Wang Xiaona, Zhao Ranran, Guo Jia, Yang Ke, Xu Bo
Department of Respiratory Medicine, Beijing Friendship Hospital, Capital Medical University, Beijing, People's Republic of China.
Nat Sci Sleep. 2025 Sep 3;17:2119-2130. doi: 10.2147/NSS.S527778. eCollection 2025.
Recent research has increasingly underscored a significant correlation between gut microbiota and obstructive sleep apnea (OSA). Probiotics have emerged as promising adjunctive interventions for OSA. Metabolites and their related biochemical pathways have emerged as important contributors to the development of OSA. This study aimed to estimate the causal association between gut microbiota and OSA and to quantify the mediating effects of metabolites.
We employed two-step, two-sample Mendelian randomization techniques, utilizing single nucleotide polymorphisms as genetic instruments for exposures and mediators. Summary statistics were obtained from genome-wide association studies of gut microbiota (the Dutch Microbiome Project, n=7,738), plasma metabolites (the Canadian Longitudinal Study on Aging cohort, n=8,299), and OSA (FinnGen database, n=410,385). To ensure the robustness of our findings, sensitivity analyses and heterogeneity tests were systematically conducted.
In the Dutch Microbiome Project, species Parabacteroides merdae, genus Faecalibacterium, species Faecalibacterium prausnitzii and species Bifidobacterium longum demonstrated a potential protective association with OSA. We included the top 10 metabolites with potential biological significance as candidate mediators. Among them, only 2-hydroxypalmitate was associated with a reduced risk of OSA. 2-hydroxypalmitate partially mediated the association between species Parabacteroides merdae and OSA, with a mediation proportion of 20.53%.
The study highlighted the protective effect of species Parabacteroides merdae against OSA. It also revealed the mediating role of 2-hydroxypalmitate in the relationship between species Parabacteroides merdae and OSA.
近期研究越来越强调肠道微生物群与阻塞性睡眠呼吸暂停(OSA)之间的显著相关性。益生菌已成为治疗OSA的有前景的辅助干预措施。代谢物及其相关生化途径已成为OSA发展的重要促成因素。本研究旨在评估肠道微生物群与OSA之间的因果关系,并量化代谢物的中介作用。
我们采用两步两样本孟德尔随机化技术,利用单核苷酸多态性作为暴露和中介的遗传工具。汇总统计数据来自肠道微生物群(荷兰微生物组计划,n = 7738)、血浆代谢物(加拿大老龄化纵向研究队列,n = 8299)和OSA(芬兰基因数据库,n = 410385)的全基因组关联研究。为确保研究结果的稳健性,系统地进行了敏感性分析和异质性检验。
在荷兰微生物组计划中,屎拟杆菌属、粪杆菌属、普拉梭菌和长双歧杆菌与OSA呈潜在的保护关联。我们纳入了具有潜在生物学意义的前10种代谢物作为候选中介。其中,只有2-羟基棕榈酸与OSA风险降低相关。第2-羟基棕榈酸部分介导了屎拟杆菌属与OSA之间的关联,中介比例为20.53%。
该研究强调了屎拟杆菌属对OSA的保护作用。它还揭示了2-羟基棕榈酸在屎拟杆菌属与OSA关系中的中介作用。