Volume 3,Issue 7
冠心病患者肠道菌的通路协同分析
冠心病（CHD）的发生与肠道菌群紊乱密切相关，但其协同作用机制尚未完全阐明。本研究通过整合多组学数据，筛选冠心病患者肠道菌群特征性物种及代谢通路，探讨菌群间协同作用对宿主代谢的影响。利用TOPSIS算法筛选出30个与CHD显著相关的核心菌群，并通过IGM平台和KEGG通路分析揭示其参与的脂代谢、炎症反应等关键通路。UniProt功能注释进一步表明，目标菌群代谢物（如短链脂肪酸、氧化三甲胺）可能通过调控宿主免疫及内皮功能影响CHD进程。本研究为揭示肠道菌群协同机制提供了新的理论依据，并为CHD的精准干预策略奠定基础。
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