Abstract:Objective To investigate the effect of probiotics combined with enteral nutrition on intestinal flora and peripheral blood miR-155 in patients with acute pancreatitis. Methods 92 patients with acute pancreatitis admitted to the Department of digestive medicine of our hospital from June 2016 to December 2018 were selected as the study subjects, according to the random number table method, the patients were divided into observation group (n=46) and control group (n=46), the control group was given enteral nutrition treatment on the basis of routine treatment, while the observation group was given Live Combined Bifidobacterium and Lactobacillus Tablets on the basis of the control group, the changes of intestinal flora, inflammatory mediators and serum miR-155 were observed before and after treatment, and the recovery of gastrointestinal function was compared between the two groups. Results After treatment, the number of bifidobacteria and lactobacillus increased and the number of enterococcus and escherichia coli decreased in observation group, and the reduced serum levels of CRP, IL-6, IL-17, TNF-α, and mi5-155 were significantly higher than those of control group (P<0.05).The gastrointestinal quality of life scale (GIQLI) score of patients in observation group was higher than that of control group, and the time for the disappearance of abdominal distension, the time for the disappearance of abdominal pain, the time for the recovery of bowel sounds, and the time for the recovery of serum amylase were all less than that of control group (P<0.05). Conclusion Probiotics combined with enteral nutrition in the treatment of acute pancreatitis can regulate the balance of intestinal flora, reduce the level of serum miR-155, alleviate inflammation and promote the recovery of intestinal function.
王燕,石剑,贡丽雅,王凤姣. 益生菌联合肠内营养对急性胰腺炎患者肠道菌群及外周血miR-155的影响[J]. 肿瘤代谢与营养电子杂志, 2020, 7(2): 199-203.
Wang Yan, Shi Jian, Gong Liya, Wang Fengjiao. Effect of probiotics combined with enteral nutrition on intestinal flora and peripheral blood miR-155 in patients with acute pancreatitis. Electron J Metab Nutr Cancer, 2020, 7(2): 199-203.
1.DUMNICKA P, MADUZIA D, CERANOWICZ P, et al.The Interplay between Inflammation, Coagulation and Endothelial Injury in the Early Phase of Acute Pancreatitis: Clinical Implications[J].Int J Mol Sci, 2017, 18(2): 354-379.
2.KRISHNAN K.Nutritional management of acute pancreatitis[J].Curr Opin Gastroenterol, 2017, 33(2): 102-106.
3.POROPAT G, GILJACA V, HAUSER G, et al.Enteral nutrition formulations for acute pancreatitis[J].Cochrane Database Syst Rev, 2015, 3(3): CD010605-CD010622.
4.顾慧媛, 高欣, 钱丽娟, 等.益生菌联合早期肠内营养治疗对重症急性胰腺炎患者血清炎性因子、肠黏膜屏障功能的影响[J].海南医学, 2017, 28(23): 3793-3795.
5.王兴鹏, 李兆申, 袁耀宗, 等.中国急性胰腺炎诊治指南(2013, 上海)[J].中国实用内科杂志, 2013, 13(7): 73-78.
6.王轶, 朱生樑. 非糜烂性反流病患者生活质量评价[J]. 广东医学, 2018, 39(3): 438-442.
7.LANKISCH PG.Acute pancreatitis[J].Lancet, 2015, 386(9988): 85-96.
8.WANG D, TANG M, ZONG P, et al.MiRNA-155 Regulates the Th17/Treg Ratio by Targeting SOCS1 in Severe Acute Pancreatitis[J].Front Physiol, 2018, 9(8): 686-696.
9.陈晓, 王鹏, 张静, 等.肠内营养支持治疗对重症急性胰腺炎合并肠源性感染患者免疫功能和炎症指标的影响研究[J].中华医院感染学杂志, 2018, 28(5): 722-725.
10.陈侣林, 李卉, 朱俊臣, 等.添加益生菌的早期肠内营养对脓毒血症休克患者血清炎症因子的影响[J].重庆医学, 2018, 47(21): 46-48.
11.江明万, 王晴雷, 于双, 等.益生菌对重症急性胰腺炎患者感染发生率的影响[J].实用临床医药杂志, 2016, 20(9): 178-179.
12.JOO K M, HEE P, GA L, et al.Multiple-unit tablet of probiotic bacteria for improved storage stability, acid tolerability, and in vivo intestinal protective effect[J].Drug Des Devel Ther, 2016, 45(10): 1355-1364.
13.赵波.益生菌联合早期肠内营养治疗重症急性胰腺炎的临床价值[J].实用临床医药杂志, 2017, 21(9): 57-60.
14.李锦春, 钱传云, 蔡乙明, 等.微生态制剂联合肠内营养对急性重症胰腺炎患者全身炎性反应、细菌移位以及免疫功能的影响[J].中国现代医学杂志, 2018, 28(6): 85-89.
15.林姝, 陈香宇, 王喜莹, 等.miR-155在急性胰腺炎患者外周血中的表达及其临床意义[J].世界华人消化杂志, 2015, 23(24): 3935-3939.
16.TIAN R, WANG R L, XIE H, et al.Overexpressed miRNA-155 dysregulates intestinal epithelial apical junctional complex in severe acute pancreatitis[J].World J Gastroenterol, 2013, 19(45): 8282-8291.
17.LI X, JI Z, LI S, et al.MiR-146a-5p antagonized AGEs- and P.g -LPS-Induced ABCA1 and ABCG1 dysregulation in macrophages via IRAK-1 downregulation[J].Inflammation, 2015, 38(5): 1761-1768.