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Loss of Airway Phylogenetic Diversity Is Associated with Clinical and Pathobiological Markers of Disease Development in Chronic Obstructive Pulmonary Disease.
Opron, Kristopher; Begley, Lesa A; Erb-Downward, John R; Li, Gen; Alexis, Neil E; Barjaktarevic, Igor; Barr, R Graham; Bleecker, Eugene R; Boucher, Richard; Bowler, Russell P; Christenson, Stephanie A; Comellas, Alejandro P; Criner, Gerard; Cooper, Christopher B; Couper, David; Galban, Craig J; Han, MeiLan K; Hastie, Annette; Hatt, Charles; Hoffman, Eric A; Kaner, Robert J; Kesimer, Mehmet; Krishnan, Jerry A; LaFon, David C; Martinez, Fernando J; Ortega, Victor E; Peters, Stephen P; Paine, Robert; Putcha, Nirupama; Woodruff, Prescott G; Huffnagle, Gary B; Kozik, Ariangela J; Curtis, Jeffrey L; Huang, Yvonne J.
  • Opron K; Department of Medicine, Division of Pulmonary and Critical Care Medicine.
  • Begley LA; Department of Medicine, Division of Pulmonary and Critical Care Medicine.
  • Erb-Downward JR; Department of Medicine, Division of Pulmonary and Critical Care Medicine.
  • Li G; Department of Biostatistics, School of Public Health.
  • Alexis NE; Center for Environmental Medicine, Asthma, and Lung Biology, Division of Allergy and Immunology.
  • Barjaktarevic I; University of California, Los Angeles, Los Angeles, California.
  • Barr RG; Department of Medicine, Division of General Medicine and.
  • Bleecker ER; Department of Epidemiology, Columbia University Medical Center, New York, New York.
  • Boucher R; University of Arizona, Tucson, Arizona.
  • Bowler RP; Marsico Lung Institute/Cystic Fibrosis and Pulmonary Research Center, and.
  • Christenson SA; Department of Medicine, National Jewish Health, Denver, Colorado.
  • Comellas AP; Department of Medicine, University of California, San Francisco, San Francisco, California.
  • Criner G; Department of Radiology.
  • Cooper CB; Department of Medicine, Division of Pulmonary and Critical Care Medicine, and.
  • Couper D; Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa.
  • Galban CJ; Temple University, Philadelphia, Pennsylvania.
  • Han MK; University of California, Los Angeles, Los Angeles, California.
  • Hastie A; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Hatt C; Department of Radiology.
  • Hoffman EA; Department of Medicine, Division of Pulmonary and Critical Care Medicine.
  • Kaner RJ; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Kesimer M; Department of Radiology.
  • Krishnan JA; Department of Radiology.
  • LaFon DC; Department of Medicine, Division of Pulmonary and Critical Care Medicine, and.
  • Martinez FJ; Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa.
  • Ortega VE; Weill Cornell, Division of Pulmonary and Critical Care Medicine, New York, New York.
  • Peters SP; Marsico Lung Institute/Cystic Fibrosis and Pulmonary Research Center, and.
  • Paine R; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Breathe Chicago Center, University of Illinois Chicago, Chicago, Illinois.
  • Putcha N; Division of Pulmonary, Allergy and Critical Care, University of Alabama at Birmingham, Alabama.
  • Woodruff PG; Weill Cornell, Division of Pulmonary and Critical Care Medicine, New York, New York.
  • Huffnagle GB; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Kozik AJ; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Curtis JL; Division of Respiratory, Critical Care, Occupational Pulmonary Medicine, University of Utah, Salt Lake City, Utah.
  • Huang YJ; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Johns Hopkins University, Baltimore, Maryland; and.
Am J Respir Crit Care Med ; 210(2): 186-200, 2024 Jul 15.
Article en En | MEDLINE | ID: mdl-38261629
ABSTRACT
Rationale The airway microbiome has the potential to shape chronic obstructive pulmonary disease (COPD) pathogenesis, but its relationship to outcomes in milder disease is unestablished.

Objectives:

To identify sputum microbiome characteristics associated with markers of COPD in participants of the Subpopulations and Intermediate Outcome Measures of COPD Study (SPIROMICS).

Methods:

Sputum DNA from 877 participants was analyzed using 16S ribosomal RNA gene sequencing. Relationships between baseline airway microbiota composition and clinical, radiographic, and mucoinflammatory markers, including longitudinal lung function trajectory, were examined. Measurements and Main

Results:

Participant data represented predominantly milder disease (Global Initiative for Chronic Obstructive Lung Disease stage 0-2 obstruction in 732 of 877 participants). Phylogenetic diversity (i.e., range of different species within a sample) correlated positively with baseline lung function, decreased with higher Global Initiative for Chronic Obstructive Lung Disease stage, and correlated negatively with symptom burden, radiographic markers of airway disease, and total mucin concentrations (P < 0.001). In covariate-adjusted regression models, organisms robustly associated with better lung function included Alloprevotella, Oribacterium, and Veillonella species. Conversely, lower lung function, greater symptoms, and radiographic measures of small airway disease were associated with enrichment in members of Streptococcus, Actinobacillus, Actinomyces, and other genera. Baseline sputum microbiota features were also associated with lung function trajectory during SPIROMICS follow-up (stable/improved, decline, or rapid decline groups). The stable/improved group (slope of FEV1 regression ⩾66th percentile) had greater bacterial diversity at baseline associated with enrichment in Prevotella, Leptotrichia, and Neisseria species. In contrast, the rapid decline group (FEV1 slope ⩽33rd percentile) had significantly lower baseline diversity associated with enrichment in Streptococcus species.

Conclusions:

In SPIROMICS, baseline airway microbiota features demonstrate divergent associations with better or worse COPD-related outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esputo / Enfermedad Pulmonar Obstructiva Crónica / Microbiota Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esputo / Enfermedad Pulmonar Obstructiva Crónica / Microbiota Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article