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Published on: April 21, 2019
Cord serum immunoglobulin E as a risk factor for allergic symptoms and sensitization in children and young adults
Maria Pesonen1, Markku J T Kallio, Martti A Siimes
1Department of Dermatology, Skin and Allergy Hospital, Helsinki University Hospital, Helsinki, Finland. maria.pesonen@luukku.com
Insights
Elevated cord serum immunoglobulin E (CS-IgE) predicts later allergy development up to age 20. This early marker helps identify infants at high risk for atopic diseases, aiding preventive strategies.
Area of Science:
- Immunology
- Allergology
- Pediatrics
Background:
- Identifying early markers for atopic predisposition is crucial for targeted allergy prevention in infants.
- Elevated cord serum immunoglobulin E (CS-IgE) is a known risk factor for childhood allergies, but its long-term predictive value is less understood.
Purpose of the Study:
- To determine if CS-IgE levels can predict atopic manifestations up to age 20 years.
- To assess the utility of CS-IgE in identifying individuals at high risk for developing allergies later in life.
Main Methods:
- Prospective follow-up of 200 newborns until age 20.
- Measurement of CS-IgE at birth, with re-examinations at ages 5, 11, and 20, including allergic symptom assessment, skin prick testing, and serum total IgE levels.
Main Results:
- Elevated CS-IgE was associated with allergic symptoms and positive skin prick tests at age 5.
- CS-IgE predicted allergic rhinoconjunctivitis at age 20 and elevated serum total IgE at ages 11 and 20.
- Sensitivity of CS-IgE for predicting atopy at age 20 was 26%; combining it with family history reduced sensitivity.
Conclusions:
- Elevated CS-IgE is a valuable predictor of subsequent atopy up to age 20 years.
- CS-IgE can aid in identifying high-risk infants for allergy prevention strategies.
Abstract:
Early markers of atopic predisposition are needed for targeting allergy preventive measures to high-risk infants. An elevated cord serum immunoglobulin E (CS-IgE) level is considered a risk factor for subsequent allergy in childhood. However, the previous studies have not assessed the predictive value of CS-IgE in a follow-up extended to adulthood. We aimed at clarifying whether CS-IgE is useful in predicting subsequent atopic manifestations up to age 20 yr. A cohort of 200 unselected, full-term newborns were prospectively followed up from birth to age 20 yr. The CS-IgE level was successfully measured in 190 subjects at birth. The subjects were re-examined at ages of 5, 11 and 20 yr with assessment of the occurrence of allergic symptoms during the preceding year, skin prick testing and measurement of serum total IgE. An elevated CS-IgE level was associated with allergic symptoms and skin prick test positivity at age 5 yr (p = 0.03 and 0.01), with allergic rhinoconjunctivitis at age 20 yr (p = 0.04) and with an elevated serum total IgE at ages of 11 and 20 yr (p = 0.02 and 0.01). The sensitivity of CS-IgE, i.e. the probability of an elevated CS-IgE in an infant who subsequently develops atopy, in predicting skin prick test-verified atopy at ages of 5 and 20 yr was 50% and 26%, respectively. The combination of elevated CS-IgE and positive family history of allergy was strongly associated with subsequent atopic manifestations. Nevertheless, it showed a reduced sensitivity as compared to CS-IgE or family history of allergy. We conclude that an elevated CS-IgE level predicts subsequent atopy up to age 20 yr.
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