Liu Liangfeng, He Guanwen, Yu Rong, Lin Bingbang, Lin Liangqing, Wei Rifu, Zhu Zhongshou, Xu Yangbin
Department of Otolaryngology, Head and Neck Surgery, Ningde Municipal Hospital of Ningde Normal University, Ningde, Fujian, China.
Department of Pediatrics, Jiaocheng District Maternal and Child Health Hospital, Ningde, Fujian, China.
Front Microbiol. 2024 Aug 23;15:1410624. doi: 10.3389/fmicb.2024.1410624. eCollection 2024.
Previous studies have identified a clinical association between gut microbiota and Obstructive sleep apnea (OSA), but the potential causal relationship between the two has not been determined. Therefore, we aim to utilize Mendelian randomization (MR) to investigate the potential causal effects of gut microbiota on OSA and the impact of OSA on altering the composition of gut microbiota.
Bi-directional MR and replicated validation were utilized. Summary-level genetic data of gut microbiota were derived from the MiBioGen consortium and the Dutch Microbiome Project (DMP). Summary statistics of OSA were drawn from FinnGen Consortium and Million Veteran Program (MVP). Inverse-variance-weighted (IVW), weighted median, MR-Egger, Simple Mode, and Weighted Mode methods were used to evaluate the potential causal link between gut microbiota and OSA.
We identified potential causal associations between 23 gut microbiota and OSA. Among them, (OR = 0.86; = 0.00013), (OR = 0.90; = 0.0090), (OR = 0.85; = 0.00016) retained a strong negative association with OSA after the Bonferroni correction. Reverse MR analyses indicated that OSA was associated with 20 gut microbiota, among them, a strong inverse association between OSA and (beta = -0.35; = 0.00032) was identified after Bonferroni correction.
Our study implicates the potential bi-directional causal effects of the gut microbiota on OSA, potentially providing new insights into the prevention and treatment of OSA through specific gut microbiota.
既往研究已确定肠道微生物群与阻塞性睡眠呼吸暂停(OSA)之间存在临床关联,但两者之间的潜在因果关系尚未确定。因此,我们旨在利用孟德尔随机化(MR)来研究肠道微生物群对OSA的潜在因果效应以及OSA对改变肠道微生物群组成的影响。
采用双向MR和重复验证。肠道微生物群的汇总水平遗传数据来自MiBioGen联盟和荷兰微生物组计划(DMP)。OSA的汇总统计数据来自芬兰基因组联盟和百万退伍军人计划(MVP)。采用逆方差加权(IVW)、加权中位数、MR-Egger、简单模式和加权模式方法来评估肠道微生物群与OSA之间的潜在因果联系。
我们确定了23种肠道微生物群与OSA之间的潜在因果关联。其中,(OR = 0.86; = 0.00013),(OR = 0.90; = 0.0090),(OR = 0.85; = 0.00016)在Bonferroni校正后与OSA保持强烈负相关。反向MR分析表明,OSA与20种肠道微生物群有关,其中,在Bonferroni校正后,OSA与(β = -0.35; = 0.00032)之间存在强烈的负相关。
我们的研究表明肠道微生物群对OSA具有潜在的双向因果效应,可能为通过特定肠道微生物群预防和治疗OSA提供新的见解。