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/mu L 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.
机构:
Univ Michigan Hlth Syst, Div Pulm & Crit Care Med, Ann Arbor, MI USAUniv Michigan Hlth Syst, Div Pulm & Crit Care Med, Ann Arbor, MI USA
Huang, Yvonne J.
Boushey, Homer A.
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Univ Calif San Francisco, Div Pulm Crit Care Allergy & Sleep Med, Box 0130,1292-M,505 Parnassus Ave, San Francisco, CA 94143 USAUniv Michigan Hlth Syst, Div Pulm & Crit Care Med, Ann Arbor, MI USA
机构:
GlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Wang, Zhang
Singh, Richa
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Singh, Richa
Miller, Bruce E.
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GlaxoSmithKline, R&D, Resp Therapy Area Unit, King Of Prussia, PA USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Miller, Bruce E.
Tal-Singer, Ruth
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GlaxoSmithKline, R&D, Resp Therapy Area Unit, King Of Prussia, PA USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Tal-Singer, Ruth
Van Horn, Stephanie
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GlaxoSmithKline, Target & Platform Validat, Target Sci, Collegeville, PA 19426 USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Van Horn, Stephanie
Tomsho, Lynn
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GlaxoSmithKline, Target & Platform Validat, Target Sci, Collegeville, PA 19426 USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Tomsho, Lynn
Mackay, Alexander
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Mackay, Alexander
Allinson, James P.
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Allinson, James P.
Webb, Adam J.
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Univ Leicester, Dept Genet & Genome Biol, Leicester, Leics, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Webb, Adam J.
Brookes, Anthony J.
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Univ Leicester, Dept Genet & Genome Biol, Leicester, Leics, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Brookes, Anthony J.
George, Leena M.
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Univ Leicester, Inst Lung Hlth, Leicester, Leics, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
George, Leena M.
Barker, Bethan
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Univ Leicester, Inst Lung Hlth, Leicester, Leics, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Barker, Bethan
Kolsum, Umme
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Univ Manchester, Ctr Resp Med & Allergy, Manchester, Lancs, England
Univ Hosp South Manchester, Manchester, Lancs, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Kolsum, Umme
Donnelly, Louise E.
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Donnelly, Louise E.
Belchamber, Kylie
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Belchamber, Kylie
Barnes, Peter J.
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Barnes, Peter J.
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Singh, Dave
Brightling, Christopher E.
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Univ Leicester, Inst Lung Hlth, Leicester, Leics, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Brightling, Christopher E.
Donaldson, Gavin C.
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Donaldson, Gavin C.
Wedzicha, Jadwiga A.
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Imperial Coll London, Natl Heart & Lung Inst, London, EnglandGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA
Wedzicha, Jadwiga A.
Brown, James R.
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GlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USAGlaxoSmithKline GSK, Computat Biol Target Sci Res & Dev R&D, Collegeville, PA 19426 USA