Volume 123, Issue 1 , Pages 131-137.e1, January 2009
The causal direction in the association between respiratory syncytial virus hospitalization and asthma
Background
Earlier studies have reported an increased risk of asthma after respiratory syncytial virus (RSV) hospitalization. Other studies found that asthmatic disposition and propensity to wheeze increase the risk of RSV hospitalization.
Objective
The current study examined the causal direction of the associations between RSV hospitalization and asthma in a population-based cohort of twins.
Methods
We conducted a prospective cohort study examining the associations between RSV hospitalization and asthma by using registry information on RSV hospitalization and asthma among 18,614 Danish twins born 1994 to 2003. The associations between RSV and asthma were examined in both directions: we examined the risk of asthma after RSV hospitalization, and the risk of RSV hospitalization in children with asthma in the same population-based cohort.
Results
Asthma hospitalization after RSV hospitalization was increased as much as 6-fold to 8-fold during the first 2 months after RSV hospitalization but was no longer increased 1 year later. Asthma increased the risk of RSV hospitalization by 3-fold, and the risk was not time-dependent. Analyzing these associations on the basis of asthma defined from use of inhaled corticosteroid did not materially change the risk estimates.
Conclusion
There is a bidirectional association between severe RSV infection and asthma. Severe RSV infection is associated with a short-term increase in the risk of subsequent asthma, suggesting that RSV induce bronchial hyperresponsiveness; and asthma is associated with a long-term increased susceptibility for severe RSV disease, suggesting a host factor being responsible for the severe response to RSV infection. This suggests that severe RSV infection and asthma may share a common genetic predisposition and/or environmental exposure.
Key words: Asthma, child, epidemiology, respiratory syncytial virus, twins
Abbreviations used: CRS, Danish Civil Registration System, DNPR, Danish National Patient Registry, RMPS, Register of Medicinal Product Statistics, RSV, Respiratory syncytial virus
Supported by the Lundbeck Foundation, the Augustinus Foundation, and an unrestricted institutional grant from MedImmune.
Disclosure of potential conflict of interest: V. Backer receives grant support from AstraZeneca, Boehringer Ingelheim, ALK-Abelló, and Novartis. H. Bisgaard has been a consultant to, has been a paid lecturer for, and holds sponsored grants from Aerocrine, AstraZeneca, Altana, GlaxoSmithKline, Merck, MedImmune, NeoLab, and Pfizer; receives grant support from Aerocrine, AstraZeneca, GlaxoSmithKline, Merck, and MedImmune; and has provided legal consultation/expert witness testimony for NeoLab. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(08)01918-0
doi:10.1016/j.jaci.2008.10.042
© 2009 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 123, Issue 1 , Pages 131-137.e1, January 2009
