Wei Haixia, Han Chunlan, Song Yongna
Pulmonary and Critical Care Medicine, Zhengzhou Central Hospital, Zhengzhou, 450000, People's Republic of China.
Int J Chron Obstruct Pulmon Dis. 2025 Aug 8;20:2801-2813. doi: 10.2147/COPD.S519630. eCollection 2025.
Idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD) are progressive lung diseases with overlapping risk factors but distinct pathologies. This study employed bidirectional two-sample Mendelian randomization (MR) to explore potential causal relationships between saliva microbiota abundance and the risk of both diseases.
Saliva microbiota abundance datasets were analyzed for forward and reverse causal associations with both diseases. Of 44 datasets, 43 met the inclusion criteria for instrumental variable selection. MR analyses were performed using inverse variance weighted (IVW), MR-Egger, weighted median, and weighted mode methods. Steiger filtering confirmed directionality. Sensitivity analyses included Cochran's Q, MR-Egger intercept, MR-PRESSO, and leave-one-out to assess heterogeneity, pleiotropy, and the influence of individual variants.
In forward MR, higher abundance of species was significantly associated with reduced COPD risk (IVW OR = 0.9546, 95% CI = 0.9224-0.9879, P = 0.0020; adjusted P = 0.019). Nominal inverse associations were observed for Bacilli, , and with IPF, though these did not remain significant after multiple testing correction. All key associations passed Steiger directionality tests, with no evidence of horizontal pleiotropy or heterogeneity. In reverse MR, COPD showed a nominal positive association with abundance.
This exploratory study suggests potential directional associations between specific salivary microbiota and chronic respiratory diseases. abundance may be protective against COPD, while Bacilli, , and may influence IPF risk. These findings support the salivary microbiome as a potential contributor to respiratory disease pathogenesis and warrant further validation in mechanistic and longitudinal studies.
特发性肺纤维化(IPF)和慢性阻塞性肺疾病(COPD)是具有重叠风险因素但病理不同的进行性肺部疾病。本研究采用双向双样本孟德尔随机化(MR)方法,探讨唾液微生物群丰度与这两种疾病风险之间的潜在因果关系。
分析唾液微生物群丰度数据集与这两种疾病的正向和反向因果关联。在44个数据集中,43个符合工具变量选择的纳入标准。使用逆方差加权(IVW)、MR-Egger、加权中位数和加权模式方法进行MR分析。Steiger过滤确认方向性。敏感性分析包括Cochran's Q、MR-Egger截距、MR-PRESSO和留一法,以评估异质性、多效性和个体变异的影响。
在正向MR中,物种丰度较高与COPD风险降低显著相关(IVW OR = 0.9546,95% CI = 0.9224 - 0.9879,P = 0.0020;校正P = 0.019)。观察到芽孢杆菌属、和与IPF存在名义上的负相关,尽管在多重检验校正后这些相关性不再显著。所有关键关联均通过Steiger方向性检验,没有水平多效性或异质性的证据。在反向MR中,COPD与丰度呈名义上的正相关。
这项探索性研究表明特定唾液微生物群与慢性呼吸道疾病之间存在潜在的方向性关联。丰度可能对COPD具有保护作用,而芽孢杆菌属、和可能影响IPF风险。这些发现支持唾液微生物群作为呼吸道疾病发病机制的潜在促成因素,值得在机制和纵向研究中进一步验证。