微生物群
医学
失调
痰
慢性阻塞性肺病
恶化
嗜酸性
肺活量
免疫学
内科学
疾病
肺
肺功能
病理
生物
扩散能力
生物信息学
肺结核
作者
Zhang Wang,Richa Singh,Bruce E. Miller,Ruth Tal‐Singer,Stephanie Van Horn,Lynn Tomsho,Alexander Mackay,James P. Allinson,Adam Webb,Anthony J. Brookes,Leena George,Bethan Barker,Umme Kolsum,Louise Donnelly,Kylie Belchamber,Peter J. Barnes,Dave Singh,Christopher E. Brightling,Gavin C. Donaldson,Jadwiga A. Wedzicha
出处
期刊:Thorax
[BMJ]
日期:2017-12-21
卷期号:73 (4): 331-338
被引量:157
标识
DOI:10.1136/thoraxjnl-2017-210741
摘要
BACKGROUND: Recent studies suggest that lung microbiome dysbiosis, the disease associated disruption of the lung microbial community, might play a key role in chronic obstructive pulmonary disease (COPD) exacerbations. However, characterising temporal variability of the microbiome from large longitudinal COPD cohorts is needed to better understand this phenomenon. METHODS: We performed a 16S ribosomal RNA survey of microbiome on 716 sputum samples collected longitudinally at baseline and exacerbations from 281 subjects with COPD at three UK clinical centres as part of the COPDMAP consortium. RESULTS: was negatively associated with bacterial alpha diversity. Microbiomes were distinct between exacerbations associated with bacteria versus eosinophilic airway inflammation. Dysbiosis at exacerbations, measured as significant within subject deviation of microbial composition relative to baseline, was present in 41% of exacerbations. Dysbiosis was associated with increased exacerbation severity indicated by a greater fall in forced expiratory volume in one second, forced vital capacity and a greater increase in CAT score, particularly in exacerbations with concurrent eosinophilic inflammation. There was a significant difference of temporal variability of microbial alpha and beta diversity among centres. The variation of beta diversity significantly decreased in those subjects with frequent historical exacerbations. CONCLUSIONS: Microbial dysbiosis is a feature of some exacerbations and its presence, especially in concert with eosinophilic inflammation, is associated with more severe exacerbations indicated by a greater fall in lung function. TRIAL REGISTRATION NUMBER: Results, NCT01620645.
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