Department of Medicine, Division of Pulmonary and Critical Care Medicine.
Department of Biostatistics, School of Public Health.
Am J Respir Crit Care Med. 2024 Jul 15;210(2):186-200. doi: 10.1164/rccm.202303-0489OC.
The airway microbiome has the potential to shape chronic obstructive pulmonary disease (COPD) pathogenesis, but its relationship to outcomes in milder disease is unestablished. To identify sputum microbiome characteristics associated with markers of COPD in participants of the Subpopulations and Intermediate Outcome Measures of COPD Study (SPIROMICS). 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. 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 ( < 0.001). In covariate-adjusted regression models, organisms robustly associated with better lung function included , , and species. Conversely, lower lung function, greater symptoms, and radiographic measures of small airway disease were associated with enrichment in members of , , , 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 FEV regression ⩾66th percentile) had greater bacterial diversity at baseline associated with enrichment in , , and species. In contrast, the rapid decline group (FEV slope ⩽33rd percentile) had significantly lower baseline diversity associated with enrichment in species. In SPIROMICS, baseline airway microbiota features demonstrate divergent associations with better or worse COPD-related outcomes.
气道微生物组有可能影响慢性阻塞性肺疾病(COPD)的发病机制,但它与更轻度疾病的结果的关系尚未确定。为了确定与COPD 研究的亚人群和中间结果测量(SPIROMICS)参与者中 COPD 标志物相关的痰微生物组特征。使用 16S 核糖体 RNA 基因测序分析了 877 名参与者的痰 DNA。检查了基线气道微生物群落组成与临床,放射学和粘蛋白炎症标志物(包括纵向肺功能轨迹)之间的关系。参与者数据主要代表更轻度的疾病(877 名参与者中有 732 名患有全球慢性阻塞性肺病倡议 0-2 期阻塞)。系统发育多样性(即在样本中不同物种的范围)与基线肺功能呈正相关,与更高的全球慢性阻塞性肺病倡议阶段呈负相关,与症状负担,气道疾病的放射学标志物和总粘蛋白浓度呈负相关(<0.001)。在协变量调整的回归模型中,与更好的肺功能相关的生物体包括 , , 和 种。相反,较低的肺功能,更多的症状和小气道疾病的放射学指标与 , , ,和其他属成员的丰度增加相关。基线痰微生物组特征也与 SPIROMICS 随访期间的肺功能轨迹相关(稳定/改善,下降或快速下降组)。稳定/改善组(FEV 回归斜率≥66 百分位数)在基线时具有更高的细菌多样性,与 , , 和 种的富集相关。相比之下,快速下降组(FEV 斜率≤33 百分位数)的基线多样性明显较低,与 种的富集相关。在 SPIROMICS 中,基线气道微生物组特征与 COPD 相关结局的改善或恶化具有不同的关联。