急性胰腺炎
微生物群
炎症
肠道菌群
肠外营养
C反应蛋白
拟杆菌
梭杆菌
医学
免疫学
胃肠病学
内科学
生物信息学
生物
细菌
遗传学
作者
F.-S. Yang,Yi‐Jing Cai,Xiaoying Niu,Shunfu Wang,Y.‐Q. Wang,Sabola Eluby Esmie,Ruicong Chen,Shengjie Dai,Hongru Kong,Hongwei Sun,Keqing Shi
标识
DOI:10.1016/j.fbio.2024.103962
摘要
Enteral nutrition (EN) represents a fundamental and efficacious therapeutic approach in acute pancreatitis (AP). Our objective is to investigate the modulation of gut microbiota through enteral nutrition. This prospective observational study enrolled 35 AP patients and implemented timely enteral nutrition intervention. Inflammatory markers, including C-reactive protein (CRP), were assessed before and after EN, while the dynamic alterations in gut microbiota were analyzed using 16S rDNA sequencing technology. Following EN, CRP significantly decreased, effectively mitigating the inflammatory response. Due to inter-individual variations in post-enteral nutrition inflammatory status, patients were further stratified into H group (CRP≥50 mg/L) and L group (CRP<50 mg/L) for subsequent analysis. Comparative evaluation of clinical characteristics between the two groups revealed that the H group exhibited a significantly higher risk of adverse prognosis including respiratory dysfunction and infectious complications. Dynamic monitoring of gut microbiota demonstrated a substantial increase in microbial diversity after EN accompanied by a decrease in opportunistic pathogens such as Enterococcus, Escherella-Shigella, and Klebsiella, along with an augmentation of beneficial bacteria including Bacteroides and Fusobacterium. The composition of gut microbiota varied according to the levels of inflammation among AP patients: Shigella predominated within Group H, while Actinomyces and Enterococcus constituted the dominant bacterial population within Group L. Furthermore, Spearman correlation analysis revealed significant associations between specific microbial communities within the gut and inflammatory markers such as neutrophil to albumin ratio (NAR) and lymphocyte to C-reactive protein ratio (LCR). EN can modify gut microbiota and alleviate inflammation, thereby affecting the severity and prognosis of AP patients.
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