Wheeze trajectories: Determinants and outcomes in the CHILD Cohort Study

J Allergy Clin Immunol. 2022 Jun;149(6):2153-2165. doi: 10.1016/j.jaci.2021.10.039. Epub 2021 Dec 30.

Abstract

Background: Wheezing in early life is associated with asthma in adulthood; however, the determinants of wheezing trajectories and their associations with asthma and lung function in childhood remain poorly understood.

Objective: In the CHILD Cohort Study, we aimed to identify wheezing trajectories and examine the associations between these trajectories, risk factors, and clinical outcomes at age 5 years.

Methods: Wheeze data were collected at 8 time points from 3 months to 5 years of age. We used group-based trajectory models to derive wheeze trajectories among 3154 children. Associations with risk factors and clinical outcomes were analyzed by weighted regression models.

Results: We identified 4 trajectories: a never/infrequent trajectory, transient wheeze, intermediate-onset (preschool) wheeze, and persistent wheeze. Higher body mass index was a common risk factor for all wheeze trajectories compared with that in the never/infrequent group. The unique predictors for specific wheeze trajectories included male sex, lower respiratory tract infections, and day care attendance for transient wheeze; paternal history of asthma, atopic sensitization, and child genetic risk score of asthma for intermediate wheeze; and maternal asthma for persistent wheeze. Blood eosinophil counts were higher in children with the intermediate wheeze trajectory than in those children with the other trajectories at the ages of 1 and 5 years. All wheeze trajectories were associated with decreased lung function and increased risk of asthma at age 5 years.

Conclusions: We identified 4 distinct trajectories in children from 3 months to 5 years of age, reflecting different phenotypes of early childhood wheeze. These trajectories were characterized by different biologic and physiologic traits and risk factors.

Keywords: CHILD Cohort Study; Wheeze trajectories; asthma; early-life determinants; genetic risk; lung function; pediatrics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma* / etiology
  • Child
  • Child, Preschool
  • Cohort Studies
  • Humans
  • Hypersensitivity, Immediate*
  • Infant
  • Male
  • Phenotype
  • Respiratory Sounds / etiology
  • Risk Factors

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