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ADOLESCENT HEALTH |
Rosângela da Costa Lima, Cesar G. Victora, and Ana Maria B. Menezes are with the Post-Graduate Programme in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil. Fernando C. Barros is with the Post-Graduate Programme in Epidemiology, Universidade Federal de Pelotas, and the Latin-American Center for Perinatology and Human Development, Pan American Health Organization/World Health Organization, Montevideo, Uruguay.
Correspondence: Requests for reprints should be sent to Rosângela da Costa Lima, MD, PhD, CP 464, 96001-970, Pelotas, RS, Brazil (e-mail: roclima{at}terra.com.br).
| ABSTRACT |
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Objectives. We studied the association between early life conditions and asthma in adolescence.
Methods. We conducted a population-based birth cohort study involving 2250 male 18-year-olds residing in Brazil.
Results. Approximately 18% of the adolescents reported having asthma. Several childhood factors were found to be significantly associated with increased asthma risk: being of high socioeconomic status, living in an uncrowded household, and children being breastfed for 9 months or longer.
Conclusions. The present results are consistent with the "hygiene hypothesis," according to which early exposure to infections provides protection against asthma. The policy implications of our findings are unclear given that risk factors for asthma protect against serious childhood diseases in developing countries.
| INTRODUCTION |
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Although genetic factors play an important role in an individuals risk of asthma, these factors probably do not account for large differences among populations.9 Thus, social, environmental, and behavioral factors must play an important role, an assertion that is confirmed by the increasing prevalence rates that have been observed. Many studies have assessed the roles of passive smoking and air pollution,10,11 dietary changes12 (including changes in breastfeeding patterns13,14), and reduced exposure to infections.11 The latter factor has been conceptualized in the "hygiene hypothesis": early exposure to infectious agents increases the production of TH1 lymphocytes, providing protection against IgE-mediated atopic diseases.
A mixture of different conditions15 with distinct etiologies and risk factors combine to cause childhood wheezing. It is important, therefore, to study the presence of wheezing among individuals of older ages, among whom atopic conditions prevail. Prospective birth cohort studies provide the ideal design for understanding the role of social, environmental, and behavioral factors in adolescent health. Few such studies have been conducted in developing countries, and the study described here is, to our knowledge, the first large cohort investigation to assess the influence of early risk factors on adolescent asthma.
| METHODS |
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In 2000, all cohort boys who still resided in Pelotas were legally required to undergo a Brazilian Army medical examination. On this occasion, they were invited to participate in the present study; if they agreed to take part, they signed an informed consent form. They then completed a standardized questionnaire and underwent anthropometric and physical examinations.
Information on the following variables was collected in the 1982 interview: monthly family income; maternal age, education level, skin color, weight gain and smoking status during pregnancy, and parity; parental tobacco use; type of delivery; gestational age; and birthweight. We assessed intrauterine growth retardation using the 10th percentile of the birthweightbygestational age curve.
In 1984, data regarding several other variables were collected via maternal reports: history of "asthma or bronchitis," expulsion of intestinal worms, or pneumonia; diphtheriapertussistetanus, polio, and measles immunization status; number of persons per bedroom; whether or not other children resided in the home; and presence of piped water and a flush toilet in the home. Also, an asset index was constructed; this variable involved a factor analysis of 5 household assets, type of residence, and number of rooms. In the case of children who could not be located in 1984, information on these variables was obtained from the 1986 questionnaire. In addition, all hospital admissions reported during the 3 interviews were recorded.
Also during the 1984 visit, children were weighed with portable scales, and their height was measured. We calculated weight-for-age, length-for-age, and weight-for-length z scores according to the standards of the National Center for Health Statistics.17
Information on breastfeeding was collected during all visits. If the child was seen in 1983 and had already been weaned, information from this interview was used; otherwise, information from the 1984 interview was used. If the child had not been seen in 1984 but was seen in 1986, the latter information was used. Few children were exclusively breastfed at any age, in that other fluids were typically introduced very early.
When children were aged 3 months, they were categorized into one of the following groups: exclusively or predominantly breastfed (breast milk in combination with water or tea), partially breastfed (breast milk in combination with nutritive fluids or semisolids), or not breastfed. Since children were seldom exclusively or predominantly breastfed after 3 months of age, we characterized feeding at older ages according to type of milk received: breast, nonbreast, or both.
In 2000, information was collected on adolescents schooling and skin color, and the scale developed for the ISAAC study was used in assessing prevalence rates of respiratory symptoms.3 This questionnaire was translated from English to Portuguese and validated by Sole et al.18 Presence of asthma was determined via a positive answer to the question "Have you ever had wheezing or whistling in the chest in the last 12 months?" We repeated all analyses using a cutoff of 6 or more positive ISAAC scale responses, the cutoff validated in Brazil.18 Our study was designed to have 80% power in terms of detecting a prevalence ratio (PR) of 1.3, at the 5% significance level, for exposures present in a 20% to 70% range of the sample.
We estimated prevalence ratios and their associated 95% confidence intervals (CIs) using Poisson regression19; we used the robust variance option in Stata 6.020 in this analysis, which allowed for the inclusion of maternal schooling, monthly family income, and the assets index. In the case of the breastfeeding variables, we included additional confounding factors in the analyses: crowding, maternal age, parental smoking, birthweight, gestational age, intrauterine growth retardation, parity, and type of delivery. When applicable, we used linear trend tests to assess ordinal variables. All statistical tests were 2 sided.
| RESULTS |
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Response rates were analyzed according to variables for which information was collected during the 1982 baseline interview (income, maternal education level, birthweight, preterm delivery, and intrauterine growth retardation). More than three quarters of respondents in the study categories were traced with the exception of those in the lowest family income group, of whom 72.5% were located (data available on request).
Among the respondents, 18.6% (95% CI = 17.0%, 20.2%) reported experiencing "wheezing in the chest" in the past year. When asthma was defined according to the ISAAC scale cutoff (6 or more positive responses), 16.1% (95% CI = 14.6%, 17.7%) of the respondents were classified as having asthma. This classification identified more severe cases than the general question on wheezing.
All 3 socioeconomic indicesfamily income, maternal education, and the asset indexwere positively associated with asthma prevalence rates in the crude analyses; when these variables were adjusted for one another, only the asset index remained significant. Two variables related to crowding were significantly associated with asthma in both the crude and adjusted analyses; children living in a home with a high number of persons per bedroom or living in a home with other children had lower asthma risks (Table 1
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Table 2
shows the effects of variables related to gestation and type of delivery. After adjustment, only type of delivery remained significant, with a 29% increase in asthma rates among babies delivered via cesarean delivery. Birthweight was not associated with risk of asthma, even when it was coded as an ordinal variable with several categories; also, there was no association with intrauterine growth retardation. Neither maternal age nor maternal skin color was associated with asthma risk (data not shown).
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Table 4
shows that children who were underweight or stunted at the age of 20 months exhibited reduced asthma prevalence rates; after adjustment, however, this association was no longer significant. Table 4
also shows data relating to morbidity. A history of having expelled intestinal worms and a history of pneumonia were not associated with later risk of asthma; however, children whose mothers reported as experiencing "asthma or bronchitis" exhibited a 40% increased risk of asthma as adolescents.
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To investigate the possibility of reporting bias, we analyzed the association between education history and asthma. Relative to boys with fewer than 6 years of schooling, those with 6 to 9 years of schooling exhibited a 15% decrease in asthma risk, and those with 10 or more years exhibited a 25% decrease (P = .19).
We repeated all analyses using the ISAAC scale cutoff (according to which 16.1% of the respondents had asthma; these individuals were included among the 18.6% who reported having experienced wheezing in the past year). In the adjusted analyses, the associations with the asset index, number of persons per bedroom, number of other children living in the home, type of delivery, breastfeeding pattern, and report of asthma in 1984 remained significant. Two variables that were not associated with respondents reports of wheezing in the past yearnormal or high weight for age (PR = 2.17; 95% CI = 1.06, 4.43) and report of expulsion of worms (PR = 0.76; 95% CI = 0.60, 0.96)were significantly associated with ISAAC scale score.
| DISCUSSION |
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Limitations of the study include its restriction to male participants, the lack of information on familial history of asthma, and the absence of data on sera immunoglobulins. The finding of a direct association between wealth indicators and asthma prevalence raised the possibility of reporting bias; however, such bias was not likely in that adolescents at higher education levels were slightly less likely to report asthma.
We found a prevalence rate of 18.6% in terms of wheezing reported in the previous 12 months, while the mean prevalence among 17 Latin American studies using the same criterion as that used here was 17%. When we used the ISAAC scale cutoff, the asthma prevalence rate was 16.1%. The only other Brazilian study involving use of the same criteria employed here revealed a 22.5% prevalence rate among São Paulo adolescents aged 13 or 14 years. Air pollution levels are high in São Paulo but very low in Pelotas, which may partly account for this difference.18
Our analyses showed that high socioeconomic status, living in an uncrowded household, and children being breastfed for 9 months or longer were associated with higher asthma risks. In addition, when the stricter definition of asthma was used, individuals of adequate weight and those not having expelled worms were both at risk for asthma. All of these variables are well-known protective factors against childhood infections. Our findings are consistent with the earlierdescribed "hygiene hypothesis," according to which early exposure to infections protects one against asthma.11 However, other variables associated with exposure to infectious agents, including history of pneumonia, hospital admissions, and immunizations, were not associated with asthma risk.
Mallol et al.21(p444) argued that the high prevalence rates of asthma found in 17 Latin American studies contradict the hygiene hypothesis: "factors that appear to protect against asthma . . . do not seem to play a protective role in this region." However, this statement was based on an ecological comparison of prevalence rates between Latin American studies and other investigations. No individual-level analyses were presented. Furthermore, the study sites were mostly in national capitals or other large polluted cities, and the samples were restricted to children attending school; thus, the results may not be representative of the poorest populations in these countries. Our results show that when a population-based sample of adolescents is analyzed at the individual level, it is possible to detect several associations supporting the hygiene hypothesis.
An interesting finding related to type of delivery. After adjustment for socioeconomic variables, babies delivered via cesarean delivery exhibited a 29% increase in asthma prevalence. Moreover, this association persisted after adjustment for breastfeeding patterns. The study of Annesi-Maesano et al.22 conducted in France produced similar results, and the authors speculated that intrauterine conditions, if adverse, could affect lung development. However, in Brazil, cesarean deliveries appear to be more strongly associated with socioeconomic status than with gestational risk.23 In a Finnish study, Kero et al.24 recently reported an association that they attributed to lower microbial exposures in surgically delivered babies. In our study, the possibility of residual confounding according to social status cannot be dismissed.
Of particular interest was the positive association between breastfeeding duration and asthma. The analyses comparing different durations of breastfeeding and those examining feeding patterns at different ages (Table 3
) produced consistent results. These findings may be regarded as counterintuitive, in that it has been proposed that breast milk may protect against atopic disorders.13 In a 1988 review, Kramer14 discussed methodological requirements for studies involving analyses of breastfeeding, including a short recall period for information on breastfeeding and the need for (1) interviewers unaware of breastfeeding history, (2) at least a 2-month assessment of breastfeeding patterns, and (3) inclusion of infants who have been exclusively breastfed (or nearly so). All of these criteria were met in the present study.
Two recent reviews assessed breastfeeding and childhood asthma. Gdalevich et al.13 carried out a meta-analysis of 12 prospective studies conducted in developed countries. The summary odds ratio for the protective effect of breastfeeding was 0.70 (95% CI = 0.60, 0.81). The effect was greater when a family history of asthma was present. Takemuras et al.25 review of asthma and other atopic conditions included 3 studies showing protective effects,2628 10 showing no association, and 2 reporting an increased risk.
The 2 studies that revealed an increased risk were those of Martin et al.29 and Savilahti et al.30 The Martin et al. Australian study, which involved respondents aged 7 to 21 years, showed that those with severe asthma had been breastfed longer than those with mild or moderate asthma and those without asthma. Savilahti et al.30 reported a higher frequency of atopic conditions in Finnish infants who were exclusively breastfed for 9 months or longer. The Takemura et al. results from their own study showed that, after adjustment for several confounding variables, Japanese children breastfed at the age of 3 months exhibited a 20% increase in asthma prevalence at the ages of 6 to 15 years.
However, as some authors have pointed out,15,31 results from childhood studies cannot necessarily be extrapolated to adolescents, in that infectious wheezing conditions and atopic asthma are combined in these studies32; since breastfeeding may protect against the former, an overall protective effect may be found. The pair of reviews just described identified 2 studiesthose of Takemura et al.25 and Martin et al.29including adolescents. We were able to identify another 6 recent studies focusing on this issue. Of the 8 combined studies, 4 reported a positive association between breastfeeding and asthma (Martin et al.,29 Takemura et al.,25 Wright et al.,33 and Sears et al.34), 2 reported a negative association (Saarinen and Kajosaari35 and Schwartz et al.36), and 2 reported no association (Gustafsson et al.37 and Lewis et al.38).
In the Wright et al. study, the association between breastfeeding and asthma was restricted to adolescents whose mothers had a history of asthma. The authors provided an extensive discussion of the possible biological mechanisms behind this association.33 First, the breast milk of allergic mothers may differ from that of nonallergic mothers in ways that affect infants subsequent susceptibility to allergens. Second, according to the hygiene hypothesis, breastfeeding may hamper the development of immune responses as a result of reduced exposure to pathogens in infancy.
As mentioned, our study is the first investigation conducted outside of a developed country to focus on risk factors for adolescent asthma. If the hygiene hypothesis is correct, factors that protect against infections are likely to be stronger risk factors for asthma in less developed countries, since the infectious burden will be greater. Furtherand betterstudies are needed on this issue.
The policy implications of the current findings are not clear cut. A number of countries are undergoing epidemiological and nutritional transitions, and changes involving the social, environmental, and behavioral factors that protect against childhood infections and malnutrition may increase the risk of chronic diseases later in life. An example of this dilemma is our recent research39 showing that rapid growth in infancy protects against early morbidity and mortality but leads to overweight and obesity in adolescence. The results described here may represent another example of this trade-off.
There is no question that breastfeeding, avoidance of malnutrition and crowding, and reductions in the presence of infections are highly beneficial for infants and children, but there may be mixed consequences later in life. Moreover, given current knowledge, there is no question that childhood risk factors should be curtailed, since the benefits for young children far outweigh later risks.
| Acknowledgments |
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We acknowledge the logistic support of the Brazilian Army, in particular Colonel J. C. Poppe, Major L. M. Coutinho, Captain J. L. Barros, and O. Petiz, and the contributions of Jaqueline Joanol Dias.
Human Participant Protection
The Medical Research Board of the Federal University of Pelotas, which is affiliated with the National Commission on Research Ethics of the Brazilian Ministry of Health, approved the study protocol. All respondents provided written informed consent.
| Footnotes |
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Accepted for publication March 2, 2003.
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