Skip to main content
Canadian Respiratory Journal logoLink to Canadian Respiratory Journal
. 2008 Apr;15(3):139–145. doi: 10.1155/2008/302407

Prevalence of asthma and risk factors for asthma-like symptoms in Aboriginal and non-Aboriginal children in the northern territories of Canada

Zhiwei Gao 1, Brian H Rowe 2, Carina Majaesic 3, Cindy O’Hara 4, A Senthilselvan 1,
PMCID: PMC2677938  PMID: 18437256

Abstract

BACKGROUND:

Few studies have investigated the prevalence and risk factors of asthma in Canadian Aboriginal children.

OBJECTIVE:

To determine the prevalence of asthma and asthma-like symptoms, as well as the risk factors for asthma-like symptoms, in Aboriginal and non-Aboriginal children living in the northern territories of Canada.

METHODS:

Data on 2404 children, aged between 0 and 11 years, who participated in the North component of the National Longitudinal Survey of Children and Youth were used in the present study. A child was considered to have an asthma-like symptom if there was a report of ever having had asthma, asthma attacks or wheeze in the past 12 months.

RESULTS:

After excluding 59 children with missing information about race, 1399 children (59.7%) were of Aboriginal ancestry. The prevalence of asthma was significantly lower (P<0.05) in Aboriginal children (5.7%) than non-Aboriginal children (10.0%), while the prevalence of wheeze was similar between Aboriginal (15.0%) and non-Aboriginal (14.5%) children. In Aboriginal children, infants and toddlers had a significantly greater prevalence of asthma-like symptoms (30.0%) than preschool-aged children (21.5%) and school-aged children (11.5%). Childhood allergy and a mother’s daily smoking habit were significant risk factors for asthma-like symptoms in both Aboriginal and non-Aboriginal children. In addition, infants and toddlers were at increased risk of asthma-like symptoms in Aboriginal children. In analyses restricted to specific outcomes, a mother’s daily smoking habit was a significant risk factor for current wheeze in Aboriginal children and for ever having had asthma in non-Aboriginal children.

CONCLUSIONS:

Asthma prevalence appears to be lower in Aboriginal children than in non-Aboriginal children. The association between daily maternal smoking and asthma-like symptoms, which has been mainly reported for children living in urban areas, was observed in Aboriginal and non-Aboriginal children living in northern and remote communities in Canada.

Keywords: Aboriginals, Asthma, Children, Remote area, Risk factors, Smoking


Asthma is one of the most common chronic disorders affecting children and adults, especially in industrialized countries (1). The prevalence of asthma increased in the 1980s and early 1990s; however, recent studies investigating temporal trends have indicated an apparent stabilization in asthma prevalence in the late 1990s and in the early part of this decade (2,3).

The cultural and lifestyle factors in Aboriginal communities may put this population at higher risk of developing asthma and asthma-like symptoms. Smoking, housing conditions and overcrowding in Aboriginal communities may also play a role in the prevalence of asthma in Aboriginal children. Only a few studies (35) have investigated the prevalence of asthma in the Aboriginal population in Canada. In the 1970s, asthma was reported to be lower in Métis populations living in northern Saskatchewan than among white people living in central Saskatchewan (4), and was reported to be rare in the Canadian Eskimo population (5). In a more recent study in Saskatchewan, the prevalence of asthma, determined from the physician services database, was lower only in children five to 14 years of age among the Registered Indian population (3). The prevalence of exercise-induced bronchospasm has also been reported to be lower in Inuit school children living in northern Quebec (6). In the present study, the prevalence of ever having had asthma, current asthma and current wheeze, and factors associated with asthma-like symptoms in Aboriginal and non-Aboriginal children living in the Northwest Territories, Yukon and Nunavut in Canada are reported.

METHODS

The National Longitudinal Survey of Children and Youth, North component (NLSCY-North), which was conducted by Statistics Canada in 1994 and 1995 (cycle 1), was used to study asthma prevalence in Aboriginal and non-Aboriginal children living in the Northwest Territories, Yukon and Nunavut (6). During the survey, Nunavut was part of the Northwest Territories, but in anticipation of the division, the survey sample was divided into two regions: the western territory and Nunavut. The western territory is referred to as the Northwest Territories in the present study. The populations from institutions, the Canadian Armed Forces and unorganized areas in the Yukon were excluded from the survey. In addition to these exclusions, populations from remote areas and very small communities in the Northwest Territories and Nunavut were also excluded.

Data collection

The National Population Health Survey for children and adults 12 years of age and older, and the NLSCY-North for children 11 years of age and younger were conducted simultaneously in the Northwest Territories, Yukon and Nunavut (7). These surveys were integrated to reduce respondent burden. The primary sampling units in the NLSCY-North were households. Randomly selected households with at least one child between 0 and 11 years of age were eligible for inclusion in the survey. The NLSCY-North sampling design for cycle 1 was constructed to guarantee that the sample size was large enough to be stratified into seven age groups: 0 to 11 months, one year, two and three years, four and five years, six and seven years, eight and nine years, 10 and 11 years.

Random samples were selected from the population of private occupied dwellings in the Northwest Territories, Yukon and Nunavut. A maximum of three children were randomly selected from each household. Specially trained persons conducted the interviews by phone or in person. Face-to-face interviews were used for data collection in the Northwest Territories and Nunavut. In the Yukon, face-to-face interviews were used during the first six months of the survey, but was replaced with random digit dialing followed by telephone survey thereafter for the majority of the population.

Questionnaires

Several questionnaires were administered as part of the survey. The household questionnaire covered basic demographic information for each household member, dwelling conditions and household income. The parent’s questionnaire was designed to collect information on age, education, employment, income and household characteristics. The child’s questionnaire was designed to collect information on several factors, including the demographics, behaviour, education and health of children selected from the household. One person was assigned as the ‘person most knowledgeable’ (PMK) about the child. The PMK was asked to complete parent and child questionnaires.

Study sample

A total of 2404 children participated in cycle 1 of the NLSCY-North. The Aboriginal ancestry of the children was determined from the response of the PMK to the question, “Do you consider the child to be a First Nation that is Indian, Métis, or Inuit?” After excluding 59 children with missing information on Aboriginal ancestry, 1399 of the 2345 children (59.7%) who were considered for the analysis were of Aboriginal ancestry.

Definition of asthma, asthma-like symptoms and allergy

A positive response to the question “Has the child ever had asthma that was diagnosed by a health professional?” was used to determine lifetime prevalence of asthma in children. The presence of current asthma was determined from a positive response to the question “Has he/she had an attack of asthma in the last 12 months?” The presence of current wheeze was determined from a positive response to the question “Has he/she had wheezing in the chest at anytime in the last 12 months?” The presence of asthma-like symptoms was determined from a positive response to any of the previous three questions on ever having had asthma, current asthma or current wheeze, respectively. The question “Does the child have any of the following long-term conditions (lasted or expected to last more than six months) that have been diagnosed by a health professional?” was used to determine the presence of a series of chronic conditions, including allergy. A positive response to the question on ‘allergies’ was used to define childhood allergy in our study.

Independent factors

Child-level predictor variables considered in the study included age group, sex, childhood allergy, living with single parent and number of siblings. Parental-level predictors considered in the study were mother’s age at the child’s birth, education level, allergy, asthma, smoking habit and marital status. Household predictors considered in the study included total income, dwelling ownership, dwelling in need of repairs and place of residence. Mother’s allergy was determined from a positive response to the second question in a series of two questions, which were asked in sequence: “Do you have any of the following long-term conditions (lasted or expected to last longer than six months) that have been diagnosed by a health professional: a) food allergies; b) other allergies?” The child’s dwelling was considered to be in need of repairs if the dwelling needed minor or major repairs other than regular maintenance (painting, furnace checking, etc).

Statistical analysis

Normalized cross-sectional weights provided by Statistics Canada were applied to adjust for the sampling design and nonresponse of selected households. The prevalence of asthma and asthma-like symptoms in the Aboriginal and non-Aboriginal samples were calculated using the normalized cross-sectional weights. The generalized estimating equation technique was used in the univariate and multivariate logistic regression analyses to adjust for the correlation among children from the same households (8). Logistic regression analyses were used to determine the significant differences in the distribution of individual and household characteristics between Aboriginal and non-Aboriginal children, and to determine the significant factors associated with asthma and asthma-like symptoms in Aboriginal and non-Aboriginal children. All of the factors that were significant at a 20% level in the univariate analysis were considered for multivariate analysis. A purposeful selection method was used to determine important factors in the multivariate regression.

RESULTS

The distribution of demographic and individual characteristics is shown in Table 1. The distribution of age group and sex was similar between Aboriginal and non-Aboriginal children. Significant differences were observed between the two groups in childhood allergy, number of siblings and number of older siblings. The distribution of parental and household characteristics is shown in Table 2. Daily smoking was significantly more prevalent among mothers of Aboriginal children than among mothers of non-Aboriginal children (Table 2). Maternal allergy and asthma were significantly lower in Aboriginal children than in non-Aboriginal children. Mother’s mean age at birth and level of education, in addition to household income, were significantly lower in Aboriginal children. A significantly greater proportion of non-Aboriginal children lived in their own homes, in homes with two or fewer rooms, and in homes needing fewer repairs.

TABLE 1.

Demographic and individual characteristics of Aboriginal and non-Aboriginal children who participated in the National Longitudinal Survey of Children and Youth-North*

Characteristics Aboriginal children, n (%) Non-Aboriginal children, n (%) P
Age group
  Infant and toddler 247 (17.7) 144 (15.2) 0.28
  Preschool-aged 372 (26.6) 264 (27.9)
  School-aged 780 (55.8) 539 (56.9)
Sex
  Male 718 (51.3) 487 (51.5) 0.94
  Female 681 (48.7) 459 (48.5)
Childhood allergy 82 (6.0) 115 (12.3) <0.0001
Living with
  One parent 204 (15.8) 143 (15.4) 0.82
  Two parents 1092 (84.3) 789 (84.6)
Number of siblings
  0 145 (11.4) 168 (18.1) <0.0001
  1 333 (26.3) 439 (47.3)
  ≥2 792 (62.3) 321 (34.6)
Number of older siblings
  0 267 (24.0) 251 (33.4) <0.0001
  1 363 (32.6) 341 (45.3)
  ≥2 483 (43.4) 161 (21.4)
*

Frequencies and proportions were weighted using normalized cross-sectional weights – frequencies do not add up to the total because of missing data;

Number of siblings includes both older and younger siblings

TABLE 2.

Parental and household characteristics of Aboriginal and non-Aboriginal children who participated in the National Longitudinal Survey of Children and Youth-North*

Characteristics Aboriginal children, n (%) Non-Aboriginal children, n (%) P
Mother’s age at birth, years
  15–24 490 (47.4) 206 (23.1) <0.0001
  25–34 469 (45.4) 561 (63.2)
  ≥35 74 (7.2) 122 (13.7)
Mother’s education level
  Less than secondary 523 (42.8) 69 (7.8) <0.0001
  Secondary 58 (4.8) 140 (15.7)
  High school 419 (34.3) 263 (30.0)
  College or higher 221 (18.1) 418 (46.9)
Mother’s allergy 106 (10.9) 221 (25.4) <0.0001
Mother’s asthma 24 (2.5) 82 (9.4) <0.0001
Mother’s smoking habit
  None 374 (28.1) 620 (68.5) <0.0001
  Occasional 184 (13.9) 49 (5.4)
  Daily 770 (58.0) 236 (26.1)
Mother’s marital status
  Married 1172 (83.7) 804 (85.0) <0.0001
  Single 128 (9.1) 40 (4.2)
  Divorced 100 (7.1) 102 (10.8)
Household income, $
  <15,000 447 (31.9) 34 (3.6) <0.0001
  15,000–40,000 443 (31.6) 151 (16.0)
  ≥40,000 510 (36.4) 761 (80.4)
Own dwelling 455 (32.8) 593 (63.0) <0.0001
Number of rooms in the dwelling
  ≤2 985 (72.2) 804 (86.4) <0.0001
  ≥3 380 (27.8) 127 (13.6)
Dwelling needing repairs 570 (41.4) 285 (30.3) <0.0001
Territory
  Northwest Territories 527 (37.7) 412 (43.5) <0.0001
  Yukon 134 (9.6) 467 (49.4)
  Nunavut 738 (52.7) 67 (7.1)
*

Frequencies and proportions were weighted using normalized cross-sectional weights – frequencies do not add up to the total because of missing data

As shown in Table 3, the prevalences of ever having had asthma and current asthma were significantly higher in non-Aboriginal than in Aboriginal children (P<0.05); however, the prevalence of wheeze was similar in the two groups. When these conditions were combined, the prevalence was also similar in the two groups. Female Aboriginal children had a significantly higher prevalence of asthma than male Aboriginal children (P<0.05); however, this pattern was reversed in male non-Aboriginal children, who had a slightly higher prevalence than female non-Aboriginal children. The prevalence of wheeze among children without health professional-diagnosed asthma was significantly higher (P=0.02) in Aboriginal children (12.2%) than in non-Aboriginal children (8.9%).

TABLE 3.

Prevalence of ever asthma, current asthma, wheeze and asthma-like symptoms in Aboriginal and non-Aboriginal children*

Condition Aboriginal children, %
Non-Aboriginal children, %
Male Female Total Male Female Total
Ever asthma 4.4 7.0 5.7 11.1 8.8 10.0
Current asthma 2.1 2.6 2.4 6.0 4.5 5.3
Current wheeze 15.7 14.2 15.0 15.1 13.9 14.5
Asthma-like symptoms 17.1 17.2 17.1 18.8 17.3 18.1
*

Prevalence estimates were weighted using normalized cross-sectional weights

The prevalence of asthma-like symptoms and the results from the univariate analysis are shown for childhood, parental and household factors in Aboriginal and non-Aboriginal children in Table 4 and Table 5. In Aboriginal children, infants and toddlers, as well as preschool children, had an increased risk of asthma-like symptoms compared with school-aged children (Table 4). In non-Aboriginal children, preschool-aged children had increased risk of asthma-like symptoms compared with school-aged children (Table 4). In both Aboriginal and non-Aboriginal children, childhood allergy was a significant risk factor for asthma-like symptoms. The number of siblings was not significantly associated with asthma-like symptoms in either Aboriginal or non-Aboriginal children. In Aboriginal children, the mother’s allergy history and daily smoking habit were significantly associated with asthma-like symptoms (Table 5). Non-Aboriginal children living in the Northwest Territories were at an increased risk of asthma-like symptoms in comparison with the non-Aboriginal children living in Nunavut (Table 5).

TABLE 4.

Prevalences and ORs of asthma-like symptoms for childhood factors in Aboriginal and non-Aboriginal children*

Factors Aboriginal children
Non-Aboriginal children
Asthma-like symptoms, % OR (95% CI) Asthma-like symptoms, % OR (95% CI)
Age group
  Infant and toddler 30.0 3.45 (2.38–5.00) 16.6 1.08 (0.63–1.82)
  Preschool-aged 21.5 1.97 (1.64–2.30) 20.8 1.41 (1.09–1.73)
  School-aged 11.5 1 17.2 1
Sex
  Female 17.2 0.99 (0.73–1.34) 17.3 0.80 (0.55–1.16)
  Male 17.1 1 18.8 1
Childhood allergy
  Yes 39.7 3.29 (1.82–5.93) 40.9 3.86 (2.41–6.11)
  No 15.9 1 14.9 1
Living with
  One parent 17.0 0.91 (0.58–1.45) 19.6 0.80 (0.48–1.34)
  Two parents 17.4 1 17.4 1
Number of siblings
  0 22.4 1.62 (0.99–2.64) 19.2 1.11 (0.61–2.01)
  1 16.7 1.09 (0.71–1.70) 17.1 0.96 (0.57–1.62)
  ≥2 15.8 1 18.2 1
*

Results are from logistic regression analysis for correlated data with normalized cross-sectional weights

TABLE 5.

Prevalences and ORs of asthma-like symptoms for parental and household factors in Aboriginal and non-Aboriginal children*

Factors Aboriginal children
Non-Aboriginal children
Asthma-like symptoms, % OR (95% CI) Asthma-like symptoms, % OR (95% CI)
Mother’s age at birth, years
  15–24 17.6 1.15 (0.58–2.27) 25.5 1.31 (0.65–2.66)
  25–34 19.0 1.38 (0.71–2.66) 15.4 0.86 (0.45–1.63)
  ≥35 15.2 1 17.8 1
Mother’s education level
  Less than secondary 14.3 0.88 (0.48–1.60) 23.3 1.49 (0.71–3.16)
  Secondary 23.1 1.62 (0.63–3.82) 21.5 1.32 (0.70–2.51)
  High school 18.9 1.30 (0.71–2.36) 14.1 0.77 (0.45–1.31)
  College or higher 15.9 1 17.5 1
Mother’s allergy
  Yes 28.3 1.97 (1.09–3.56) 20.3 1.26 (0.75–2.12)
  No 15.6 1 16.6 1
Mother’s asthma
  Yes 27.1 1.70 (0.57–5.05) 18.2 1.08 (0.58–2.03)
  No 16.7 1 17.5 1
Mother’s smoking habit
  Daily 19.3 1.61 (1.05–2.50) 21.7 1.47 (0.95–2.33)
  Occasional 15.5 1.34 (0.87–1.81) 21.7 1.46 (0.21–2.71)
  None 12.8 1 16.1 1
Mother’s marital status
  Married 17.0 1.16 (0.59–2.29) 17.8 1.04 (0.58–1.88)
  Single 21.6 1.63 (0.74–3.60) 28.7 2.03 (0.79–5.31)
  Divorced 13.8 1 16.3 1
Household income, $
  <15,000 15.2 0.98 (0.63–1.54) 24.4 1.75 (0.73–4.18)
  15,000–40,000 19.8 1.27 (0.82–1.95) 18.1 1.05 (0.64–1.73)
  ≥40,000 16.5 1 17.8 1
Own dwelling
  Yes 16.8 0.97 (0.64–1.45) 16.5 0.70 (0.45–1.07)
  No 17.0 1 20.5 1
Number of rooms in the dwelling
  ≥3 16.0 0.77 (0.52–1.13) 18.5 1.17 (0.66–2.07)
  ≤2 19.9 1 15.8 1
Dwelling needs repair
  Yes 18.7 1.21 (0.84–1.75) 19.2 1.11 (0.70–1.72)
  No 15.9 1 17.7 1
Territory
  Yukon 20.0 1.08 (0.71–1.67) 15.9 1.38 (0.56–3.39)
  Northwest Territories 13.4 0.63 (0.41–1.03) 21.3 1.92 (1.36–4.96)
  Nunavut 19.3 1 12.9 1
*

Results are from logistic regression analysis for correlated data with normalized cross-sectional weights

As shown in Table 6, statistically significant factors from the multivariate analysis in Aboriginal children were age group (infant/toddler versus school-aged: OR 3.72, 95% CI 2.51 to 5.52; preschool-aged versus school-aged: OR 1.93, 95% CI 1.34 to 2.77), childhood allergy (OR 2.91, 95% CI 1.55 to 5.49) and the mother’s smoking habit (daily versus none: OR 1.88, 95% CI 1.18 to 3.01). In non-Aboriginal children, factors associated with asthma-like symptoms were childhood allergy (OR 3.77, 95% CI 2.30 to 6.19) and the mother’s smoking habit (daily versus none: OR 1.66, 95% CI 1.05 to 2.63).

TABLE 6.

Factors associated with asthma-like symptoms in the multivariate logistic regression analysis in Aboriginal and non-Aboriginal children*

Factors Aboriginal children
Non-Aboriginal children
OR (95% CI) P OR (95% CI) P
Age group
  Infant and toddler 3.72 (2.51–5.52) <0.0001 1.15 (0.64–2.06) 0.64
  Preschool-aged 1.93 (1.34–2.77) 0.0004 1.41 (0.96–2.09) 0.08
  School-aged 1 1
Sex
  Female 0.91 (0.65–1.26) 0.57 0.86 (0.58–1.27) 0.44
Male 1 1
Childhood allergy
  Yes 2.91 (1.55–5.49) 0.0009 3.77 (2.30–6.19) <0.0001
  No 1 1
Mother’s smoking habit
  Daily 1.88 (1.18–3.01) 0.008 1.66 (1.05–2.63) 0.03
  Occasionally 1.58 (0.86–2.90) 0.14 1.17 (0.38–3.64) 0.79
  None 1 1
*

Results from logistic regression analysis for correlated data with normalized cross-sectional weights

In analyses restricted to wheeze outcome, after controlling for age group, sex and childhood allergy, the mother’s daily smoking habit was a significant risk factor for current wheeze in Aboriginal children (OR 2.55, 95% CI 1.45 to 4.48) but not in non-Aboriginal children (OR 1.21, 95% CI 0.69 to 2.14). In analyses restricted to asthma outcome, after controlling for age group, sex and childhood allergy, mother’s daily smoking habit was a significant risk factor for ever having had asthma in non-Aboriginal children (OR 1.96, 95% CI 1.05 to 3.66) but not in Aboriginal children (OR 0.87, 95% CI 0.45 to 1.66).

DISCUSSION

Using a large population-based database, the present study found that Aboriginal children had a significantly lower prevalence of health professional-diagnosed asthma than non-Aboriginal children. However, the prevalence of asthma-like symptoms was similar in Aboriginal and non-Aboriginal children. In addition, the prevalence of asthma in non-Aboriginal children (10%) was similar to that reported in Canadian children (12.2%) (9). In our study, the overall prevalence of asthma was 5.7% in Aboriginal children. The lower prevalence of health care professional-diagnosed asthma among Aboriginal children might have been related to differences in access to health care services between Aboriginal and non-Aboriginal populations. The higher prevalence of wheeze among Aboriginal children without an asthma diagnosis indicated that these Aboriginal children might have had reduced access to health care services, and might not have had an opportunity to meet with a health care professional and thus receive a diagnosis of asthma. In a study based on the 1991 Aboriginal Peoples Survey and the 1991 General Social Survey, Aboriginals were much less likely to use physician services than the total Canadian population, even though both populations ranked their health similarly (10).

In the 1970s, asthma was a rare condition in the Eskimo population (5). In Saskatchewan, the prevalence of asthma, determined from the physician services database, was higher in children between 0 and four years of age and lower in children five to 14 years of age in the Registered Indian population in comparison with other Saskatchewan populations (3). In our study, the sample size was too small to investigate the asthma prevalence in children younger than four years of age. In another study, the prevalence of exercise-induced bronchospasm in boys and girls among Inuit school children living in northern Quebec was lower than that observed among a group of urban school children in Montreal, Quebec (6). Hospitalization rates for asthma in Aboriginal and Torres Strait Islander children aged one to nine years were also reported to be significantly lower than in the rest of the population in Australia (11). In a study of 287,329 children between 0 and 14 years of age in China, asthma prevalence was found to be 1.5% (12), which was much lower than the corresponding asthma prevalence in developed countries, including Canada. In our study, the prevalence of asthma was higher in non-Aboriginal boys than non-Aboriginal girls, but this was reversed in Aboriginal children. However, when ever having had asthma, current asthma and current wheeze were combined into asthma-like symptoms, boys were at reduced risk of asthma-like symptoms than girls in both Aboriginal and non-Aboriginal children. Aboriginal women appear to receive diagnoses of diseases from health care professionals more often than Aboriginal men. In a study examining the sex differences in Canadian Aboriginal individuals admitted to an inpatient, hospital-based substance abuse detoxification program, women received a greater proportion of cocaine or opiate detoxification diagnoses than men, even though alcohol was the most frequent primary drug of detoxification for both sexes (13). Several studies have reported that boys have a higher prevalence of asthma than girls (3,14,15). In the Avon Longitudinal Study of Parents and Children (ALSPAC) – a birth cohort study conducted in the United Kingdom – maternal reports of child wheezing that persisted from birth to six months of age were significantly more common in boys than girls in the first three-and-a-half years of their lives (14). In Canada, sex differences in the prevalence of asthma have also been reported among Aboriginal populations in Saskatchewan (3). Boys are at greater risk of developing asthma than girls, approximately until the age of puberty. The reasons for the sex differences in asthma morbidity are not well understood. However, in a review article (15), differences in hormonal changes between boys and girls at puberty, in addition to smaller airways relative to lung volume in boys, were discussed as possible pathophysiological mechanisms for the sex differences in the prevalence of asthma (15).

In our study, the prevalence of asthma-like symptoms in infants and toddlers was higher than that in older age groups of Aboriginal children. These differences may be related to exposure to second-hand smoke at home. In a 1995 survey of the Aboriginal population, the smoking rate was 57%, which was twofold that of people in the general Canadian population (27%). In Aboriginals, the highest smoking rate was in Inuit (72%), followed by 57% in Métis and 56% in First Nations people (16). In a 1997 survey of the Aboriginal population, adults reported that they started smoking at approximately 16 years of age, with some as early as 11 years of age, and a few as young as eight years of age (17). In a study comparing American Indian and Alaskan Native children using Washington State (United States) hospitalization data for 1987 to 1999 (18), there were no significant differences in asthma hospitalization rates in children between one and five years of age. Conversely, Indian and Alaskan Native children younger than one year of age had two- to threefold higher rates of asthma hospitalization in comparison with overall asthma hospitalization rates in Washington State (18).

In our study, the prevalence of parental reports of childhood allergy in Aboriginal children was 5.9%, which was comparable with those reported in children aged six to 13 years in four Inuit communities in northern Quebec (diagnosis was based on skin prick testing and varied between 2.1% and 7.1%) (6). Childhood allergy showed a significant association with prevalence of asthma-like symptoms in both Aboriginal and non-Aboriginal children. A study of twins conducted in Finland found that among asthmatic children with at least one asthmatic parent, genetic factors explained 87% of the variation in susceptibility to asthma (19,20). Childhood allergy is another important factor associated with asthma, which has been reported in many studies (21,22). Childhood allergy history has also been reported to be strongly associated with asthma among children from ethnic minority groups, such as African-American and Mexican-American groups (23,24). In a study of 4164 children aged six to 16 years who participated in allergen testing in the Third National Health and Nutrition Examination Survey conducted in the United States from 1988 to 1994, African-American and Mexican-American children were substantially more likely to be sensitized to allergens than Caucasian children (23). Childhood allergy has also been reported to be a significant risk factor for asthma in countries where the prevalence of asthma is very low. In a study of 10,902 school children aged nine to 11 years in China, atopic sensitization, determined by skin-prick tests, was significantly associated with asthma (24).

In our study, the mother’s daily smoking habit was a significant factor associated with the prevalence of asthma-like symptoms in both Aboriginal and non-Aboriginal children. In analyses restricted to specific outcomes, the mother’s daily smoking habit was a significant risk factor for current wheeze in Aboriginal children and for ever having had asthma in non-Aboriginal children. Several studies have shown that parental cigarette smoking, especially maternal smoking, is a significant risk factor for asthma and wheeze in children. Cotinine levels in saliva and the child’s smoking habit were not significantly associated with exercise-induced bronchospasm in a study of Inuit school children living in northern Quebec (6). Maternal smoking was associated with a twofold higher incidence of transient and persistent wheezing only among the children aged 0 to three years; maternal smoking was less associated with the incidence of late-onset wheezing (25). A study of children (six to seven years of age) and adolescents (13 to 14 years of age) in Italy showed that parental smoking was associated with current asthma and wheeze in children, and maternal smoking during pregnancy was a significant risk factor for current asthma symptoms, including wheezing in children (26). In a study from southern California, United States, investigating the effect of maternal smoking during pregnancy and childhood environmental smoke in 5762 children aged 10 years or younger, in utero exposure to maternal smoking without postnatal exposure to environmental smoke was associated with an increased prevalence of physician-diagnosed asthma, wheeze-related symptoms, asthma severity and emergency room visits (27). In the present study, current and previous environmental smoke exposure was associated with wheeze-related symptoms but not with asthma prevalence. In a birth cohort study of 4089 infants conducted in Sweden, maternal smoking during pregnancy was associated with recurrent wheezing and physician-diagnosed asthma until two years of age, but exposure to environmental smoke was not associated with these outcomes (28). There have been extensive studies of the effects of tobacco smoke exposure on childhood asthma, particularly when the mother is a smoker (2932). There is also evidence showing that tobacco smoke exposure can increase asthma severity in both children and adults (33,34).

There are several limitations that need to be considered in the present study. The survey was a general health survey, and did not specifically focus on asthma and/or wheeze. Questions related to episodes of chest tightness, nocturnal shortness of breath and cough were not included in the questionnaire. Information on several risk factors, including exposure to animals, as well as types of heating and cooking apparatus, were not available.

In the present study, reports from the PMK on physician-diagnosed asthma, current asthma and current wheeze were used to determine asthma prevalence. Bootstrap weights were not available to obtain efficient estimates in the statistical analysis. Sample sizes of both Aboriginal and non-Aboriginal children may not have been adequate to determine the statistical significance of factors that had weak associations with asthma-like symptoms.

CONCLUSIONS

Asthma prevalence appears to be lower in Aboriginal children than in non-Aboriginal children in remote northern communities of Canada. The association between maternal daily smoking and asthma-like symptoms, which has been mainly reported for children living in urban areas, was observed in Aboriginal and non-Aboriginal children living in the northern and remote communities of Canada.

Footnotes

FUNDING: This study was supported by a grant from the Canadian Institutes for Health Research (grant number 62909).

DISCLAIMER: The research and analysis in this study are based on data from Statistics Canada, and the opinions expressed herein do not represent the views of Statistics Canada.

REFERENCES

  • 1.The International Study of Asthma and Allergies in Childhood (ISAAC) Steering Committee. Worldwide variation in prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and atopic eczema: ISAAC. Lancet. 1998;351:1225–32. [PubMed] [Google Scholar]
  • 2.Lawson JA, Senthilselvan A. Asthma epidemiology: Has the crisis passed? Curr Opin Pulm Med. 2005;11:79–84. doi: 10.1097/01.mcp.0000147861.60768.24. [DOI] [PubMed] [Google Scholar]
  • 3.Senthilselvan A, Lawson J, Rennie DC, Dosman JA. Stabilization of an increasing trend in physician-diagnosed asthma prevalence in Saskatchewan, 1991 to 1998. Chest. 2003;124:438–48. doi: 10.1378/chest.124.2.438. [DOI] [PubMed] [Google Scholar]
  • 4.Gerrard JW, Geddes CA, Reggin PL, Gerrard CD, Horne S. Serum IgE levels in white and metis communities in Saskatchewan. Ann Allergy. 1976;37:91–100. [PubMed] [Google Scholar]
  • 5.Herxheimer H, Schaefer O. Asthma in Canadian Eskimos. N Engl J Med. 1974;291:1419. doi: 10.1056/NEJM197412262912621. (Lett) [DOI] [PubMed] [Google Scholar]
  • 6.Hemmelgarn B, Ernst P. Airway function among Inuit primary school children in far northern Quebec. Am J Respir Crit Care Med. 1997;156:1870–5. doi: 10.1164/ajrccm.156.6.9704083. [DOI] [PubMed] [Google Scholar]
  • 7.Statistics Canada Indicators based on Statistics Canada (STC) surveys. < http://www.statcan.ca/> (Version current at March 14, 2008).
  • 8.Statistics Canada Data sets and research tools. < http://www.statcan.ca/english/rdc/whatdata.htm> (Version current at March 14, 2008).
  • 9.Public Health Agency of Canada Measuring up: A health surveillance update on Canadian children and youth. < http://www.phac-aspc.gc.ca/publicat/meas-haut/mu_r_e.html> (Version current at March 14, 2008).
  • 10.Newbold KB. Aboriginal physician use in Canada: Location, orientation and identity. Health Econ. 1997;6:197–207. doi: 10.1002/(sici)1099-1050(199703)6:2<197::aid-hec260>3.0.co;2-k. [DOI] [PubMed] [Google Scholar]
  • 11.Whybourne A, Lesnikowski C, Ruben A, Walker A. Low rates of hospitalization for asthma among Aboriginal children compared to non-Aboriginal children of the top end of the northern territory. J Paediatr Child Health. 1999;35:438–41. doi: 10.1046/j.1440-1754.1999.355393.x. [DOI] [PubMed] [Google Scholar]
  • 12.Chen YZ. Comparative analysis of the state of asthma prevalence in children from two nation-wide surveys in 1990 and 2000 year. Zhonghua Yi Xue Ke Xue Za Zhi. 2004;27:112–6. [PubMed] [Google Scholar]
  • 13.Callaghan RC, Cull R, Vettese LC, Taylor L. A gendered analysis of Canadian Aboriginal individuals admitted to inpatient substance abuse detoxification: A three-year medical chart review. Am J Addict. 2006;15:380–6. doi: 10.1080/10550490600860270. [DOI] [PubMed] [Google Scholar]
  • 14.Sherriff A, Peters TJ, Henderson J, Strachan D, Avon Longitudinal Study of Parents and Children Risk factor associations with wheezing patterns in children followed longitudinally from birth to 3(1/2) years. Int J Epidemiol. 2001;30:1473–84. doi: 10.1093/ije/30.6.1473. [DOI] [PubMed] [Google Scholar]
  • 15.Bjornson CL, Mitchell I. Gender differences in asthma in childhood and adolescence. J Gend Specif Med. 2000;3:57–61. [PubMed] [Google Scholar]
  • 16.Godel J, Chatel N. Tobacco use among Aboriginal children and youth. Paediatr Child Health. 1999;4:277–81. [Google Scholar]
  • 17.Ottawa: National Aboriginal Health Organization; 2004. First Nations and Inuit Health Surveys, 1997: A Synthesis of the National and Regional Reports. [Google Scholar]
  • 18.Liu LL, Stout JW, Sullivan M, Solet D, Shay DK, Grossman DC. Asthma and bronchiolitis hospitalizations among American Indian children. Arch Pediatr Adolesc Med. 2000;154:991–6. doi: 10.1001/archpedi.154.10.991. [DOI] [PubMed] [Google Scholar]
  • 19.Räsänen M, Kaprio J, Laitinen T, Winter T, Koskenvuo M, Laitinen LA. Perinatal risk factors for asthma in Finnish adolescent twins. Thorax. 2000;55:25–31. doi: 10.1136/thorax.55.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Laitinen T, Räsänen M, Kaprio J, Koskenvuo M, Laitinen LA. Importance of genetic factors in adolescent asthma: A population-based twin-family study. Am J Respir Crit Care Med. 1998;157:1073–8. doi: 10.1164/ajrccm.157.4.9704041. [DOI] [PubMed] [Google Scholar]
  • 21.Nickel R, Lau S, Niggemann B, et al. MAS Group Messages from the German Multicentre Allergy Study. Pediatr Allergy Immunol. 2002;13:7–10. doi: 10.1034/j.1399-3038.13.s.15.4.x. [DOI] [PubMed] [Google Scholar]
  • 22.Illi S, von Mutius E, Lau S, et al. Multicenter Allergy Study Group The natural course of atopic dermatitis from birth to age 7 years and the association with asthma. J Allergy Clin Immunol. 2004;113:925–31. doi: 10.1016/j.jaci.2004.01.778. [DOI] [PubMed] [Google Scholar]
  • 23.Stevenson LA, Gergen PJ, Hoover DR, Rosenstreich D, Mannino DM, Matte TD. Sociodemographic correlates of indoor allergen sensitivity among United States children. J Allergy Clin Immunol. 2001;108:747–52. doi: 10.1067/mai.2001.119410. [DOI] [PubMed] [Google Scholar]
  • 24.Wong GW, Hui DS, Chan HH, et al. Prevalence of respiratory and atopic disorders in Chinese schoolchildren. Clin Exp Allergy. 2001;31:1225–31. doi: 10.1046/j.1365-2222.2001.01140.x. [DOI] [PubMed] [Google Scholar]
  • 25.Martinez FD, Wright AL, Taussig LM, Holberg CJ, Halonen M, Morgan WJ. Asthma and wheezing in the first six years of life. The Group Health Medical Associates. N Engl J Med. 1995;332:133–8. doi: 10.1056/NEJM199501193320301. [DOI] [PubMed] [Google Scholar]
  • 26.Agabiti N, Mallone S, Forastiere F, et al. The impact of parental smoking on asthma and wheezing. SIDRIA Collaborative Group. Studi Italiani sui Disturbi Respiratori nell’Infanzia e l’Ambiente. Epidemiology. 1999;10:692–8. doi: 10.1097/00001648-199911000-00005. [DOI] [PubMed] [Google Scholar]
  • 27.Gilliland FD, Li YF, Peters JM. Effects of maternal smoking during pregnancy and environmental tobacco smoke on asthma and wheezing in children. Am J Respir Crit Care Med. 2001;163:429–36. doi: 10.1164/ajrccm.163.2.2006009. [DOI] [PubMed] [Google Scholar]
  • 28.Lannerö E, Wickman M, Pershagen G, Nordvall L. Maternal smoking during pregnancy increases the risk of recurrent wheezing during the first years of life (BAMSE) Respir Res. 2006;7:3. doi: 10.1186/1465-9921-7-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.United States Environmental Protection Agency . Washington, District of Columbia: Office of Research and Development, Office of Health and Environmental Assessment; 1992. Respiratory Health Effects of Passive Smoking: Lung Cancer and Other Disorders. [Google Scholar]
  • 30.Department of Health and Human Services . Washington, District of Columbia: United States Public Health Service; 1986. The Health Consequences of Involuntary Smoking: A Report of the Surgeon General. [Google Scholar]
  • 31.National Research Council . Washington, District of Columbia: National Academy Press; 1986. Environmental Tobacco Smoke: Measuring Exposures and Assessing Health Effects. [PubMed] [Google Scholar]
  • 32.Samet JM, Lange P. Longitudinal studies of active and passive smoking. Am J Respir Crit Care Med. 1996;154:S257–65. doi: 10.1164/ajrccm/154.6_Pt_2.S257. [DOI] [PubMed] [Google Scholar]
  • 33.Mannino DM, Homa DM, Redd SC. Involuntary smoking and asthma severity in children: Data from the Third National Health and Nutrition Examination Survey. Chest. 2002;122:409–15. doi: 10.1378/chest.122.2.409. [DOI] [PubMed] [Google Scholar]
  • 34.Althuis MD, Sexton M, Prybylski D. Cigarette smoking and asthma symptom severity among adult asthmatics. J Asthma. 1999;36:257–64. doi: 10.3109/02770909909075409. [DOI] [PubMed] [Google Scholar]

Articles from Canadian Respiratory Journal : Journal of the Canadian Thoracic Society are provided here courtesy of Wiley

RESOURCES