Endotoxin exposure in inner-city schools and homes of children with asthma Academic Article Article uri icon


MeSH Major

  • Irritable Bowel Syndrome
  • Primary Health Care
  • Risk Assessment


  • Background: Endotoxins are stimulators of the immune system and, despite their potential to protect against allergy, have been associated with early wheezing and asthma morbidity. Objective: To compare inner-city school endotoxin exposure with home endotoxin exposure in children with asthma. Methods: Students with asthma were recruited from 12 urban elementary schools. Settled and airborne dust samples, linked to enrolled students, were collected from school classrooms, gymnasiums, and cafeterias twice during the academic year. For comparison, settled dust was collected once from the bedrooms of students with asthma. Results: Two hundred twenty-nine school settled dust samples and 118 bedroom settled dust samples were collected and analyzed for endotoxin. The median endotoxin concentration for school samples was 13.4 EU/mg (range, 0.7-360.7 EU/mg) and for home samples was 7.0 EU/mg (range = LLOD-843.0 EU/mg). The median concentration within each individual school varied from 6.6 EU/mg to 24.0 EU/mg. One hundred four students with asthma had matched classroom and bedroom endotoxin exposure measurements performed in the same season and demonstrated significantly higher concentrations of endotoxin in the students' classrooms (mean log value, 1.13 vs 0.99, P =.04). The median of the classrooms was 12.5 EU/mg compared with their bedrooms, with a median of 7.0 EU/mg. Within the school environment, no significant difference was seen between the fall and spring samples (mean log value 1.14 vs 1.09; P =.35). Conclusion: Inner-city children with asthma were exposed to higher concentrations of endotoxin in their classrooms as compared with their bedrooms. Further studies are needed to evaluate school endotoxin exposure as a factor in asthma morbidity. © 2012 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

publication date

  • June 2012



  • Academic Article


Digital Object Identifier (DOI)

  • 10.1016/j.anai.2012.04.003

PubMed ID

  • 22626594

Additional Document Info

start page

  • 418

end page

  • 422


  • 108


  • 6