Xia Xian-Xin, Li Chuan-Xiang, Guo Hong-Rong
Department of Respiratory and Critical Care Medicine, The Third Hospital of Wuhan, Wuhan, 430030, People's Republic of China.
J Transl Med. 2025 May 17;23(1):557. doi: 10.1186/s12967-025-06553-9.
There is a dearth of population-based studies on the association between the diversity of the oral microbiome and the risk of chronic obstructive pulmonary disease (COPD). The study aims to investigate the association between oral microbiome diversity and COPD.
In this cross-sectional study, data from the National Health and Nutrition Examination Survey (NHANES 2009-2012) were analyzed. The association between the oral microbiome α-diversity and COPD risk was examined via multivariable logistic regression, with Restricted cubic splines revealing potential non-linear trends. The β-diversity disparities between COPD and non-COPD groups were delineated using Principal Coordinate Analysis (PCoA) and Permutational Multivariate Analysis of Variance (PERMANOVA).
A total of 6061 participants were included in this study. For α-diversity, the observed ASVs were significantly associated with COPD risk (OR = 0.964, 95%CI: 0.936-0.993, P = 0.016). Similarly, Faith's phylogenetic Diversity showed a significant association with COPD risk (OR = 0.955, 95%CI: 0.919-0.993, P = 0.020). The Shannon-Weiner index was also associated with COPD risk (OR = 0.829, 95%CI: 0.702-0.981, P = 0.029). For β-diversity, PCoA and PERMANOVA analysis showed statistically significant differences in Bray-Curtis, unweighted, and weighted UniFrac distances (all P < 0.01) between the COPD and non-COPD groups.
Significant differences in oral microbiome α-diversity and β-diversity were found between COPD and non-COPD populations, with α-diversity (observed ASVs, Faith's Phylogenetic Diversity, Shannon-Weiner index) being negatively associated with the risk of COPD.
关于口腔微生物群多样性与慢性阻塞性肺疾病(COPD)风险之间关联的基于人群的研究匮乏。本研究旨在调查口腔微生物群多样性与COPD之间的关联。
在这项横断面研究中,分析了来自国家健康与营养检查调查(NHANES 2009 - 2012)的数据。通过多变量逻辑回归检验口腔微生物群α多样性与COPD风险之间的关联,受限立方样条显示潜在的非线性趋势。使用主坐标分析(PCoA)和置换多变量方差分析(PERMANOVA)来描述COPD组和非COPD组之间的β多样性差异。
本研究共纳入6061名参与者。对于α多样性,观察到的可操作分类单元(ASVs)与COPD风险显著相关(OR = 0.964,95%CI:0.936 - 0.993,P = 0.016)。同样,费思系统发育多样性与COPD风险显著相关(OR = 0.955,95%CI:0.919 - 0.993,P = 0.020)。香农 - 韦纳指数也与COPD风险相关(OR = 0.829,95%CI:0.702 - 0.981,P = 0.029)。对于β多样性,PCoA和PERMANOVA分析显示,COPD组和非COPD组之间在布雷 - 柯蒂斯、未加权和加权的非加权 UniFrac 距离上存在统计学显著差异(所有P < 0.01)。
在COPD人群和非COPD人群之间发现口腔微生物群α多样性和β多样性存在显著差异,α多样性(观察到的ASVs、费思系统发育多样性、香农 - 韦纳指数)与COPD风险呈负相关。