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Lower airway microbiota in COPD and healthy controls.
Tangedal, Solveig; Nielsen, Rune; Aanerud, Marianne; Drengenes, Christine; Husebø, Gunnar R; Lehmann, Sverre; Knudsen, Kristel S; Hiemstra, Pieter S; Eagan, Tomas Ml.
Afiliación
  • Tangedal S; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway stangedal@gmail.com.
  • Nielsen R; Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.
  • Aanerud M; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway.
  • Drengenes C; Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.
  • Husebø GR; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway.
  • Lehmann S; Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.
  • Knudsen KS; Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.
  • Hiemstra PS; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway.
  • Eagan TM; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway.
Thorax ; 2024 Feb 08.
Article en En | MEDLINE | ID: mdl-38331579
ABSTRACT

BACKGROUND:

The lower airway microbiota in patients with chronic obstructive pulmonary disease (COPD) are likely altered compared with the microbiota in healthy individuals. Information on how the microbiota is affected by smoking, use of inhaled corticosteroids (ICS) and COPD severity is still scarce.

METHODS:

In the MicroCOPD Study, participant characteristics were obtained through standardised questionnaires and clinical measurements at a single centre from 2012 to 2015. Protected bronchoalveolar lavage samples from 97 patients with COPD and 97 controls were paired-end sequenced with the Illumina MiSeq System. Data were analysed in QIIME 2 and R.

RESULTS:

Alpha-diversity was lower in patients with COPD than controls (Pielou evenness COPD=0.76, control=0.80, p=0.004; Shannon entropy COPD=3.98, control=4.34, p=0.01). Beta-diversity differed with smoking only in the COPD cohort (weighted UniFrac permutational analysis of variance R2=0.04, p=0.03). Nine genera were differentially abundant between COPD and controls. Genera enriched in COPD belonged to the Firmicutes phylum. Pack years were linked to differential abundance of taxa in controls only (ANCOM-BC (Analysis of Compositions of Microbiomes with Bias Correction) log-fold difference/q-values Haemophilus -0.05/0.048; Lachnoanaerobaculum -0.04/0.03). Oribacterium was absent in smoking patients with COPD compared with non-smoking patients (ANCOM-BC log-fold difference/q-values -1.46/0.03). We found no associations between the microbiota and COPD severity or ICS.

CONCLUSION:

The lower airway microbiota is equal in richness in patients with COPD to controls, but less even. Genera from the Firmicutes phylum thrive particularly in COPD airways. Smoking has different effects on diversity and taxonomic abundance in patients with COPD compared with controls. COPD severity and ICS use were not linked to the lower airway microbiota.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Thorax Año: 2024 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Thorax Año: 2024 Tipo del documento: Article País de afiliación: Noruega