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Published on: August 7, 2017
Recurrent wheeze in early childhood and asthma among children at risk for atopy
Ngoc P Ly1, Diane R Gold, Scott T Weiss
1Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Children with recurrent early wheeze face a fourfold increase in asthma risk. Frequent early wheeze significantly elevates asthma risk, highlighting the need for close clinical follow-up in at-risk children.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Epidemiology
Background:
- The natural history of wheezing disorders in children at risk for atopy is not well understood.
- Children with a parental history of asthma or allergies are at increased risk for developing atopic diseases.
Purpose of the Study:
- To investigate the relationship between early wheezing patterns and the development of asthma by age 7 in high-risk children.
- To identify early indicators of childhood asthma in genetically predisposed individuals.
Main Methods:
- Prospective cohort study of children with parental history of asthma or allergies, followed from birth.
- Wheezing was monitored bimonthly until age 2, then every 6 months until age 7.
- Recurrent early wheeze defined as >=2 episodes in the first 3 years; frequent early wheeze as >=2 episodes/year.
- Asthma at age 7 defined as physician diagnosis with prior year wheezing.
Main Results:
- Over 50% of children experienced wheeze before age 3.
- Recurrent early wheeze was observed in 26% and frequent early wheeze in 2.7% of participants.
- Children with recurrent early wheeze had a fourfold increased odds of asthma at age 7.
- Children with frequent early wheeze had a twelvefold increased odds of asthma at age 7.
Conclusions:
- Absence of recurrent early wheeze suggests a low risk of school-age asthma in children with atopic predisposition.
- Early wheezing patterns, particularly frequent early wheeze, are strong predictors of childhood asthma.
- Close clinical monitoring is recommended for children with frequent early wheeze and a family history of atopy.
Objectives:
Little is known about the natural history of wheezing disorders among children at risk for atopy. We examined the relation between early wheeze and asthma at 7 years of age among children with parental history of asthma or allergies followed from birth.
Methods:
Information on wheeze was collected bimonthly from birth to age 24 months and every 6 months thereafter. Recurrent early wheeze was defined as > or =2 reports of wheezing in the first 3 years of life. Frequent early wheeze was defined as > or =2 reports of wheezing per year in the first 3 years of life. At 7 years of age, asthma was defined as physician-diagnosed asthma and wheezing in the previous year.
Results:
Of the 440 participating children, 223 (50.7%) had > or =1 report of wheeze before 3 years old, 111 (26.0%) had recurrent early wheeze, and 12 (2.7%) had frequent early wheeze. Whereas only 31 (13.9%) of 223 children with > or =1 report of wheeze developed asthma at 7 years of age, 24 (21.6%) of 111 children with recurrent early wheeze developed asthma at 7 years of age. Among the 12 children with frequent early wheeze, 6 (50%) had asthma at 7 years of age. After adjustment for other covariates, recurrent early wheeze in children at risk for atopy was associated with a fourfold increase in the odds of asthma at 7 years of age, and frequent early wheeze was associated with an approximately 12-fold increase in the odds of asthma at 7 years of age. Most (94%) of the children without frequent early wheeze did not develop asthma at 7 years of age.
Conclusions:
The absence of recurrent early wheeze indicates a very low risk of asthma at school age among children with parental history of asthma or allergies. Early identification of children who will develop asthma at school age is difficult, even in children at risk for atopy. However, children with parental history of asthma or allergies who have frequent early wheeze, in particular, are at greatly increased risk of asthma and merit close clinical follow-up.
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