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Article

Future Health Risk Assessment of Exposure to PM2.5 in Different Age Groups of Children in Northern Thailand

by
Teerachai Amnuaylojaroen
1,2 and
Nichapa Parasin
3,*
1
Department of Environmental Science, School of Energy and Environment, University of Phayao, Phayao 56000, Thailand
2
Atmospheric Pollution and Climate Research Unit, School of Energy and Environment, University of Phayao, Phayao 56000, Thailand
3
School of Allied Health Science, University of Phayao, Phayao 56000, Thailand
*
Author to whom correspondence should be addressed.
Toxics 2023, 11(3), 291; https://doi.org/10.3390/toxics11030291
Submission received: 14 February 2023 / Revised: 17 March 2023 / Accepted: 21 March 2023 / Published: 22 March 2023
(This article belongs to the Special Issue Ambient Air Pollution Exposure and Human Health)

Abstract

:
Particulate matter with a diameter less than 2.5 (PM2.5) is one of the major threats posed by air pollution to human health. It penetrates the respiratory system, particularly the lungs. In northern Thailand, the PM2.5 concentrations have significantly increased in the past decade, becoming a major concern for the health of children. This study aimed to assess the health risk of PM2.5 in different age groups of children in northern Thailand between 2020 and 2029. Based on the PM2.5 data from the simulation of the Nested Regional Climate Model with Chemistry (NRCM-Chem), the hazard quotient (HQ) was used to estimate the possible risk from PM2.5 exposure in children. In general, all age groups of children in northern Thailand will tend to experience the threat of PM2.5 in the future. In the context of age-related development periods, infants are at a higher risk than other groups (toddlers, young children, school age and adolescents), but adolescents also have a lower risk of exposure to PM2.5, albeit maintaining a high HQ value (>1). Moreover, the analysis of risk assessment in different age groups of children revealed that PM2.5 exposure might indeed affect adolescent risk differently depending on gender, with males generally at a heightened risk than females in adolescence.

1. Introduction

PM2.5 is a significant air contaminant that has a significant impact on human health [1]. Due to their small sizes and large interfacial areas, PM2.5 particles can be transported by a wide variety of toxic substances, passing through the nose’s purification process, attaining the tip of the nasal passages with the movement of air, and acquiring through spread, permanent havoc toward other parts of the human body via the respiratory system’s air exchange [2]. Fine particulate exposure could potentially impair pulmonary function and aggravate asthma and cardiovascular disease [3]. According to recent reports of global premature mortality rates, Southeast Asia (SEA) accounts for around 25% of global deaths [4]. Asia is a region that has gained notoriety for its stated susceptibility to a greater mortality of about more than 59% of the total global deaths due to poor air quality [5,6,7]. In recent years, significant haze outbreaks in Southeast Asia (SEA) have become increasingly common and severe due to particle pollution. Periodic biomass burning and airborne contaminants from anthropogenic activities greatly pollute the atmosphere in Southeast Asia (SEA) and northern Thailand [8,9].
Air pollution has a severe impact on the health of children. Air pollution contributes to unfavorable preterm birth, infant mortality, impaired respiratory symptoms, allergies, delay gross motor development, cancers, and raising the chance of neurological diseases [10,11]. Because their brains, lungs, and other systems are still growing, children are biologically more susceptible to air pollution than adults [11]. In addition, children are physiologically more vulnerable to polluted air than adults because they inhale twice as fast and frequently through their mouths, absorbing more toxins [11]. Recent research has found that both sudden and long-term exposure to particulate matter increases the risk of death and mortality, with a significant positive relation between PM2.5 and child mortality [12]. For instance, Lien et al. [12] demonstrated a positive correlation between infants and PM2.5 and premature death in 45 Asian and African nations. Gouveia et al. [13], who assessed the influence of air pollution, found that their outcome indicates a correlation between air pollution and childhood mortality in Latin America. Sarkodie et al. [14] investigated the association between PM2.5, mortality, and life expectancy in Europe and North America. Their results demonstrated a statistically strong positive correlation between air pollution, death, and living standards in the nations under consideration. Furthermore, health impacts vary based on the metal’s oxidation state (i.e., copper (Cu), iron (Fe), manganese (Mn), and zinc (Zn)0, altering the absorption, membrane transport, excretion, and toxicity at the cellular or molecular target [15,16]. Children are a particularly vulnerable population to PM2.5 exposure and associated metal components. Children inhale more pollutants per unit body weight than adults, and their lungs are still developing, therefore pollutants ingested can interfere with normal lung function development [17]. Additionally, children have narrower airways than adults; while PM2.5 may cause moderate irritation in adult airways, it can create significant blockages in children [18]. Children have substantially higher rates of heavy metal absorption and hemoglobin sensitivity to these metals than adults. Studies on Asian countries that have investigated the connection between PM2.5 and childhood mortality in children under the age of five found the highest incidence of death as a result of biomass and dust mixture in PM2.5 [12]. This is despite the fact that Asian countries experience disastrous air pollution and its influence on mortality rates in children. Studies have classified PM2.5 as the most harmful fine particulates in relation to child death [19,20], noting that newborns (0–1 year) and children between the ages of five became more vulnerable to poor air quality [21]. Children are more affected by polluted air than adults because they spend more time outdoors and breathe through their mouths, which increases their exposure [13].
This study evaluated the children’s exposure to PM2.5 in northern Thailand from 2020 to 2029. This is because a prior study conducted by Amnuaylojaroen et al. [1] to analyze the health risks related to PM2.5 in northern Thailand over 2020–2029 indicated that children tend to be at a greater risk than adults. However, the outcomes in the context of children were limited. In the study, no specific age range of children was considered because specific age groups of children are differently exposed to ambient toxins via breathing. Infants and children, for instance, have a faster metabolism at rest and a greater amount of oxygen uptake per unit body weight than adolescents because of their larger cooling surface per unit body weight and rapid growth [11]. Therefore, the effects of either indoor or outdoor air pollution might differ depending on the age and mobility of a child. To successfully protect and promote better health in children, risk assessments of air contaminants in specific age groups of children should be considered when planning and improving air quality policies. The exposure of pollutants to human can occur through different pathways, which include ingestion, dermal, and inhalation [22]. The exposure of particulate matter (PM) has been recognized as a well-known human health risk factor [22]. In this study, we addressed the non-carcinogenic risk factors of future PM2.5 via the inhalation exposure of different age groups in children evaluated in northern Thailand between 2020 and 2029. As a result, the findings of this study will provide health care professionals and the general public with a better understanding of air quality, promoting awareness about the toxicity of PM2.5 in children.

2. Materials and Methods

To study the health risks of PM2.5 exposure in different age groups of children in northern Thailand during 2020–2029, we calculated the HQ value using the PM2.5 input data from the previous simulation [22] by the NRCM-Model to quantify the risks resulting from PM2.5 exposure in northern Thailand.

2.1. Description of Study Area

Figure 1 shows the study area in northern Thailand that is generally located in the northern peninsula of SEA and is geographically defined by many mountain ranges bordering Laos and Burma. This region has traditionally experienced air pollution driven by the burning of agriculture waste and forest fires, which release many sizes of particles over the entire year. The primary sources of air pollution in northern Thailand come from both transboundary and domestic burning [8]. Most of the air pollution in northern Thailand is caused by the burning of forests, which primarily occur in deciduous forests. Several regions in northern Thailand were forced to close in 2023 because of haze pollution. According to the Ministry of Public Health, 376,165 people were affected by air pollution-related health concerns, a rise of 163,491. More than 165,000 of these people suffered from respiratory issues, 80,248 from skin issues, and 70,206 from eye discomfort. The PM2.5 concentration in February 2023 was 84.7 μg/m3, which exceeded the safety standards of both USEPA (35 μg/m3) and the Thai (50 μg/m3) guidelines, potentially leading to major health consequences (http://air4thai.com/webV3/#/Report, accessed on 20 March 2023).

2.2. Data of Future PM2.5 Concentration

The data of future PM2.5 used in this study was obtained from Amnuaylojaroen et al. [22]. The data were generated using the simulation of the NRCM-Chem modeling system under a climate scenario based on the representative concentration pathway (RCP8.5). The biomass-burning and anthropogenic emission inventories from RCPs were included in the simulation. When compared to the observations, the performance of the PM2.5 dataset accurately represents the PM2.5 pattern in northern Thailand. The statistical examination of the PM2.5 concentrations between the modeled PM2.5 dataset and the observation were acceptable, with an index of agreement (0.82), mean-bias (21.9), fractional error (0.043), and residue standard deviation (30.2), and an uncertainty of data with ±6.27 μg/m3 [22]. However, the model captures the overestimation of PM2.5 predictions. The high bias in PM2.5 can impact the prediction of HQ values. Because the average daily dosage (ADD) that is directly related to PM2.5 concentration was used to estimate the HQ value, a higher PM2.5 concentration would also tend to overpredict the HQ.
Figure 1. Map of Thailand demonstrating the study area in northern Thailand.
Figure 1. Map of Thailand demonstrating the study area in northern Thailand.
Toxics 11 00291 g001

2.3. Health Risk Assessment

The assessment of health risks is an essential tool for determining the possible negative consequences of pollutant exposure on human health [23,24,25]. This prediction tool examines the measurable data of exposure to assess the risk factor from pollution on human health. The exposure to humans was described by the average daily dosage (ADD), which was calculated as follows in Equation (1):
ADD = C   ×   IR   ×   EF   ×   ED BW   ×   AT
where IR is the inhalation rate (m3/day); C is the pollutant concentration (μg/m3); EF is the exposure frequency (days/year); ED is the exposure duration (years); ET is the exposure time (24 h/day); AT is the average exposure time (days); BW is the body weight of the children (kg). The values for these variables were derived from the previous studies, as indicated in Table 1 and Table 2.
Given that individuals in Asia, particularly in Thailand and China, have comparable physical circumstances, the precise values are shown in Table 1. The body weight (BW) and inhalation rate (IR) of children were used by Layton et al. [26] (Table 2), while the average time (AT) included some of the parameters used by Liang et al. [27]. The lifelong exposure of human receptors in children was calculated using an EF of 350 days per year and the hypothesis that the whole population in the research region spends no more than 14 days away from the study area [28,29].
Table 1. PM2.5 exposure factors used for uptake through the respiratory system.
Table 1. PM2.5 exposure factors used for uptake through the respiratory system.
FactorExposure Frequency (EF) (Days/Year)Exposure Duration (ED) (Years)Averaging Time (AT) (Days)
Value350124380
ReferenceMorakinyo et al. [28]; Olufemi et al. [29]Morakinyo et al. [28]; Olufemi et al. [29]Liang et al. [27]
Table 2. Body weight and inhalation in the different age groups of children.
Table 2. Body weight and inhalation in the different age groups of children.
Cohort/Age (Years)Body Weight (kg)Inhalation (m3/day)
Infant (<1)7.64.5
1–213.06.8
3–518.08.3
6–826.010
Male
9–1136.014
12–1450.015
15–1866.017
Female
9–1136.013
12–1449.012
15–1856.012
To determine the non-carcinogenic health risks, the HQ, that is, the ratio of ADD to the reference dose (RfD), was calculated as follows in Equation (2) [11]:
Hazard   Quotient   ( HQ ) = Average   Daily   Dose   ( ADD ) ( μ g kg · day ) Inhalation   Reference   Dose   ( RfD ) ( μ g kg · day )
The inhalation reference dose (RfD) was calculated as follows in Equation (3):
RfD = RfC   ×   IR   ×   ET   ×   EF   ×   ED BW   ×   AT
where the exposure time (ET) = 24 h/day; the inhalation rate (IR) = 0.83 m3/h; the exposure frequency (EF) = 350 days/year; the averaging time (AT) = ED ∗ 365 days/year; body weight (BW) = 70 kg; and ED = 30 years. RfC is the safe limit of the inhalation reference proposed by the USEPA National Ambient Air Quality Standard (NAAQS) for PM2.5 in 2006, which is 35 μg/m3.
The standard for safety is an HQ of 1.0. An HQ less than 1.0 denotes insignificance or “negligible risk”, implying that the pollutant under consideration is unlikely to have unfavorable health consequences, even in a susceptible individual. An HQ greater than 1.0 suggests that there might be certain levels of threat to sensitive persons as a consequence of exposure [11]; however, an HQ greater than 10 implies a substantial chronic risk [30,31].

3. Results

3.1. Situation of PM2.5 Concentrations between 2020 and 2029

The daily and monthly average between 2020 and 2029 of the PM2.5 concentration in northern Thailand is shown in Figure 2 and Figure 3. Between 2020 and 2029, the average daily PM2.5 concentrations will greatly surpass both the Thai (50 μg/m3) and USEPA (35 μg/m3) guidelines, especially during the dry season. The highest daily average PM2.5 concentrations were at the beginning of February and ended in April with ranges of 40–400 μg/m3 in the future (Figure 2) while the PM2.5 concentrations dropped in the rainy season (May to October) and peaked in the dry season (November to December and January to April) (2020–2029) (Figure 3). The worst PM2.5 values were detected predominantly between February and March. In northern Thailand, biomass burning emissions govern the seasonal variance of PM2.5 [8,22]. PM2.5 is extensively distributed by biomass burning including open and waste burning, in advance of the forthcoming rain and rice seeding during the dry season [8].

3.2. Hazard Quote in Different Age Groups of Children in Northern Thailand between 2020 and 2029

In this study, the values of HQ were estimated for children in order to evaluate the non-carcinogenic threat of PM2.5 in northern Thailand. Figure 3a depicts the daily averages of the HQ associated with PM2.5 in northern Thailand throughout the age-related development period of 2020–2029. Militaru and Martinovici [32] classified the age-related development phase. Infants were 1 month to 1 year old, toddlers were 1 to 3 years old, young children were 3 to 6 years old, school-age children were 6 to 12 years old, and adolescents were 12 to 18 years old. During January and April, the daily mean of the HQ was greater than 1. The highest HQ value was discovered in March, suggesting that all age groups of children in northern Thailand face significant danger in the near future. When comparing the age-related development periods, infants had a larger risk than other groups, with an HQ value of 23.96, whereas adolescents had a decreased risk of exposure to PM2.5, although the HQ value remained quite high (10.28 for adolescents). Figure 3b depicts the monthly averages of the HQ associated with PM2.5 in different age groups of children in northern Thailand between 2020 and 2029. From February through April, the monthly averages of the HQ values were larger than one, suggesting a high risk for all children in northern Thailand. In March, the highest HQ value was discovered in a group of infants. In the dry season, the HQ values between February and April were higher than during November and January. This is likely due to the emissions from the massive biomass burnings from agricultural and waste burning in preparation for the rice planting season. Along with the long-range transport of air pollutants from neighboring countries such as Laos, Vietnam, and Burma, which is induced by meteorological conditions, these factors contribute to the high air pollution in northern Thailand [8].
Table 3 displays the calculated HQ values for PM2.5 based on age-related development. HQ values greater than one indicate hazardous exposure situations. Over the entire year, the mean of the HQ was 2.93 ± 1.20, 2.59 ± 1.06, 2.28 ± 0.93, 1.88 ± 0.77, 1.26 ± 0.51 for newborn, toddlers, young children, school age, and adolescents, respectively (Table 3). The averages of the HQ for PM2.5 were in the range of 0.48–13.89, 0.42–12.27, 0.37–10.82, 0.31–8.91, and 0.21–5.96 for infants, toddlers, young children, school age, and adolescents, respectively, which were all greater than 1, indicating an intolerable risk to human health. The maximum HQ for infants, toddlers, young children, school age, and adolescents was 0.57–23.96, 0.50–21.16, 0.44–18.66, 0.37–15.37, and 0.24–10.28, respectively. The minimum HQ level for infants, toddlers, young children, school age, and adolescents was 0.38–7.12, 0.34–6.29, 0.30–5.55, 0.24–4.57, and 0.16–3.06, respectively. The HQ values were shown to be greater in February and March than in other months between 2020 and 2029, with March having the highest value (mean HQ = 13.89 for babies, 12.27 for toddlers, 10.82 for young children, 8.91 for school age, and 5.96 for adolescents). Despite the fact that school age and adolescents were at a lower risk than other age groups, the HQ value remained at an undesirable level for human health. Males had greater HQ values than females, as seen by the mean, maximum, and lowest HQ values in Table 4, Table 5 and Table 6. For adolescent males aged 9 to 11 years, 12 to 14 years, and 15 to 18 years, the mean HQ values were 1.92 ± 0.79, 1.48 ± 0.61, and 1.27 ± 0.52, respectively. Females in those age categories had mean HQ values of 1.79 ± 0.73, 1.21 ± 0.50, and 1.06 ± 0.43, respectively (Table 4). For males aged 9 to 11 years, 12 to 14 years, and 15 to 18 years, the minimum HQ values were 0.87 ± 1.54, 0.67 ± 1.19, and 0.58 ± 1.02, respectively. Females in the same age categories had mean HQ values of 0.81 ± 1.43, 0.55 ± 0.97, and 0.48 ± 0.85, respectively (Table 5). The maximum HQ values for males in the age ranges of 9–11 years, 12–14 years, and 15–18 years were 3.66 ± 0.36, 2.82 ± 0.28, and 2.42 ± 0.24, respectively. Females in these age categories had mean HQ values of 3.40 ± 0.33, 2.30 ± 0.23, and 2.02 ± 0.20, respectively (Table 6).

4. Discussion

The results of this study indicate that the HQ values of infants were acutely high-risk and higher in comparison to the other groups. This is most likely due to a mix of behavior, environment, and physical factors. They are highly susceptible to the developing fetus and the early years of their lives, when their respiratory systems, organ systems, and brains are still growing. It is uncertain what biological processes induce PM2.5 inhalation to cause infant death. Nevertheless, Brook et al. [33] reported that PM2.5 exposure likely promotes oxidative stress, systemic inflammation, and blood clotting. As a result, Kannan et al. [34] explained that if a pregnant woman becomes exposed to PM2.5, a chain reaction of unfavorable biological reactions may endanger the health of the fetus. Previous studies by Feng et al. [31], and Valentino et al. [35] discovered that PM exposure changed the placental function and structure, potentially impairing fetal development and growth. Simultaneously, Wick et al. [36] revealed that PM2.5 was able to pass the cell membrane. As a result, fine particulates that penetrate directly through the placenta would impair the fetus because the immune system of the fetus is still developing [37]. Prenatal exposure to a toxic drug can disrupt the development of many systems necessary for life. For instance, prenatal PM2.5 exposure may hinder the development of the cardiovascular and central nervous systems [38]. Furthermore, prenatal PM2.5 exposure may disrupt lung maturation by interacting with lung growth, neurogenesis, and differentiation [39]. Prenatal exposure to PM2.5 might well be associated with infant mortality, provided that disruptions in the formation and function of biological systems before birth are associated with negative health consequences later in life. Due to the role of exposure time on fetal susceptibility, the magnitude of the adverse effects of PM2.5 can fluctuate during the perinatal period [40]. With regard to cognitive function, PM2.5 exposure during earlier stages of pregnancy may be associated with severe issues, whereas exposure during the later stages of pregnancy may be associated with inadequacies [38].
Particulate matter is likely to be associated with gender [41]. Due to differences in respiratory symptom rates of growth, disentangling the role of gender in particle pollution connections in children may be more difficult [42]. It has been postulated that observed disparities in poor air quality consequences between males and females were caused by sex-related biological factors such as hormone balancing and body structure or sex differences in behavior patterns, doses, or the accuracy of measurements [43]. Furthermore, because males have a greater death rate than females, the lag in fetal respiratory system development in males might explain their high susceptibility to PM2.5 exposure [44,45]. Moreover, long-term prenatal PM2.5 exposure disrupts the Ras homolog gene family member A (RhoA) pathway in males [46]. Since the enhanced production of reactive oxygen species is a putative stimulation process of the RhoA system for PM2.5, males might be more prone to heart disease when exposed to PM2.5 [46,47]. Furthermore, some studies have found that male and female lungs respond differently to air pollution exposure [48,49,50,51]. This likely occurred because male and female lungs differed earlier in fetal and maternal growth all through their lives, with female lungs maturing earlier in terms of surfactant production [52,53]. Women have smaller lungs than men throughout their lives, but their respiratory anatomy is more beneficial, with a larger airway size in comparison to the amount of pulmonary parenchyma. As a result, airway hyperreactivity and asthma are more prevalent in boys than in girls during childhood.
Furthermore, PM2.5 does not only have a non-carcinogenic risk on human health; its chemical composition also has an effect on carcinogenic risk on human health. The latest studies demonstrate that the composition of particulate matter is related to human health. For example, Phairuang et al. [54,55] investigated the health risk of PM0.1 and its trace elements such as aluminum (Al), barium (Ba), potassium (K), iron (Fe), chromium (Cr), copper (Cu), nickel (Ni), sodium (Na), manganese (Mn), magnesium (Mg), titanium (Ti), lead (Pb), and zinc (Zn) on humans in Bangkok and Hat Yai, Thailand. They discovered that biomass burning was the predominant source of PM and had a high risk for human health in those areas. Additionally, Insian et al. [56] evaluated the respiratory health risk posed by size-fractionated PM-bound polycyclic aromatic hydrocarbons (PAHs) in urban and rural Chiang Mai, northern Thailand. They discovered a rather high respiratory health risk during the smoky haze season in Chiang Mai, Thailand based on toxicity equivalent concentrations of the PAH-bound size-fractionated particulate matters (SPMs) and inhalation cancer risk (ICR). Wang et al. [57] revealed that the health risk assessment of heavy metals showed that non-carcinogenic hazards are not expected to occur, while Cr contributed the highest cancer risk in the industrial areas of China.

5. Conclusions

The purpose of this study was to examine health risks among different age groups of children in northern Thailand between 2020 and 2029. The analysis of PM2.5 concentrations in the future found that they tended to exceed both the USEPA and Thai guidelines, mainly in the dry season. The air quality in the wet season is expected to be better than the dry season, when PM2.5 concentrations tend to be lower. The highest future PM2.5 concentrations were detected in ranges of 40 to 400 μg/m3 in the dry season, especially in February and March. As a result, the highest concentration of PM2.5 was found in March. At the same time, the highest average of HQ values was found with 13.89, 12.27, 10.82, 8.91, and 5.96 for infants, toddlers, young children, school age, and adolescents, respectively, while the HQ of different age groups of children showed the highest value in March with 13.89, 12.27, 10.82, and 9.02 for children aged less than 1 year, 1 to 2 years, 3 to 5 years, and 6 to 8 years, respectively. Meanwhile, the HQ of children aged 9 to 11 years, 12 to 14 years, and 15 to 18 years was in the range of 6.04 to 9.12 for males and 5.03 to 8.47 for females. In conclusion, in general, children of all ages are likely to suffer from PM2.5 in the future. Infants are especially at higher risk than other groups of children. Simultaneously, adolescent males tend to be at higher risk than females.

Author Contributions

Conceptualization, T.A. and N.P.; Methodology, T.A.; Software, T.A.; Validation, T.A. and N.P.; Formal analysis, T.A.; Investigation, T.A. and N.P.; Resources, T.A.; Data curation, T.A.; Writing—original draft preparation, T.A.; Writing—review and editing, T.A. and N.P.; Visualization, T.A.; Supervision, T.A.; Project administration, T.A.; Funding acquisition, T.A. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by the Thailand Science Research and Innovation Fund and the University of Phayao (Grant No. FF66-UoE010).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data generated or analyzed during this study are included in this published article.

Acknowledgments

The author would like to thank the Thai Pollution Control Department for supporting ground-based measurement data.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Amnuaylojaroen, T.; Parasin, N.; Limsakul, A. Health risk assessment of exposure near-future PM2. 5 in Northern Thailand. Air Qual. Atmos. Health 2022, 15, 1963–1979. [Google Scholar] [CrossRef]
  2. Zhang, S.; Liu, X.; Bae, J. Does trade openness affect CO2 emissions: Evidence from ten newly industrialized countries? Environ. Sci. Pollut. Res. 2017, 24, 17616–17625. [Google Scholar] [CrossRef] [PubMed]
  3. Wu, Z.; Zhang, Y.; Zhang, L.; Huang, M.; Zhong, L.; Chen, D.; Wang, X. Trends of outdoor air pollution and the impact on premature mortality in the Pearl River Delta region of southern China during 2006–2015. Sci. Total Environ. 2019, 690, 248–260. [Google Scholar] [CrossRef]
  4. Lelieveld, J.; Barlas, C.; Giannadaki, D.; Pozzer, A. Model calculated global, regional and megacity premature mortality due to air pollution. Atmos. Chem. Phys. 2013, 13, 7023–7037. [Google Scholar] [CrossRef] [Green Version]
  5. Cohen, A.J.; Brauer, M.; Burnett, R.; Anderson, H.R.; Frostad, J.; Estep, K.; Balakrishnan, K.; Brunekreef, B.; Dandona, L.; Dandona, R.; et al. Estimates and 25-year trends of the global burden of disease attributable to ambient air pollution: An analysis of data from the Global Burden of Diseases Study 2015. Lancet 2017, 389, 1907–1918. [Google Scholar] [CrossRef] [Green Version]
  6. Shi, Y.; Matsunaga, T.; Yamaguchi, Y.; Zhao, A.; Li, Z.; Gu, X. Long-term trends and spatial patterns of PM2.5-induced premature mortality in South and Southeast Asia from 1999 to 2014. Sci. Total Environ. 2018, 631, 1504–1514. [Google Scholar] [CrossRef]
  7. Amnuaylojaroen, T.; Inkom, J.; Janta, R.; Surapipith, V. Long range transport of southeast asian PM2.5 pollution to northern Thailand during high biomass burning episodes. Sustainability 2020, 12, 10049. [Google Scholar] [CrossRef]
  8. Khodmanee, S.; Amnuaylojaroen, T. Impact of biomass burning on ozone, carbon monoxide, and nitrogen dioxide in Northern Thailand. Front. Environ. Sci. 2021, 8, 641877. [Google Scholar] [CrossRef]
  9. Parasin, N.; Amnuaylojaroen, T.; Saokaew, S. Effect of air pollution on obesity in children: A systematic review and meta-analysis. Children 2021, 8, 327. [Google Scholar] [CrossRef]
  10. U.S. EPA. Child-Specific Exposure Factors Handbook; EPA: Washington, DC, USA, 2008.
  11. Liu, J.; Kiesewetter, G.; Klimont, Z.; Cofala, J.; Heyes, C.; Schöpp, W.; Zhu, T.; Cao, G.; Sanabria, A.G.; Sander, R.; et al. Mitigation pathways of air pollution from residential emissions in the Beijing-Tianjin-Hebei region in China. Environ. Int. 2019, 125, 236–244. [Google Scholar] [CrossRef]
  12. Lien, W.-H.; Owili, P.O.; Muga, M.A.; Lin, T.-H. Ambient particulate matter exposure and under-five and maternal deaths in Asia. Int. J. Environ. Res. Public Health 2019, 16, 3855. [Google Scholar] [CrossRef] [Green Version]
  13. Gouveia, N.; Junger, W.L.; Romieu, I.; Cifuentes, L.A.; de Leon, A.P.; Vera, J.; Strappa, V.; Hurtado-Díaz, M.; Miranda-Soberanis, V.; Rojas-Bracho, L.; et al. Effects of air pollution on infant and children respiratory mortality in four large Latin-American cities. Environ. Pollut. 2018, 232, 385–391. [Google Scholar] [CrossRef]
  14. Sarkodie, S.A.; Strezov, V.; Jiang, Y.; Evans, T. Proximate determinants of particulate matter (PM2.5) emission, mortality and life expectancy in Europe, Central Asia, Australia, Canada and the US. Sci. Total Environ. 2019, 683, 489–497. [Google Scholar] [CrossRef]
  15. Chowdhury, S.; Dey, S.; Smith, K.R. Ambient PM2.5 exposure and expected premature mortality to 2100 in India under climate change scenarios. Nat. Commun. 2018, 9, 318. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Huggins, F.E.; Huffman, G.P.; Robertson, J.D. Speciation of elements in NIST particulate matter SRMs 1648 and 1650. J. Hazard. Mater. 2000, 74, 1–23. [Google Scholar] [CrossRef] [PubMed]
  17. Majestic, B.J.; Schauer, J.J.; Shafer, M.M. Development of a manganese speciation method for atmospheric aerosols in biologically and environmentally relevant fluids. Aerosol Sci. Technol. 2007, 41, 925–933. [Google Scholar] [CrossRef]
  18. Kulkarni, N.; Grigg, J. Effect of air pollution on children Paediatr. Child Health 2008, 18, 238–243. [Google Scholar] [CrossRef]
  19. Bruce, N.G.; Dherani, M.K.; Das, J.K.; Balakrishnan, K.; Adair-Rohani, H.; Bhutta, Z.A.; Pope, D. Control of household air pollution for child survival: Estimates for intervention impacts. BMC Public Health 2013, 13, S8. [Google Scholar] [CrossRef] [Green Version]
  20. Zheng, X.; Xu, X.; Yekeen, T.A.; Zhang, Y.; Chen, A.; Kim, S.S.; Dietrich, K.N.; Ho, S.-M.; Lee, S.-A.; Reponen, T.; et al. Ambient air heavy metals in PM2.5 and potential human health risk assessment in an informal electronic-waste recycling site of China. Aerosol Air Qual. Res. 2016, 16, 388–397. [Google Scholar] [CrossRef] [Green Version]
  21. Anwar, A.; Ayub, M.; Khan, N.; Flahault, A. Nexus between air pollution and neonatal deaths: A case of Asian countries. Int. J. Environ. Res. Public Health 2019, 16, 4148. [Google Scholar] [CrossRef] [Green Version]
  22. Amnuaylojaroen, T.; Surapipith, V.; Macatangay, R.C. Projection of the near-future PM2.5 in Northern Peninsular Southeast Asia under RCP8.5. Atmosphere 2022, 13, 305. [Google Scholar] [CrossRef]
  23. Zheng, N.; Liu, J.; Wang, Q.; Liang, Z. Health risk assessment of heavy metals exposure to street dust in the zinc smelting district, Northeast of China. Sci. Total Environ. 2010, 408, 726–733. [Google Scholar] [CrossRef] [PubMed]
  24. Yarmohammadi, H.; Poursadeghiyan, M.; Shorabi, Y.; Ebrahimi, M.H.; Rezaei, G.; Biglari, H.; Rostami, R. Risk assessment in a wheat winnowing factory based on ET and BA method. J. Eng. Appl. Sci. 2016, 11, 334–338. [Google Scholar]
  25. Ghaderpoori, M.; Paydar, M.; Zarei, A.; Alidadi, H.; Najafpoor, A.A.; Gohary, A.H.; Shams, M. Health risk assessment of fluoride in water distribution network of Mashhad, Iran. Hum. Ecol. Risk Assess. Int. J. 2019, 25, 851–862. [Google Scholar] [CrossRef]
  26. Layton, D.W. Metabolically consistent breathing rates for use in dose assessments. Health Phys. 1993, 64, 22–36. [Google Scholar] [CrossRef]
  27. Liang, B.; Li, X.-L.; Ma, K.; Liang, S.-X. Pollution characteristics of metal pollutants in PM2.5 and comparison of risk on human health in heating and non-heating seasons in Baoding, China. Ecotoxicol. Environ. Saf. 2019, 170, 166–171. [Google Scholar] [CrossRef] [PubMed]
  28. Morakinyo, O.M.; Adebowale, A.S.; Mokgobu, M.I.; Mukhola, M.S. Health risk of inhalation exposure to sub-10 µm particulate matter and gaseous pollutants in an urban-industrial area in South Africa: An ecological study. BMJ Open 2017, 7, e013941. [Google Scholar] [CrossRef]
  29. Olufemi, A.C.; Mji, A.; Mukhola, M.S. Health risks of exposure to air pollutants among students in schools in the vicinities of coal mines. Energy Explor. Exploit. 2019, 37, 1638–1656. [Google Scholar] [CrossRef] [Green Version]
  30. Fang, W.; Yang, Y.; Xu, Z. PM10 and PM2. 5 and health risk assessment for heavy metals in a typical factory for cathode ray tube television recycling. Environ. Sci. Technol. 2013, 47, 12469–12476. [Google Scholar] [CrossRef]
  31. Feng, S.; Gao, D.; Liao, F.; Zhou, F.; Wang, X. The health effects of ambient PM2.5 and potential mechanisms. Ecotoxicol. Environ. Saf. 2016, 128, 67–74. [Google Scholar] [CrossRef]
  32. Militaru, M.; Martinovici, D. Our experience in pediatric sepsis. J. Pediatrului 2005, 8, 29–30. [Google Scholar]
  33. Brook, R.D.; Rajagopalan, S.; Pope, C.A., III; Brook, J.R.; Bhatnagar, A.; Diez-Roux, A.V.; Holguin, F.; Hong, Y.; Luepker, R.V.; Mittleman, M.A.; et al. Particulate matter air pollution and cardiovascular disease: An update to the scientific statement from the American Heart Association. Circulation 2010, 121, 2331–2378. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Kannan, S.; Misra, D.P.; Dvonch, J.T.; Krishnakumar, A. Exposures to airborne particulate matter and adverse perinatal outcomes: A biologically plausible mechanistic framework for exploring potential effect modification by nutrition. Environ. Health Perspect. 2006, 114, 1636–1642. [Google Scholar] [CrossRef]
  35. Valentino, S.A.; Tarrade, A.; Aioun, J.; Mourier, E.; Richard, C.; Dahirel, M.; Rousseau-Ralliard, D.; Fournier, N.; Aubrière, M.-C.; Lallemand, M.-S.; et al. Maternal exposure to diluted diesel engine exhaust alters placental function and induces intergenerational effects in rabbits. Part. Fibre Toxicol. 2015, 13, 39. [Google Scholar] [CrossRef] [Green Version]
  36. Wick, P.; Malek, A.; Manser, P.; Meili, D.; Maeder-Althaus, X.; Diener, L.; Diener, P.-A.; Zisch, A.; Krug, H.F.; von Mandach, U. Barrier capacity of human placenta for nanosized materials. Environ. Health Perspect. 2010, 118, 432–436. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. West, L. Defining critical windows in the development of the human immune system. Hum. Exp. Toxicol. 2002, 21, 499–505. [Google Scholar] [CrossRef] [PubMed]
  38. Moore, K.L.; Persaud, T.V.N.; Torchia, M.G. Before We are Born E-Book: Essentials of Embryology and Birth Defects with Student Consult Online Access; Elsevier Health Sciences: Amsterdam, The Netherlands, 2015. [Google Scholar]
  39. Schittny, J.C. Development of the lung. Cell Tissue Res. 2017, 367, 427–444. [Google Scholar] [CrossRef] [Green Version]
  40. Selevan, S.G.; Kimmel, C.A.; Mendola, P. Identifying critical windows of exposure for children’s health. Environ. Health Perspect. 2000, 108 (Suppl. 3), 451–455. [Google Scholar] [PubMed]
  41. Xia, T.; Fang, F.; Montgomery, S.; Fang, B.; Wang, C.; Cao, Y. Sex differences in associations of fine particulate matter with non-accidental deaths: An ecological time-series study. Air Qual. Atmos. Health 2021, 14, 863–872. [Google Scholar] [CrossRef]
  42. Berhane, K.; McConnell, R.; Gilliland, F.; Islam, T.; James Gauderman, W.; Avol, E.; London, S.J.; Rappaport, E.; Margolis, H.G.; Peters, J.M. Sex-specific effects of asthma on pulmonary function in children. Am. J. Respir. Crit. Care Med. 2000, 162, 1723–1730. [Google Scholar] [CrossRef] [Green Version]
  43. Clougherty, J.E. A growing role for gender analysis in air pollution epidemiology. Environ. Health Perspect. 2010, 118, 167–176. [Google Scholar] [CrossRef] [Green Version]
  44. Drevenstedt, G.L.; Crimmins, E.M.; Vasunilashorn, S.; Finch, C.E. The rise and fall of excess male infant mortality. Proc. Natl. Acad. Sci. USA 2008, 105, 5016–5021. [Google Scholar] [CrossRef] [Green Version]
  45. Torday, J.S.; Nielsen, H.C.; Fencl, M.D.M.; Avery, M.E. Sex differences in fetal lung maturation. Am. Rev. Respir. Dis. 1981, 123, 205–208. [Google Scholar]
  46. Winckelmans, E.; Vrijens, K.; Tsamou, M.; Janssen, B.G.; Saenen, N.D.; Roels, H.A.; Kleinjans, J.; Lefebvre, W.; Vanpoucke, C.; de Kok, T.M.; et al. Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: Findings from the ENVIRONAGE birth cohort. Environ. Health 2017, 16, 52. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Lodovici, M.; Bigagli, E. Oxidative stress and air pollution exposure. J. Toxicol. 2011, 2011, 487074. [Google Scholar] [CrossRef]
  48. Gauderman, W.J.; Vora, H.; McConnell, R.; Berhane, K.; Gilliland, F.; Thomas, D.; Lurmann, F.; Avol, E.; Kunzli, N.; Jerrett, M.; et al. Effect of exposure to traffic on lung development from 10 to 18 years of age: A cohort study. Lancet 2007, 369, 571–577. [Google Scholar] [CrossRef]
  49. Gehring, U.; Cyrys, J.; Sedlmeir, G.; Brunekreef, B.; Bellander, T.; Fischer, P.; Bauer, C.P.; Reinhardt, D.; Wichmann, H.E.; Heinrich, J. Traffic-related air pollution and respiratory health during the first 2 yrs of life. Eur. Respir. J. 2002, 19, 690–698. [Google Scholar] [CrossRef] [Green Version]
  50. Peters, J.M.; Avol, E.; Navidi, W.; London, S.J.; Gauderman, W.J.; Lurmann, F.; Linn, W.S.; Margolis, H.; Rappaport, E.; Gong, H.; et al. A study of twelve Southern California communities with differing levels and types of air pollution: I. Prevalence of respiratory morbidity. Am. J. Respir. Crit. Care Med. 1999, 159, 760–767. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Rojas-Martinez, R.; Perez-Padilla, R.; Olaiz-Fernandez, G.; Mendoza-Alvarado, L.; Moreno-Macias, H.; Fortoul, T.; McDonnell, W.; Loomis, D.; Romieu, I. Lung function growth in children with long-term exposure to air pollutants in Mexico City. Am. J. Respir. Crit. Care Med. 2007, 176, 377–384. [Google Scholar] [CrossRef] [PubMed]
  52. Becklake, M.R.; Kauffmann, F. Gender differences in airway behaviour over the human life span. Thorax 1999, 54, 1119–1138. [Google Scholar] [CrossRef] [Green Version]
  53. Polgar, G.; Weng, T.R. The functional development of the respiratory system: From the period of gestation to adulthood. Am. Rev. Respir. Dis. 1979, 120, 625–695. [Google Scholar]
  54. Phairuang, W.; Suwattiga, P.; Hongtieab, S.; Inerb, M.; Furuuchi, M.; Hata, M. Characteristics, sources, and health risks of ambient nanoparticles (PM0.1) bound metal in Bangkok Thailand. Atmos. Environ. X 2021, 12, 100141. [Google Scholar] [CrossRef]
  55. Phairuang, W.; Inerb, M.; Hata, M.; Furuuchi, M. Characteristics of trace elements bound to ambient nanoparticles (PM0.1) and a health risk assessment in southern Thailand. J. Hazard. Mater. 2022, 425, 127986. [Google Scholar] [CrossRef] [PubMed]
  56. Insian, W.; Yabueng, N.; Wiriya, W.; Chantara, S. Size-fractionated PM- bound PAHs in urban and rural atmospheres of Northern Thailand for respiratory health risk assessment. Environ. Pollut. 2022, 293, 118488. [Google Scholar] [CrossRef] [PubMed]
  57. Wang, N.; Zhao, X.; Wang, J.; Yin, B.; Geng, C.; Niu, D.; Yang, W.; Yu, H.; Li, W. Chemical composition of PM2.5 and its impact on inhalation health risk evaluation in a city with light industry in central China. Atmosphere 2020, 11, 340. [Google Scholar] [CrossRef] [Green Version]
Figure 2. (a) Daily and (b) monthly means of the PM2.5 concentrations in northern Thailand during 2020–2029.
Figure 2. (a) Daily and (b) monthly means of the PM2.5 concentrations in northern Thailand during 2020–2029.
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Figure 3. (a) Daily means of the HQ related to PM2.5 concentrations in the age-related development period and (b) the monthly means of the HQ related to PM2.5 concentrations in specific groups of ages in children in northern Thailand during 2020–2029 (black line is HQ = 1).
Figure 3. (a) Daily means of the HQ related to PM2.5 concentrations in the age-related development period and (b) the monthly means of the HQ related to PM2.5 concentrations in specific groups of ages in children in northern Thailand during 2020–2029 (black line is HQ = 1).
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Table 3. Mean, maximum, and minimum of the monthly means of the HQ related to PM2.5 according to the age-related development period in children during 2020–2029.
Table 3. Mean, maximum, and minimum of the monthly means of the HQ related to PM2.5 according to the age-related development period in children during 2020–2029.
MonthMeanMaxMin
InfantsToddlersYoung ChildrenSchool AgeAdolescentsInfantsToddlersYoung ChildrenSchool AgeAdolescentsInfantsToddlersYoung ChildrenSchool AgeAdolescents
January1.771.571.381.140.762.832.502.211.821.220.860.760.670.550.37
February7.987.056.215.123.4314.0712.4310.969.036.042.372.091.841.521.02
March13.8912.2710.828.915.9623.9621.1618.6615.3710.287.126.295.554.573.06
April5.234.624.073.362.2517.4815.4413.6111.217.501.050.930.820.670.45
May0.770.680.600.490.331.471.291.140.940.630.440.390.340.280.19
June0.480.420.370.310.210.630.560.490.410.270.380.340.300.240.16
July0.490.430.380.310.210.570.500.440.370.240.390.340.300.250.17
August0.620.550.480.400.270.800.700.620.510.340.440.390.340.280.19
September0.840.740.660.540.361.151.010.890.730.490.580.510.450.370.25
October1.020.890.810.650.431.201.031.050.790.530.670.670.570.480.32
November0.990.880.760.640.421.201.100.970.740.490.650.580.540.490.34
December1.100.950.860.690.471.381.271.120.860.590.710.700.690.530.35
Mean2.93 ± 1.202.59 ± 1.062.28 ± 0.931.88 ± 0.771.26 ± 0.515.56 ± 2.344.92 ± 2.074.35 ± 1.823.56 ± 1.502.39 ± 1.011.31 ± 0.551.17 ± 0.491.03 ± 0.430.85 ± 0.350.57 ± 0.24
Table 4. Mean of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Table 4. Mean of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Month<1 y1 y–2 y3 y–5 y6 y–8 y9 y–11 y12 y–14 y15 y–18 y
MaleFemaleMaleFemaleMaleFemale
January1.771.571.381.151.161.080.900.730.770.64
February7.987.056.215.185.244.874.043.303.472.89
March13.8912.2710.829.029.128.477.045.746.045.03
April5.234.624.073.403.443.192.652.162.281.89
May0.770.680.600.500.500.470.390.320.330.28
June0.480.420.370.310.320.290.240.200.210.17
July0.490.430.380.320.320.300.250.200.210.18
August0.620.550.480.400.410.380.310.260.270.22
September0.840.740.660.550.550.510.430.350.370.31
October1.020.890.810.650.680.620.510.420.430.36
November0.990.880.760.650.640.600.500.410.430.35
December1.100.950.860.690.700.660.550.440.480.40
Mean2.93 ± 1.202.59 ± 1.062.28 ± 0.931.90 ± 0.781.92 ± 0.791.79 ± 0.731.48 ± 0.611.21 ± 0.501.27 ± 0.521.06 ± 0.43
Table 5. Minimum of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Table 5. Minimum of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Month<1 y1 y–2 y3 y–5 y6 y–8 y9 y–11 y12 y–14 y15 y–18 y
MaleFemaleMaleFemaleMaleFemale
January0.860.760.670.560.570.530.440.360.380.31
February2.372.091.841.541.551.441.200.981.030.86
March7.126.295.554.634.684.343.612.953.102.58
April1.050.930.820.680.690.640.530.430.460.38
May0.440.390.340.290.290.270.220.180.190.16
June0.380.340.300.250.250.230.190.160.170.14
July0.390.340.300.250.250.240.200.160.170.14
August0.440.390.340.290.290.270.220.180.190.16
September0.580.510.450.380.380.350.290.240.250.21
October0.670.670.570.460.470.460.330.300.330.26
November0.650.580.540.510.470.470.390.320.300.28
December0.710.700.690.550.500.470.430.330.360.28
Mean1.31 ± 2.341.17 ± 2.071.03 ± 1.820.86 ± 1.520.87 ± 1.540.81 ± 1.430.67 ± 1.190.55 ± 0.970.58 ± 1.020.48 ± 0.85
Table 6. Maximum of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Table 6. Maximum of the monthly means of the HQ related to PM2.5 according to the different age groups of children during 2020–2029.
Month<1 y1 y–2 y3 y–5 y6 y–8 y9 y–11 y12 y–14 y15 y–18 y
MaleFemaleMaleFemaleMaleFemale
January2.832.502.211.841.861.731.431.171.231.02
February14.0712.4310.969.149.248.587.135.826.125.09
March23.9621.1618.6615.5615.7314.6112.149.9110.428.67
April17.4815.4413.6111.3511.4810.668.867.237.606.33
May1.471.291.140.950.960.890.740.610.640.53
June0.630.560.490.410.410.390.320.260.270.23
July0.570.500.440.370.370.350.290.240.250.21
August0.800.700.620.520.520.490.400.330.350.29
September1.151.010.890.740.750.700.580.470.500.41
October1.201.031.050.830.840.760.640.500.560.48
November1.201.100.970.790.770.780.610.490.510.44
December1.381.271.120.860.900.820.750.560.640.50
Mean5.56 ± 0.554.92 ± 0.494.35 ± 0.433.61 ± 0.363.66 ± 0.363.40 ± 0.332.82 ± 0.282.30 ± 0.232.42 ± 0.242.02 ± 0.20
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Amnuaylojaroen, T.; Parasin, N. Future Health Risk Assessment of Exposure to PM2.5 in Different Age Groups of Children in Northern Thailand. Toxics 2023, 11, 291. https://doi.org/10.3390/toxics11030291

AMA Style

Amnuaylojaroen T, Parasin N. Future Health Risk Assessment of Exposure to PM2.5 in Different Age Groups of Children in Northern Thailand. Toxics. 2023; 11(3):291. https://doi.org/10.3390/toxics11030291

Chicago/Turabian Style

Amnuaylojaroen, Teerachai, and Nichapa Parasin. 2023. "Future Health Risk Assessment of Exposure to PM2.5 in Different Age Groups of Children in Northern Thailand" Toxics 11, no. 3: 291. https://doi.org/10.3390/toxics11030291

APA Style

Amnuaylojaroen, T., & Parasin, N. (2023). Future Health Risk Assessment of Exposure to PM2.5 in Different Age Groups of Children in Northern Thailand. Toxics, 11(3), 291. https://doi.org/10.3390/toxics11030291

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