Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma
By M. Kusel, N. de Klerk, T. Kebadze, Vaike Vohma, P. Holt, S. Johnston, P. Sly. Journal of Allergy and Clinical Immunology, 2007
757 citations recorded by the source corpus.
Background Severe lower respiratory infections (LRIs) and atopic sensitization have been identified as independent risk factors for asthma. Objective The nature of potential interactions between these risk factors was the subject of this study. Methods A community-based cohort of 198 children at high atopic risk was followed from birth to 5 years. All episodes of acute respiratory illness in the first year were recorded and postnasal aspirates were collected for viral identification. History of wheeze and asthma was collected annually, and atopy was assessed at 6 months, 2 years, and 5 years. Results A total of 815 episodes of acute respiratory illness were reported, and 33% were LRIs. Viruses were detected in 69% of aspirates, most commonly rhinoviruses (48.3%) and respiratory syncytial virus (10.9%). At 5 years, 28.3%(n = 56) had current wheeze, and this was associated with wheezy [odds ratio (OR), 3.4 (1.2-9.7); P = .02] and/or febrile LRI [OR, 3.9 (1.4-10.5); P = .007], in particular those caused by respiratory syncytial virus or rhinoviruses [OR, 4.1 (1.3-12.6); P = .02]. Comparable findings were made for current asthma. Strikingly these associations were restricted to children who displayed early sensitization (≤2 years old) and not observed in nonatopic patients or those sensitized later. Conclusion These data suggest viral infections interact with atopy in infancy to promote later asthma. Notably the occurrence of both of these events during this narrow developmental window is associated with maximal risk for subsequent asthma, which suggests a contribution from both classes of inflammatory insults to disease pathogenesis. Clinical implications Protection of “high-risk” children against the effects of severe respiratory infections during infancy may represent an effective strategy for primary asthma prevention. The potential benefits of these strategies merit more careful evaluation in this age group.
Subfields: Emergency Medical Services, Epidemiology, Physiology
View Paper: https://www.semanticscholar.org/paper/581a6d089e4a9985696f24cfa612d6483ecb92b2
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- D. Jackson
- N. Sigurs
- M. Kusel
- S. Teo
- P. Gustafsson
- R. Lemanske
- R. Gangnon
- R. Bjarnason
Citations in the corpus
- Asthma and allergy patterns over 18 years after severe RSV bronchiolitis in the first year of life (2010, background): “Viral airway infections and atopy may interact in a multiplicative way to promote asthma development in young childhood.(26) In addition, predisposition to both early severe RSV bronchiolitis and allergic sensitisation may be related to the interleukin (IL)-13/IL-4 gene locus.”
- The infant airway microbiome in health and disease impacts later asthma development (2015, methodology): “We and others have previously shown that development of persistent atopic (allergic) wheeze in children is linked to the number of virus-associated febrile and/or wheezy LRIs experienced during infancy (Jackson et al., 2008; Kusel et al., 2007, 2012; Oddy et al., 2002).”
- Wheezing rhinovirus illnesses in early life predict asthma development in high-risk children. (2008, background): “Kusel and colleagues also recently demonstrated an association between infantilewheezingRSVandRVillnessesandcurrentwheezingat age 5 years; however, their finding was limited to children with earlyallergicsensitization( 6 ).TheyalsoassociatedRVwheezing in infancy and asthma at age 5 years, but this a”