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Longitudinal profiling of the lung microbiome in the AERIS study demonstrates repeatability of bacterial and eosinophilic COPD exacerbations.
Mayhew, David; Devos, Nathalie; Lambert, Christophe; Brown, James R; Clarke, Stuart C; Kim, Viktoriya L; Magid-Slav, Michal; Miller, Bruce E; Ostridge, Kristoffer K; Patel, Ruchi; Sathe, Ganesh; Simola, Daniel F; Staples, Karl J; Sung, Ruby; Tal-Singer, Ruth; Tuck, Andrew C; Van Horn, Stephanie; Weynants, Vincent; Williams, Nicholas P; Devaster, Jeanne-Marie; Wilkinson, Tom M A.
Afiliação
  • Mayhew D; Computational Biology, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Devos N; GSK Vaccines, Rixensart, Belgium.
  • Lambert C; GSK Vaccines, Rixensart, Belgium.
  • Brown JR; Computational Biology, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Clarke SC; Clinical and Experimental Sciences, University of Southampton Faculty of Medicine, Southampton General Hospital, Southampton, UK.
  • Kim VL; Southampton NIHR Respiratory Biomedical Research Unit, Southampton General Hospital, Southampton, UK.
  • Magid-Slav M; Southampton NIHR Respiratory Biomedical Research Unit, Southampton General Hospital, Southampton, UK.
  • Miller BE; Computational Biology, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Ostridge KK; Respiratory Therapy Area Unit, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Patel R; Southampton NIHR Respiratory Biomedical Research Unit, Southampton General Hospital, Southampton, UK.
  • Sathe G; Target and Pathway Validation, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Simola DF; Target and Pathway Validation, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Staples KJ; Computational Biology, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Sung R; Clinical and Experimental Sciences, University of Southampton Faculty of Medicine, Southampton General Hospital, Southampton, UK.
  • Tal-Singer R; Southampton NIHR Respiratory Biomedical Research Unit, Southampton General Hospital, Southampton, UK.
  • Tuck AC; Wessex Investigational Sciences Hub, University of Southampton Faculty of Medicine, Southampton General Hospital, Southampton, UK.
  • Van Horn S; Respiratory Therapy Area Unit, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Weynants V; Respiratory Therapy Area Unit, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Williams NP; Clinical and Experimental Sciences, University of Southampton Faculty of Medicine, Southampton General Hospital, Southampton, UK.
  • Devaster JM; Target and Pathway Validation, Target Sciences, GSK R&D, King of Prussia, Pennsylvania, USA.
  • Wilkinson TMA; GSK Vaccines, Rixensart, Belgium.
Thorax ; 73(5): 422-430, 2018 05.
Article em En | MEDLINE | ID: mdl-29386298
ABSTRACT

BACKGROUND:

Alterations in the composition of the lung microbiome associated with adverse clinical outcomes, known as dysbiosis, have been implicated with disease severity and exacerbations in COPD.

OBJECTIVE:

To characterise longitudinal changes in the lung microbiome in the AERIS study (Acute Exacerbation and Respiratory InfectionS in COPD) and their relationship with associated COPD outcomes.

METHODS:

We surveyed 584 sputum samples from 101 patients with COPD to analyse the lung microbiome at both stable and exacerbation time points over 1 year using high-throughput sequencing of the 16S ribosomal RNA gene. We incorporated additional lung microbiology, blood markers and in-depth clinical assessments to classify COPD phenotypes.

RESULTS:

The stability of the lung microbiome over time was more likely to be decreased in exacerbations and within individuals with higher exacerbation frequencies. Analysis of exacerbation phenotypes using a Markov chain model revealed that bacterial and eosinophilic exacerbations were more likely to be repeated in subsequent exacerbations within a subject, whereas viral exacerbations were not more likely to be repeated. We also confirmed the association of bacterial genera, including Haemophilus and Moraxella, with disease severity, exacerbation events and bronchiectasis.

CONCLUSIONS:

Subtypes of COPD have distinct bacterial compositions and stabilities over time. Some exacerbation subtypes have non-random probabilities of repeating those subtypes in the future. This study provides insights pertaining to the identification of bacterial targets in the lung and biomarkers to classify COPD subtypes and to determine appropriate treatments for the patient. TRIAL REGISTRATION NUMBER Results, NCT01360398.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eosinofilia Pulmonar / Progressão da Doença / Doença Pulmonar Obstrutiva Crônica / Microbiota / Pulmão Tipo de estudo: Observational_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Thorax Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eosinofilia Pulmonar / Progressão da Doença / Doença Pulmonar Obstrutiva Crônica / Microbiota / Pulmão Tipo de estudo: Observational_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Thorax Ano de publicação: 2018 Tipo de documento: Article