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. 2016 Apr 15;50:15. doi: 10.1590/S1518-8787.2016050005100

Risk factors for recurrent wheezing in infants: a case-control study

Fatores de risco para sibilância recorrente em lactentes: estudo caso-controle

Roberta Barros de Sousa I, Décio Medeiros II, Emanuel Sarinho II, José Ângelo Rizzo III, Almerinda Rêgo Silva II, Ana Carolina Dela Bianca II
PMCID: PMC4904490  PMID: 27143615

ABSTRACT

OBJECTIVE

To evaluate the association between recurrent wheezing and atopy, the Asthma Predictive Index, exposure to risk factors, and total serum IgE levels as potential factors to predict recurrent wheezing.

METHODS

A case-control study with infants aged 6-24 months treated at a specialized outpatient clinic from November 2011 to March 2013. Evaluations included sensitivity to inhalant and food antigens, positive Asthma Predictive Index, and other risk factors for recurrent wheezing (smoking during pregnancy, presence of indoor smoke, viral infections, and total serum IgE levels).

RESULTS

We evaluated 113 children: 65 infants with recurrent wheezing (63.0% male) with a mean age of 14.8 (SD = 5.2) months and 48 healthy infants (44.0% male) with a mean age of 15.2 (SD = 5.1) months. In the multiple analysis model, antigen sensitivity (OR = 12.45; 95%CI 1.28–19.11), positive Asthma Predictive Index (OR = 5.57; 95%CI 2.23–7.96), and exposure to environmental smoke (OR = 2.63; 95%CI 1.09–6.30) remained as risk factors for wheezing. Eosinophilia ≥ 4.0% e total IgE ≥ 100 UI/mL were more prevalent in the wheezing group, but failed to remain in the model. Smoking during pregnancy was identified in a small number of mothers, and secondhand smoke at home was higher in the control group.

CONCLUSIONS

Presence of atopy, positive Asthma Predictive Index and exposure to environmental smoke are associated to recurrent wheezing. Identifying these factors enables the adoption of preventive measures, especially for children susceptible to persistent wheezing and future asthma onset.

Keywords: Infant, Asthma, Risk Factors, Respiratory Sounds, Allergens, Smoke, Case-Control Studies

INTRODUCTION

Wheezing resulting from peripheral airway narrowing is a frequent occurrence in the pediatric age group and may be a sign of systemic disease. Although asthma is the main cause of wheezing in infancy, this must always be a diagnosis of exclusion 16 . Many children have recurrent coughing and wheezing episodes early in life, normally during viral respiratory infections 15 . In most cases, there is a spontaneous remission of wheezing. Nevertheless, approximately 50.0% of infants and pre-school children are still wheezing at the age of six 20 . Wheezing infants are defined as children with a history of three or more wheezing episodes over a six-month period 16 .

In the International Study of Wheezing in Infants (EISL), a multi-center study to develop epidemiological knowledge of wheezing infants, prevalence of wheezing in Brazil among first-year infants varied from 43.0% to 61.0%, with 28.0% of recurrent wheezing infants 8 . This study also showed that some factors, such as early onset and number of viral infections and maternal smoking during pregnancy, had a strong correlation with cases of recurrent wheezing 18 .

The association between recurrent symptoms and personal or family history of atopy helps the early diagnosis of asthma a , an inflammatory disease 24 that may lead to airway remodeling and decreased lung function in the first months of life 19 . Diagnostic criteria have been proposed for the early diagnosis of children with a high risk of developing asthma 7 . The Asthma Predictive Index (API) aims to identify wheezing infants at risk of developing the disease. Family history of atopy and atopic dermatitis are considered major criteria, while diagnosis of personal allergic rhinitis, wheezing with no upper airway infection, and blood eosinophilia ≥ 4.0% are considered minor criteria. The presence of one major or two minor criteria in an infant with three or more wheezing episodes is considered high risk for the development of asthma 7 .

Allergen sensitivity before the age of five, an important atopy marker, has been related to the development of childhood asthma 13 . However, previous studies have only investigated the prevalence of allergy in children over four years old 11 , 29 . The early diagnosis of asthma is essential to prevent chronic consequences of recurrent wheezing, by introducing appropriate therapy and secondary prevention. This study aims to evaluate the association between recurrent wheezing and potential predicting factors such as atopy, Asthma Predictive Index, exposure to risk factors for allergic diseases, and total serum IgE levels.

METHODS

This is a case-control study with infants aged 6-24 months treated at the outpatient clinic of the Hospital das Clínicas of the Universidade Federal de Pernambuco (HC/UFPE) from November 2011 to March 2013. Recurrent wheezing infants from the hospital’s Allergy and Immunology Clinic composed the case group. Infants of the same age group from the Pediatrics and Childcare Clinic, with no history of wheezing, constituted the control group. The individuals were selected as they arrived for routine health care in the respective clinics.

The study enrolled children whose parents or legal guardians signed an informed consent form. The following were considered exclusion criteria: other chronic respiratory conditions, aspiration diseases, congenital anomalies, immunodeficiency disorders, prematurity, contraindication for skin testing and technical failure in blood test or collection.

Following the examination, the children’s parents or guardians answered questions based on the EISL 9 questionnaire investigating the presence, without quantifying, of clinical parameters (airway infections, use of paracetamol and antibiotics) and risk factors related to allergic diseases (passive smoking or smoking during pregnancy, exposure to smoke – wood-burning stoves, factory chimneys or agricultural burning near home, day-care attendance, presence of dust accumulators – carpets, curtains, cushions, stuffed animals – or mold, cockroaches, and pets in the house). The Asthma Predictive Index 7 was applied, indicating major (family history of asthma and atopic dermatitis) and minor (allergic rhinitis, peripheral eosinophilia ≥ 4.0%, and wheezing with no upper airway infection) criteria for the future onset of asthma. It was considered positive when at least one major or two minor criteria were present.

Sensitization to inhalant and food antigens was assessed by skin prick tests using standardized extracts (FDA Allergenic®, Rio de Janeiro, Brazil). The following inhalant antigens were evaluated: Dermatophaghoides pteronyssinus, Dermatophaghoides farinae, Blomia tropicalis, fungal mix (Aspergillus fumigatus and Alternaria alternata), dog, cat and cockroach epithelium mix (Blattella germanica and Periplaneta americana). Regarding food allergens, alpha-lactalbumin, beta-lactoglobulin, casein, soy, egg, and peanut were assessed. Blood was collected from infants for eosinophil count by the automated method of leukocyte differentiation in blood count and total serum IgE levels by electrochemiluminescence.

A logistic regression model was applied to the independent variables presenting p < 0.10 in the univariate analysis. The strength of the association between wheezing condition and the various outcomes was evaluated by odds ratio. Pearson’s Chi-square test was used for the categorical variables. Fisher’s exact test was used when the expected values were lower than five. Student’s t-test was used to compare the mean age between both groups. A significance level of 5% was considered.

The study was approved by the Ethics Committee for Research Involving Human Subjects of the Health Sciences Center of the Universidade Federal de Pernambuco (CEP/CCS/UFPE), CAAE registration number 0338.0.172.000-10.

RESULTS

We evaluated 113 patients, 65 wheezing infants with a mean age of 14.8 (SD = 5.2) months and 50 controls with a mean age of 15.2 (SD = 5.1) months (p > 0.05). Two subjects from the control group were excluded due to venous access difficulties after signing the consent form and answering the questionnaire, resulting in n = 48 in this group. Males were prevalent in the wheezing group (p = 0.041). Among wheezing infants, symptoms onset age varied from one month to 18 months, with an average of 8 (SD = 5.6) months (Table 1).

Table 1. Characteristics of evaluated infants. Pernambuco, Northeastern Brazil, 2013.

Characteristic Wheezing infants (n = 65) Non-wheezing infants (n = 48) p


n/mean %/SD n/mean %/SD
Sex (male)a 41 63,1 21 43.8 0.041
Age in monthsb 14.8 5.2 15.2 5.1 0.701
Age of symptoms onset in monthsb 8 5.6 NA - -

NA: not applicable

a n and %.

b mean and SD.

We found sensitization to inhalant and food allergens in 11.0% and 6.0% of wheezing infants, respectively. The most prevalent inhalant allergen was Blomia tropicalis (6.2%) and the most prevalent food allergen was egg (3.1%). We found no combined sensitization to inhalant and food allergens in the same patient. Only one non-wheezing infant (2.1%) showed sensitization to an inhalant allergen (fungal mix) and none to food allergens (Table 2).

Table 2. Sensitization to inhalant and food allergens in evaluated infants. Pernambuco, Northeastern Brazil, 2013.

Allergen Wheezing infants Non-wheezing infants

n % n %
Inhalant allergens 7/65 10.7 1/48 2.1
Dermatophaghoides pteronyssinus 2/7 28.6 0 -
Dermatophaghoides farinae 1/7 14.3 0 -
Blomia tropicalis 4/7 57.1 0 -
Fungal mix* 0 - 1/1 100
Food allergens 4/65 6.2 - -
Cow’s milk 1/4 25.0 0 -
Egg 2/4 50.0 0 -
Peanut 1/4 25.0 0 -

* Fungal mix (Alternaria alternata and Aspergillus fumigatus).

Forty-eight percent of recurrent wheezing infants and 30.0% of non-wheezing subjects showed total serum IgE equal to or above 100 UI/mL (variation of 3 to 3.859 UI/mL) (p = 0.059) (data not shown). Peripheral blood eosinophilia greater than or equal to 4.0% of leukocytes was observed in 46.2% of recurrent wheezers and in 18.8% of infants with no previous wheezing history (p = 0.002), with an average percentage of 3.65% (SD = 1.48%; variation of 0.4% to 18.2%) (data not shown).

API was positive for 81.5% of recurrent wheezing infants and 44.8% of non-wheezers (p < 0.001). The presence of atopic dermatitis was the sole factor with no difference between both groups (Table 3).

Table 3. API in evaluated infants. Pernambuco, Northeastern Brazil, 2013.

API Wheezing infants Non-wheezing infants p

n % n %
Positive 53 81.5 21 43.8 < 0.001
Major criteria
Family history of asthma 43 66.2 18 37.5 0.003
Atopic dermatitis 6 9.2 5 10.4 1.0
Minor criteria
Allergic rhinitis 23 35.4 6 12.5 0.006
Eosinophilia ≥ 4.0% 30 46.2 9 18.8 0.002
Wheezing without URI 35 53.9 NA -

API: Asthma Predictive Index; URI: upper respiratory tract infection; NA: not applicable

Among the risk factors investigated, only the presence of pets in the house and exposure to smoke caused by environmental pollution were individually associated with the occurrence of wheezing (Table 4).

Table 4. Risk factors associated to recurrent wheezing in evaluated infants. Pernambuco, Northeastern Brazil, 2013.

Risk factor Wheezing infants Non-wheezing infants p

n % n %
Day care attendance 8 12.3 7 14.6 0.725
Dust accumulators 53 81.4 41 85.4 0.586
Mold at home 27 41.5 21 43.8 0.814
Cockroaches at home 46 70.8 36 75.0 0.618
Pets 18 27.7 22 45.8 0.046
Smoking during pregnancy 6 9.2 5 10.4 > 0.999
Passive smoking 17 26.2 19 39.6 0.130
Exposure to smoke 39 60.0 17 35.4 0.010
Caesarean section 36 55.4 20 41.7 0.149
EB ≥ 6 months 19 29.2 20 41.7 0.169
Repeated URI 48 73.8 31 64.6 0.289

EB: exclusive breastfeeding; URI: upper respiratory tract infection

In the multiple analysis model, sensitization to allergens (OR = 12.45; 95%CI 1.28–19.11), positive API (OR = 5.57; 95%CI 2.23–7.96) and exposure to smoke (OR = 2.63; 95%CI 1.09–6.30) persisted as important risk factors for wheezing (Table 5). We excluded variables that could adjust the model based on previous knowledge, such as smoking during pregnancy, passive smoking after birth, upper airway infections, total IgE, and day care attendance 4 , 22 , since their p-value was greater than 1.

Table 5. Multiple analysis of factors associated with wheezing in evaluated infants. Pernambuco, Northeastern Brazil, 2013.

Associated factor OR 95%CI p
Sensitization to allergens 12.45 1.28–19.11 0.029
Positive API 5.57 2.23–7.96 < 0.001
Exposure to smoke 2.63 1.09–6.30 0.030

API: Asthma Predictive Index

DISCUSSION

In this study evaluating infants aged 6-24 months, sensitization to inhalant and food allergens, positive Asthma Predictive Index and exposure to smoke were associated with recurrent wheezing.

Longitudinal studies established early sensitization to allergens as one of the main risk factors for persistent wheezing 25 , 28 , sensitization to inhalant household allergens being the most important 8 . In addition, asthma severity is increased in atopic patients exposed to high levels of allergens 17 .

Similarly to this study, several other authors have observed a greater prevalence of wheezing among male infants, an intrinsic risk factor. The average age for the onset of symptoms in Brazil in the EISL was five months 18 . In our study, the average age was slightly higher.

In Germany, a multicenter study assessing 1,290 children with a family history of atopy investigated the relation between the presence of IgE specific to inhalant and food allergens at 12 months and the development of atopic disease at the age of six. The authors observed that children with early sensitization to inhalant allergens presented greater risk of developing allergic disease 6 .

A study carried out in different Brazilian localities observed that sensitization to food was prevalent in the first years of life, and to inhalants in older age groups 23 . These findings were also observed in other countries 2 , 27 , but not in this study. In this case, sensitization to the house dust mite was prevalent, with Blomia tropicalis being the main allergen. The high levels of sensitization to mites in Brazil may be associated to the high level of exposure to these allergens at home 26 . The incidence of specific sensitization to the house dust mite tends to increase progressively with age, while sensitization to food decreases 11 . However, the design of this study does not allow us to reach such an assessment.

Total serum IgE and peripheral blood eosinophilia 3 , 19 have been associated to a persistent wheezing condition. Similarly to Naspitz et al. 23 , we also observed a wide variation in total IgE levels, the highest occurring in the case group (p = 0.059). Medeiros et al. 21 concluded that total serum IgE can be influenced by current or past presence of intestinal parasites. Peripheral blood eosinophilia count was also higher in the group of wheezing infants (p = 0.002).

In this study, infants with positive API showed a higher probability of persistent wheezing. This outcome was expected, since this scoring system was developed to identify among recurrent wheezing infants those with greater risk to continue wheezing until school age 7 . We observed, however, two recurrent wheezing infants with positive skin tests but negative API, which might suggest a limitation of this index.

Among avoidable risk factors, exposure to smoke from environmental pollution was most strongly associated with the occurrence of wheezing. Children exposed to smoke were 2.6 times more likely to be recurrent wheezers than children who had no contact with smoke. Indeed, air pollution, whether from the use of biomass fuels (wood, coal, animal manure, among others) or from vehicles, increases the risk and severity of asthma a . Environmental tobacco smoke and or smoking during pregnancy were not identified as risks factors in this study. This may be due to the low prevalence of smoking during pregnancy and the fact that passive smoking was more prevalent in the control group. Nevertheless, exposure to tobacco smoke must be avoided.

The association between viral respiratory infection and atopy, despite still being controversial, has also been considered a risk factor for persistent wheezing and later asthma onset 15 . In this study, prevalence of viral infection was high in both groups, although there was no significant difference between them.

Reduced inflammatory response or non-exposure to allergens may have led to the higher percentage of negative results in the immediate hypersensitivity test 14 . This may have affected our findings. A further limitation concerns data interpretation, since no stool and specific anti-ascaris IgE tests were carried out, which would be necessary to eliminate any present or past geohelmynth infection that could alter the peripheral blood eosinophilia count, total serum IgE levels, and positive response to immediate allergen hypersensitivity 1 .

Fitzpatrick et al. 12 showed the importance of atopy in defining pediatric asthma. Atopy can be confirmed by detecting allergen-specific IgE by in vivo immediate hypersensitivity skin testing 23 .

The higher frequency of positive reaction to allergy skin tests in wheezing infants suggests that early sensitization influences recurrent wheezing. Such findings suggest that immediate response skin tests, which present good sensitivity, specificity and safety, should be carried out when assessing wheezing infants, alongside API assessment.

The identification of allergen sensitivity allows asthma diagnoses in infants and pre-school children to be guided by more objective parameters, supporting the adoption of drug treatment and directing environmental control measures, thus reducing allergen exposure by children susceptible to persistent wheezing. Early asthma diagnosis and treatment in these children, alongside objective measures to prevent exposure, improve their quality of life and the prognosis of asthma a . This context enables the development of studies to ascertain the atopic profile and assess the routine use of skin testing in early wheezing infants.

Footnotes

a

Global Initiative for Asthma. Global Strategy for the diagnosis and management of asthma in children 5 years and younger. Update 2009 [cited 2013 nov 25]. Available from: http://www.ginasthma.org/local/uploads/files/GINA_Under5_2009_CorxAug11.pdf

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