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Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease

BACKGROUND: The eosinophilic chronic obstructive pulmonary disease (COPD) is known to be more sensitive to corticosteroid. The sputum microbiome has been shown to affect COPD prognosis, but its role in acute exacerbations of eosinophilic COPD is unclear. This study aimed to investigate the dynamic c...

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Autores principales: Qi, Yu-Jing, Sun, Xue-Jiao, Wang, Zhe, Bin, Yan-Fei, Li, Ying-Hua, Zhong, Xiao-Ning, Bai, Jing, Deng, Jing-Min, He, Zhi-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065869/
https://www.ncbi.nlm.nih.gov/pubmed/32053571
http://dx.doi.org/10.1097/CM9.0000000000000677
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author Qi, Yu-Jing
Sun, Xue-Jiao
Wang, Zhe
Bin, Yan-Fei
Li, Ying-Hua
Zhong, Xiao-Ning
Bai, Jing
Deng, Jing-Min
He, Zhi-Yi
author_facet Qi, Yu-Jing
Sun, Xue-Jiao
Wang, Zhe
Bin, Yan-Fei
Li, Ying-Hua
Zhong, Xiao-Ning
Bai, Jing
Deng, Jing-Min
He, Zhi-Yi
author_sort Qi, Yu-Jing
collection PubMed
description BACKGROUND: The eosinophilic chronic obstructive pulmonary disease (COPD) is known to be more sensitive to corticosteroid. The sputum microbiome has been shown to affect COPD prognosis, but its role in acute exacerbations of eosinophilic COPD is unclear. This study aimed to investigate the dynamic changes of the airway microbiome in patients with acute exacerbations of eosinophilic COPD. METHODS: Fifty-seven patients with acute exacerbations of COPD from the First Affiliated Hospital of Guangxi Medical University between June 2017 and June 2018 were divided into two groups. Patients with eosinophils ≥300 cells/μL in the peripheral venous blood were assigned to the eosinophilic group (Eos) and the rest to the non-eosinophilic group (Noneos). All patients received similar treatment including inhaled budesonide according to the guidelines. The induced sputum microbiome was analyzed on the 1st and 7th day of treatment using the 16S ribosomal RNA (rRNA) method. The levels of interleukin (IL)-6 and IL-8 were measured in the plasma and the sensitivity to corticosteroids was determined in isolated peripheral blood mononuclear cells. Quantitative data were compared between the two groups using the independent samples t test or Mann-Whitney U test. Categorical data were evaluated using Chi-squared test or Fisher's exact test. RESULTS: Twenty-six patients were classified into Eos group and 31 patients were classified into Noneos group. Prior to treatment, the alpha diversity (Shannon index) (2.65 ± 0.63 vs. 2.56 ± 0.54, t = 0.328, P = 0.747) and the structure of the sputum microbiome were similar in the Eos group and the Noneos group. After 7 days of treatment, alpha diversity increased in both groups, while the microbiome richness (Ace index) was significantly lower in the Eos group (561.87 ± 109.13 vs. 767.88 ± 148.48, t = −3.535, P = 0.002). At the same time, IL-6 (12.09 ± 2.85 pg/mL vs. 15.54 ± 2.45 pg/mL, t = −4.913, P < 0.001) and IL-8 (63.64 ± 21.69 pg/mL vs. 78.97 ± 17.13 pg/mL, t = −2.981, P = 0.004) decreased more significantly in the Eos group, and the percentages of inhibition of IL-8 at dexamethasone concentrations 10(−8) to 10(−6) mol/L were significantly higher in the Eos group than those in the Noneos group (all P < 0.05). CONCLUSIONS: The induced sputum microbiome richness decreased more significantly following treatment in the Eos patients compared to the Noneos patients. The lower plasma inflammatory factor levels and the higher percentage of inhibition of IL-8 might be due to higher corticosteroid sensitivity in Eos patients.
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spelling pubmed-70658692020-03-24 Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease Qi, Yu-Jing Sun, Xue-Jiao Wang, Zhe Bin, Yan-Fei Li, Ying-Hua Zhong, Xiao-Ning Bai, Jing Deng, Jing-Min He, Zhi-Yi Chin Med J (Engl) Original Articles BACKGROUND: The eosinophilic chronic obstructive pulmonary disease (COPD) is known to be more sensitive to corticosteroid. The sputum microbiome has been shown to affect COPD prognosis, but its role in acute exacerbations of eosinophilic COPD is unclear. This study aimed to investigate the dynamic changes of the airway microbiome in patients with acute exacerbations of eosinophilic COPD. METHODS: Fifty-seven patients with acute exacerbations of COPD from the First Affiliated Hospital of Guangxi Medical University between June 2017 and June 2018 were divided into two groups. Patients with eosinophils ≥300 cells/μL in the peripheral venous blood were assigned to the eosinophilic group (Eos) and the rest to the non-eosinophilic group (Noneos). All patients received similar treatment including inhaled budesonide according to the guidelines. The induced sputum microbiome was analyzed on the 1st and 7th day of treatment using the 16S ribosomal RNA (rRNA) method. The levels of interleukin (IL)-6 and IL-8 were measured in the plasma and the sensitivity to corticosteroids was determined in isolated peripheral blood mononuclear cells. Quantitative data were compared between the two groups using the independent samples t test or Mann-Whitney U test. Categorical data were evaluated using Chi-squared test or Fisher's exact test. RESULTS: Twenty-six patients were classified into Eos group and 31 patients were classified into Noneos group. Prior to treatment, the alpha diversity (Shannon index) (2.65 ± 0.63 vs. 2.56 ± 0.54, t = 0.328, P = 0.747) and the structure of the sputum microbiome were similar in the Eos group and the Noneos group. After 7 days of treatment, alpha diversity increased in both groups, while the microbiome richness (Ace index) was significantly lower in the Eos group (561.87 ± 109.13 vs. 767.88 ± 148.48, t = −3.535, P = 0.002). At the same time, IL-6 (12.09 ± 2.85 pg/mL vs. 15.54 ± 2.45 pg/mL, t = −4.913, P < 0.001) and IL-8 (63.64 ± 21.69 pg/mL vs. 78.97 ± 17.13 pg/mL, t = −2.981, P = 0.004) decreased more significantly in the Eos group, and the percentages of inhibition of IL-8 at dexamethasone concentrations 10(−8) to 10(−6) mol/L were significantly higher in the Eos group than those in the Noneos group (all P < 0.05). CONCLUSIONS: The induced sputum microbiome richness decreased more significantly following treatment in the Eos patients compared to the Noneos patients. The lower plasma inflammatory factor levels and the higher percentage of inhibition of IL-8 might be due to higher corticosteroid sensitivity in Eos patients. Wolters Kluwer Health 2020-03-05 2020-03-05 /pmc/articles/PMC7065869/ /pubmed/32053571 http://dx.doi.org/10.1097/CM9.0000000000000677 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Articles
Qi, Yu-Jing
Sun, Xue-Jiao
Wang, Zhe
Bin, Yan-Fei
Li, Ying-Hua
Zhong, Xiao-Ning
Bai, Jing
Deng, Jing-Min
He, Zhi-Yi
Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title_full Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title_fullStr Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title_full_unstemmed Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title_short Richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
title_sort richness of sputum microbiome in acute exacerbations of eosinophilic chronic obstructive pulmonary disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065869/
https://www.ncbi.nlm.nih.gov/pubmed/32053571
http://dx.doi.org/10.1097/CM9.0000000000000677
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