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Impact of community respiratory viral infections in urban children with asthma
BACKGROUND: Upper respiratory tract viral infections cause asthma exacerbations in children. However, the impact of natural colds on children with asthma in the community, particularly in the high-risk urban environment, is less well defined. OBJECTIVE: We hypothesized that children with high-sympto...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American College of Allergy, Asthma, and Immunology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360098/ https://www.ncbi.nlm.nih.gov/pubmed/30385348 http://dx.doi.org/10.1016/j.anai.2018.10.021 |
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author | Lewis, Toby C. Metitiri, Ediri E. Mentz, Graciela B. Ren, Xiaodan Goldsmith, Adam M. Eder, Breanna N. Wicklund, Kyra E. Walsh, Megan P. Comstock, Adam T. Ricci, Jeannette M. Brennan, Sean R. Washington, Ginger L. Owens, Kendall B. Mukherjee, Bhramar Robins, Thomas G. Batterman, Stuart A. Hershenson, Marc B. |
author_facet | Lewis, Toby C. Metitiri, Ediri E. Mentz, Graciela B. Ren, Xiaodan Goldsmith, Adam M. Eder, Breanna N. Wicklund, Kyra E. Walsh, Megan P. Comstock, Adam T. Ricci, Jeannette M. Brennan, Sean R. Washington, Ginger L. Owens, Kendall B. Mukherjee, Bhramar Robins, Thomas G. Batterman, Stuart A. Hershenson, Marc B. |
author_sort | Lewis, Toby C. |
collection | PubMed |
description | BACKGROUND: Upper respiratory tract viral infections cause asthma exacerbations in children. However, the impact of natural colds on children with asthma in the community, particularly in the high-risk urban environment, is less well defined. OBJECTIVE: We hypothesized that children with high-symptom upper respiratory viral infections have reduced airway function and greater respiratory tract inflammation than children with virus-positive low-symptom illnesses or virus-negative upper respiratory tract symptoms. METHODS: We studied 53 children with asthma from Detroit, Michigan, during scheduled surveillance periods and self-reported respiratory illnesses for 1 year. Symptom score, spirometry, fraction of exhaled nitric oxide (FeNO), and nasal aspirate biomarkers, and viral nucleic acid and rhinovirus (RV) copy number were assessed. RESULTS: Of 658 aspirates collected, 22.9% of surveillance samples and 33.7% of respiratory illnesses were virus-positive. Compared with the virus-negative asymptomatic condition, children with severe colds (symptom score ≥5) showed reduced forced expiratory flow at 25% to 75% of the pulmonary volume (FEF(25%-75%)), higher nasal messenger RNA expression of C-X-C motif chemokine ligand (CXCL)-10 and melanoma differentiation-associated protein 5, and higher protein abundance of CXCL8, CXCL10 and C-C motif chemokine ligands (CCL)-2, CCL4, CCL20, and CCL24. Children with mild (symptom score, 1-4) and asymptomatic infections showed normal airway function and fewer biomarker elevations. Virus-negative cold-like illnesses demonstrated increased FeNO, minimal biomarker elevation, and normal airflow. The RV copy number was associated with nasal chemokine levels but not symptom score. CONCLUSION: Urban children with asthma with high-symptom respiratory viral infections have reduced FEF(25%-75%) and more elevations of nasal biomarkers than children with mild or symptomatic infections, or virus-negative illnesses. |
format | Online Article Text |
id | pubmed-6360098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American College of Allergy, Asthma, and Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63600982020-02-01 Impact of community respiratory viral infections in urban children with asthma Lewis, Toby C. Metitiri, Ediri E. Mentz, Graciela B. Ren, Xiaodan Goldsmith, Adam M. Eder, Breanna N. Wicklund, Kyra E. Walsh, Megan P. Comstock, Adam T. Ricci, Jeannette M. Brennan, Sean R. Washington, Ginger L. Owens, Kendall B. Mukherjee, Bhramar Robins, Thomas G. Batterman, Stuart A. Hershenson, Marc B. Ann Allergy Asthma Immunol Article BACKGROUND: Upper respiratory tract viral infections cause asthma exacerbations in children. However, the impact of natural colds on children with asthma in the community, particularly in the high-risk urban environment, is less well defined. OBJECTIVE: We hypothesized that children with high-symptom upper respiratory viral infections have reduced airway function and greater respiratory tract inflammation than children with virus-positive low-symptom illnesses or virus-negative upper respiratory tract symptoms. METHODS: We studied 53 children with asthma from Detroit, Michigan, during scheduled surveillance periods and self-reported respiratory illnesses for 1 year. Symptom score, spirometry, fraction of exhaled nitric oxide (FeNO), and nasal aspirate biomarkers, and viral nucleic acid and rhinovirus (RV) copy number were assessed. RESULTS: Of 658 aspirates collected, 22.9% of surveillance samples and 33.7% of respiratory illnesses were virus-positive. Compared with the virus-negative asymptomatic condition, children with severe colds (symptom score ≥5) showed reduced forced expiratory flow at 25% to 75% of the pulmonary volume (FEF(25%-75%)), higher nasal messenger RNA expression of C-X-C motif chemokine ligand (CXCL)-10 and melanoma differentiation-associated protein 5, and higher protein abundance of CXCL8, CXCL10 and C-C motif chemokine ligands (CCL)-2, CCL4, CCL20, and CCL24. Children with mild (symptom score, 1-4) and asymptomatic infections showed normal airway function and fewer biomarker elevations. Virus-negative cold-like illnesses demonstrated increased FeNO, minimal biomarker elevation, and normal airflow. The RV copy number was associated with nasal chemokine levels but not symptom score. CONCLUSION: Urban children with asthma with high-symptom respiratory viral infections have reduced FEF(25%-75%) and more elevations of nasal biomarkers than children with mild or symptomatic infections, or virus-negative illnesses. American College of Allergy, Asthma, and Immunology 2019-02 2018-10-29 /pmc/articles/PMC6360098/ /pubmed/30385348 http://dx.doi.org/10.1016/j.anai.2018.10.021 Text en 38; Immunology. 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 Lewis, Toby C. Metitiri, Ediri E. Mentz, Graciela B. Ren, Xiaodan Goldsmith, Adam M. Eder, Breanna N. Wicklund, Kyra E. Walsh, Megan P. Comstock, Adam T. Ricci, Jeannette M. Brennan, Sean R. Washington, Ginger L. Owens, Kendall B. Mukherjee, Bhramar Robins, Thomas G. Batterman, Stuart A. Hershenson, Marc B. Impact of community respiratory viral infections in urban children with asthma |
title | Impact of community respiratory viral infections in urban children with asthma |
title_full | Impact of community respiratory viral infections in urban children with asthma |
title_fullStr | Impact of community respiratory viral infections in urban children with asthma |
title_full_unstemmed | Impact of community respiratory viral infections in urban children with asthma |
title_short | Impact of community respiratory viral infections in urban children with asthma |
title_sort | impact of community respiratory viral infections in urban children with asthma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360098/ https://www.ncbi.nlm.nih.gov/pubmed/30385348 http://dx.doi.org/10.1016/j.anai.2018.10.021 |
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