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Circulating microRNAs and prediction of asthma exacerbation in childhood asthma

BACKGROUND: Circulating microRNAs have shown promise as non-invasive biomarkers and predictors of disease activity. Prior asthma studies using clinical, biochemical and genomic data have not shown excellent prediction of exacerbation. We hypothesized that a panel of circulating microRNAs in a pediat...

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Autores principales: Kho, Alvin T., McGeachie, Michael J., Moore, Kip G., Sylvia, Jody M., Weiss, Scott T., Tantisira, Kelan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020199/
https://www.ncbi.nlm.nih.gov/pubmed/29940952
http://dx.doi.org/10.1186/s12931-018-0828-6
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author Kho, Alvin T.
McGeachie, Michael J.
Moore, Kip G.
Sylvia, Jody M.
Weiss, Scott T.
Tantisira, Kelan G.
author_facet Kho, Alvin T.
McGeachie, Michael J.
Moore, Kip G.
Sylvia, Jody M.
Weiss, Scott T.
Tantisira, Kelan G.
author_sort Kho, Alvin T.
collection PubMed
description BACKGROUND: Circulating microRNAs have shown promise as non-invasive biomarkers and predictors of disease activity. Prior asthma studies using clinical, biochemical and genomic data have not shown excellent prediction of exacerbation. We hypothesized that a panel of circulating microRNAs in a pediatric asthma cohort combined with an exacerbation clinical score might predict exacerbation better than the latter alone. METHODS: Serum samples from 153 children at randomization in the Childhood Asthma Management Program were profiled for 754 microRNAs. Data dichotomized for asthma exacerbation one year after randomization to inhaled corticosteroid treatment were used for binary logistic regression with miRNA expressions and exacerbation clinical score. RESULTS: 12 of 125 well-detected circulating microRNAs had significant odd ratios for exacerbation with miR-206 being most significant. Each doubling of expression of the 12 microRNA corresponded to a 25–67% increase in exacerbation risk. Stepwise logistic regression yielded a 3-microRNA model (miR-146b, miR-206 and miR-720) that, combined with the exacerbation clinical score, had excellent predictive power with a 0.81 AUROC. These 3 microRNAs were involved in NF-kβ and GSK3/AKT pathways. CONCLUSIONS: This combined circulating microRNA-clinical score model predicted exacerbation in asthmatic subjects on inhaled corticosteroids better than each constituent feature alone. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00000575. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0828-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-60201992018-07-06 Circulating microRNAs and prediction of asthma exacerbation in childhood asthma Kho, Alvin T. McGeachie, Michael J. Moore, Kip G. Sylvia, Jody M. Weiss, Scott T. Tantisira, Kelan G. Respir Res Research BACKGROUND: Circulating microRNAs have shown promise as non-invasive biomarkers and predictors of disease activity. Prior asthma studies using clinical, biochemical and genomic data have not shown excellent prediction of exacerbation. We hypothesized that a panel of circulating microRNAs in a pediatric asthma cohort combined with an exacerbation clinical score might predict exacerbation better than the latter alone. METHODS: Serum samples from 153 children at randomization in the Childhood Asthma Management Program were profiled for 754 microRNAs. Data dichotomized for asthma exacerbation one year after randomization to inhaled corticosteroid treatment were used for binary logistic regression with miRNA expressions and exacerbation clinical score. RESULTS: 12 of 125 well-detected circulating microRNAs had significant odd ratios for exacerbation with miR-206 being most significant. Each doubling of expression of the 12 microRNA corresponded to a 25–67% increase in exacerbation risk. Stepwise logistic regression yielded a 3-microRNA model (miR-146b, miR-206 and miR-720) that, combined with the exacerbation clinical score, had excellent predictive power with a 0.81 AUROC. These 3 microRNAs were involved in NF-kβ and GSK3/AKT pathways. CONCLUSIONS: This combined circulating microRNA-clinical score model predicted exacerbation in asthmatic subjects on inhaled corticosteroids better than each constituent feature alone. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00000575. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0828-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-26 2018 /pmc/articles/PMC6020199/ /pubmed/29940952 http://dx.doi.org/10.1186/s12931-018-0828-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kho, Alvin T.
McGeachie, Michael J.
Moore, Kip G.
Sylvia, Jody M.
Weiss, Scott T.
Tantisira, Kelan G.
Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title_full Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title_fullStr Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title_full_unstemmed Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title_short Circulating microRNAs and prediction of asthma exacerbation in childhood asthma
title_sort circulating micrornas and prediction of asthma exacerbation in childhood asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020199/
https://www.ncbi.nlm.nih.gov/pubmed/29940952
http://dx.doi.org/10.1186/s12931-018-0828-6
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