Li Xiaxi, Li Xiaoling, Xiao Haowei, Xu Jiaying, He Jianquan, Xiao Chuanxing, Zhang Bangzhou, Cao Man, Hong Wenxin
Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
College of Rehabilitation Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Front Microbiol. 2024 Dec 24;15:1492349. doi: 10.3389/fmicb.2024.1492349. eCollection 2024.
Irritable bowel syndrome (IBS) is a common chronic disorder of gastrointestinal function with a high prevalence worldwide. Due to its complex pathogenesis and heterogeneity, there is urrently no consensus in IBS research.
We collected and uniformly reanalyzed 1167 fecal 16S rRNA gene sequencing samples (623 from IBS patients and 544 from healthy subjects) from 9 studies. Using both a random effects (RE) model and a fixed effects (FE) model, we calculated the odds ratios for metrics including bacterial alpha diversity, beta diversity, common genera and pathways between the IBS and control groups.
Significantly lower alpha-diversity indexes were observed in IBS patients by random effects model. Twenty-six bacterial genera and twelve predicted pathways were identified with significant odds ratios and classification potentials for IBS patients. Based on these feature, we used transfer learning to enhance the predictive capabilities of our model, which improved model performance by approximately 10%. Moreover, through correlation network analysis, we found that Ruminococcaceae and Christensenellaceae were negatively correlated with vitamin B6 metabolism, which was decreased in the patients with IBS. Ruminococcaceae was also negatively correlated with tyrosine metabolism, which was decreased in the patients with IBS.
This study revealed the dysbiosis of fecal bacterial diversity, composition, and predicted pathways of patients with IBS by meta-analysis and identified universal biomarkers for IBS prediction and therapeutic targets.
肠易激综合征(IBS)是一种常见的胃肠功能慢性疾病,在全球范围内具有较高的患病率。由于其发病机制复杂且具有异质性,目前IBS研究尚无共识。
我们收集并统一重新分析了来自9项研究的1167份粪便16S rRNA基因测序样本(623份来自IBS患者,544份来自健康受试者)。使用随机效应(RE)模型和固定效应(FE)模型,我们计算了IBS组和对照组之间包括细菌α多样性、β多样性、常见菌属和通路等指标的优势比。
通过随机效应模型观察到IBS患者的α多样性指数显著降低。确定了26个细菌属和12条预测通路,它们对IBS患者具有显著的优势比和分类潜力。基于这些特征,我们使用迁移学习来增强模型的预测能力,模型性能提高了约10%。此外,通过相关网络分析,我们发现瘤胃球菌科和克里斯滕森菌科与维生素B6代谢呈负相关,IBS患者中维生素B6代谢降低。瘤胃球菌科也与酪氨酸代谢呈负相关,IBS患者中酪氨酸代谢降低。
本研究通过荟萃分析揭示了IBS患者粪便细菌多样性、组成和预测通路的失调,并确定了用于IBS预测的通用生物标志物和治疗靶点。