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Int. J. Environ. Res. Public Health 2012, 9(8), 2620-2635; doi:10.3390/ijerph9082620
Published: 27 July 2012
Abstract: Eight candidate genes selected in this study were previously associated with gene-environment interactions in asthma in an urban area. These genes were analyzed in a familial collection from a founder and remote population (Saguenay–Lac-Saint-Jean; SLSJ) located in an area with low air levels of ozone but with localized areas of relatively high air pollutant levels, such as sulphur dioxide, when compared to many urban areas. Polymorphisms (SNPs) were extracted from the genome-wide association study (GWAS) performed on the SLSJ familial collection. A transmission disequilibrium test (TDT) was performed using the entire family sample (1,428 individuals in 254 nuclear families). Stratification according to the proximity of aluminium, pulp and paper industries was also analyzed. Two genes were associated with asthma in the entire sample before correction (CAT and NQO1) and one was associated after correction for multiple analyses (CAT). Two genes were associated when subjects were stratified according to the proximity of aluminium industries (CAT and NQO1) and one according to the proximity of pulp and paper industries (GSTP1). However, none of them resisted correction for multiple analyses. Given that the spatial pattern of environmental exposures can be complex and inadequately represented by a few stationary monitors and that exposures can also come from sources other than the standard outdoor air pollution (e.g., indoor air, occupation, residential wood smoke), a new approach and new tools are required to measure specific and individual pollutant exposures in order to estimate the real impact of gene-environment interactions on respiratory health.
Asthma is a chronic inflammatory disease of the airways characterized by airway hyperresponsiveness, inflammation and remodelling. Asthma is a complex trait and many risk factors have been identified. These risk factors can be divided into two main categories: genetics and environmental factors . The mechanisms underlying the implication of these two categories in the development and the expression of asthma have not been completely clarified. However, it has been found that the interactions between genetic and environmental factors can induce the expression of the disease phenotype . Studies evaluating the impact of ambient air pollution in the development of the disease have shown growing evidence that exposure to ambient air pollution can lead to the development of the asthma phenotype .
As reviewed by London and Romieu in 2009 , different genes associated with the disease phenotype in interaction with air pollution have been identified in the past few years. These studies have contributed to the understanding of the pathophysiology of asthma and to the comprehension of how different environments can have a protective or deleterious effect on the disease. In the literature, different categories of genes were associated with asthma in populations exposed to a polluted urban environment. The principal categories reported are immune signalling (mediators) molecules such as: tumor necrosis factor (TNF) and transforming growth factor, beta 1 (TGFB1) [3,4,5,6]; immune response molecule: myeloperoxidase (MPO); free radical metabolism molecules: catalase (CAT), epoxide hydrolase 1, microsomal (EPHX1), glutathione S-transferase pi 1 (GSTP1) and NAD(P)H dehydrogenase, quinone 1 (NQO1) [7,8,9,10,11,12,13,14,15] that protect against reactive oxygen species (ROS) produced by air pollutants ; and metabolic enzyme like arginase (ARG1).
The objective of this study was to evaluate the association between asthma-related phenotypes and eight genes selected from the literature based on their interaction with asthma in an environment characterized by a higher level of air pollution. The analyses were performed on a familial asthma collection located in the Saguenay–Lac-Saint-Jean region (SLSJ)—a region located in the northeastern Quebec province of Canada. This sample is a distinct, remote population, which is exposed to different levels of air pollutants compared to urban populations. Many industries influence the levels of air pollutants of this region: industries associated with aluminium, pulp and paper. Wood products industries are also present.
A well-characterized family sample of asthmatic patients from the founder population of SLSJ was used to investigate the association between genes selected based on interaction reported with specific environmental exposure and asthma. Asthma phenotype was described following the American Thoracic Society standards : all participants had a respiratory health questionnaire and function tests. Participants were defined as having asthma if (1) they had a reported history of asthma (validated by a physician); or (2) they showed asthma-related symptoms and a positive PC20 at the time of recruitment. Subjects with a PC20 greater than 8 mg/mL; without history of physician-diagnosed asthma, and without symptoms of asthma; and with no positive response on skin prick test were considered unaffected for asthma. Detailed recruitment method is described in the paper by Bégin et al. 2007 . Probands were included in the study if they met two of the three following criteria: (1) a minimum of three clinic visits for acute asthma within one year; (2) two or more asthma related hospital admissions within one year; (3) steroid dependency, defined by either a use of oral corticosteroids for six months, or a year for inhaled corticosteroids. Families were included in the study if phenotypic assessment was available for at least one parent, at least one parent was unaffected, and if all grandparents were French-Canadian descendants. Family members were considered asthmatics if both a self-reported history of asthma and a history of physician diagnosed asthma were recorded, or by clinical evaluation following a methacholine provocation test. Spirometry, methacholine challenge and IgE measurements are detailed in Bégin et al. 2007 . Spirometry was performed to measure the expiratory flow (FEV1) using a Morgan spirometer (Morgan Spiro 232, P.K. Morgan Ltd.) following the American Thoracic Society’s recommendations . Methacholine challenges (bronchoprovocation) were performed for participants of 12 years and older according to the method described by Juniper et al. . The PC20 is described as the dose of methacholine that resulted in a 20% fall in FEV1. Serum IgE was measured with enzyme immunofluorometry. The investigators performed all of the measures for each participant (except for bronchoprovocation) at the University of Montreal Community Genomic Medicine Centre in Saguenay, Québec, Canada. All subjects signed the informed consent approved by the local hospital (Centre de santé et de service sociaux de Chicoutimi) ethics committee. A total of 1,428 individuals from 254 nuclear families were included the study (Table 1).
2.2. Gene Selection and Genotypes
Eight genes were selected from the literature: immune signalling molecules (TGFB1 and TNF), immune response molecule (MPO), genes implicated in free radical metabolism (CAT, EPHX1, GSTP1 and NQO1) and metabolic enzyme (ARG1). The specific genes were selected in the literature using PubMed. Genes had to have one or more polymorphisms (SNPs) associated to asthma in an environment related to air pollution (pollutant related to industries or other pollutant found in the SLSJ region). Key words used were: air pollution, carbon monoxide, ozone, nitrogen oxide, particulate matter, sulfur dioxide and industries.
|Table 1. Clinical characteristics of the Saguenay-Lac-Saint-Jean asthma study.|
|All samples (n = 1,428)||Probands a (n = 254)||Family members (n = 1,174)||Exposed b|
|Children (na = 327) (np = 194)||Family members (na = 729)(np = 431)|
|General descriptive data|
|Age, mean (range) c||39 (2–93)||18 (3–62)||43 (2–93)||22 (2–71)||47 (3–93)|
|25 (2–75)||47 (3–88)|
|Smoking status, n (%) d|
|non smoker||721 (51)||208 (84)||512 (44)||239 (74)||279 (39)|
|139 (74)||163 (39)|
|ex smoker||405 (29)||14 (6)||391 (34)||38(12)||277 (39)|
|22 (12)||157 (37)|
|smoker||283 (20)||27 (11)||256 (22)||47 (14)||162 (22)|
|27 (14)||103 (24)|
|Clinical descriptive data|
|FEV1, % pred. (SD) e||94 (42)||93 (34)||95 (43)||93 (18)||96 (18)|
|PC20, mg/mL (SD) f||7.76 (5.21)||2.50 (3.61)||10.06 (5.04)||6.40 (10.85)||27.83 (26.4)|
|7.60 (13.02)||29.30 (26.98)|
|IgE, μg/L (SD) g||135 (5)||236 (5)||118 (4)||693 (1738)||260 (517.1)|
|891 (3063.9)||394 (1975.6)|
|Asthma, n (%) h||693 (49)||253 (100)||440 (38)||327 (100)||192 (27)|
|194 (100)||116 (27)|
a Probands are first affected family member recruited in the familial collection and family members refers to other family members who joined the study; b Exposed refers to the stratification according to the proximity of aluminium (na (upper line)) and pulp and paper (np (lower line)) industries. A total of 382 individuals (168 children) are exposed to both aluminium and pulp and paper industries; c Mean and median age calculated for 1,425 subjects (254 probands and 1,172 family members); d Smoking status available for 1409 subjects (250 probands and 1159 family members) and passive smoking available for 1,240 subjects (239 probands and 1001 family members). Ex smoker are defined as subjects who have stopped smoking 3 months or more; e FEV1 = Mean and standard deviation (SD) calculated for the Forced expiratory volume in one second in % of predicted value for 1133 subjects (221 probands and 912 family members); f PC20 = Provocative concentration of methacholine that induces a 20% fall in FEV1. Geometric mean and SD calculated for 1,045 subjects (196 probands and 849 family members); g IgE = Immunoglobulin E serum concentration. Geometric mean and SD; h Present asthma or past documented clinical history of asthma. The reported mean age of onset is 7 years old among probands and 22 years old among asthmatic family members. Asthma phenotype is available for 1,166 of the 1,174 family members.
SNPs were extracted using the PLINK software from the genome-wide association study (GWAS) performed on the SLSJ familial collection in the context of the large-scale, consortium-based genome wide association study of asthma GABRIEL . SNPs extracted were located in the selected genes and their 5’ and 3’ untranslated regions (UTR) (which may contain gene expression regulation sites and promoter regions). A total of 90 SNPs were extracted and a total of 72 were kept for analysis (criteria are mentioned in the statistical analysis section): 64 in the total sample, 69 when stratified according to proximity of aluminium industries and 69 when stratified according to pulp and paper industries. All SNPs are described in Table 1 in the supplementary material.
2.3. Environment Characteristics and Air Pollution Data
Subjects of the SLSJ sample were recruited from 1998 to 2001. During these years, only outdoor ozone and sulphur dioxide concentrations were measured routinely in four different places in the SLSJ area. Table 2 is a brief summary of the measures for ozone and sulphur dioxide among these four sites between 1997 and 2000. Both of these pollutants are known to pose a risk to human health and thus ambient air quality standards are in place provincially, federally and also in other countries [22,23]. Air pollutant measures are in part per billion (ppb) and are assessed during a defined period of time (8 hours or 24 hours for longer periods and 1 h for peaks). For example, standards set by the Ministère du Développement durable, de l’Environnement et des Parcs, indicate that the acceptable limits are a maximum value of ozone of 65 ppb for 8 hours and/or 80 ppb for 1 h. The maximum acceptable limits for sulphur dioxide (SO2) are set at 20 ppb for an annual average, 110 ppb for a 24 h average and 500 ppb for 1 h. The levels observed in U.S. cities exceed the standards: the average range of ozone is 0 to 125 ppb for 8 h and the average for SO2 is 0.5 to 50 ppb for 24 h. Also peaks of 200 ppb for 1 h of ozone and 150 ppb for 1 h of SO2 are typically observed in U.S. cities that are not located in areas where there are direct emission sources .
As shown in Table 2, ozone and SO2 levels cannot be considered low in SLSJ region because the concentrations are close to the limit value set by the Canadian government and to levels measured in more populated areas of Canada, as well as in the United States . In particular, the magnitude of the SO2 peaks occurring indicates that the industries known to operate in the area have a significant impact on air quality. Additionally, they are potentially leading to at least some exposure for the study population depending upon the prevailing winds.
The majority of the subjects live within a 10 km radius of aluminium industries (73.93%), which are known to emit significant amounts of fluoride, polycyclic aromatic hydrocarbons (PAH), SO2, carbon monoxide (CO) and particulate matter (PM2.5 and PM10) (NPRI Google Earth tool) (Table 2, supplementary material). There is also a good proportion of the individuals living near pulp and paper industries (44.59%) and wood product industries (11.80%). Such facilities are known to emit a range of air pollutants, such as volatile organic compound (VOC), PM2.5 and PM10, sulphur oxides (SOx), and nitrogen oxides (NOx) etc. [26,27]. There was also a small proportion of the individuals living within a 10 km radius of a niobium mine and other industries, including milk transformation, iron and steel, petroleum refining, chemicals, plastic and rubber etc. Air pollution emissions in tones during the year 2002 are indicated in Table 3 in the supplementary material for each industry located in the SLSJ area.
|Table 2. Levels of air pollutants measured in four places in the SLSJ area.|
|Air pollutant||Years||Mean annual value (ppb)||Period (hour) a||Median (ppb)||Maximum (ppb)|
|Ozone||1997 to 2000||27.7||1||28||76.2|
a Periods are defined as: 1 h = mean value hourly, 8 h = mean value during 8 hours and 24 h = mean value during 24 hours. Areas where sulphur dioxide was measured were influenced by different industries .
2.4. Statistical Analysis
SNPs were tested for association with asthma using the transmission disequilibrium test (TDT) performed with PLINK analysis software [28,29]. The association study was performed on a familial collection. Thus, to test if SNPs are associated to the trait, transmission disequilibrium is observed between generations. Differential allele transmission to affected offspring from heterozygous parents was calculated to determine the association. SNPs included in the study must fulfill these quality criteria: a cut off for minor allele frequency of 5%, a genotyping rate of 5%, a p value > 0.05 for the Hardy-Weinberg equilibrium and < 1% of Mendelian errors. TDT analyses were performed for SNPs and haplotypes employing a chi-square distribution followed by permutations to determine the significance. Permutations were used to test the accuracy of the estimated p value and to palliate lack of power and false positive results. The number of permutations was chosen according to the significance level of the p values of the TDT analyses (for example: 10,000 permutations for p < 0.05 and 20,000 permutations for p < 0.01). Haplotypes (combination of alleles transmitted together) and strength of linkage disequilibrium between SNPs (the more these alleles are transmitted together, the more they are dependent and thus in linkage disequilibrium, values shown as D’) were obtained using the Haploview software (version 3.31; Broad Institute of MIT and Harvard University, Boston, MA, USA). Association between different haplotype blocks of SNPs and asthma was also done using the TDT analysis in the PLINK software. According to the number of SNPs considered in the TDT analyses, multiple analyses correction was performed to avoid false positive results. This correction was done considering the number of independent tagSNPs (SNPs that represent a region with high linkage disequilibrium) for each gene separately using the Nyholt method . For example, for CAT, there were 11 independent tagSNPs and the corrected threshold was 0.0047 (0.05/11 tagSNPs).
TDT for SNPs and haplotype blocks were repeated after stratification for the proximity of aluminium or pulp and paper industries (10 km radius around the subject’s house location). For these analyses, only the nuclear trios, for which the children were exposed to one industry or the other, were kept for analyses.
Association results for SNPs that had a significant p-value before correction (p < 0.05) for the whole sample and for the sample stratified according to the proximity of aluminium or pulp and paper industries are shown in Table 3. Five SNPs from two genes (CAT (rs11032703, rs2300181, rs511895) and NQO1 (rs1800566, rs1437135)) were associated before correction and one SNP located in CAT gene was still associated after correction (indicated in bold in Table 3). The minor allele of the CAT rs11032703T SNP was transmitted more often to asthmatic subjects and could be a risk factor of asthma. Results for the TDT with the stratified sample that had a p-value less than the 0.05 thresholds are indicated in Table 3. Three SNPs located in two genes were associated when stratified according to proximity to aluminium industries (CAT (rs1132703) and NQO1 (rs1800566 and rs1437135)) and only one SNP in the GSTP1 gene (rs1695) was associated in the pulp and paper sample. None of the SNPs resisted the correction for multiple analyses.
Haplotypes of the selected genes were also analyzed to look for association with asthma in the whole sample and the stratified ones. A TDT was then performed on linkage disequilibrium plot located in the eight genes selected for this study and obtained with the Haploview software. Five haplotypes located in three different genes (CAT, EPHX1 and NQO1) were associated to asthma before correction (p < 0.05) and are shown in Table 4. One haplotype located in the CAT gene was still associated after correction. The haplotype was transmitted more often to asthmatic patients, which indicates a potential deleterious effect on the phenotype. This haplotype also contains the SNP rs11032703 that has been associated alone with asthma, but also other SNPs that had a p value under 0.05, but did not remain significant after correction (rs2300181 (intron 6) and rs511895 (intron 10)). Linkage disequilibrium plot for the CAT gene is shown in Figure S1 in the supplementary materials. Two haplotypes located in two genes (CAT and NQO1) were associated to asthma before correction when the sample was stratified according to proximity to aluminium industries. When stratified according to proximity to pulp and paper industries there were also two haplotype blocks located in two genes (EPHX1 and GSTP1) that were associated to asthma before correction. None of these haplotypes resisted correction for multiple analyses.
|Table 3. Transmission disequilibrium test (TDT) results with p value < 0.05 for genes selected in the literature and stratified according to proximity to aluminium or pulp and paper industries.|
|Industry||Gene symbol/position||SNP/position a||Allele b||T||U||OR||CHISQ||p value a||p value with permutations||p value threshold (Meff) c|
|All samples||CAT/11p13||rs11032703/intron 1||T/C||90||52||1.731||10.17||0.001428||0.0029||0.00474|
|NQO1/16q22.1||rs1800566/exon 5 (Pro187Ser)||A/G||86||118||0.7288||5.02||0.02506||0.03135||0.01686|
|NQO1/16q22.1||rs1800566/exon 5 (Pro187Ser)||A/G||63||90||0.7||4.765||0.02905||0.03595||0.01827|
|Pulp and Paper||GSTP1/11q13||rs1695/exon 5 (Ile105Val)||G/A||46||70||0.6571||4.966||0.02586||0.0354||0.02072|
Definition of abbreviations: SNP= single nucleotide polymorphism, T = Transmitted minor allele count, U = Untransmitted allele count, OR = odds ratio, CHISQ = chi-square statistic, CAT = catalase, GSTP1 = Glutathione S-transferase, NQO1 = NAD(P)H dehydrogenase quinone 1; a Significant results after corrections are indicated in bold; b Ancestral alleles are indicated in bold when available in National Centre for Biotechnology Information (NCBI); c Corrected p value threshold for each gene considering only tagSNPs . Meff = Effective number of independent marker loci.
|Table 4. Transmission Disequilibrium Test (TDT) results with p value < 0.05 for haplotypes and stratified according to the proximity of aluminium of pulp and paper industries.|
|Industry||Gene symbol/position||Locus||Haplotype||T||U||CHISQ||p value a||p value Threshold b(Meff)|
|All samples||CAT/11p13||H1||rs208679A rs7118388G rs7944397A rs208682C rs554518C||162.5||123.8||5.223||0.0223||0.00474 (10.5509)|
|H1||rs208679A rs7118388A rs7944397A rs208682C rs554518C||113.5||148.9||4.779||0.0288|
|H2||rs1001179C rs480575A rs2284369A rs11032703T rs769218G rs2300181C rs7933285C rs511895T rs10488736C||91||54.4||9.221||0.002406|
|EPHX1/1q42.1||H3||rs4653695A rs2740174A rs360063A rs1009668C||150.8||114.9||4.842||0.02777||0.00352 (14.2206)|
|NQO1/16q22.1||H1||rs1800566A rs4986998G rs689452G rs1437135G rs689457C rs2917682T||86||119||5.312||0.02118||0.01686 (2.9652)|
|Aluminium||CAT/11p13||H2||rs1001179C rs480575A rs2284369A rs11032703T rs769218G rs2300181C rs7933285C rs511895T rs10488736C||71||42||7.442||0.00637||0.00442 (11.3167)|
|NQO1/16q22.1||H1||rs1800566A rs4986998G rs689452G rs1437135G rs689457C rs2917682T||63||91||5.091||0.02405||0.01827 (2.7369)|
|Pulp and Paper||EPHX1/1q42.1||H4||rs360063A rs1009668C||62||41||4.282||0.03853||0.00311|
|GSTP1/ 11q13||H1||rs1695A rs1138272C||69||45||5.053||0.02459||0.02072 (2.4134)|
Haplotypes were selected from all the genes selected for this study. Definition of abbreviations: T = transmitted minor allele count, U = untransmitted allele count, NQO1 = NAD(P)H dehydrogenase quinone 1, CAT = catalase, EPHX1 = epoxide hydrolase 1, microsomal, CHISQ = chi-square statistic; a Significant results after correction; b Corrected p value considering the number of independent tagSNPs . Meff = Effective number of independent marker loci.
We performed a genetic family based association study between asthma and genes that were previously associated with air pollution in an urban environment. Our study focused on a population residing in a relatively unpopulated area but where the air quality is influenced by the presence of several industries. The principal strength of this study is the well-defined population. Every subject has gone through different analyses of their respiratory capacity and they were questioned on different aspects related to respiratory diseases like their smoking status. It is also a homogeneous population with similar lifestyles (same religion, language, activities, etc.) .
This study also has some limitations. First, the familial collection was not designed to study gene-environment interactions. The main purpose is to study the impact of genetic variants on asthma phenotypes.
Also, the presence of a significant number of smokers (11% of probands and 20% of family members) or ex-smokers (6% of probands and 29% of family members) might have influenced the results of the gene-environment interactions examined in this study. For example, the two associated genes (CAT and NQO1) have been associated with asthma and tobacco smoke exposures [32,33]. NQO1 Pro187Ser mutation was associated in our study, but was also associated with asthma and exposure to tobacco smoke in a previous study. Unfortunately, excluding smokers in this study would have significantly affected its power.
Potential environmental exposures for this study were complex and difficult to describe given the lack of information on true spatial concentration patterns and subject activity. Thus, while it would have been interesting to consider exposure of each individual, such detail was beyond the scope of the present study. Compounding these challenges, the concentration of some key air pollutants, like PM10, PM2.5, PAH, CO and VOC, were not measured in the area during the recruitment years. However, as described above data on total release of different pollutants were available for the year 2002. Furthermore, even if data were not available during the recruitment years (1998 to 2001), the 2002 data are still relevant as an indication of the general air conditions in the area. This is because the air pollutants emitted by the different industries generally do not show significant differences from one year to the next. Decreasing trends are only apparent over multiple years.
Even if the distances between the industries and the homes of the subjects were measured and the dispersion of the emitted pollutants were known so that more accurate air pollutant exposures could be assigned there are other potential exposures in this population. For example, occupational exposures or local activities can be significant, but with current information these cannot be quantified. There are also other types of oxidizing pollutants like indoor air exposures (e.g., environmental tobacco smoke) or wood smoke from residential burning that can influence individual exposures and these are also not known for our population. Many contaminant from wood smoke can have an impact on health like CO, PM2,5, NOx, PAH, etc. .
Another limitation with this familial collection is that some of the genes were not evaluated because few SNPs located in these genes were not analyzed in the ILLUMINA 610K arrays or these SNPs did not respond to criteria mentioned in the statistical analysis section. This was the case for the MPO gene (rs2333227) that was previously associated with asthma in gene-environment interactions studies .
Candidate gene studies have a low replication rate , that can be explained by the difference in recruitment (case-control studies compared to familial studies or birth cohorts, different age of onset in cohorts, etc.), by the presence of difference in linkage disequilibrium between populations (a founder population compared to a cosmopolitan population) and in the characterization of the subjects at the phenotypic and exposition to environment levels. In this study, we tried to reduce the impact of the difference in the characterization of exposure to the environment by selecting genes that were previously associated to asthma in similar environment (urban area with pollutant related to industries or other pollutant found in the SLSJ region). Gene selection was well defined and based on their previous association with asthma and air pollution in the literature and criteria are mentioned in the Gene Selection and Genotypes section. This strict selection allowed replicating selected genes in a precise environment to address the impact of their interaction with this environment in the context of asthma pathogenesis.
This study showed an association for the CAT gene and asthma in the whole sample of the SLSJ study. The CAT gene is located on the chromosome 11p13 and expresses the catalase protein implicated in defense against oxidative stress . It is an antioxidant enzyme that protects the cell from oxidative stress by decomposition of hydrogen peroxide into water and oxygen . Reactive oxygen species and hydrogen peroxide are known to have an impact on many characteristic elements of the asthma phenotype such as contracting airway smooth muscle, increasing airway reactivity and the synthesis and release of chemoattractants [36,37,38,39]. There are different external and cellular sources of hydrogen peroxide like ozone or inflammatory cells and the respiratory chain located in the mitochondria . Catalase may play a role on the oxidant-antioxidant imbalance in asthma because studies have shown a higher activity of the enzyme in affected people .
Our results show an association between CAT rs11032703 and asthma in the SLSJ sample and show that the minor allele might be a risk factor for the disease phenotype. Two studies have previously associated this gene with exposure to air pollutants [15,41]. Wenten et al. found an epistasic effect between SNPs in CAT (rs1001179) and MPO (rs2333227) genes when subjects were exposed to air pollutants (NO2 and ozone)  but neither of the two SNPs alone was associated with the phenotype combined with the environment. Strict replication (same gene and same SNP) was not possible in our sample since rs2333227 was not present in the GWAS database, thus not evaluated in this study and, as found by Wenten et al., rs10001179 alone was not associated with asthma in our study (p = 0.942). Gene-gene interactions were evaluated between these two genes (CAT and MPO) to look at possible epistatic effects between other SNPs of these genes and asthma in a context of air pollution, but no association was found (results not shown). The haplotype block 2 of the CAT gene is also associated with asthma in this sample. This haplotype block is more transmitted to asthmatic subjects compared to controls and appears to be a susceptibility factor for asthma. Interestingly, this haplotype block includes the only SNP associated after correction (rs11032703), for which the minor allele is also transmitted more often to the asthmatic subjects. However, it is important to note that the associated SNPs may not be the causal one and other SNPs in linkage disequilibrium with the associated one may explain the impact on the trait.
These results indicate the importance of this locus and of the CAT gene in asthma. The fact that SNPs located in the CAT gene were not associated after correction when the sample was stratified according to the proximity of aluminium industries and that no association was observed when the sample was stratified according to the proximity of pulp and paper industries may indicate that the association of this gene is not restricted to a specific environment. As previously mentioned, the origin of the causal SNP may not be the one associated in this study and its impact on asthma needs to be assessed. However, since the exposition measure is not perfect, this clearly points out the importance of measuring and modeling individual-level exposures to air pollutants in order to properly study gene-environment interactions so that firm conclusions can be drawn.
In conclusion, in this study we evaluated the association of genes that were previously associated with asthma in the literature within a gene-environment interaction with air pollution context. CAT gene previously associated with urban environments and air pollution was associated with asthma after correction in our sample. Interestingly, the familial collection used in this study is characterized by being composed of a remote/rural population. However, subjects tend to live in an area with variable, but potentially significant air pollutant exposures because there are aluminium, pulp and paper, and wood product industries in the region which emit a range of pollutants like SO2 and particulate matter. However, while these are important pollution sources, the surrounding background pollutant levels are generally low. This differs from the environment in urban areas where there are many sources (e.g., traffic) leading to higher overall levels of air pollutants, but which are less variable and potentially with less intense peaks typically associated with industrial plumes. In order to determine if the genes found to be important in this study were indeed implicated because of environmental (air pollutant) exposures and not because of other unknown factors, future efforts need to focus on accurate characterization of individual exposures from all potential sources. This added information would allow for a more complete assessment of the impact of gene-environment interactions in asthma and could lead to better insight regarding what types and quantities of exposures are harmful with respect to different asthma phenotypes. Finally, this study gives first exploratory results of gene-environment interactions in this area and shows that this kind of study is important to better understand asthma pathogenesis. However, better characterization tools will be needed to correctly answer those questions. This study also emphasizes the challenge that these types of studies represent and raises some questions regarding a few points that need to be taken into consideration for future approaches: (1) How to measure the environment; (2) when to measure it (what period of life); (3) how long do we measure it; and (4) what environment (in this case what air pollutant) to consider.
This study was possible with the support of: GABRIEL, Canadian Centre for Health and Safety in Agriculture, Canadian Institutes of Health Research. We express gratitude to all subjects who accepted to participate in the study. Andréanne Morin is supported by the Réseau en Médecine Génétique Appliqué (RMGA) of the Fonds de recherche du Québec en santé (FRQS). Catherine Laprise is the chair holder of the Canada Research Chair for genetic determinants in asthma (www.chairs.gc.ca) and the director of the Inflammation and Remodeling Strategic Group of the Respiratory Health Network (RHN). Catherine Laprise and Jeffrey R. Brook are members of the AllerGen NCE Inc. (the Allergy, Genes and Environment Network) a national multidisciplinary research network supporting research, networking, commercialization, knowledge mobilization and capacity building activities that contribute to reducing the morbidity, mortality and socio-economic impact of allergic diseases. AllerGen is a member of the Networks of Centres of Excellence (NCE), a Government of Canada program that funds partnerships between universities, industry, government and non-profit organizations to connect leading-edge research with industrial know-how and strategic investment. All the genotypes were available due to the GABRIEL project.
Conflict of Interest
The authors declare that they have no competing interests.
- Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention; GINA: Cape Town, South Africa, 2008.
- London, S.J.; Romieu, I. Gene by environment interaction in asthma. Annu. Rev. Public Health 2009, 30, 55–80. [Google Scholar] [CrossRef]
- Lee, Y.L.; McConnell, R.; Berhane, K.; Gilliland, F.D. Ambient ozone modifies the effect of tumor necrosis factor g-308a on bronchitic symptoms among children with asthma. Allergy 2009, 64, 1342–1348. [Google Scholar]
- Li, Y.F.; Gauderman, W.J.; Avol, E.; Dubeau, L.; Gilliland, F.D. Associations of tumor necrosis factor g-308a with childhood asthma and wheezing. Am. J. Respir. Crit. Care Med. 2006, 173, 970–976. [Google Scholar]
- Salam, M.T.; Gauderman, W.J.; McConnell, R.; Lin, P.C.; Gilliland, F.D. Transforming growth factor-1 c-509t polymorphism, oxidant stress, and early-onset childhood asthma. Am. J. Respir. Crit. Care Med. 2007, 176, 1192–1199. [Google Scholar]
- Yang, I.A.; Holz, O.; Jorres, R.A.; Magnussen, H.; Barton, S.J.; Rodriguez, S.; Cakebread, J.A.; Holloway, J.W.; Holgate, S.T. Association of tumor necrosis factor-alpha polymorphisms and ozone-induced change in lung function. Am. J. Respir. Crit. Care Med. 2005, 171, 171–176. [Google Scholar]
- Castro-Giner, F.; Kunzli, N.; Jacquemin, B.; Forsberg, B.; de Cid, R.; Sunyer, J.; Jarvis, D.; Briggs, D.; Vienneau, D.; Norback, D.; et al. Traffic-related air pollution, oxidative stress genes, and asthma (echrs). Environ. Health Perspect. 2009, 117, 1919–1924. [Google Scholar]
- David, G.L.; Romieu, I.; Sienra-Monge, J.J.; Collins, W.J.; Ramirez-Aguilar, M.; del Rio-Navarro, B.E.; Reyes-Ruiz, N.I.; Morris, R.W.; Marzec, J.M.; London, S.J. Nicotinamide adenine dinucleotide (phosphate) reduced: Quinone oxidoreductase and glutathione s-transferase m1 polymorphisms and childhood asthma. Am. J. Respir. Crit. Care Med. 2003, 168, 1199–1204. [Google Scholar]
- Islam, T.; Berhane, K.; McConnell, R.; Gauderman, W.J.; Avol, E.; Peters, J.M.; Gilliland, F.D. Glutathione-s-transferase (gst) p1, gstm1, exercise, ozone and asthma incidence in school children. Thorax 2009, 64, 197–202. [Google Scholar]
- Lee, Y.L.; Lin, Y.C.; Lee, Y.C.; Wang, J.Y.; Hsiue, T.R.; Guo, Y.L. Glutathione s-transferase p1 gene polymorphism and air pollution as interactive risk factors for childhood asthma. Clin. Exp. Allergy 2004, 34, 1707–1713. [Google Scholar]
- Melen, E.; Nyberg, F.; Lindgren, C.M.; Berglind, N.; Zucchelli, M.; Nordling, E.; Hallberg, J.; Svartengren, M.; Morgenstern, R.; Kere, J.; et al. Interactions between glutathione s-transferase p1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease. Environ. Health Perspect. 2008, 116, 1077–1084. [Google Scholar]
- Romieu, I.; Ramirez-Aguilar, M.; Sienra-Monge, J.J.; Moreno-Macias, H.; del Rio-Navarro, B.E.; David, G.; Marzec, J.; Hernandez-Avila, M.; London, S. Gstm1 and gstp1 and respiratory health in asthmatic children exposed to ozone. Eur. Respir. J. 2006, 28, 953–959. [Google Scholar]
- Romieu, I.; Sienra-Monge, J.J.; Ramirez-Aguilar, M.; Moreno-Macias, H.; Reyes-Ruiz, N.I.; Estela del Rio-Navarro, B.; Hernandez-Avila, M.; London, S.J. Genetic polymorphism of gstm1 and antioxidant supplementation influence lung function in relation to ozone exposure in asthmatic children in mexico city. Thorax 2004, 59, 8–10. [Google Scholar]
- Schroer, K.T.; Biagini Myers, J.M.; Ryan, P.H.; LeMasters, G.K.; Bernstein, D.I.; Villareal, M.; Lockey, J.E.; Reponen, T.; Grinshpun, S.; Khurana Hershey, G.K. Associations between multiple environmental exposures and glutathione s-transferase p1 on persistent wheezing in a birth cohort. J. Pediatr. 2009, 154, 401–408. [Google Scholar]
- Wenten, M.; Gauderman, W.J.; Berhane, K.; Lin, P.C.; Peters, J.; Gilliland, F.D. Functional variants in the catalase and myeloperoxidase genes, ambient air pollution, and respiratory-related school absences: An example of epistasis in gene-environment interactions. Am. J. Epidemiol. 2009, 170, 1494–1501. [Google Scholar]
- Bowler, R.P.; Crapo, J.D. Oxidative stress in allergic respiratory diseases. J. Allergy Clin. Immunol. 2002, 110, 349–356. [Google Scholar] [CrossRef]
- Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease (copd) and asthma. This official statement of the american thoracic society was adopted by the ats board of directors, November 1986. Am. Rev. Respir. Dis. 1987, 136, 225–244.
- Begin, P.; Tremblay, K.; Daley, D.; Lemire, M.; Claveau, S.; Salesse, C.; Kacel, S.; Montpetit, A.; Becker, A.; Chan-Yeung, M.; et al. Association of urokinase-type plasminogen activator with asthma and atopy. Am. J. Respir. Crit. Care Med. 2007, 175, 1109–1116. [Google Scholar] [CrossRef]
- Ats statement—Snowbird workshop on standardization of spirometry. Am. Rev. Respir. Dis. 1979, 119, 831–838.
- Standardization of spirometry, 1994 update. American Thoracic Society. Am. J. Respir. Crit. Care Med. 1995, 152, 1107–1136.
- Moffatt, M.F.; Gut, I.G.; Demenais, F.; Strachan, D.P.; Bouzigon, E.; Heath, S.; von Mutius, E.; Farrall, M.; Lathrop, M.; Cookson, W.O. A large-scale, consortium-based genomewide association study of asthma. N. Engl. J. Med. 2010, 363, 1211–1221. [Google Scholar]
- Environment Canada. Air Quality. 2011. Available online: http://www.ec.gc.ca/Air/default.asp?lang=En&n=04104DB7-1 (accessed on 8 August 2011).
- Environment Canada. Pollutants. 2011. Available online: http://www.ec.gc.ca/Air/default.asp?lang=En&n=BCC0B44A-1 (accessed on 8 August 2011).
- Brook, R.D.; Rajagopalan, S.; Pope, C.A., 3rd; 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]
- CESPA. Banque de Données sur la Connaissance et la Surveillance de la Pollution Atmosphérique—Données Préliminaires; Ministère du Développement durable, de l’Environnement et des Parcs, Direction du suivi de l’état de l’environnement: Québec, QC, Canada, 2010.
- Environment Canada. Pulp and Paper; 2011. Available online: http://www.ec.gc.ca/Air/default.asp?lang=En&n=CB1E071C-1 (accessed on 15 September 2011).
- Environment Canada. Lumber and Allied Wood Products; 2011. Available online: http://www.ec.gc.ca/Air/default.asp?lang=En&n=542779CB-1 (accessed on 15 September 2011).
- Purcell, S.; Neale, B.; Todd-Brown, K.; Thomas, L.; Ferreira, M.A.R.; Bender, D.; Maller, J.; Sklar, P.; de Bakker, P.I.W.; Daly, M.J.; Sham, P.C. PLINK: A toolset for whole-genome association and population-based linkage analysis. A. J. Hum. Genet. 2007, 81, 559–575. [Google Scholar]
- PLINK. Version 1.07. Shaun Purcell. Available online: http://pngu.mgh.harvard.edu/purcell/plink/ (accessed on 20 August 2010).
- Nyholt, D.R. A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am. J. Hum. Genet. 2004, 74, 765–769. [Google Scholar] [CrossRef]
- Roy-Gagnon, M.H.; Moreau, C.; Bherer, C.; St-Onge, P.; Sinnett, D.; Laprise, C.; Vezina, H.; Labuda, D. Genomic and genealogical investigation of the French Canadian founder population structure. Hum. Genet. 2011, 129, 521–531. [Google Scholar]
- Li, Y.F.; Tseng, P.J.; Lin, C.C.; Hung, C.L.; Lin, S.C.; Su, W.C.; Huang, Y.L.; Sung, F.C.; Tai, C.K. Nad(p)h: Quinone oxidoreductase 1, glutathione s-transferase m1, environmental tobacco smoke exposure, and childhood asthma. Mutat. Res. 2009, 678, 53–58. [Google Scholar]
- Polonikov, A.V.; Ivanov, V.P.; Solodilova, M.A.; Kozhuhov, M.A.; Panfilov, V.I. Tobacco smoking, fruit and vegetable intake modify association between −21a>t polymorphism of catalase gene and risk of bronchial asthma. J. Asthma 2009, 46, 217–224. [Google Scholar] [CrossRef]
- Environment Canada. Residential Wood Heating; 2011. Available online: http://www.ec.gc.ca/residentiel-residential/default.asp?lang=En&n=E9FE1750-1 (accessed on 2 October 2012).
- Ober, C.; Hoffjan, S. Asthma genetics 2006: The long and winding road to gene discovery. Genes Immun. 2006, 7, 95–100. [Google Scholar] [CrossRef]
- Rahman, I.; Biswas, S.K.; Kode, A. Oxidant and antioxidant balance in the airways and airway diseases. Eur. J. Pharmacol. 2006, 533, 222–239. [Google Scholar] [CrossRef]
- Barnes, P.J. Cytokines as mediators of chronic asthma. Am. J. Respir. Crit. Care Med. 1994, 150, S42–S49. [Google Scholar]
- Barnes, P.J.; Chung, K.F.; Page, C.P. Inflammatory mediators of asthma: An update. Pharmacol. Rev. 1998, 50, 515–596. [Google Scholar]
- Nadeem, A.; Masood, A.; Siddiqui, N. Oxidant-antioxidant imbalance in asthma: Scientific evidence, epidemiological data and possible therapeutic options. Ther. Adv. Respir. Dis. 2008, 2, 215–235. [Google Scholar] [CrossRef]
- Mak, J.C.; Leung, H.C.; Ho, S.P.; Ko, F.W.; Cheung, A.H.; Ip, M.S.; Chan-Yeung, M.M. Polymorphisms in manganese superoxide dismutase and catalase genes: Functional study in Hong Kong Chinese asthma patients. Clin. Exp. Allergy 2006, 36, 440–447. [Google Scholar]
- Islam, T.; McConnell, R.; Gauderman, W.J.; Avol, E.; Peters, J.M.; Gilliland, F.D. Ozone, oxidant defense genes, and risk of asthma during adolescence. Am. J. Respir. Crit. Care Med. 2008, 177, 388–395. [Google Scholar]
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