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Release date：2019-09-23

JACI

[IF:13.1]

Relationships among aeroallergen sensitization, peripheral blood eosinophils, and periostin in pediatric asthma development
https://dio.org/10.1016/j.jaci.2016.05.033
Abstract:
Background: Biomarkers, preferably noninvasive, that predict asthma inception in children are lacking.
Objective: Little is known about biomarkers of type 2 inflammation in early life in relation to asthma inception. We evaluated aeroallergen sensitization, peripheral blood eosinophils, and serum periostin as potential biomarkers of asthma in children.
Methods: Children enrolled in the Childhood Origins of Asthma study were followed prospectively from birth. Blood samples were collected at ages 2, 4, 6, and 11 years, and serum- specific IgE levels, blood eosionophil counts, and periostin levels were measured in 244 children. Relationships among these biomarkers, age, and asthma were assessed.
Results: Serum periostin levels were approximately 2- to 3-fold higher in children than previously observed adult levels. Levels were highest at 2 years (145 ng/mL), and did not change significantly between 4 and 11 years (128 and 130 ng/mL). Age2 year periostin level of 150 ng/mL or more predicted asthma at age 6 years (odds ratio [OR], 2.3; 95% CI, 1.3-4.4). Eosinophil count of 300 cells/mL or more and aeroallergen sensitization at age 2 years were each associated with increased risk of asthma at age 6 years (OR, 3.1; 95% CI, 1.7-6.0 and OR, 3.3; 95% CI,1.7-6.3). Children with any 2 of the biomarkers had a significantly increased risk of developing asthma by school age (>_2 biomarkers vs none: OR, 6.6; 95% CI, 2.7-16.0).
Conclusions: Serum periostin levels are significantly higher in children than in adults, likely due to bone turnover, which impairs clinical utility in children. Early life aeroallergen sensitization and elevated blood eosinophils are robust predictors of asthma development. Children with evidence of activation of multiple pathways of type 2 inflammation in early life are at greatest risk for asthma development. (J Allergy Clin Immunol 2016;nnn:nnn-nnn.)
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All Author:
Halie M. Anderson, MD,a Robert F. Lemanske, Jr, MD,a Joseph R. Arron, MD, PhD,b Cecile T. J. Holweg, PhD,b Victoria Rajamanickam, MS,c Ronald E. Gangnon, PhD,c James E. Gern, MD,a and Daniel J. Jackson

2019-9-11 Article

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Release date：2019-09-23