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Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125611/ https://www.ncbi.nlm.nih.gov/pubmed/17353039 http://dx.doi.org/10.1016/j.jaci.2006.12.669 |
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author | Kusel, Merci M.H. de Klerk, Nicholas H. Kebadze, Tatiana Vohma, Vaike Holt, Patrick G. Johnston, Sebastian L. Sly, Peter D. |
author_facet | Kusel, Merci M.H. de Klerk, Nicholas H. Kebadze, Tatiana Vohma, Vaike Holt, Patrick G. Johnston, Sebastian L. Sly, Peter D. |
author_sort | Kusel, Merci M.H. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7125611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71256112020-04-08 Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma Kusel, Merci M.H. de Klerk, Nicholas H. Kebadze, Tatiana Vohma, Vaike Holt, Patrick G. Johnston, Sebastian L. Sly, Peter D. J Allergy Clin Immunol Article 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. American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. 2007-05 2007-03-13 /pmc/articles/PMC7125611/ /pubmed/17353039 http://dx.doi.org/10.1016/j.jaci.2006.12.669 Text en Copyright © 2007 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Kusel, Merci M.H. de Klerk, Nicholas H. Kebadze, Tatiana Vohma, Vaike Holt, Patrick G. Johnston, Sebastian L. Sly, Peter D. Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title | Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title_full | Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title_fullStr | Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title_full_unstemmed | Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title_short | Early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
title_sort | early-life respiratory viral infections, atopic sensitization, and risk of subsequent development of persistent asthma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125611/ https://www.ncbi.nlm.nih.gov/pubmed/17353039 http://dx.doi.org/10.1016/j.jaci.2006.12.669 |
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