Wang Zhenjiang, Guo Mingyi, Yang Sen, Chen Yuping, Cheng Jianbin, Huang Zaiwei, Wang Tongxu, Luo Xiaobei, He Xingxiang, Wang Dali, Xu Xiaohong
Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University), Zhuhai, China.
Nanfang Hospital, Southern Medical University, Guangzhou, China.
Gut Pathog. 2024 Oct 30;16(1):64. doi: 10.1186/s13099-024-00652-6.
Specific intestinal metabolites are closely associated with the classification, severity, and necrosis of acute pancreatitis (AP) and provide novel insights for in-depth clinical investigations. In this study, the gut microbiota and metabolites of 49 AP patients at different treatment stages and severities were analysed via 16S rDNA sequencing and untargeted metabolomics to investigate the trends in gut microbiota composition and metabolome profiles observed in patients with severe AP. These findings revealed an imbalance in intestinal flora homeostasis among AP patients characterized by a decrease in probiotics and an increase in opportunistic pathogens, which leads to damage to the intestinal mucosal barrier through reduced short-chain fatty acid (SCFA) secretion and disruption of the intestinal epithelium. This dysbiosis influences energy metabolism, anti-inflammatory responses, and immune regulation, and these results highlight significant differences in energy metabolism pathways. These findings suggest that the differential composition of intestinal flora, along with alterations in intestinal metabolites and metabolic pathways, contribute to the compromised integrity of the intestinal mucosal barrier and disturbances in energy metabolism in patients with severe AP.
特定的肠道代谢产物与急性胰腺炎(AP)的分类、严重程度及坏死密切相关,为深入的临床研究提供了新的见解。在本研究中,通过16S rDNA测序和非靶向代谢组学分析了49例处于不同治疗阶段和严重程度的AP患者的肠道微生物群和代谢产物,以研究重症AP患者肠道微生物群组成和代谢组谱的变化趋势。这些发现揭示了AP患者肠道菌群稳态失衡,其特征为益生菌减少和机会致病菌增加,这通过短链脂肪酸(SCFA)分泌减少和肠上皮破坏导致肠黏膜屏障受损。这种生态失调影响能量代谢、抗炎反应和免疫调节,这些结果突出了能量代谢途径的显著差异。这些发现表明,肠道菌群的差异组成以及肠道代谢产物和代谢途径的改变,导致了重症AP患者肠黏膜屏障完整性受损和能量代谢紊乱。