2019.

Methods

Study area

Hainan Province lies in the south of China between latitude 3°35′ to 20°10’N and longitude 108°37′ to 118°45′E with a land area of 35,354 square kilometers. In 2019, the total resident population of Hainan Province was 9,447,200 (25). From 2016 to 2019, PM2.5 and PM10 exceeded the levels of 75 μg/m3 and 150 μg/m3 (class two standard according to Chinese National Ambient Air Quality Standards [GB3095-2012]) in 0.6 and 0% of the days, respectively, which was lower than the national average (12.5, 7.7%).

Data collection

We obtained the individual data of all PTB patients hospitalized in the top three largest hospitals that serve PTB patients in Hainan Province (i.e., Hainan General Hospital, The Second Affiliated Hospital of Hainan Medical University, and Haikou Municipal People’s Hospital) from January 1st, 2016 to December 31st, 2019. The collected data included the date of admission, age, sex, marital status, residential address, and primary diagnosis, coded according to the International Statistical Classification of Diseases and Related Health Problems, 10th edition (ICD-10). We included all patients whose primary discharge diagnosis was PTB (ICD-10 codes A15–A16). This study was approved by the Research Ethics Committee of Hainan General Hospital (No. 2021–314).

Data on daily average concentrations of PM2.5 and PM10 with a spatial resolution of 1 km × 1 km were obtained from the National Earth System Science Data Center, National Science & Technology Infrastructure of China.1 Daily meteorological data (i.e., mean temperature and relative humidity) were downloaded from the National Meteorological Information Center.2

Study design and exposure assignment

A time-stratified case-crossover design was applied in this study to assess the short-term effects of PM2.5 and PM10 on hospital admission for PTB. For each hospital admission, the case day was the day of admission, whereas the control day was the same day of other weeks within the same month. This self-pairing case–control design has the unique advantage of controlling for long-term and seasonal trends as well as time-invariant subject-specific variables or those that change slowly over time.

In addition, we matched each patient to the nearest 1 km × 1 km PM grid and meteorological monitoring station based on the patient’s residential address (Figure 1), generating 2,157 strata of exposure proxies for PM and meteorological factors (including mean temperature and relative humidity). Patients shared the same exposure proxy if they were in the same stratum.

FIGURE 1
www.frontiersin.org

Figure 1. Locations of patients admitted to the top three largest hospitals in Hainan for pulmonary tuberculosis.

Statistical analysis

Conditional logistic regression models were used to investigate the effects of PM2.5 and PM10 on hospital admission for PTB. The model is expressed as follows:

logit(Pi)=αi+βPM+NS(Temp014,df=3) +NS(RH,df=3)+δHoliday

Where Pi is the probability of hospital admission for PTB in stratum i. αi is the intercept for stratum i. Here, we considered single-day lags from 0 to 14 days and multi-day lags from 0–1 to 0–14 days (0–1 and 0–14 days mean the 2–day and 15–day moving average, respectively) for the concentration of PM (i.e., PM2.5 or PM10) (26). We added each lag term to the model separately and selected the lags corresponding to the models with the strongest effects of PM2.5 and PM10 (2729). Many previous studies have suggested that the effect of temperature on health outcomes is limited to 2 weeks (3032). In addition, previous studies controlled for the potential confounding effects of current–day relative humidity when assessing the health effects of air pollution (28, 33). Therefore, natural cubic splines with three degrees of freedom (dfs) were applied to the 15–day moving average temperature and current-day relative humidity. An indicator variable for holidays is also included in the model. The reported effects for the risk of PTB hospitalization were expressed as odds ratios (ORs) and corresponding 95% confidence intervals (CIs), which were associated with each interquartile range (IQR) increase in PM concentration.

We classified Hainan Province into two administrative regions: prefecture-level cities and county-level divisions (including county-level cities, counties, and autonomous counties). Stratified analyses were conducted by age at admission (<65 and ≥ 65 years), sex, marital status (married and others), administrative division (prefecture-level city and county-level division), and season of admission (warm [May–October] and cold [November–April]). Differences in the estimated effects of PM between subgroups were tested using a Z test (34):

Z=β1β2SE2(β1)+SE2(β2)

Where β1 and β2 are the regression coefficients of PM for two comparative subgroups. SE (β1) and SE (β2) are the standard errors of β1 and β2, respectively.

Sensitivity analyses were performed to verify the robustness of the findings by changing the dfs of the natural cubic splines for temperature and relative humidity to 4–6. Two-sided p < 0.05 was regarded as statistically significant. R software version 4.2.2 (R Foundation for Statistical Computing) was used for all analyses.

Results

Table 1 shows the number and percentage of hospital admission for PTB in different subgroups in Hainan Province from 2016 to 2019. A total of 4,562 hospital admission for PTB were included in this study, all of which occurred on Hainan Island (Figure 1). Patients aged < 65, male, married, and those living in county-level divisions accounted for 76.2, 76.6, 79.7, and 67.7% of admissions, respectively. There were slightly more patients in the warm season (54.0%) than in the cold season. The average concentrations of PM2.5 and PM10 were 20.2 μg/m3 and 36.2 μg/m3, respectively during the study period (Table 2).

TABLE 1
www.frontiersin.org

Table 1. Number and percentage of PTB hospitalization in different subgroups in Hainan Province, China, 2016–2019.

TABLE 2
www.frontiersin.org

Table 2. Summary statistics of PM2.5, PM10, and meteorological factors in Hainan Province, China, 2016–2019.

Figure 2 illustrates the ORs of hospital admission for PTB associated with each IQR increase in PM2.5 and PM10 across various lag days. We found that the effect of PM2.5 at lag 0–8 days was the highest among the effects at different lags, and the same finding was observed for PM10. Therefore, we mainly explored the effects of PM2.5 and PM10 at a lag of 0–8 days. Specifically, the risk of PTB hospitalization were, respectively, 1.155 (95% confidence interval [CI]: 1.041–1.282) and 1.142 (95% CI: 1.033–1.263) for an IQR increase in PM2.5 and PM10 at a lag of 0–8 days.

FIGURE 2
www.frontiersin.org

Figure 2. Odds ratios of PTB hospitalization associated with an interquartile range increase in PM2.5 and PM10 concentration. Points are the point estimates of odds ratios, while lines represent the corresponding 95% confidence intervals. Lag 01-014 are moving averages of the concentrations of PM2.5 and PM10 over 0–1 to 0–14 days. PTB, pulmonary tuberculosis; PM2.5, particulate matter with aerodynamic diameters <2.5 μm; PM10, particulate matter with aerodynamic diameters <10 μm.

Figure 3 presents the effects of PM2.5 on hospital admission for PTB in different subgroups. An IQR increase in PM2.5 was associated with 1.323 (95% CI: 1.073–1.631), 1.149 (95% CI: 1.021–1.293), 1.160 (95% CI: 1.032–1.303), and 1.277 (95% CI: 1.089–1.498) hospital admission risks for PTB among patients aged ≥65 years, male patients, married individuals, and those living in prefecture-level cities, respectively. As for the disparity by season, the effect of PM2.5 on hospital admission for PTB was statistically significant in the warm season (OR = 1.260, 95% CI: 1.066–1.488) but not in the cold season. The trends in the differences in the effects of PM10 across subgroups were similar to those of PM2.5, although the subgroup differences were not statistically significant (p > 0.05; Figures 3, 4). The effects of PM2.5 on hospital admission for PTB seemed to be greater than those of PM10 for most of the subgroups.

FIGURE 3
www.frontiersin.org

Figure 3. Odds ratios for PTB hospitalization among subgroups associated with an interquartile range increase in PM2.5 concentration. Subgroups were stratified by age, sex, marital status, administrative division, and season. p values were obtained with Z tests. Points are the point estimates of odds ratios, while lines represent the corresponding 95% confidence intervals. PTB, pulmonary tuberculosis; PM2.5, particulate matter with aerodynamic diameters <2.5 μm; CI, confidence interval.

FIGURE 4
www.frontiersin.org

Figure 4. Odds ratios for PTB hospitalization among subgroups associated with an interquartile range increase in PM10 concentration. Subgroups were stratified by age, sex, marital status, administrative division, and season. p values were obtained with Z tests. Points are the point estimates of odds ratios, while lines represent the corresponding 95% confidence intervals. PTB, pulmonary tuberculosis; PM10, particulate matter with aerodynamic diameters <10 μm; CI, confidence interval.

The sensitivity analysis results suggested that the main analysis findings were robust when changing the dfs for the natural cubic splines of temperature and relative humidity to 4–6 (Supplementary Tables S1, S2).

Discussion

The present study evaluated the short-term effects of ambient PM2.5 and PM10 exposure on hospital admission for PTB in a tropical Chinese province. It was found that both PM2.5 (OR = 1.155) and PM10 (OR = 1.142) were positively associated with hospital admission for PTB, which was partially in line with the findings of previous studies that reported adverse effects of PM on PTB outcomes, such as incidence (19, 35) and mortality (36). However, Álvaro-Meca et al. found that the effect of PM10 on hospital admission for PTB was not statistically significant in HIV-infected patients (22). The health impact of PM on PTB hospitalization may vary across different populations, warranting further investigation.

The mechanism linking PM exposure to hospital admission for PTB remains unclear, however, several plausible explanations exist. Fine PM can irritate the lung tissue, damage the tracheobronchial mucosa, and impair the body’s anti-mycobacterial immunity by inhibiting the synthesis and secretion of various key inflammatory mediators in the fight against M. tuberculosis (37). The susceptibility and infection of M. tuberculosis may be aggravated when exposed to high concentrations of PM because it induces alterations in protective host immune responses (38). Meanwhile, an experimental study suggested that exposure to PM2.5 and PM10 increased the intracellular growth of M. tuberculosis (39). Therefore, PM exposure may exacerbate M. tuberculosis infections in the lungs and increase risk of hospital admission for PTB.

We found that the effect of PM2.5 on hospital admission for PTB was higher than that of PM10, which was consistent with previous studies on respiratory disease hospitalizations (28, 40). An experimental study also reported that PM2.5 induced higher oxidative stress and more malondialdehyde in rat lung epithelial cells and cells treated with PM2.5 were more susceptible to apoptosis than PM10 (41). The stronger effect of PM2.5 on PTB outcomes may be attributed to its physicochemical characteristics such as a larger surface area and longer atmospheric suspension (42). At the same time, PM2.5 can carry external impurities, such as metal ions, minerals, and polycyclic aromatic hydrocarbons into the fine bronchi and alveoli (43, 44), which may lead to various forms of inflammatory responses and impair cellular immune function in the lungs (45, 46).

In accordance with previous research (16), we found that patients aged ≥65 years were vulnerable to PM exposure. Older adults infected with M. tuberculosis, a potent stimulator of numerous inflammatory cytokines, tend to develop a range of inflammatory responses (47). With a decline in the innate immune response, PM inhalation may lead to overwhelming inflammation when superimposed on the inflammation associated with aging in the older adults patients with PTB (48).

Consistent with a previous study on TB incidence conducted in Shanghai (16), we found that PM significantly affected hospital admission for PTB in male patients but not in female patients. Polymorphisms of the Toll-like receptor 8 gene (gene identity: 51311) on the X chromosome are associated with susceptibility to PTB in males, and susceptibility to PTB also increases in male carriers of rs3764880 allele A (49). Additionally, males tend to consume alcohol and nicotine (50), which may have a significant inhibitory effect on tumor necrosis factor-α production and cell-mediated immunity, thereby exacerbating the PTB progression (51).

Our study found that the association between PM and hospital admission for PTB was statistically significant for married patients but not for others. Married people have less time to perform stress-relieving healthy physical activity for family-related tasks, including childcare (52). An Indian study found that single TB patients had higher quality of life scores (53). A cross-sectional study of treated PTB patients suggested that married PTB patients had lower mental-domain scores (54). Less physical activity, lower quality of life, and poor mental health may weaken the immune system, in which case PM inhalation may have more harmful health effects.

In our study, the effect of PM on hospital admission for PTB varied according to administrative division, with PM having a greater impact on patients living in prefecture-level cities. This finding is similar to that of a national study in China that explored the associations between major PM2.5 components and TB incidence and mortality (55). Inconsistent socioeconomic characteristics across administrative regions may explain this result. The higher population density of prefecture-level cities (Supplementary Table S3) may facilitate the spread of respiratory viruses, such as influenza (56). Higher respiratory virus incidence and ambient PM concentration may exacerbate PTB (20, 38). Therefore, the effect of PM in prefecture-level cities tends to be more detrimental than that in county-level divisions.

We found that the effect of PM on hospital admission for PTB was statistically significant in the warm season but not in the cold season. The result can be interpreted as follows: First, M. tuberculosis’s rate of proliferation and growth increases significantly with increasing temperature (57). Second, on average, people spend more time outdoors (or with windows open) during the warm season, which can expose them to outdoor PM more often. Third, PM may reduce the phagocytosis of M. tuberculosis by peripheral blood mononuclear cells in warmer months but not in colder months (58).

Limitations

Our study has a few limitations. First, we included 4,562 PTB hospital admissions. Although the participating hospitals are the top three largest hospitals and the PTB patients came from 3/4 prefecture-level cities and all 15 county-level divisions directly under the provincial government in Hainan, the sample size may be insufficient for the statistical inference of the association between exposure to ambient PM and hospital admission for PTB in some subgroups. More reliable results can be obtained using data from more hospital patients. Second, we only examined the association between PTB hospital admission with PM2.5 and PM10. It will be interesting to further assess the effects of PM2.5 components and PM1. Third, measurement errors may exist in the exposure proxy for the PM concentration. Nevertheless, we used PM data with 1 km × 1 km resolution in this study. Effect estimates derived from such exposure data may be more accurate than those based on data collected from only a few monitoring stations. Finally, this ecological study sheds light on the link between PM exposure and hospital admission for PTB, however, the underlying mechanisms of this link warrant further investigation.

Conclusion

Taken together, exposure to ambient PM2.5 and PM10 increases the risk of PTB hospital admission. PM with a smaller aerodynamic diameter is more hazardous. Our findings highlight the importance of reducing ambient PM concentrations to alleviate the PTB burden.

Data availability statement

The data sets generated during and/or analyzed during the current study are available from the corresponding authors on reasonable request.

Ethics statement

This study was approved by the Research Ethics Committee of Hainan General Hospital (No. 2021-314). Written informed consent was not required as the data was anonymized for the study. Consent was waived by the Research Ethics Committee.

Author contributions

P-PZ: formal analysis, methodology, software, visualization, and writing – original draft. YG: conceptualization, funding acquisition, investigation, project administration, resources, validation, and writing – original draft. G-ZZ: resources and writing – original draft. RL, X-BL, X-XF, JF, and FL: data curation. Y-PZ: conceptualization, supervision, and writing – review and editing. LL: conceptualization, funding acquisition, methodology, supervision, and writing – review and editing. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the National Natural Science Foundation of China [82003555] and Hainan Province Science and Technology Special Fund [ZDYF2021SHFZ079].

Acknowledgments

We thank the staff of the three participating hospitals for collecting data.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2023.1252741/full#supplementary-material

Footnotes

References

1. Gagneux, S. Ecology and evolution of Mycobacterium tuberculosis. Nat Rev Microbiol. (2018) 16:202–13. doi: 10.1038/nrmicro.2018.8

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Glassroth, JL. Letter: transmission of tuberculosis. JAMA. (1976) 236:1578. doi: 10.1001/jama.1976.03270150016016

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Gengenbacher, M, and Kaufmann, SH. Mycobacterium tuberculosis: success through dormancy. FEMS Microbiol Rev. (2012) 36:514–32. doi: 10.1111/j.1574-6976.2012.00331.x

PubMed Abstract | CrossRef Full Text | Google Scholar

4. World Health Organization. Global Tuberculosis Report; (2020). Available at: https://www.who.int/publications/i/item/9789240013131 (Accessed July 01, 2023).

Google Scholar

5. National Center for Tuberculosis Control and Prevention. Chinese Center for Disease Control and Prevention; (2023). Available at: https://tb.chinacdc.cn/ (Accessed July 01, 2023).

Google Scholar

6. Furin, J, Cox, H, and Pai, M. Tuberculosis. Lancet. (2019) 393:1642–56. doi: 10.1016/S0140-6736(19)30308-3

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Lönnroth, K, Jaramillo, E, Williams, BG, Dye, C, and Raviglione, M. Drivers of tuberculosis epidemics: the role of risk factors and social determinants. Soc Sci Med. (2009) 68:2240–6. doi: 10.1016/j.socscimed.2009.03.041

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Lönnroth, K, Castro, KG, Chakaya, JM, Chauhan, LS, Floyd, K, Glaziou, P, et al. Tuberculosis control and elimination 2010-50: cure, care, and social development. Lancet. (2010) 375:1814–29. doi: 10.1016/S0140-6736(10)60483-7

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Cohen, A, and Mehta, S. Pollution and tuberculosis: outdoor sources. PLoS Med. (2007) 4:e142. doi: 10.1371/journal.pmed.0040142

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Brunekreef, B, and Holgate, ST. Air pollution and health. Lancet. (2002) 360:1233–42. doi: 10.1016/S0140-6736(02)11274-8

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Jalava, PI, Salonen, RO, Pennanen, AS, Sillanpää, M, Hälinen, AI, Happo, MS, et al. Heterogeneities in inflammatory and cytotoxic responses of RAW 264.7 macrophage cell line to urban air coarse, fine, and ultrafine particles from six European sampling campaigns. Inhal Toxicol. (2007) 19:213–25. doi: 10.1080/08958370601067863

CrossRef Full Text | Google Scholar

12. Mehta, M, Chen, LC, Gordon, T, Rom, W, and Tang, MS. Particulate matter inhibits DNA repair and enhances mutagenesis. Mutat Res. (2008) 657:116–21. doi: 10.1016/j.mrgentox.2008.08.015

CrossRef Full Text | Google Scholar

13. Xing, YF, Xu, YH, Shi, MH, and Lian, YX. The impact of PM2.5 on the human respiratory system. J Thorac Dis. (2016) 8:E69–74. doi: 10.3978/j.issn.2072-1439.2016.01.19

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Huang, K, Ding, K, Yang, XJ, Hu, CY, Jiang, W, Hua, XG, et al. Association between short-term exposure to ambient air pollutants and the risk of tuberculosis outpatient visits: a time-series study in Hefei. China Environ Res. (2020) 184:109343. doi: 10.1016/j.envres.2020.109343

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Xu, M, Liao, J, Yin, P, Hou, J, Zhou, Y, Huang, J, et al. Association of air pollution with the risk of initial outpatient visits for tuberculosis in Wuhan. China Occup Environ Med. (2019) 76:560–6. doi: 10.1136/oemed-2018-105532

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Xiong, Y, Yang, M, Wang, Z, Jiang, H, Xu, N, Tong, Y, et al. Association of daily exposure to air pollutants with the risk of tuberculosis in Xuhui district of Shanghai, China. Int J Environ Res Public Health. (2022) 19:6085. doi: 10.3390/ijerph19106085

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Lai, TC, Chiang, CY, Wu, CF, Yang, SL, Liu, DP, Chan, CC, et al. Ambient air pollution and risk of tuberculosis: a cohort study. Occup Environ Med. (2016) 73:56–61. doi: 10.1136/oemed-2015-102995

CrossRef Full Text | Google Scholar

18. Smith, GS, Van Den Eeden, SK, Garcia, C, Shan, J, Baxter, R, Herring, AH, et al. Air pollution and pulmonary tuberculosis: a nested case-control study among members of a northern California health plan. Environ Health Perspect. (2016) 124:761–8. doi: 10.1289/ehp.1408166

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Liu, F, Zhang, Z, Chen, H, and Nie, S. Associations of ambient air pollutants with regional pulmonary tuberculosis incidence in the central Chinese province of Hubei: a Bayesian spatial-temporal analysis. Environ Health. (2020) 19:51. doi: 10.1186/s12940-020-00604-y

CrossRef Full Text | Google Scholar

20. Chong, KC, Yeoh, EK, Leung, CC, Lau, SYF, Lam, HCY, Goggins, WB, et al. Independent effect of weather, air pollutants, and seasonal influenza on risk of tuberculosis hospitalization: an analysis of 22-year hospital admission data. Sci Total Environ. (2022) 837:155711. doi: 10.1016/j.scitotenv.2022.155711

CrossRef Full Text | Google Scholar

21. Popovic, I, Soares Magalhaes, RJ, Ge, E, Marks, GB, Dong, GH, Wei, X, et al. A systematic literature review and critical appraisal of epidemiological studies on outdoor air pollution and tuberculosis outcomes. Environ Res. (2019) 170:33–45. doi: 10.1016/j.envres.2018.12.011

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Álvaro-Meca, A, Díaz, A, de Miguel, DJ, Resino, R, and Resino, S. Environmental factors related to pulmonary tuberculosis in HIV-infected patients in the combined antiretroviral therapy (cART) era. PLoS One. (2016) 11:e0165944. doi: 10.1371/journal.pone.0165944

PubMed Abstract | CrossRef Full Text | Google Scholar

23. National Health Commission of the People’s Republic of China; (2023). Available at: http://www.nhc.gov.cn/jkj/s3578/202004/b1519e1bc1a944fc8ec176db600f68d1.shtml (Accessed July 01, 2023).

Google Scholar

24. The China Disease Prevention and Control Information System; (2023). Available at: https://www.phsciencedata.cn/Share/edtShareNew.jsp?id=39208 (Accessed July 10, 2023).

Google Scholar

25. The People's Government of Hainan Province; (2023). Available at: https://www.hainan.gov.cn/hainan/tjnj/list3.shtml (Accessed July 01, 2023).

Google Scholar

26. Huang, S, Xiang, H, Yang, W, Zhu, Z, Tian, L, Deng, S, et al. Short-term effect of air pollution on tuberculosis based on kriged data: a time-series analysis. Int J Environ Res Public Health. (2020) 17:1522. doi: 10.3390/ijerph17051522

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Gu, X, Guo, T, Si, Y, Wang, J, Zhang, W, Deng, F, et al. Association between ambient air pollution and daily hospital admissions for depression in 75 Chinese cities. Am J Psychiatry. (2020) 177:735–43. doi: 10.1176/appi.ajp.2020.19070748

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Peng, W, Li, H, Peng, L, Wang, Y, and Wang, W. Effects of particulate matter on hospital admissions for respiratory diseases: an ecological study based on 12.5 years of time series data in Shanghai. Environ Health. (2022) 21:12. doi: 10.1186/s12940-021-00828-6

CrossRef Full Text | Google Scholar

29. Wang, X, Wang, W, Jiao, S, Yuan, J, Hu, C, and Wang, L. The effects of air pollution on daily cardiovascular diseases hospital admissions in Wuhan from 2013 to 2015. Atmos Environ. (2018) 260:113776. doi: 10.1016/j.atmosenv.2018.03.036

CrossRef Full Text | Google Scholar

30. Yang, J, Yin, P, Zhou, M, Ou, CQ, Guo, Y, Gasparrini, A, et al. Cardiovascular mortality risk attributable to ambient temperature in China. Heart. (2015) 101:1966–72. doi: 10.1136/heartjnl-2015-308062

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Yang, J, Yin, P, Zhou, M, Ou, CQ, Li, M, Li, J, et al. The burden of stroke mortality attributable to cold and hot ambient temperatures: epidemiological evidence from China. Environ Int. (2016) 92–93:232–8. doi: 10.1016/j.envint.2016.04.001

CrossRef Full Text | Google Scholar

32. Yang, J, Ou, CQ, Ding, Y, Zhou, YX, and Chen, PY. Daily temperature and mortality: a study of distributed lag non-linear effect and effect modification in Guangzhou. Environ Health. (2012) 11:63. doi: 10.1186/1476-069X-11-63

CrossRef Full Text | Google Scholar

33. Li, L, Yang, J, Song, YF, Chen, PY, and Ou, CQ. The burden of COPD mortality due to ambient air pollution in Guangzhou. China Sci Rep. (2016) 6:25900. doi: 10.1038/srep25900

CrossRef Full Text | Google Scholar

34. Jin, JQ, Han, D, Tian, Q, Chen, ZY, Ye, YS, Lin, QX, et al. Individual exposure to ambient PM2.5 and hospital admissions for COPD in 110 hospitals: a case-crossover study in Guangzhou, China. Environ Sci Pollut Res Int. (2022) 29:11699–706. doi: 10.1007/s11356-021-16539-x

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Smith, GS, Schoenbach, VJ, Richardson, DB, and Gammon, MD. Particulate air pollution and susceptibility to the development of pulmonary tuberculosis disease in North Carolina: an ecological study. Int J Environ Health Res. (2014) 24:103–12. doi: 10.1080/09603123.2013.800959

CrossRef Full Text | Google Scholar

36. Liu, Y, Zhao, S, Li, Y, Song, W, Yu, C, Gao, L, et al. Effect of ambient air pollution on tuberculosis risks and mortality in Shandong, China: a multi-city modeling study of the short-and long-term effects of pollutants. Environ Sci Pollut Res Int. (2021) 28:27757–68. doi: 10.1007/s11356-021-12621-6

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Hiramatsu, K, Saito, Y, Sakakibara, K, Azuma, A, Takizawa, H, and Sugawara, I. The effects of inhalation of diesel exhaust on murine mycobacterial infection. Exp Lung Res. (2005) 31:405–15. doi: 10.1080/01902140590918786

CrossRef Full Text | Google Scholar

38. Torres, M, Carranza, C, Sarkar, S, Gonzalez, Y, Osornio Vargas, A, Black, K, et al. Urban airborne particle exposure impairs human lung and blood Mycobacterium tuberculosis immunity. Thorax. (2019) 74:675–83. doi: 10.1136/thoraxjnl-2018-212529

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Rivas-Santiago, CE, Sarkar, S, Cantarella, P 4th, Osornio-Vargas, Á, Quintana-Belmares, R, Meng, Q, et al. Air pollution particulate matter alters antimycobacterial respiratory epithelium innate immunity. Infect Immun. (2015) 83:2507–17. doi: 10.1128/IAI.03018-14

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Tian, Y, Liu, H, Wu, Y, Si, Y, Li, M, Wu, Y, et al. Ambient particulate matter pollution and adult hospital admissions for pneumonia in urban China: a national time series analysis for 2014 through 2017. PLoS Med. (2019) 16:e1003010. doi: 10.1371/journal.pmed.1003010

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Choi, JH, Kim, JS, Kim, YC, Kim, YS, Chung, NH, and Cho, MH. Comparative study of PM2.5- and PM10- induced oxidative stress in rat lung epithelial cells. J Vet Sci. (2004) 5:11–8. doi: 10.4142/jvs.2004.5.1.11

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Dimala, CA, and Kadia, BM. A systematic review and meta-analysis on the association between ambient air pollution and pulmonary tuberculosis. Sci Rep. (2022) 12:11282. doi: 10.1038/s41598-022-15443-9

CrossRef Full Text | Google Scholar

43. Aust, AE, Ball, JC, Hu, AA, Lighty, JS, Smith, KR, Straccia, AM, et al. Particle characteristics responsible for effects on human lung epithelial cells. Res Rep Health Eff Inst. (2002) 110:1–65.

Google Scholar

44. Brugha, R, and Grigg, J. Urban air pollution and respiratory infections. Paediatr Respir Rev. (2014) 15:194–9. doi: 10.1016/j.prrv.2014.03.001

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Bai, L, Su, X, Zhao, D, Zhang, Y, Cheng, Q, Zhang, H, et al. Exposure to traffic-related air pollution and acute bronchitis in children: season and age as modifiers. J Epidemiol Community Health. (2018) 72:426–33. doi: 10.1136/jech-2017-209948

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Mumtaz, A, Rehman, E, Rehman, S, and Hussain, I. Impact of environmental degradation on human health: an assessment using multicriteria decision making. Front Public Health. (2022) 9:812743. doi: 10.3389/fpubh.2021.812743

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Sia, JK, and Rengarajan, J. Immunology of Mycobacterium tuberculosis infections. Microbiol Spectr. (2019) 7:10.1128. doi: 10.1128/microbiolspec.GPP3-0022-2018

CrossRef Full Text | Google Scholar

48. Piergallini, TJ, and Turner, J. Tuberculosis in the elderly: why inflammation matters. Exp Gerontol. (2018) 105:32–9. doi: 10.1016/j.exger.2017.12.021

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Davila, S, Hibberd, ML, Hari Dass, R, Wong, HE, Sahiratmadja, E, Bonnard, C, et al. Genetic association and expression studies indicate a role of toll-like receptor 8 in pulmonary tuberculosis. PLoS Genet. (2008) 4:e1000218. doi: 10.1371/journal.pgen.1000218

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Przybylski, G, Nowakowska-Arendt, A, Pilaczyńska-Ceme, M, and Gołda, R. 10 years comparative clinico-epidemiological analysis of smoking and alcohol consumption in TB patients (Myc. Tuberculosis) and with mycobacteriosis (Myc Kansas). Przegl Lek. (2014) 71:576–80.

PubMed Abstract | Google Scholar

51. Sopori, ML, Kozak, W, Savage, SM, Geng, Y, and Kluger, MJ. Nicotine-induced modulation of T cell function. Implications for inflammation and infection. Adv Exp Med Biol. (1998) 437:279–89. doi: 10.1007/978-1-4615-5347-231

CrossRef Full Text | Google Scholar

52. Puciato, D, and Rozpara, M. Physical activity and socio-economic status of single and married urban adults: a cross-sectional study. Peer J. (2021) 9:e12466. doi: 10.7717/peerj.12466

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Unalan, D, Soyuer, F, Ceyhan, O, Basturk, M, and Ozturk, A. Is the quality of life different in patients with active and inactive tuberculosis? Indian J Tuberc. (2008) 55:127–37.

PubMed Abstract | Google Scholar

54. Adeyeye, OO, Ogunleye, OO, Coker, A, Kuyinu, Y, Bamisile, RT, Ekrikpo, U, et al. Factors influencing quality of life and predictors of low quality of life scores in patients on treatment for pulmonary tuberculosis: a cross sectional study. J Public Health Afr. (2014) 5:366. doi: 10.4081/jphia.2014.366

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Wang, S, Wu, G, Du, Z, Wu, W, Ju, X, Yimaer, W, et al. The causal links between long-term exposure to major PM2.5 components and the burden of tuberculosis in China. Sci Total Environ. (2023) 870:161745. doi: 10.1016/j.scitotenv.2023.161745

CrossRef Full Text | Google Scholar

56. Dalziel, BD, Kissler, S, Gog, JR, Viboud, C, Bjørnstad, ON, Metcalf, CJE, et al. Urbanization and humidity shape the intensity of influenza epidemics in U.S. cities. Science. (2018) 362:75–9. doi: 10.1126/science.aat6030

CrossRef Full Text | Google Scholar

57. Wards, BJ, and Collins, DM. Electroporation at elevated temperatures substantially improves transformation efficiency of slow-growing mycobacteria. FEMS Microbiol Lett. (1996) 145:101–5. doi: 10.1111/j.1574-6968.1996.tb08563.x

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Sarkar, S, Rivas-Santiago, CE, Ibironke, OA, Carranza, C, Meng, Q, Osornio-Vargas, Á, et al. Season and size of urban particulate matter differentially affect cytotoxicity and human immune responses to Mycobacterium tuberculosis. PLoS One. (2019) 14:e0219122. doi: 10.1371/journal.pone.0219122

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: particulate matter, hospitalization, pulmonary tuberculosis, case-crossover design, tropical region

Citation: Zhu P-P, Gao Y, Zhou G-Z, Liu R, Li X-B, Fu X-X, Fu J, Lin F, Zhou Y-P and Li L (2023) Short-term effects of high-resolution (1-km) ambient PM2.5 and PM10 on hospital admission for pulmonary tuberculosis: a case-crossover study in Hainan, China. Front. Public Health. 11:1252741. doi: 10.3389/fpubh.2023.1252741

Received: 04 July 2023; Accepted: 16 August 2023;
Published: 05 September 2023.

Edited by:

Shazia Rehman, Central South University, China

Reviewed by:

Arthit Phosri, Mahidol University, Thailand
Muhammad Nasir Khan, Government College University, Lahore, Pakistan

Copyright © 2023 Zhu, Gao, Zhou, Liu, Li, Fu, Fu, Lin, Zhou and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Li Li, lylygdsg@163.com; Yuan-Ping Zhou, yuanpingzhou@163.com

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.