The association between Acute Lymphoblastic Leukemia in children and Helicobacter pylori as the marker for sanitation
 Pengiran Hishamuddin^{1}Email author
https://doi.org/10.1186/175605005345
© Hishamuddin; licensee BioMed Central Ltd. 2012
Received: 8 March 2012
Accepted: 18 June 2012
Published: 3 July 2012
Abstract
Background
Greaves “delayed infection” hypothesis suggested that Acute Lymphoblastic Leukemia (ALL) in children is caused by a lack of exposure to infection in infancy, which may be due higher standards of sanitation. We have conducted an ecologic analysis of the relationship between sanitation, using Helicobacter pylori (H. pylori) as the marker, and the incidence of childhood ALL in 127 cancer registries from 28 countries.
Results
There were inverse associations between H. pylori prevalence and ALL incidence rates in children. These associations were minor and only significant for ALL incidence rates for all cancer registries. They became nonsignificant and smaller in magnitude when the population source and/or the GNP per capita were added to the relationship. Furthermore, these results were unchanged when the associations were examined using the Generalized Estimating Equations.
Conclusions
Although the findings showed lower prevalence of H. pylori and improved sanitation is associated with increased incidence of childhood ALL, they do not conclusively support Greaves “delayed infection” hypothesis.
Keywords
Public health Epidemiology OncologyBackground
Leukemia is the most common cancer in children [1]. The major types of childhood leukemia are acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML) [1, 2]. ALL accounts for the majority of childhood leukemia [1, 2]. The incidence of childhood ALL has increased over the past 20 years [1, 2]. This trend is more apparent among 2 to 5 years and in developed countries [1–3].
Genetic alterations occurring during fetal development increase the risk of childhood ALL [4, 5]. However, these genetic factors are insufficient for leukemogenesis, which appears to require a “second hit” [6]. One potential mechanisms of such “second hit” transition is proposed by the “delayed infection” (or Greaves) hypothesis [7]. According to the Greaves’ hypothesis, ALL in children is caused by a lack of exposure to infections in infancy. This inadequate exposure to infections in infancy leads to failure of modulation in the immune system, which involves changes to certain Tcells [7]. Exposure to one or more common bacterial or viral infections later in life, for example after mixing with carriers such as children in playgroups or schools [8, 9], then results in an abnormal immune response and eventually ALL. This delayed infection may be due to improved sanitary conditions found in modern lifestyles [7]. Greaves’ “delayed infection” hypothesis is conceptually similar to the “hygiene hypothesis” that has been proposed to explain allergies, asthma and type 1 diabetes [10]. The “hygiene hypothesis” suggests that early childhood infections are needed to promote the development of the immune system and to suppress allergic and autoimmune disorders.
This study examines Greaves’ “delayed infection” hypothesis by looking at whether level of sanitation is associated with the incidence rates of childhood ALL in different countries. In this study we use Helicobacter pylori (H. pylori) as a marker of sanitation. H. pylori is an ubiquitous bacterium affecting a large percentage of the world’s population [11]. Prevalence of H. pylori is greater in people who reside in conditions with inadequate saniation [12]. Therefore, lower prevalence of H. pylori is associated with improved sanitation and lack of exposure to infections. Under the “delayed infection” hypothesis countries with lower prevalence of H. pylori are expected to have a higher incidence rate of childhood ALL and vice versa.
Methods
ALL incidence rates
The ALL incidence rates (per 100, 000 persons) in 0 to 4 years old children obtained from the monograph, Cancer Incidence in Five Continents, Volume VIII, published jointly by the International Agency for Research on Cancer (IARC) and the International Association of Cancer Registries (IARC) [13]. Data were available from 185 cancer registries in 56 countries. However, the analyses were confined to those countries in which corresponding H. pylori prevalence rates for children were available. These comprised 28 countries that include 127 cancer registries. All the data were collected between 1991 and 1998, with the majority (78%) collected between 1993 and 1997.
Weighted ALL incidence rates
Weighted ALL incidence rates, which is the pooled estimate of the ALL incidence rates for cancer registries in a country, were calculated using the inverse variance method where larger studies are given more weight than smaller studies [14]. If I_{i}, (i = 1,2 …), is the ALL incidence rate for the i^{th} cancer registry in a country, then the weighted ALL incidence rate for the entire country is defined as (∑ I_{ i }w_{ i }) / (∑ w_{ i }), where the registryspecific weight (w_{i}) equals 1/(s_{i}^{2}) and s_{i}^{2} represents the variance of the I_{i} estimate. As ALL incidence rates are binomially distributed, the variance (s_{i}^{2}) for the ALL incidence rate for each individual cancer registry was obtained using the formula s^{2}_{ i } = n_{ i }I_{ i }(1I_{ i }), where n_{i} (i = 1, 2 …) is the population size of children aged 0 to 4 years old in the i^{th} cancer registry, and I_{i} (i = 1, 2 …) is the ALL incidence rate for the i^{th} cancer registry in a country [15].
H. pylori prevalence rates
The prevalence rates (per 100 persons) of H. pylori infection in children from 26 countries were obtained from studies reviewed by Torres et al [16]. To supplement these data, a Medline search of articles using the search term Helicobacter pylori and prevalence was conducted and H. pylori prevalence rates for two additional countries, Singapore [17] and Thailand [18], were found.

Studies which looked exclusively at infants aged 0 to 1 years old were excluded, as the H. pylori prevalence in this age group, especially when measured using the serological assays, could be influenced by maternal IgG antibodies that were transferred to the child [16].

The maximum age of children in the studies was limited to 10 years old as the most relevant group for ALL children is under this age [1–3].

Studies with children 1 to 4 years old were preferred, and if this was not available then the next youngest age group was selected.
Covariates
Certain characteristics of the H. pylori studies were considered as potential confounders. All H. pylori surveys were characterized as either clinicbased or populationbased. Clinicbased surveys can be affected by selection bias because participants in these studies may have higher socioeconomic status and live in better sanitary conditions [16]. As a result H. pylori prevalence rates are more likely to be lower in clinicbased samples. Another potential confounder was the method of H. pylori detection. The studies used either the urea breath test or serological assays of IgG antibodies. The H. pylori prevalence rates differ depending on which method was utilized, and this is due to the different sensitivities and specificities associated with these diagnostic tests [19]. The degree of urbanization in the area where the studies were conducted was also a potential confounder as H. pylori prevalence rates have been shown to be higher in more urban areas [16]. The minimum and maximum ages of children in the studies, were considered potential confounders as H. pylori prevalence rates and ALL incidence rates are known to change according to age groups [16]. H. pylori prevalence rates also vary according to geographic locations [16, 19], and therefore the regional location of a country was considered a potential confounder. To examine this, all countries that provided the data for analyses were categorized according to the World Health Organization (WHO) regions [20]. The data for each country also included the interval between the year of the ALL incidence and the year when the H. pylori survey was conducted.
Characteristics of the countries considered in this study included the Gross National Product (GNP) per capita, Human Development Index (HDI) and the population size. GNP per capita is defined as the dollar value of a country’s final output of goods and services in a year, divided by its population size [21]. This reflects the average income of a country’s citizens. HDI measures a country’s average achievements in human development [22]. It consists of three components – life expectancy at birth, education levels, and standards of living as measured by the Gross Domestic Product per capita. GNP per capita and HDI are considered to be markers for the level of affluence and development of a country, and also potential confounders for H. pylori prevalence and ALL incidence rates. This is because countries with higher GNP per capita and HDI typically have improved levels of sanitation and healthcare, and are likely to have lower H. pylori prevalence and higher ALL incidence rates. For each country, the analytic dataset included the GNP per capita and the population size corresponding to the year the H. pylori study [21]. The United Nations Development Program releases HDI data every 5 years [22]. The specific HDI value was selected based in its proximity to the H. pylori survey.
Statistical analyses
The ALL incidence rates were considered using two methods: the weighted method combined the data from all cancer registries is each country (n = 28) and the nonweighted method included data from each cancer registry separately (n = 127). The H. pylori prevalence rate was continuously entered into all the models.
The minimum and maximum age of children in the H. pylori studies, the interval between the ALL incidence and H. pylori surveys, the GNP per capita, the HDI, and the population size were treated as continuous variables. The method of H. pylori detection (urea breath test versus serological assay), the population source (clinicbased versus communitybased), the level of urbanization (urban, rural or both) and the WHO region (Africa, Americas, South East Asia, Europe and Western Pacific) were treated as categorical variables.
All analyses were performed using the software SAS 9.1.3.
Univariate analyses
PROC UNIVARIATE was used to look at the normal distributions, mean, median, and standard deviation of all continuous variables. PROC FREQ was used to produce counts and cross tabulation tables for all categorical variables. Both the continuous and categorical variables were examined for missing values and extreme outliers.
Both outcome variables (the weighted ALL incidence rates for each country and the ALL incidence rates for all cancer registries) were normally distributed. Only one other continuous covariate, the interval between ALL incidence and H. pylori surveys, was normally distributed. No issues with regards to missing values were found in all the continuous and categorical variables. No problems with extreme outliers were identified in continuous variables.
Bivariate analyses

Both outcome variables and the H. pylori prevalence rates.

Both outcome variables and the other continuous covariates.

The H. pylori prevalence rates and the other continuous covariates.

The other continuous covariates with each other.
The r^{2} value, which denotes the percentage of variation in the dependent outcome variable which is accounted for by the independent exposure variable or covariates, and the significance of the correlation (pvalue of less than 0.05) was looked at. Pearson’s method was used to look at the correlation between both outcome variables and the interval between ALL incidence and H. pylori surveys. This method was applied as both the outcome variables and this continuous covariate were normally distributed. Spearman’s method was used for all other correlations as at least one continuous variable then was not normally distributed. For categorical variables, PROC GLM or PROC ANOVA was performed to look at the mean, standard deviation and significance (pvalue of less than 0.05) of the prevalence of both outcome variables, H. pylori prevalence rate, the other continuous and categorical covariates, in each category of the categorical covariates.
Bivariate analyses: the correlations between ALL incidence, H. pylori prevalence and characteristics of H. pylori studies/countries (n = 28)

H. pylori prevalence rates and GNP per capita (r^{2} = −0.60, pvalue = 0.0007).

H. pylori prevalence rates and HDI (r^{2} = −0.57, pvalue = 0.002).

GNP per capita and HDI (r^{2} = 0.95, pvalue = <0.0001)
Bivariate analyses: the correlations between ALL incidence, H. pylori prevalence and characteristics of H. pylori studies/countries (n = 127)
The correlations between all continuous variables when the ALL incidence rates for all cancer registries in all countries (n = 127) were modeled were calculated using PROC CORR. Pearson’s method was used for the correlations between the ALL incidence rates for all cancer registries in all countries and the interval between the ALL incidence and the H. pylori surveys, as both these variables were normally distributed. Spearman’s method was used for all other correlations as at least one continuous variable then was not normally distributed. The ALL incidence rates for all cancer registries in all countries was negatively correlated to the H. pylori prevalence rates but this was not significant (r^{2} = −0.17, pvalue = 0.05). The covariates which were not significantly correlated with both the ALL incidence rates for all cancer registries and the H. pylori prevalence rates were the maximum age of children in the H. pylori studies and the interval between the ALL incidence and the H. pylori surveys. These 2 covariates could potentially be excluded from the model.

ALL incidence rates for all cancer registries and GNP per capita (r^{2} = 0.38, pvalue = <0.0001)

ALL incidence rates for all cancer registries and HDI (r^{2} = 0.41, pvalue = <0.0001)

ALL incidence rates for all cancer registries and population size of countries (r^{2} = −0.21, pvalue = 0.019).

H. pylori prevalence rates and GNP per capita (r^{2} = −0.43, pvalue = <0.0001).

H. pylori prevalence rates and the HDI (r^{2} = −0.40, pvalue = <0.0001).

H. pylori prevalence rates and the population size of countries (r^{2} = 0.54, pvalue = <0.0001).

H. pylori prevalence rates and the minimum age of children in the H. pylori studies (r^{2} = 0.24, pvalue = 0.003).

GNP per capita and the HDI (r2 = 0.97, pvalue = <0.0001).

GNP per capita and population size (r2 = −0.25, pvalue = 0.005).

HDI and population size of countries (r2 = −0.26, pvalue = 0.003).
Bivariate analyses: the relation of ALL incidence, H. pylori prevalence, the minimum and maximum age of children, the interval between ALL incidence and H. pylori surveys, GNP per capita, HDI and population size to various characteristics of H. pylori studies (n = 28)
PROC GLM was performed to look at the mean, standard deviation and significance (pvalue of less than 0.05) of the prevalence of the weighted ALL incidence rates for each country, the H. pylori prevalence rates and the other continuous covariates, in each category of the categorical covariates (which were certain characteristics of the H. pylori studies). The prevalence of both the weighted ALL incidence rates for each country and the H. pylori prevalence rates was not significant in the method of H. pylori used in the H. pylori studies. This covariate could potentially be excluded from the model.

The prevalence of H. pylori prevalence rates in the population source used in the H. pylori survey (p = 0.04), the level of urbanization in the H. pylori studies (p = 0.02) and the region a country is situated (p = 0.0003).

The prevalence of GNP per capita in the level of urbanization in the H. pylori studies (p = 0.02).

The prevalence of HDI in the level of urbanization in the H. pylori studies (p = 0.008) and the region a country is situated (p = <0.0001).
Bivariate analyses: the relation of ALL incidence, H. pylori prevalence, the minimum and maximum age of children, the interval between ALL incidence and H. pylori surveys, GNP per capita, HDI and population size to various characteristics of H. pylori studies (n = 127)
PROC GLM were performed to look at the mean, standard deviation and significance (pvalue of less than 0.05) of the prevalence of the ALL incidence rates for all cancer registries, the H. pylori prevalence rates and the other continuous covariates, in each category of the categorical covariates (which were certain characteristics of the H. pylori studies). The prevalence of both the ALL incidence rates for all cancer registries and the H. pylori prevalence rates was not significant in the method of H. pylori detection used in the H. pylori studies. This covariate could potentially be excluded from the model.

The prevalence of the ALL incidence rates for all cancer registries in the population source used in the H. pylori survey (p = 0.038), the level of urbanization in the H. pylori studies (p = 0.002) and the region a country is situated (p = 0.0008).

The prevalence of H. pylori prevalence rates in the population source used in the H. pylori survey (p = <0.0001), the level of urbanization in the H. pylori studies (p = <0.0001) and the region a country is situated (p = <0.0001).

The prevalence of GNP per capita in the level of urbanization in the H. pylori studies (p = <0.0001) and the region a country is situated (p = <0.0001).

The prevalence of HDI in the population source used in the H. pylori survey (p = 0.004), the level of urbanization in the H. pylori studies (p = <0.0001) and the region a country is situated (p = <0.0001).

The prevalence of the population size of countries in the population source used in the H. pylori survey (p = 0.0006), the level of urbanization in the H. pylori studies (p = <0.0001) and the region a country is situated (p = <0.0001).
Bivariate analyses: the associations among various characteristics of H. pylori studies (n = 28)
PROC ANOVA were performed to look at the mean, standard deviation and significance (pvalue of less than o.05) of the prevalence of the categorical covariates in each other, when the weighted ALL incidence rates in each country was modeled.

The prevalence of the population source used in the H. pylori survey in the level of urbanization in the H. pylori studies (p = 0.007).
Bivariate analyses: the associations among various characteristics of H. pylori studies (n = 127)
PROC ANOVA were performed to look at the mean, standard deviation and significance (pvalue of less than 0.05) of the prevalence of the categorical covariates in each other, when the ALL incidence rates in all cancer registries were modeled.

The population source used in the H. pylori survey in the level of urbanization in the H. pylori studies (p = <0.0001).

The level of urbanization in the H. pylori studies in the population source used in the H. pylori survey (p = 0.002) and the region a country is situated (p = <0.0001).
Covariates or confounders excluded from further analyses
Covariates which were not correlated or associated with either H. pylori prevalence of ALL incidence rates were not included in the model. The confounders that remained were examined for collinearity. When this existed one confounder was chosen to be included in the model based on the strength of its correlation or association to either H. pylori prevalence or ALL incidence rates.
Continuous covariates or confounders excluded from further analyses
GNP per capita and the HDI were positively correlated with ALL incidence rates. This correlation was not significant when weighted ALL incidence rates were modeled (GNP per capita: r^{2} = 0.22, pvalue = 0.26; HDI: r^{2} = 0.18, pvalue = 0.36) but was significant when the ALL incidence rates for all cancer registries were modeled (GNP per capita: r^{2} = 0.38, pvalue = <0.0001; HDI: r^{2} = 0.41, pvalue = <0.0001). GNP per capita and the HDI were negatively correlated with the H. pylori prevalence rates. For example, when the ALL incidence rates for all cancer registries were used as the outcome variable, the correlation between H. pylori prevalence rates and GNP per capita had a r^{2} of −0.43 and a pvalue of <0.0001 whereas the correlation between H. pylori prevalence rates and HDI had a r^{2} of −0.40 and a pvalue of <0.0001. GNP per capita and HDI were highly correlated to each other. For example, when the weighted ALL incidence rates for each country were used in the model, the correlation between these two was significantly positive with a r^{2} of 0.95 and a pvalue of <0.0001. This meant that both covariates could not be considered in the same model as doing so might lead to potential collinearity. GNP per capita was the covariate used in the further analyses based on its higher correlation to the H. pylori prevalence and ALL incidence rates.
The population size of the countries was negatively correlated with the ALL incidence rates. This correlation was significant when the ALL incidence rates for all cancer registries were modeled (r^{2} = −0.21, pvalue = 0.019). The population size of countries was positively correlated with the H. pylori prevalence rates. This correlation was significant when the outcome variable was the ALL incidence rates in all cancer registries (r^{2} = 0.54, pvalue = <0.0001). The population size of a country was negatively correlated with a confounder, GNP per capita. This correlation was significant when the ALL incidence rates for all cancer registries were modeled (r^{2} = −0.25, pvalue = 0.005). This is not surprising as the denominator in the calculation of the GNP per capita of a country is its population size. The population size of a country was therefore excluded from further analysis.
The minimum age of children in the H. pylori studies was positively correlated with the H. pylori prevalence rates. This correlation was significant when the outcome variable was the ALL incidence rates for all cancer registries (r^{2} = 0.24, pvalue = 0.003). This covariate was not consistently correlated with both ALL incidence rates. When the weighted ALL incidence rates for each country were modeled, the correlation had a r^{2} of 0.34 with a pvalue of 0.08 and when the ALL incidence rates for all cancer registries were modeled, the correlation had a r^{2} of −0.008 with a pvalue of 0.93. Therefore, the minimum age of children in the H. pylori studies was excluded from further analysis.
The maximum age of children in the H. pylori studies was not consistently correlated with both ALL incidence rates. When the weighted ALL incidence rates for each country were modeled, the correlation had a r2 of −0.23 with a pvalue of 0.24 and when the ALL incidence rates for all cancer registries were modeled, the correlation had a r2 of 0.10 with a pvalue of 0.29. This covariate was also not consistently correlated with the H. pylori prevalence rates. When the weighted ALL incidence rates for each country were modeled, the correlation with the H. pylori prevalence rates had a r^{2} of 0.24 with a pvalue of 0.21 and when the ALL incidence rates for all cancer registries were modeled, the correlation with the H. pylori prevalence rates had a r^{2} of −0.08 with a pvalue of 0.38. Therefore, the maximum age of children in the H. pylori studies was not used in the further analysis.
The interval between the ALL incidence and the H. pylori surveys was not consistently correlated with both ALL incidence rates. When the weighted ALL incidence rates for each country were modeled, the correlation had a r^{2} of 0.21 with a pvalue of 0.27 and when the ALL incidence rates for all cancer registries were modeled, the correlations had a r2 of −0.15 with a pvalue of 0.08. The interval between the ALL incidence and the H. pylori surveys was not consistently correlated with the H. pylori prevalence rates. When the weighted ALL incidence rates for each country were modeled, the correlation with the H. pylori prevalence rates had a r^{2} of −0.01 with a pvalue of 0.94 and when the outcome variable was the ALL incidence rates for all cancer registries, the correlation with the H. pylori prevalence rates had a r^{2} of −0.009 with a pvalue of 0.92. Therefore the interval between the ALL incidence and the H. pylori surveys was not used in the further analysis. This meant that the only continuous confounder in the model was GNP per capita.
Categorical covariates or confounders excluded from further analyses
The method of H. pylori detection used in the H. pylori studies was not associated with H. pylori prevalence for both ALL incidence rates. For example when the weighted ALL incident rates for each country were modeled, the association between the method of H. pylori detection used in the H. pylori studies and the H. pylori prevalence rates had a pvalue of 0.14 and between the method of H. pylori detection used in the H. pylori studies and ALL incidence rates had a pvalue of 0.08. This covariate was therefore excluded from further analysis.
The population source used in the H. pylori survey was associated with ALL incidence rates for all cancer registries (pvalue = 0.038). The type of population source used in the H. pylori survey was also associated H. pylori prevalence rates for both outcomes. For example, when the ALL incidence rates for all cancer registries were modeled, the associations between the population source used in the H. pylori survey and H. pylori prevalence rates had a pvalue of <0.0001.
The level of urbanization in the H. pylori studies was associated with ALL incidence rates for all cancer registries (pvalue = 0.002). The level of urbanization in the H. pylori studies was also associated with H. pylori prevalence rates for both outcomes. For example, when the ALL incidence rate for all cancer registries were modeled, the association between level of urbanization in the H. pylori studies and the H. pylori prevalence rates had a pvalue of <0.0001.
The region each country was situated in was associated with ALL incidence rates for all cancer registries (pvalue = 0.0008). The region each country was situated in was also associated H. pylori prevalence rates for both outcomes. For example, when the ALL incidence rates for all cancer registries were modeled, the association between region each country was situated in and H. pylori prevalence rates had a pvalue of <0.0001.
The level of urbanization in the H. pylori studies and the region each country was situated in were associated with GNP per capita. For example when the ALL incidence rates for all cancer registries were modeled, the association between GNP per capita and the level of urbanization in the H. pylori studies and between GNP per capita and the region in each country was situated both had a pvalue of <0.0001. The level of urbanization in the H. pylori studies and the region each country was situated in were excluded from further analyses as GNP per capita had a higher correlation to the H. pylori prevalence and ALL incidence rates.
Confounders included in further analyses
Therefore, confounders that remained and which did not have collinearity with each other, were GNP per capita (continuous) and the population source used in the H. pylori survey (clinicbased or communitybased samples). These two confounders were included in the final analyses.
Linear regression – unadjusted and adjusted analyses
The population source used in the H. pylori survey was analyzed using a new categorical covariate (population1) which was created using dummy variables, where the reference group is communitybased population samples. PROC REG was used to perform unadjusted linear regression analyses between the outcome variables and the H. pylori prevalence rates, and the confounders – the GNP per capita and the population source used in the H. pylori survey. PROC REG was then repeated to perform adjusted linear regression analyses between the outcome variables and the H. pylori prevalence rates, controlling for both confounders separately, and then simultaneously. For each step of the analyses the parameter estimate (coefficient), standard error and significance (pvalue of less than 0.05) was looked at. All linear regression analyses were performed twice, initially with the weighted ALL incidence rates for each country (n = 28) as the outcome variable and then repeated with the ALL incidence rates for all the cancer registries (n = 127).
Generalized Estimating Equations
Generalized Estimating Equations (GEE) [14], were used to assess the relationship between H. pylori prevalence and ALL incidence rates among the 127 cancer registries in the 28 countries, accounting for the dependency and repeated observations within countries. PROC GENMOD was used to perform unadjusted analyses between the outcome variable (which in this method is the ALL incidence rates in all cancer registries belonging to the same country) and the H. pylori prevalence rates, and the confounders – the GNP per capita and the population source used in the H. pylori survey. PROC GENMOD was then repeated to perform adjusted analyses between the outcome variable and the H. pylori prevalence rates, controlling for both confounders separately and then simultaneously. For each step of the analyses the parameter estimate (coefficient), standard error and significance (pvalue of less than 0.05) was looked at.
Regression diagnostics

The values of the outcome variable against its predicted values. This plot should look like a 45° line when the X and Y axes are scaled the same.

The studentized residuals against the predicted values for the outcome variable. If the assumption for the constant variance of errors is true then this plot should show a random scatter about 0 and the width of the scatter should be the same.

The studentized residuals against the values of the predictor variables. If the assumption for the constant variance of errors is true then this plot should show a random scatter about 0 and the width of the scatter should be the same. This plot was done for each predictor variable in the model.

Normal probability plot of errors. This checks the normality assumption.
In addition, issues with regards to influential outliers and collinearity were addressed. The assumptions for the linear regression models were met and there were no issues with regards to influential outliers and collinearity.
Ethical approval
As this study was an ecological study which utilized previously published data and which was not research involving human subjects or animals, it required no submission to IRB. This was determined in consultation with the Communicable Diseases Division, Ministry of Health, Singapore.
Results and discussion
Characteristics of H. pylori studies
Country  H. pylori prevalence^{a}  Min. age^{b}  Max. age^{c}  No.^{d}  Method^{f}  Population source^{g}  Level of urbanization^{h}  Year^{i}  Region^{k}  Reference 

Algeria  45  0  9  42  Serology  Clinic  Urban  1987  Africa  Megraud et al. [23] 
Brazil  36.7  3  5  60  Serology  Clinic  Urban  1992  Americas  Oliveira et al. [24] 
Colombia  61  2  5  373  UBT  Community  Rural  1992  Americas  Goodman et al. [25] 
Costa Rica  60  7  10  60  Serology  Community  Rural  19841988  Americas  Sierra et al. [26] 
USA  35  1  5  182  Serology  Clinic  Both  1998  Americas  Elitsur et al. [27] 
China  53  3  4  19  UBT  Community  Rural  1994  Western Pacific  Ma et al. [28] 
India  6  3  10  30  Serology  Clinic  Urban  1989  Southeast Asia  Graham et al. [29] 
Japan  12.5  1  4  56  Serology  Clinic  Urban  1994  Western Pacific  Matsukura et al. [30] 
Korea  6  1  3  52  Serology  Clinic  Both  1998^{j}  Western Pacific  Malaty et al. [31] 
Vietnam  13  0  9  61  Serology  Clinic  Urban  1987  Western Pacific  Megraud et al. [23] 
Belgium  6.4  1  5  n/a^{e}  Serology  Clinic  Both  1995 ^{j}  Europe  Blecker et al. [32] 
Estonia  4.9  9  9  94  Serology  Community  Both  19931996  Europe  Vorobja et al. [33] 
Finland  6  3  3  131  Serology  Community  Both  1980  Europe  Ashorn et al. [34] 
France  4  0  9  113  Serology  Clinic  Urban  1987  Europe  Megraud et al. [23] 
Germany  8.3  3  5  36  Serology  Clinic  Urban  1984  Europe  Hornemann et al. [35] 
Iceland  9  0  9  13  Serology  Clinic  Both  19911992  Europe  Bergenzaum et al. [36] 
Italy  22  1  10  32  Serology  Clinic  Urban  1995  Europe  Luzza et al. [37] 
Netherlands  9  6  8  80  Serology  Clinic  Urban  1993  Europe  Roosendaal et al. [38] 
Poland  16.6  3  5  60  Serology  Clinic  Urban  1996  Europe  Czkwianianc et al. [39] 
Portugal  42.6  3  6  n/a^{e}  Serology  Clinic  Urban  1994 ^{j}  Europe  Quina et al. [40] 
Russia  30  1  4  44  Serology  Community  Urban  1996  Europe  Malaty et.al [41] 
Spain  11  2  9  203  Serology  Clinic  Both  19911992  Europe  Cilla et al. [42] 
Sweden  7.7  1  4  661  Serology  Clinic  Urban  19841995  Europe  Grandstorm et al. [43] 
Switzerland  7  5  7  432  UBT  Community  Both  1998  Europe  Boltshauser et al. [44] 
Australia  25  2  4  20  Serology  Clinic  Urban  1991  Western Pacific  Hardikar et al. [45] 
Gambia  31  0  5  353  Serology  Community  Rural  1990  Africa  Sullivan et al. [46] 
Singapore  3  0  4  305  Serology  Community  Urban  1992  Western Pacific  [17] 
Thailand  74  1  4  27  Serology  Community  Urban  1990  Southeast Asia  PerezPerez et al. [18] 
Descriptive statistics for characteristics of ALL incidence and H. pylori prevalence studies/countries
ALL incidence rate (per 100,000 persons)  Mean  Median  s.d.^{b}  Frequency  (%) 

Weighted ALL incidence ^{a} (28 countries)  17.61  16.40  11.75     
Nonweighted ALL incidence rate (127 cancer registries)  21.68  21.25  12.62     
Characteristics of included countries (n = 28)  
Gross National Product per capita for countries (USD$)  11375.79  9520.00  1182.10     
Human Development Index for countries  0.80  0.87  0.14     
Population size for countries  118137528  36416282  265588002     
Characteristics of H. pylori studies (n = 28)  
H. pylori prevalence (%)  26.56  19.30  21.46     
Minimum age of children (years)  2.21  1.50  2.25     
Maximum age of children (years)  6.21  5.00  2.43     
Interval between ALL incidence and H. pylori surveys (years)  4.11  3.00  4.78     
Method of H. pylori detection  
Serological assays using IgG        25  89.29 
Urea breath test        3  10.71 
Population source  
Communitybased        10  35.71 
Clinicbased        18  64.29 
Level of urbanization  
Rural        4  14.29 
Urban        16  57.14 
Both rural and urban        8  28.57 
Region  
Africa        2  7.14 
Americas        4  14.29 
Southeast Asia        2  7.14 
Europe        14  50.00 
Western Pacific        6  21.43 
Confounders which did not have any collinearity with each other were GNP per capita (continuous) and the population source used in the H. pylori surveys (clinicbased or communitybased samples). These were included in the further analyses.
There was a negative association between H. pylori prevalence and ALL incidence rates. This was nonsignificant when the weighted ALL incidence rates for each country were used in the model (parameter estimate = −0.10, standard error = 0.11, pvalue = 0.35), However when the ALL incidence rates for all cancer registries were modelled this association became significant (parameter estimate = −0.14, standard error = 0.05, pvalue = 0.01, R^{2} = 0.0485).
There was a positive association between ALL incidence rates and both confounders – the population source in the H. pylori surveys and the GNP per capita. This association was nonsignificant for the weighted ALL incidence rates (the population source used in the H. pylori surveys: parameter estimate = 2.98, standard error = 4.69, pvalue = 0.53; GNP per capita: parameter estimate = 0.0001, standard error = 0.0002, pvalue = 0.55), but became significant when the ALL incidence rates for all cancer registries were included separately (the population source used in the H. pylori surveys: parameter estimate = 5.40, standard error = 2.57, pvalue = 0.04; GNP per capita: parameter estimate = 0.0003, standard error = 0.00009, pvalue = 0.0004, R^{2} = 0.0953).
The effect of the association between the ALL incidence rates for all cancer registries and the H. pylori prevalence rates were attenuated (became nonsignificant) slightly when it was adjusted for the population source used in the H. pylori surveys (parameter estimate = −0.11, standard error = 0.06, pvalue = 0.06). This attenuation was more pronounced when the analysis was adjusted for GNP per capita (parameter estimate = −0.05, standard error = 0.06, pvalue = 0.41) and changed further when the analysis was adjusted for both the population source used in the H. pylori surveys and GNP per capita (parameter estimate = −0.02, standard error = 0.07, pvalue = 0.82).
Generalized Estimating Equations (GEE) [14] were used to assess the relationship between H. pylori prevalence and ALL incidence rates among the 127 cancer registries in the 28 countries, accounting for the repeated observations within countries. The results were similar to the associations found in both the unadjusted and adjusted linear regression analyses when the ALL incidence rate for all cancer registries were modelled. For example, the unadjusted analyses for the association between ALL incidence and H. pylori prevalence rates had a parameter estimate of −0.14, standard error of 0.05 and pvalue of 0.01 using both methods.
Conclusion
Smith et al. [47] showed that improved hygiene, as measured by decreased prevalence of Hepatitis A virus, is associated with higher childhood ALL incidence rates. In our study we examined whether the level of sanitation, using H. pylori as the marker, is associated with incidence rates of childhood ALL in different countries. Our analyses demonstrated inverse association between H. pylori prevalence and ALL incidence rates in children. This implies that countries, where children live in better sanitary conditions and have lower H. pylori prevalence rates, are expected to experience increased childhood ALL incidence rates. However these associations were minor and only significant for ALL incidence rates for all cancer registries (n = 127). These associations became nonsignificant and smaller in magnitude, when the population source and/or the GNP per capita were added to the relationship. Furthermore, these results were unchanged when the association were examined using the Generalised Estimating Equations. Therefore, although we showed that lower prevalence of H. pylori and improved sanitation is associated with increased incidence of childhood ALL, our findings do not conclusively support Greaves’ [9] “ delayed infection” hypothesis.
One of the strengths in our study is the use of H. pylori as a biomarker for sanitation. However, as ours was an ecological study, various weaknesses are associated with the study design [14]. One is ecologic bias. This means that even though inverse associations between H. pylori prevalence and incidence rates of childhood ALL among populations were shown, this cannot be translated into an increased risk of incidence of ALL in an individual child known to be infected by H. pylori. Doing so would be erroneous and leads to ecologic fallacy. Ecologic bias can arise as a result of biases within the group studied, confounding by groups or effect modification by groups [14]. There are also more problems in ecologic studies as compared to individuallevel studies with regards to the selection, control and analysis of confounders [14]. This was experienced in our study. In addition, ecologic studies do not provide assurance that disease occurrence did not precede exposure [14]. Temporality is an important criterion that needs to be met for causality in an exposuredisease relationship. Collinearity is another limitation as certain predictors, such as sociodemographic and environmental factors, tend to be highly correlated with each other than they are at individual level [14]. This is illustrated in our study, for example, between the level of urbanization and GNP per capita. Ecologic studies are also limited by lack of adequate data or if available, these data may not be comparable [14]. This was certainly seen in our study as there were insufficient data on H. pylori prevalence and when available, they were not comparable due to the different methodologies used in the various H. pylori studies. Another limitation is ALL incidence, especially in developing countries, may actually be higher since ALL may not have been diagnosed and recorded for all cases.
In view of the numerous weaknesses associated with ecologic studies, future studies looking at the association between sanitation and the incidence of childhood ALL should be done employing individuallevel study designs, such as case–control studies. This will be ideal as childhood ALL is a rare disease and sanitation and H. pylori are not rare exposures.
Author’s contribution
I performed all the steps involved in this study including the conceptualisation, design, acquisition of data, analysis and interpretation, including the drafting and submission of this manuscript.
Declarations
Authors’ Affiliations
References
 IARC Scientific Publications, Volume 144. International Incidence of Childhood Cancer, Vol. II. Edited by: Parkin DM, Kramaírovaí E, Draper GJ, Masuyer E, Michaelis J, Neglia J, Qureshi S, Stiller CA. 1998, Lyon, France: International Agency on Research on CancerGoogle Scholar
 Smith MA, Ries LAG, Gurney JG, Ross JA: Cancer Incidence and Survival Among Children and Adolescents: United States SEER Program 1975 – 1995. 1999, Bethesda, Maryland: National Cancer Institute, Surveillance Epidemiology and End Results (SEER) Program, Leukemia, NIH PublicationsGoogle Scholar
 Linet MS, Devesa SS: Descriptive epidemiology of childhood leukemia. Br J Cancer. 1991, 63: 424429. 10.1038/bjc.1991.98.PubMedPubMed CentralView ArticleGoogle Scholar
 Greaves MF, Wiemels J: Origins of chromosome translocations in childhood leukemia. Nat Rev Cancer. 2003, 3: 639649. 10.1038/nrc1164.PubMedView ArticleGoogle Scholar
 Greaves M: Childhood leukemia. Br Med J. 2002, 324: 283287. 10.1136/bmj.324.7332.283.View ArticleGoogle Scholar
 Greaves M: Molecular genetics, natural history and the demise of childhood leukemia. Eur J Cancer. 1991, 35: 173185.View ArticleGoogle Scholar
 Greaves MF: Aetiology of acute leukemia. Lancet. 1997, 349: 344349. 10.1016/S01406736(96)094123.PubMedView ArticleGoogle Scholar
 Ma X, Buffler PA, Selvin S, Matthay KK, Wiencke JK, Wiemels JL, Reynolds P: Daycare attendance and risk of childhood acute lymphoblastic leukemia. Br J Cancer. 2002, 86: 14191424. 10.1038/sj.bjc.6600274.PubMedPubMed CentralView ArticleGoogle Scholar
 Perrillat F, Clavel J, Auclerc MF, Baruchel A, Leverger G, Nelken B, Philippe N, Schaison G, Sommelet D, Vilmer E, Hemon D: Daycare, early common infections and childhood acute leukemia: a multicentre French case–control study. Br J Cancer. 2002, 86: 10641069. 10.1038/sj.bjc.6600091.PubMedPubMed CentralView ArticleGoogle Scholar
 WillsKarp M, Santeliz J, Karp CL: The germless theory of allergic disease: revisiting the hygiene hypothesis. Nat Rev Immunol. 2001, 1: 6975. 10.1038/35095579.PubMedView ArticleGoogle Scholar
 Go MF: Review article: natural history and epidemiology of Helicobacter pylori infection. Aliment Pharmacol Ther. 2002, 16: 315.PubMedView ArticleGoogle Scholar
 Brown LM: Helicobacter pylori: epidemiology and routes of transmission. Epidemiol Rev. 2000, 22: 283297. 10.1093/oxfordjournals.epirev.a018040.PubMedView ArticleGoogle Scholar
 Cancer Incidence in Five Five Continents. Edited by: Parkin DM, Whelan SL, Ferlay J, Teppo L, Thomas DB. 2002, France: International Agency on Research on Cancer, (IARC Scientific Publications no. 155)Google Scholar
 Modern Epidemiology. Edited by: Rothman KJ, Greenland S. 1998, Philadelphia: LippincottRaven, 2Google Scholar
 Weiss NA: Introductory Statistics. 2004, Boston: Addison Wesley, 7Google Scholar
 Torres J, PerezPerez G, Goodman KJ, Atherton JC, Gold BD, Harris PR, la Garza AM, Guarner J, Munoz O: A comprehensive review of the natural history of Helicobacter pylori infection in children. Arch Med Res. 2000, 31: 431469. 10.1016/S01884409(00)000990.PubMedView ArticleGoogle Scholar
 Committee on Epidemic Diseases Ministry of Health, Singapore: Seroprevalence of H. pylori infection in Singapore. Epidemiol News Bull. 1996, 22: 3132.Google Scholar
 PerezPerez GI, Taylor DN, Bodhidatta L, Wongsrichanalai J, Baze WB, Dunn BE, Echeverria PD, Blaser MJ: Seroprevalence of Helicobacter pylori infections in Thailand. J Infect Dis. 1990, 161: 12371241. 10.1093/infdis/161.6.1237.PubMedView ArticleGoogle Scholar
 Mittal SK, Mathew JL: Helicobacter pylori infection in children: a review. Trop Gastroenterol. 2003, 24: 106115.PubMedGoogle Scholar
 World Health Organization Regional Offices: Retrieved February 15 2010 from www.who.int
 Gross National Product per capita: Retrieved February 15 2010 from: www.worldbank.org
 Human Development Index: Retrieved February 15 2010 from: hdr.undp.org
 Megraud F, BrassensRabbe MP, Denis F, Belbouri A, Hoa DQ: Seroepidemiology of Campylobacter pylori infection in various populations. J Clin Microbiol. 1989, 27: 18701873.PubMedPubMed CentralGoogle Scholar
 Oliveira AM, Queiroz DM, Rocha GA, Mendes EN: Seroprevalence of Helicobacter pylori infection in children of low socioeconomic level in Belo Horizonte, Brazil. Am J Gastroenterol. 1994, 89: 22012204.PubMedGoogle Scholar
 Goodman KJ, Correa P, Tengana Aux HJ, Ramirez H, DeLany JP, Guerrero Pepinosa O, Lopez Quinones M, Collazos Parra T: Helicobacter pylori infection in the Colombian Andes: a populationbased study of transmission pathways. Am J Epidemiol. 1996, 144 (3): 290299. 10.1093/oxfordjournals.aje.a008924.PubMedView ArticleGoogle Scholar
 Sierra R, Munoz N, Pena AS, Biemond I, van Duijin W, Lamers CB, Teuchmann S, Hernandez S, Correa P: Antibodies to Helicobacter pylori and pepsinogen levels in children from Costa Rica: comparison of two areas with different risks for stomach cancer. Cancer Epidemiol Biomarkers Prev. 1992, 1: 449454.PubMedGoogle Scholar
 Elitsur Y, Short JP, Neace C: Prevalence of Helicobacter pylori infection in children from urban and rural West Virginia. Dig Dis Sci. 1998, 43: 773778. 10.1023/A:1018866030977.PubMedView ArticleGoogle Scholar
 Ma JL, You WC, Gail MH, Zhang L, Blot WJ, Chang YS, Jiang J, Liu WD, Hu YR, Brown LM, Xu GW, Fraumeni JF: Helicobacter pylori infection and mode of transmission in a population at high risk of stomach cancer. Int J Epidemiol. 1998, 27: 570573. 10.1093/ije/27.4.570.PubMedView ArticleGoogle Scholar
 Graham DY, Adam E, Reddy GT, Agarwal JP, Agarwal R, Evans DJ, Malaty HM, Evans DG: Seroepidemiology of Helicobacter pylori infection in India. Comparison of developing and developed countries. Dig Dis Sci. 1991, 36: 10841088. 10.1007/BF01297451.PubMedView ArticleGoogle Scholar
 Matsukura N, Onda M, Tokunaga A, Teramoto T, Fujita I, Okuda T, Yamashita K: Detection of serum IgG antibody against Helicobacter pylori from childhood in a Japanese population. J Gastroenterol. 1994, 29: 403405. 10.1007/BF02361235.PubMedView ArticleGoogle Scholar
 Malaty HM, Kim JG, Kim SD, Graham DY: Prevalence of Helicobacter pylori infection in Korean children: inverse relation to socioeconomic status despite a uniformly high prevalence in adults. Am J Epidemiol. 1996, 143: 257262. 10.1093/oxfordjournals.aje.a008736.PubMedView ArticleGoogle Scholar
 Blecker U, Lanciers S, Hauser B, Vandenplas Y: Helicobacter pylori positivity in Belgium. Acta Gastroenterol Belg. 1995, 58: 3134.PubMedGoogle Scholar
 Vorobjova T, Grunberg H, Oona M, Maaroos HI, Nilsson I, Wadstrom T, Covacci A, Uibo R: Seropositivity to Helicobacter pylori and CagA protein in schoolchildren of different ages living in urban and rural areas in Southern Estonia. Eur J Gastroenterol Hepatol. 2000, 12: 97101. 10.1097/0004273720001201000018.PubMedView ArticleGoogle Scholar
 Ashorn M, Maki M, Hallstrom M, Uhari M, Akerblom HK, Viikari J, Miettinen A: Helicobacter pylori infection in Finnish children and adolescents. A serologic crosssectional and followup study. Scand J Gastroenterol. 1995, 30: 876879. 10.3109/00365529509101594.PubMedView ArticleGoogle Scholar
 Hornemann F, Nilius M, Malfertheiner P, Bartmann P: Seroprevalence of Helicobacter pylori in German infants and children. Helicobacter. 1997, 2: 176179. 10.1111/j.15235378.1997.tb00083.x.PubMedView ArticleGoogle Scholar
 Bergenzaun P, Kristinsson KG, Thjodleifsson B, Sigvaldadottir E, Molstad S, Held M, Wadstrom T: Seroprevalence of Helicobacter pylori in south Sweden and Iceland. Scand J Gastroenterol. 1996, 31: 11571161. 10.3109/00365529609036904.PubMedView ArticleGoogle Scholar
 Luzza F, Imeneo M, Maletta M, Paluccio G, Giancotti A, Perticone F, Foca A, Pallone F: Seroepidemiology of Helicobacter pylori infection and Hepatitis A in a rural area: evidence against a common mode of transmission. Gut. 1997, 41: 164168. 10.1136/gut.41.2.164.PubMedPubMed CentralView ArticleGoogle Scholar
 Roosendaal R, Kuipers EJ, Buitenwerf J, van Uffelen C, Meuwissen SG, van Kamp GJ, VandenbrouckeGrauls CM: Helicobacter pylori and the birth cohort effect: evidence of a continuous decrease of infection rates in childhood. Am J Gastroentereol. 1997, 92: 14801482.Google Scholar
 Czkwiamiamc E, BakRomaniszyn L, MaleckaPanas E, Suski S, Woch G: Prevalence of Helicobacter pylori in children dependently on age and living conditions. J Physiol Pharmacol. 1996, 47: 203207.Google Scholar
 Quina MG: Helicobacter pylori: the Portuguese scene. Grupo de Estudo Portugues do Helicobacter pylori (GEPHP). Eur J Cancer Prev. 1994, 3 (Suppl 2): 6567.PubMedView ArticleGoogle Scholar
 Malaty HM, Paykov V, Bykova O, Ross A, Graham DP, Anneger JF, Graham DY: Helicobacter pylori and socioeconomic factors in Russia. Helicobacter. 1996, 1: 8287. 10.1111/j.15235378.1996.tb00015.x.PubMedView ArticleGoogle Scholar
 Cilla G, PerezTrallero E, GarciaBengoechea M, Marimon JM, Arenas JI: Helicobacter pylori infection: a seroepidemiology study in Gipuzkoa Basque County, Spain. Eur J Epidemiol. 1997, 13: 945949. 10.1023/A:1007480625665.PubMedView ArticleGoogle Scholar
 Granstrom M, Tindberg Y, Blennow M: Seroepidemiology of Helicobacter pylori infection in a cohort of children monitored from 6 months to 11 years of age. J Microbiol. 1997, 35: 468470.Google Scholar
 Boltshauser S, Herzog D: Prevalence of Helicobacter pylori infection in asymptomatic 5 – 7year old children of St. Gallen canton (German) Schweizerische Medizinische Wochenschrift. Schweiz Med Wschr. J Suisse de Med. 1999, 129: 579584.Google Scholar
 Hardikar W, Grimwood K: Prevalence of Helicobacter pylori infection in asymptomatic children. J Paediatr Child Health. 1995, 31: 537541. 10.1111/j.14401754.1995.tb00879.x.PubMedView ArticleGoogle Scholar
 Sullivan PB, Thomas JE, Wight DG, Neale G, Eastham EJ, Corrah T, LloydEvans N, Greenwood BM: Helicobacter pylori in Gambian children with chronic diarrhoea and malnutrition. Arch Dis Child. 1990, 65: 189191. 10.1136/adc.65.2.189.PubMedPubMed CentralView ArticleGoogle Scholar
 Smith MA, Simon R, Strickler HD, McQuillan G, Ries LA, Linet MS: Evidence that childhood acute lymphoblastic leukemia is associated with an infectious agent linked to hygiene conditions. Cancer Causes Control. 1998, 9: 285298. 10.1023/A:1008873103921.PubMedView ArticleGoogle Scholar
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