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Article

Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China

1
Department of Environmental Health, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing 210009, China
2
Department of Environmental Health, Jintan Center for Disease Control and Prevention, Changzhou 213200, China
3
National Center for Rural Water Supply Technical Guidance, Chinese Center for Disease Control and Prevention, Beijing 102200, China
4
School of Public Health and Social Work, Queensland University of Technology, Brisbane, Queensland 4059, Australia
*
Authors to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2018, 15(5), 924; https://doi.org/10.3390/ijerph15050924
Submission received: 12 April 2018 / Revised: 29 April 2018 / Accepted: 3 May 2018 / Published: 6 May 2018
(This article belongs to the Special Issue Environmental Determinants of Infectious Disease Transmission)

Abstract

:
The epidemiological features of Cryptosporidium infection among school-age children in China still remain unclear. Hereby, a cross-sectional study of 1637 children aged 3–9 years was designed to investigate the risk factors and spatial clusters of Cryptosporidium infection in a rural region of Eastern China. Stool specimens collected from participants were examined using the auramine-phenol and modified acid-fast staining. Univariable and multivariable analyses were performed to identify the risk factors of Cryptospordium infection. The spatial clusters were analyzed by a discrete Poisson model using SaTScan software. Our results showed that the overall prevalence of Cryptosporidium infection was 11‰ in the research region. At the age of 3–6 years (odds ratios (OR) = 3.072, 95% confidence intervals (CI): 1.001–9.427), not washing hands before eating and after defecation (OR = 3.003, 95% CI: 1.060–8.511) were recognized as risk factors. Furthermore, a high-risk spatial cluster (relative risk = 4.220, p = 0.025) was identified. These findings call for effective sustainable interventions including family and school-based hygienic education to reduce the prevalence of Cryptosporidium infection. Therefore, an early warning system based spatiotemporal models with risk factors is required to further improve the effectiveness and efficiency of cryptosporidiosis control in the future.

1. Introduction

The intestinal protozoan Cryptosporidium is considered to be a leading cause of the diarrheal diseases affecting humans globally. Since the first human cryptosporidiosis was found in 1976, it has been estimated that the prevalence of Cryptosporidium infection is <3% in industrialized regions and between 5 and ≥10% in developing regions [1,2,3]. Prior studies inferred that the high prevalence occurred more in socioeconomically-disadvantaged countries. The Cryptosporidium oocysts can remain infectious for several months owing to a high resistance to a variety of environmental pressures, such as disinfectants or pesticides. Individuals may be infected with oocysts directly or indirectly, through person-to-person transmission, consumption of contaminated food and water, or contact with contagious animals or domestic pets [4].
The clinical features of Cryptosporidium infection differ from asymptomatic status to a severe fatal outcome. Possible symptoms include diarrhea, vomiting, abdominal pain and fever. The severity of cryptosporidiosis depends on the age and immune status of individuals, varying from no symptoms or self-limiting diarrhea in immunocompetent persons to life-threatening outcomes in immunocompromised individuals [4]. Children are more vulnerable to Cryptosporidium infection than older age groups [5,6]. It is recognized that Cryptosporidium infection contributes to 30–50% of diarrhea mortality for children under five years in developing countries [2,7]. The results of a global multicenter study indicated that Cryptosporidium was second only to the rotavirus pathogen in leading to moderate-to-severe diarrhea among children younger than two years in developing countries [7]. Epidemiological studies revealed that early childhood cryptosporidiosis might be linked with malnutrition, growth impairment, and long-term cognitive function deficits [8,9,10].
In China, the first human case of cryptosporidiosis was confirmed in Nanjing, Jiangsu Province in 1987 [11]. After that, a number of studies concerning the epidemiology of cryptosporidiosis in different regions have been reported, estimating that the Cryptosporidium contributed to 1.40% to 5.66% of diarrhea episodes in China [12,13,14]. However, to date, cryptosporidiosis has not been involved in the national reported diseases systems. Furthermore, the examination of Cryptosporidium oocysts is not a routine check for the fecal samples of patients with diarrhea, which can lead to an underestimation of the prevalence. The main targeted groups of previous studies have been limited to patients with diarrhea or immunodeficiency diseases [13,14,15]. However, the epidemiology of Cryptosporidium infection among school-age children remains largely unclear, although children have been widely recognized as one of the most susceptible groups to Cryptosporidium infection. Furthermore, to facilitate the development of tailored and cost-effective cryptosporidiosis control and prevention strategies, it is desirable to delineate the spatial distribution of Cryptosporidium infection and to identify possible high-risk spatial clusters. This cross-sectional study attempted to fill these existing knowledge gaps. The specific objectives were two-fold: (a) to investigate the prevalence and possible risk factors of Cryptosporidium infection, and (b) to analyze spatial clusters of Cryptosporidium infection among school-age children in Jintan County, Jiangsu Province of Eastern China.

2. Materials and Methods

2.1. Study Area

The cross-sectional study was carried out between July and October 2013 in a rural region of Jintan County, Jiangsu Province of Eastern China (Figure 1). Jintan County covers an area of 975 km2 and has a population of approximately 500,000 inhabitants, including 300,000 rural populations. Its coordinates are between 31.33° to 31.53° N and 119.17° to 119.44° E. The district is in the subtropical climate area. The average annual temperature is 15.3 °C (5–9 °C in winter, 29–32 °C in summer), and the annual average rainfall is between 900 and 1600 mm. Topographically, Western Jintan is high and Eastern Jintan is low. This district features relatively high-level socioeconomic status in China. Its economic income is mainly based on the production of basic grains, tourism, and commercial activities.

2.2. Data Collection

In 2013, there were 37 public primary schools and 41 kindergartens in Jintan County, and there were a total of 19,406 children aged 3 to 9 years in Jintan County (data provided by Jintan Education Bureau). In this study, four public primary schools and four kindergartens, located in four rural townships (Township A, B, C, and D), were randomly selected from all public primary schools and kindergartens in Jintan County (Figure 1). Using a stratified cluster sampling method, a total of 1651 children aged from 3 to 9 years were randomly selected from the above eight sites. Specifically, in the selected schools/kindergartens, children aged 3 to 9 years were identified first, and all these children were chosen as the participants in the investigation. To better perform the investigation, parents or guardians were first informed the purposes and procedures of the study, and written informed consent was provided to each of them. Further, a clean plastic container with a tag number was delivered to each parent or guardian to collect the stool samples of their children. When the written informed consent was completed, a self-administered questionnaire with demographic, environmental, and personal characteristics was filled in by the parents or guardians. The details of the questionnaire are summarized in Supplementary Table S1. Ultimately, only 1637 met the requirements, including written informed consent, questionnaires and fecal samples. There is no statistical difference between the included and excluded children in terms of age, gender and location.
Fecal samples (20–30 g) from each child were collected on the next day, and all feces were then sent to Jintan Center for Disease Control and Prevention (CDC) for determination and stored at 4 °C immediately. The oocysts of Cryptosporidium were examined using auramine-phenol and modified acid-fast staining [16]. In this method, Cryptosporidium oocysts were identified as pink to red on a blue background under fluorescence microscope. A stool was considered as positive if the oocysts fell with the size range of 4 to 6 µm. Each specimen was separately examined twice by two experienced technicians for quality control, and each run used one positive and two negative controls. Ten percent of the total examined smears were randomly selected, and then were sent to National Center for Rural Water Supply Technical Guidance, Chinese CDC for rechecking.
The study was performed in line with the Declaration of Helsinki. This study protocol was approved by the Ethics Committee of National Center for Rural Water Supply Technical Guidance, Chinese CDC (No. 201201). Children with Cryptosporidium infection were advised to go to the local hospital for further examination.

2.3. Descriptive and Risk Factors Analysis

Data were double input to EpiData software (version 3.0; The EpiData Association, Odense, Denmark). The prevalence of Cryptosporidium infection was expressed as permillage. The univariable analysis was performed by Pearson’s Chi-square test to identify the association between potential risk factors and Cryptosporidium infection, and the results were presented as crude odds ratios (cOR) with 95% confidence intervals (CI). Multivariable analysis was conducted to confirm the risk factors by logistic regression analysis (Enter), and the results were presented as adjusted odds ratios (aOR) with 95% CI. Cryptosporidium infection was used as the dependent variable and the demographic, environmental, and personal characteristics were taken as the independent variables. Factors with p values < 0.1 in the Pearson’s chi-square test were chosen as the independent variables in the logistic regression analysis. All statistical analyses were carried out using SPSS software (version 20.0; IBM SPSS Institute, Inc., Armonk, NY, USA). Differences were considered significant at p values ≤ 0.05.

2.4. Cluster Analysis and Spatial Visualization

To identify the high-risk spatial clusters, we employed a discrete Possion model using the SatScan software (version 9.4; Martin Kulldorff, Boston, MA, USA). The discrete Possion model requires cases and populations for a set of data districts. In this study, all cases were sorted into different villages according to the address of each case. Each village was marked using geographical coordinates on the map. Demographic information on Jintan County was provided by the local government. We input the details (number of cases, geographical coordinates, and populations) of the each village into Excel (version Office 2010; Microsoft Inc., Redmond, WA, USA), and then imported the file into the SatScan software. We chose a discrete Possion model with high rates to output the results of the spatial cluster analysis. We assumed the age group structures in each village were similar and used the total population of each village in the discrete Possion model. The results were shown using ArcGIS software (version 10.2; ESRI Inc., Redlands, CA, USA). The spatial distribution was estimated based on the observed cases in this study using the empirical Bayesian Kriging (EBK) method with the ArcGIS software. EBK is a geostatistical interpolation method that is widely used to estimate the spatial distribution of targeted diseases. In this method, the location (displayed by the latitude and longitude) of each case was marked on the map, and then we choose the EBK method to analyze the spatial distribution in Jintan County. Spatial visualization was shown on the map by ArcGIS.

3. Results

3.1. Characteristics of the Participants

A total of 1, 637 school-age children from four townships (A, B, C and D) were enrolled in the present study. These children were categorized into two groups by age: 3–6 years in the kindergarten stage (n = 863, 52.7%) and 7–9 years in the primary school stage (Grade 1 to Grade 3) (n = 774, 47.3%). The average age of the children was 6.4 ± 1.7 years.
In total, 864 (52.8%) were male and 773 (47.2%) were female. The sex ratios of male/female in 3–6 years and 7–9 years were 1.16 and 1.07, respectively. There was a higher proportion of participants from Township D (n = 741, 45.3%) compared with the other townships. The majority of the participants had access to piped water (97.4%, n = 1594) and household toilets (96.5%, n = 1580). Almost half of the participants (46.2%, n = 756) raised livestock or poultry. About a quarter of the children (25.4%, n = 416) reported that they had contact with pets. The general characteristics of the participants are presented in Table 1.

3.2. Prevalence and Risk Factors Associated with Cryptosporidium Infection

The results of the univariable and multivariable analyses of the risk factors associated with Cryptosporidium infection are presented in Table 2. Overall, 18 of 1637 fecal samples (11‰) were positive for Cryptosporidium infection. In terms of age and gender, the prevalence was 16‰ (14/863) among children aged 3–6 years and 5‰ (4/774) aged 7–9 years; 9‰ (8/864) for male and 13‰ (10/773) for female.
The results of the univariable analysis revealed that for the age group of 3–6 years (cOR = 3.175, 95% CI: 1.041–9.709, p = 0.032), location (F = 8.07, p = 0.031), and not washing hands before eating and after defecation (cOR = 3.088, 95% CI: 1.096–8.703, p = 0.025) were possible risk factors. In addition, the prevalence of infection in males was slightly lower than that of female children, although the difference was not statistically significant. The risks of Cryptosporidium infection did not differ according to the factors supply of piped water, presence of toilets in the household, raising livestock or poultry, contact with pets, boiling water before drinking, swimming in one month, travelling in six months, contact with water facilities in one month, and contact with a person with diarrhea in three months.
As gender may be a confounding factor, it was therefore controlled for in the multivariable logistic regression. Finally, the results of the multivariable logistic regression confirmed that participants aged 3–6 years were 3.072 times more likely to be infected with Cryptosporidium infection (aOR = 3.072, 95% CI: 1.001–9.427, p = 0.050). Children who did not wash their hands before eating or after defecation were 3.003 times more likely to be infected with Cryptosporidium infection (aOR = 3.003, 95% CI: 1.060–8.511, p = 0.039).

3.3. Cluster Analysis and Spatial Visualization

A total of 18 cases were confirmed in this study. The location of each case was marked on the map according to the address reported in the questionnaires. The total of 18 cases was distributed in seven villages and the number of cases from each village is shown on the map. As shown in Figure 2, the prevalence in Township A, C, and D was 9‰, 3‰, 19‰, respectively. No cases were found in Township B. The details of each village were input into the SatScan software to identify the spatial clusters. The results of a discrete Possion model analysis identified a high-risk primary cluster with a radius of 2.86 km in Township D (Relative Risk (RR) = 4.220, p = 0.025). This spatial cluster was composed of three villages (Village a, b, and c), and the observed and expected cases were 14 and 8.16 respectively. The number of cases in Village a, b, and c was 3, 9, and 2, respectively. Among the total of 14 cases in the cluster confirmed in Township D, 10 cases were from the same kindergarten, and two pairs of students are classmates. The details of the spatial cluster are shown in Table 3 and Figure 2.
A spatial visualization of Cryptosporidium infection is delineated in Figure 3. It shows that the predicted cases increased from East Jintan to West Jintan gradually. The number of estimated cases increased from 1.3 to 2.6 in Jintan County.

3.4. Association of Cryptosporidium Infection with Gastrointestinal Symptoms

Most of the children (90.1%, 1475/1637) had no complaints about gastrointestinal signs or symptoms. Of the overall 18 cases, most cases (72.2%, 13/18) were asymptomatic. The remaining five cases reported diarrhea, and three cases were accompanied by nausea and vomiting symptoms. The prevalence of Cryptosporidium infection was significantly higher among children who had gastrointestinal symptoms than their asymptomatic counterparts (31‰ vs. 9‰, F = 4.656, p = 0.031).

4. Discussion

The present study investigated the prevalence and risk factors of Cryptosporidium infection among school-age children in Jintan County of Eastern China. Furthermore, the study identified a spatial cluster in Township D, and estimated the spatial visualization based on the observed cases. Previous studies revealed a possible association between increased temperature and precipitation and Cryptosporidium infection [17,18]. Accordingly, this investigation was chosen to be carried out during a rainy season with high temperature.
The prevalence of Cryptosporidium infection has been extensively reported in developing countries. Previous studies estimated that the prevalence ranged from 0.79 to 5.06% among the general population in China [12,16,19,20]. However, a recent community-based investigation reported that the prevalence was 12.0% among the general population (1–60 years) in a rural resource-limited region [21]. Al-Delaimy et al. found that the prevalence was 5.2% among school children in Malaysia [22]. Two studies performed in Ethiopia reported that the prevalence was 7.3% and 4.6% among school children, respectively [23,24]. Quihui-Cota et al. reported a high prevalence of 27% among children in Mexico [25]. The heterogeneity of the previously documented prevalence might to some extent be due to the socioeconomic level of the study site, the immune status of the targeted groups, and the sensitivity of the examining techniques. Our study suggested the overall prevalence was 11‰ among school-age children in the research region, which was lower than previous studies reported in other countries, and this might be attributable to two reasons. First, as discussed above, the site of this study features a relatively high socioeconomic level in China. Second, we detected the Cryptosporidium oocysts via the traditional microscopic examination, which may underestimate the true prevalence owing to low sensitivity.
Our finding indicated that children aged 3–6 years were more likely to be infected with Cryptosporidium infection than those aged 7–9 years. A similar result was found among infants and children in Xuzhou City, China [20]. This may be explained by the higher vulnerability of younger children and the relatively better personal hygiene awareness in older children. In our study, children between 3–6 years were still at kindergarten stage, and they may not receive as much hygienic education as those in primary schools. Besides, younger children may have a higher opportunistic exposure to contaminated sources of infection. The association between younger age and higher chance of Cryptosporidium infection was well-established in a number of studies in other countries [22,26,27].
In addition, we found that not washing hands before eating and after defecation was a significant risk factor for Cryptosporidium infection. This finding is also in line with similar studies reported in other regions [22,27,28,29]. Exposure to contaminated food and hand and skin penetration is an important transmission route for Cryptosporidium infection. Owing to a high resistance to the environment, infectious Cryptosporidium oocysts can survive for a long time. The absence of a good personal hygiene may facilitate transmission, and consequently increase the risks of Cryptosporidium infection. Despite the rapid development of the economy, family and school-based hygienic education is urgently needed for the children in this region.
No statistical difference was found between male and female children in terms of Cryptosporidium infection in our study. This is in agreement with observations in similar studies [22,23]. In addition, we did not observe any association between “supplied with piped water” and Cryptosporidium infection. Previous studies revealed that tap water was a risk factor for Cryptosporidium infection in other regions [25,30]. In our study, supplied drinking water covered most of the households. Furthermore, this region had a qualified drinking-water quality that meets the National Drinking Water Quality Standard. The drinking water quality surveillance also demonstrated the absence of Cryptosporidium oocysts. Finally, the majority of participants were used to boiling water before drinking in daily life. These reasons may remarkably decrease the risk of transmission via drinking water.
In this study, we identified a high-risk spatial cluster in Township D. In addition, children with Cryptosporidium infection also clustered in the same kindergarten (71.4%, 10/14), highlighting the importance of disease prevention in homes and schools. Besides, a very famous scenic location called Mao Mountain is mainly located in Township D. The scenic location attracts more than a million visitors every year. The intense mobility of persons, consequently, may increase the risk of transmission. Finally, high temperature during the rainy season with a mountainous topography generates a humid environment, which may increase the likelihood of infection. However, the reasons for the cluster still remain unclear in our study. Further studies considering the molecular techniques may help us to explore the exact reasons behind this in the future.
The results of the spatial visualization showed a high to low tendency of estimated cases from West to East of Jintan County. The results suggest that West Jintan County has a higher risk of infection than other parts. Therefore, this region may be taken as a priority site for future investigation. This finding is consistent with the results above. However, in the process of spatial analysis, we only considered the locations of the cases. Other potential factors such as socioeconomic and travelling information were not taken into account in the present study. Therefore, large-scale and comprehensive studies are required to explore the epidemiological features.
Our study also found that 72.2% (13/18) of Cryptosporidium-positive children were asymptomatic. A cohort study performed in Peru indicated that even if asymptomatic cryptosporidiosis has a less severe effect on weight gain than symptomatic counterparts, it still has a more adverse effect on child growth [31]. Symptomless children can act as potential sources of infection by excreting contagious oocysts in feces. Intimate individuals at home or school may cause fecal–oral route infection. In view of the strong resistance of Cryptosporidium oocysts to the environment, the infection can last for a long time. In light of the ubiquity of asymptomatic cryptosporidiosis, more attention is needed from public health officials.
To the best of our knowledge, this is the first cross-sectional study of school-age children in Jintan County. The spatial cluster analysis suggested a potentially high-risk cluster in Township D requiring further study. We found that “children aged 3–6 years” and “not washing hands before eating and after defecation” significantly increased the likelihood of infection compared with other factors. Intervention measures such as family and school-based hygienic education needs to be strengthened among the susceptible population in this region.
There are several limitations in this study. Firstly, owing to limited of resources, only one single fecal sample was collected from each child, although three consecutive samples would have been more ideal. Secondly, the prevalence might be underestimated due to the low sensitivity of the stool sample examination technique. However, the auramine-phenol and modified acid-fast staining method used in the study is more sensitive than modified acid-fast staining alone [19]. Furthermore, we took strict quality control measures (the details were described in the Methods section) to overcome this limitation. Finally, this study was restricted to four rural townships, which hardly represents the overall status of the whole region. The study had relatively little sampling, so the distribution of sampling could be biased if interpolating the whole county. In future research, more evenly distributed sampling sites are required to confirm these results.

5. Conclusions

Despite the relatively low prevalence reported in this study, Cryptosporidium infection still remains an important public health issue in Jintan County. These findings call for effective sustainable interventions, including family and school-based hygienic education, to be strengthened to reduce the risk of infection among the susceptible population. Based on these findings, molecular techniques are recommended to explore the sources of infection. An early warning system based on a spatiotemporal model with risk factors is required to further improve the effectiveness and efficiency of cryptosporidiosis control in the future.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-4601/15/5/924/s1, Table S1: Details of the questionnaire in the study.

Author Contributions

Zhen Ding and Wenbiao Hu conceived and designed the study. Hao Zheng, Li Wang, and Jianfeng He performed all the procedures. Hao Zheng was responsible for literature review, statistical analysis, and wrote the manuscript. Wenbiao Hu, Zhen Ding, and Rong Zhang contributed to the interpretation and discussion of the results, and edited the manuscript. All authors read and approved the final manuscript.

Acknowledgments

The authors are grateful for the valued help of the staff of Jintan CDC. The study was supported by Jiangsu Health International Exchange Program sponsorship (JSH-2017-003) and Key Talent Project for Medical Young Scholar of Jiangsu Province (QNRC2016551).

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

The following abbreviations are used in the manuscript:
OROdds Ratios
CIConfidence Intervals
CDCCenter for Disease Control and Prevention
cORcrude Odds Ratios
aORadjusted Odds Ratios
EBKEmpirical Bayesian Kriging
RRRelative Risk

References

  1. White, A.C., Jr. Cryptosporidiosis and the ears of the hippopotamus. Clin. Infect. Dis. 2010, 50, 1373–1374. [Google Scholar] [PubMed]
  2. Mahmoudi, M.R.; Ongerth, J.E.; Karanis, P. Cryptosporidium and cryptosporidiosis: The Asian perspective. Int. J. Hyg. Environ. Health 2017, 220, 1098–1109. [Google Scholar] [CrossRef] [PubMed]
  3. Laupland, K.B.; Church, D.L. Population-based laboratory surveillance for Giardia sp. and Cryptosporidium sp. Infections in a large canadian health region. BMC Infect. Dis. 2005, 5, 72. [Google Scholar] [CrossRef] [PubMed]
  4. Chen, X.M.; Keithly, J.S.; Paya, C.V.; LaRusso, N.F. Cryptosporidiosis. N. Engl. J. Med. 2002, 346, 1723–1731. [Google Scholar] [CrossRef] [PubMed]
  5. Mor, S.M.; Tzipori, S. Cryptosporidiosis in children in sub-saharan africa: A lingering challenge. Clin. Infect. Dis. 2008, 47, 915–921. [Google Scholar] [CrossRef] [PubMed]
  6. Tumwine, J.K.; Kekitiinwa, A.; Nabukeera, N.; Akiyoshi, D.E.; Rich, S.M.; Widmer, G.; Feng, X.; Tzipori, S. Cryptosporidium parvum in children with diarrhea in Mulago hospital, Kampala, Uganda. Am. J. Trop. Med. Hyg. 2003, 68, 710–715. [Google Scholar] [PubMed]
  7. Kotloff, K.L.; Nataro, J.P.; Blackwelder, W.C.; Nasrin, D.; Farag, T.H.; Panchalingam, S.; Wu, Y.; Sow, S.O.; Sur, D.; Breiman, R.F.; et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the global enteric multicenter study, gems): A prospective, case-control study. Lancet 2013, 382, 209–222. [Google Scholar] [CrossRef]
  8. Checkley, W.; Epstein, L.D.; Gilman, R.H.; Black, R.E.; Cabrera, L.; Sterling, C.R. Effects of cryptosporidium parvum infection in Peruvian children: Growth faltering and subsequent catch-up growth. Am. J. Epidemiol. 1998, 148, 497–506. [Google Scholar] [CrossRef] [PubMed]
  9. Agnew, D.G.; Lima, A.A.; Newman, R.D.; Wuhib, T.; Moore, R.D.; Guerrant, R.L.; Sears, C.L. Cryptosporidiosis in northeastern Brazilian children: Association with increased diarrhea morbidity. J. Infect. Dis. 1998, 177, 754–760. [Google Scholar] [CrossRef] [PubMed]
  10. Checkley, W.; White, A.C., Jr.; Jaganath, D.; Arrowood, M.J.; Chalmers, R.M.; Chen, X.M.; Fayer, R.; Griffiths, J.K.; Guerrant, R.L.; Hedstrom, L.; et al. A review of the global burden, novel diagnostics, therapeutics, and vaccine targets for Cryptosporidium. Lancet Infect. Dis. 2015, 15, 85–94. [Google Scholar] [CrossRef]
  11. Han, F.; Tan, W.X.; Zhou, X.L. Two case reports of cryptosporidiosis in Nanjing. Jiangsu Med. J. 1987, 13, 692. [Google Scholar]
  12. Lv, S.; Tian, L.G.; Liu, Q.; Qian, M.B.; Fu, Q.; Steinmann, P.; Chen, J.X.; Yang, G.J.; Yang, K.; Zhou, X.N. Water-related parasitic diseases in China. Int. J. Environ. Res. Public Health 2013, 10, 1977–2016. [Google Scholar] [CrossRef] [PubMed]
  13. Jiang, Y.; Ren, J.; Yuan, Z.; Liu, A.; Zhao, H.; Liu, H.; Chu, L.; Pan, W.; Cao, J.; Lin, Y.; et al. Cryptosporidium andersoni as a novel predominant Cryptosporidium species in outpatients with diarrhea in jiangsu province, China. BMC Infect. Dis. 2014, 14, 555. [Google Scholar] [CrossRef] [PubMed]
  14. Liu, H.; Shen, Y.; Yin, J.; Yuan, Z.; Jiang, Y.; Xu, Y.; Pan, W.; Hu, Y.; Cao, J. Prevalence and genetic characterization of Cryptosporidium, enterocytozoon, giardia and cyclospora in diarrheal outpatients in China. BMC Infect. Dis. 2014, 14, 25. [Google Scholar] [CrossRef] [PubMed]
  15. Yu, Z.; Li, F.; Zeng, Z.; Huang, Z.; Fan, Z.; Jin, Y.; Luo, W.; Xiang, X.; Deng, Q. Prevalence and clinical significance of Cryptosporidium infection in patients with hepatitis b virus-associated acute-on-chronic liver failure. Int. J. Infect. Dis. 2011, 15, e845–848. [Google Scholar] [CrossRef] [PubMed]
  16. Wang, K.X.; Li, C.P.; Wang, J.; Pan, B.R. Epidemiological survey of cryptosporidiosis in Anhui province China. World J. Gastroenterol. 2002, 8, 371–374. [Google Scholar] [CrossRef] [PubMed]
  17. Muchiri, J.M.; Ascolillo, L.; Mugambi, M.; Mutwiri, T.; Ward, H.D.; Naumova, E.N.; Egorov, A.I.; Cohen, S.; Else, J.G.; Griffiths, J.K. Seasonality of Cryptosporidium oocyst detection in surface waters of meru, kenya as determined by two isolation methods followed by pcr. J. Water Health 2009, 7, 67–75. [Google Scholar] [CrossRef] [PubMed]
  18. Jagai, J.S.; Castronovo, D.A.; Monchak, J.; Naumova, E.N. Seasonality of cryptosporidiosis: A meta-analysis approach. Environ. Res. 2009, 109, 465–478. [Google Scholar] [CrossRef] [PubMed]
  19. Lu, J.; Li, C.P. The survey of cryptosporidium infection among young children in kindergartens in Anhui province. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi 2004, 22, 331–333. [Google Scholar] [CrossRef]
  20. Chen, Y.G.; Yao, F.B.; Li, H.S.; Shi, W.S.; Dai, M.X.; Lu, M. Cryptosporidium infection and diarrhea in rural and urban areas of jiangsu, people's republic of china. J. Clin. Microbiol. 1992, 30, 492–494. [Google Scholar] [PubMed]
  21. Yang, Y.; Zhou, Y.B.; Xiao, P.L.; Shi, Y.; Chen, Y.; Liang, S.; Yihuo, W.L.; Song, X.X.; Jiang, Q.W. Prevalence of and risk factors associated with cryptosporidium infection in an underdeveloped rural community of southwest China. Infect. Dis. Poverty 2017, 6, 2. [Google Scholar] [CrossRef] [PubMed]
  22. Al-Delaimy, A.K.; Al-Mekhlafi, H.M.; Nasr, N.A.; Sady, H.; Atroosh, W.M.; Nashiry, M.; Anuar, T.S.; Moktar, N.; Lim, Y.A.; Mahmud, R. Epidemiology of intestinal polyparasitism among orang asli school children in rural Malaysia. PLoS Negl. Trop. Dis. 2014, 8, e3074. [Google Scholar] [CrossRef] [PubMed]
  23. Wegayehu, T.; Adamu, H.; Petros, B. Prevalence of giardia duodenalis and cryptosporidium species infections among children and cattle in north Shewa zone, Ethiopia. BMC Infect. Dis. 2013, 13, 419. [Google Scholar] [CrossRef] [PubMed]
  24. de Lucio, A.; Amor-Aramendia, A.; Bailo, B.; Saugar, J.M.; Anegagrie, M.; Arroyo, A.; Lopez-Quintana, B.; Zewdie, D.; Ayehubizu, Z.; Yizengaw, E.; et al. Prevalence and genetic diversity of giardia duodenalis and Cryptosporidium spp. Among school children in a rural area of the Amhara region, north-west Ethiopia. PLoS ONE 2016, 11, e0159992. [Google Scholar] [CrossRef] [PubMed]
  25. Quihui-Cota, L.; Morales-Figueroa, G.G.; Javalera-Duarte, A.; Ponce-Martinez, J.A.; Valbuena-Gregorio, E.; Lopez-Mata, M.A. Prevalence and associated risk factors for giardia and cryptosporidium infections among children of northwest Mexico: A cross-sectional study. BMC Public Health 2017, 17, 852. [Google Scholar] [CrossRef] [PubMed]
  26. Ajjampur, S.S.; Liakath, F.B.; Kannan, A.; Rajendran, P.; Sarkar, R.; Moses, P.D.; Simon, A.; Agarwal, I.; Mathew, A.; O’Connor, R.; et al. Multisite study of cryptosporidiosis in children with diarrhea in India. J. Clin. Microbiol. 2010, 48, 2075–2081. [Google Scholar] [CrossRef] [PubMed]
  27. Al-Mohammed, H.I.; Amin, T.T.; Aboulmagd, E.; Hablus, H.R.; Zaza, B.O. Prevalence of intestinal parasitic infections and its relationship with socio–demographics and hygienic habits among male primary schoolchildren in Al–Ahsa, Saudi Arabia. Asian Pac. J. Trop. Med. 2010, 3, 906–912. [Google Scholar] [CrossRef]
  28. Speich, B.; Croll, D.; Furst, T.; Utzinger, J.; Keiser, J. Effect of sanitation and water treatment on intestinal protozoa infection: A systematic review and meta-analysis. Lancet Infect. Dis. 2016, 16, 87–99. [Google Scholar] [CrossRef]
  29. Wani, S.A.; Ahmad, F.; Zargar, S.A.; Ahmad, Z.; Ahmad, P.; Tak, H. Prevalence of intestinal parasites and associated risk factors among schoolchildren in Srinagar city, Kashmir, India. J. Parasitol. 2007, 93, 1541–1543. [Google Scholar] [CrossRef] [PubMed]
  30. Chin, Y.T.; Lim, Y.A.; Chong, C.W.; Teh, C.S.; Yap, I.K.; Lee, S.C.; Tee, M.Z.; Siow, V.W.; Chua, K.H. Prevalence and risk factors of intestinal parasitism among two indigenous sub-ethnic groups in Peninsular Malaysia. Infect. Dis. Poverty 2016, 5, 77. [Google Scholar] [CrossRef] [PubMed]
  31. Checkley, W.; Gilman, R.H.; Epstein, L.D.; Suarez, M.; Diaz, J.F.; Cabrera, L.; Black, R.E.; Sterling, C.R. Asymptomatic and symptomatic cryptosporidiosis: Their acute effect on weight gain in Peruvian children. Am. J. Epidemiol. 1997, 145, 156–163. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The study area, involving townships A, B, C, and D, studied public primary schools, and studied kindergartens in the study.
Figure 1. The study area, involving townships A, B, C, and D, studied public primary schools, and studied kindergartens in the study.
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Figure 2. Spatial cluster and prevalence of Cryptosporidium infection in the study.
Figure 2. Spatial cluster and prevalence of Cryptosporidium infection in the study.
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Figure 3. Spatial visualization of Cryptosporidium infection in Jintan County.
Figure 3. Spatial visualization of Cryptosporidium infection in Jintan County.
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Table 1. Characteristics of the participants in this study.
Table 1. Characteristics of the participants in this study.
VariablesNo. of Participants%
Total1637100
Gender
 Male86452.8
 Female77347.2
Age (years)
 3–686352.7
 7–977447.3
Location (Township)
 A33020.2
 B24214.8
 C32419.8
 D74145.3
Supplied with piped water
 Yes159497.4
 No432.6
Presence of toilets at household
 Yes158096.5
 No573.5
Raising livestock or poultry (e.g., cattle, sheep, chicken)
 Yes75646.2
 No88153.8
Contact with pets (e.g., dog, cat)
 Yes41625.4
 No122174.6
Table 2. Univariable and multivariable analyses of risk factors associated with Cryptosporidium infection in this study (n = 1637).
Table 2. Univariable and multivariable analyses of risk factors associated with Cryptosporidium infection in this study (n = 1637).
VariablesExamined nInfected n (‰)cOR (95% Cl)paOR (95% Cl)p
Gender
 Male8648 (9)0.713 (0.280–1.815)0.4760.713(0.278–1.828)0.481
 Female77310 (13)1
Age (years)
 3–686314 (16)3.175 (1.041–9.709)0.0323.072 (1.001–9.427)0.050
 7–97744 (5)1
Location (Township)
 A3303 (9)1.000.03110.244
 B2420 (0)0.000.2660.000.995
 C3241 (3)0.337 (0.035–3.261)0.6240.354 (0.036–3.438)0.371
 D74114 (19)2.099 (0.599–7.354)0.2362.196 (0.624–7.734)0.221
Supplied with piped water
 No430 (0.0)0.001.000
 Yes159418 (11)1
Presence of toilets at household
 Yes158017 (11)0.609 (0.080–4.651)0.473
 No571 (18)1
Raising livestock or poultry
 Yes7567 (9)0.739 (0.285–1.915)0.533
 No88111 (12)1
Contact with pets (e.g., dog, cat)
 Yes4163 (7)0.584 (0.168–2.028)0.559
 No122115 (12)1
Boiling water before drinking
 Yes136115 (11)1.014 (0.292–3.521)1.000
 No2763 (11)1
Swimming in one month
 Yes1041 (10)0.866 (0.114–6.579)1.000
 No153317 (11)1
Travelling in six months
 Yes2692 (7)0.632 (0.145–2.770)0.770
 No136816 (12)1
Contact with water facilities in one month
 Yes740 (0)0.001.000
 No156318 (12)1
Contact with a person with diarrhea in three months
 Yes2644 (15)1.492 (0.488–4.566)0.700
 No137314 (10)1
Washing hands before eating and after defecation
 No75313 (17)3.088 (1.096–8.703)0.0253.003 (1.060–8.511)0.039
 Yes8845 (6)1
Table 3. Details of spatial cluster of Cryptosporidium infection in Township D.
Table 3. Details of spatial cluster of Cryptosporidium infection in Township D.
ClusterRadius (km)Number of Observed CasesNumber of Expected CasesPopulationRRp
Primary2.86148.16156024.2200.025

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MDPI and ACS Style

Zheng, H.; He, J.; Wang, L.; Zhang, R.; Ding, Z.; Hu, W. Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China. Int. J. Environ. Res. Public Health 2018, 15, 924. https://doi.org/10.3390/ijerph15050924

AMA Style

Zheng H, He J, Wang L, Zhang R, Ding Z, Hu W. Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China. International Journal of Environmental Research and Public Health. 2018; 15(5):924. https://doi.org/10.3390/ijerph15050924

Chicago/Turabian Style

Zheng, Hao, Jianfeng He, Li Wang, Rong Zhang, Zhen Ding, and Wenbiao Hu. 2018. "Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China" International Journal of Environmental Research and Public Health 15, no. 5: 924. https://doi.org/10.3390/ijerph15050924

APA Style

Zheng, H., He, J., Wang, L., Zhang, R., Ding, Z., & Hu, W. (2018). Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China. International Journal of Environmental Research and Public Health, 15(5), 924. https://doi.org/10.3390/ijerph15050924

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