Asthma Heredity, Cord Blood IgE and Asthma-Related Symptoms and Medication in Adulthood: A Long-Term Follow-Up in a Swedish Birth Cohort

PLoS One. 2013 Jun 21;8(6):e66777. doi: 10.1371/journal.pone.0066777. Print 2013.

Abstract

Cord blood IgE has previously been studied as a possible predictor of asthma and allergic diseases. Results from different studies have been contradictory, and most have focused on high-risk infants and early infancy. Few studies have followed their study population into adulthood. This study assessed whether cord blood IgE levels and a family history of asthma were associated with, and could predict, asthma medication and allergy-related respiratory symptoms in adults. A follow-up was carried out in a Swedish birth cohort comprising 1,701 consecutively born children. In all, 1,661 individuals could be linked to the Swedish Prescribed Drug Register and the Medical Birth Register, and 1,227 responded to a postal questionnaire. Cord blood IgE and family history of asthma were correlated with reported respiratory symptoms and dispensed asthma medication at 32-34 years. Elevated cord blood IgE was associated with a two- to threefold increased risk of pollen-induced respiratory symptoms and dispensed anti-inflammatory asthma medication. Similarly, a family history of asthma was associated with an increased risk of pollen-induced respiratory symptoms and anti-inflammatory medication. However, only 8% of the individuals with elevated cord blood IgE or a family history of asthma in infancy could be linked to current dispensation of anti-inflammatory asthma medication at follow-up. In all, 49 out of 60 individuals with dispensed anti-inflammatory asthma medication at 32-34 years of age had not been reported having asthma at previous check-ups of the cohort during childhood. Among those, only 5% with elevated cord blood IgE and 6% with a family history of asthma in infancy could be linked to current dispensation of anti-inflammatory asthma medication as adults. Elevated cord blood IgE and a positive family history of asthma were associated with reported respiratory symptoms and dispensed asthma medication in adulthood, but their predictive power was poor in this long-time follow-up.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Adrenergic beta-2 Receptor Agonists / therapeutic use
  • Adult
  • Allergens / immunology
  • Asthma / blood
  • Asthma / drug therapy
  • Asthma / epidemiology
  • Asthma / genetics*
  • Child
  • Cohort Studies
  • Female
  • Fetal Blood / metabolism*
  • Follow-Up Studies
  • Humans
  • Hypersensitivity / drug therapy
  • Hypersensitivity / epidemiology
  • Hypersensitivity / etiology
  • Immunoglobulin E / blood*
  • Male
  • Medical History Taking
  • Prevalence
  • Registries
  • Risk
  • Sweden / epidemiology

Substances

  • Adrenal Cortex Hormones
  • Adrenergic beta-2 Receptor Agonists
  • Allergens
  • Immunoglobulin E

Grants and funding

LB was supported by the Umeå SIMSAM Node (Microdata research on childhood for lifelong health and welfare) financed by the Swedish Research Council. KFM was supported by the Swedish Research Council. LN and HV were supported by The Swedish Asthma and Allergy Association (Stockholm, Sweden). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.