Association of Picornavirus Infections With Acute Otitis Media in a Prospective Birth Cohort Study

Author:

Seppälä Elina M1,Oikarinen Sami1,Lehtonen Jussi P1,Neupane Subas2,Honkanen Hanna1,Tyni Iiris1,Siljander Heli34,Ilonen Jorma56,Sillanpää Saara7,Laranne Jussi8,Knip Mikael349,Hyöty Heikki110

Affiliation:

1. Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland

2. Unit of Health Sciences, Faculty of Social Sciences, Tampere University, Tampere, Finland

3. Children’s Hospital, University of Helsinki, Helsinki, Finland

4. Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland

5. Immunogenetics Laboratory, Institute of Biomedicine, University of Turku, Turku, Finland

6. Clinical Microbiology, Turku University Hospital, Turku, Finland

7. Department of Otorhinolaryngology, Tampere University Hospital, Tampere, Finland

8. Department of Otorhinolaryngology, Central Ostrobothnia Central Hospital, Kokkola, Finland

9. Folkhälsan Research Center, University of Helsinki, Helsinki, Finland

10. Fimlab Laboratories, Pirkanmaa Hospital District, Tampere, Finland

Abstract

Abstract Background Human rhinoviruses (HRVs), human enteroviruses (HEVs) and human parechoviruses (HPeVs) have been linked to acute otitis media (AOM). We evaluated this association in a prospective birth cohort setting. Methods A total of 324 healthy infants were followed up from birth to age 3 years. Nasal swab samples were collected at age 3, 6, 12, 18, 24, and 36 months and screened for HRV and HEV using real-time reverse-transcription quantitative polymerase chain reaction. Stool samples were collected monthly and analyzed for HRV, HEV, and HPeV. AOM episodes diagnosed by physicians were reported by parents in a diary. The association of viruses with AOM was analyzed using generalized estimation equations, and their relative contributions using population-attributable risk percentages. Results A clear association was found between AOM episodes and simultaneous detection of HEV (adjusted odds ratio for the detection of virus in stools, 2.04; 95% confidence interval, 1.06–3.91) and HRV (1.54; 1.04–2.30). HPeV showed a similar, yet nonsignificant trend (adjusted odds ratio, 1.44; 95% confidence interval, .81–2.56). HRV and HEV showed higher population-attributable risk percentages (25% and 20%) than HPeV (11%). Conclusions HEVs and HRVs may contribute to the development of AOM in a relatively large proportion of cases.

Funder

Academy of Finland

Centre of Excellence in Molecular Systems Immunology and Physiology Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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