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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Respiratory morbidity 20 years after RSV infection in infancy
M Korppi1, E Piippo-Savolainen, K Korhonen
1Department of Pediatrics, Kuopio University and University Hospital, Finland. matti.korppi@uku.fi
Insights
Infants hospitalized with respiratory syncytial virus (RSV) infection show increased risk for abnormal lung function in adulthood. Early RSV infection is an independent risk factor for reduced lung function, but not asthma or bronchial reactivity.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Epidemiology
Background:
- Early-life respiratory syncytial virus (RSV) infection is a suspected risk factor for adult asthma.
- Prospective studies tracking RSV infection from infancy through adulthood are lacking.
Purpose of the Study:
- To evaluate early-life RSV infection as a risk factor for adult asthma, bronchial reactivity, and lung function abnormalities.
- To investigate the long-term respiratory health outcomes in young adults previously hospitalized for RSV bronchiolitis or pneumonia.
Main Methods:
- A prospective cohort study followed children hospitalized for RSV before age 24 months until ages 18-20 years.
- Methods included questionnaires, spirometry (FVS), methacholine challenge (MIC), home peak expiratory flow (PEF) monitoring, and skin prick tests (SPT).
Main Results:
- 17-22% of RSV-exposed subjects had asthma; 44% had abnormal lung function compared to 11% of controls.
- RSV infection in infancy was an independent risk factor for lung function abnormality (OR, 5.27) and decreased FEV% and MEF50.
- No significant association was found between early RSV infection and asthma or bronchial reactivity.
Conclusions:
- Hospitalization for RSV in infancy is an independent risk factor for developing lung function abnormalities in young adulthood.
- While not directly linked to asthma or bronchial hyperresponsiveness, early RSV infection has lasting impacts on lung function.
Abstract:
Epidemiological data suggest that respiratory syncytial virus (RSV) infection in early life is a risk factor for later asthma. There are no prospective studies on RSV infection starting from infancy progressing through childhood into adulthood. We followed up a cohort of children, hospitalized for RSV bronchiolitis or RSV pneumonia before age 24 months, until age 18-20 years. The aim of the study was to evaluate early RSV infection as a risk factor for asthma, bronchial reactivity, and lung function abnormalities in young adults. The participants filled in a questionnaire on asthma and asthma-like symptoms. The clinical study included flow-volume spirometry (FVS), methacholine inhalation challenge (MIC), home PEF (peak expiratory flow) monitoring, and skin prick tests (SPT) to common allergens. Asthma was present in 17-22% of 36 index subjects, depending on asthma definition, compared to 11% of 45 controls. Furthermore, FEV% and MEF25 were lower, and MEF50 tended to be lower, in index than in control subjects. One or more abnormal lung function results were found in 16 (44%) index subjects, but only in 5 (11%) controls (P < 0.01). Bronchial reactivity (PD20 <4,900 microg methacholine) was demonstrated in 16 (46%) index subjects and 14 (32%) controls (NS). At least one positive SPT result was present in 21 (60%) index subjects; 6 (29%) had asthma (NS vs. nonatopic index subjects); 13 (62%) had abnormal lung function (P < 0.05); and 14 (67%) had bronchial reactivity (P < 0.01). In the logistic regression adjusted for atopy, as defined by SPT positivity, RSV infection in infancy was an independent risk factor for lung function abnormality (one or more abnormal results in FVS; OR, 5.27; 95% CI, 1.60-17.36), and also for decreased FEV% and MEF50 when these were analyzed separately. However, RSV infection in infancy was not a significant risk factor for asthma or bronchial reactivity. In young adults, lung function abnormalities may be associated with RSV infection which required hospitalization in infancy.
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