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Prematurity at birth reduces the long-term risk of atopy
M Siltanen1, M Kajosaari, M Pohjavuori
1Hospital for Children and Adolescents, University of Helsinki, Finland.
Insights
Children born preterm showed significantly less atopy by age 10 compared to those born at term. Premature birth appears linked to a reduced long-term risk of developing atopic sensitization.
Area of Science:
- Pediatric Allergy and Immunology
- Neonatal Outcomes and Long-Term Health
Background:
- Early life antigen exposure significantly influences atopic sensitization.
- Children born preterm may have a different predisposition to atopy compared to full-term infants.
Purpose of the Study:
- To investigate the association between premature birth and the development of atopy in children.
Main Methods:
- A cohort of 10-year-old children, including 72 born preterm (birth weight < 1500g) and 65 born at term (birth weight > 2500g), were evaluated.
- Atopy assessment involved questionnaires, skin prick testing, and measurement of serum total IgE, allergen-specific IgE, eosinophil cationic protein, and blood eosinophil levels.
- Perinatal and neonatal data for preterm infants were retrieved from hospital records.
Main Results:
- Children born preterm exhibited significantly lower rates of atopy (15%) compared to term-born children (31%) by age 10 (P = .03).
- The mean total IgE level was higher in the term group (74 kU/L) than in the preterm group (41 kU/L) (P = .02).
- Skin prick testing revealed positive reactions in 37% of term-born children versus 17% of preterm-born children (P = .007).
Conclusions:
- Premature birth is associated with a reduced long-term risk of atopic sensitization.
- These findings highlight a potential protective effect of prematurity against the development of atopy later in childhood.
Background:
Antigen exposure in early life has long-lasting effects on atopic sensitization. Thus the predisposition to atopy of children born preterm can be assumed to differ from that of children born at term.
Objective:
The aim of this study was to evaluate the association between premature birth and atopy.
Methods:
At an outpatient clinic, we examined 2 groups of 10-year-old children, 72 who were born preterm (birth weight < 1500 g) and 65 who were born at term (birth weight > 2500 g). The atopy data were collected with a questionnaire, by performing skin prick testing, and by measuring the serum total IgE level, 3 allergen-specific IgE levels, the eosinophil cationic protein level, and the blood eosinophil level. The data on perinatal and neonatal events affecting the preterm children were collected from the hospital records.
Results:
By the age of 10 years, the children born preterm had significantly less atopy than the children born at term: 15% versus 31% of children in the 2 groups were defined as having had obvious atopy (P = .03, odds ratio 0.41, 95% CI 0.18-0.93). The mean value of total IgE level was significantly higher in the term group, 74 kU/L versus 41 kU/L (P = .02). By skin prick testing, the children born at term had positive reactions 2 to 3 times more often; 37% versus 17% of children in the groups had at least 1 positive reaction (P = .007).
Conclusion:
Our data show that prematurity at birth is linked with a decreased long-term risk of atopic sensitization.
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