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福克 23 益生菌治疗丙型肝炎病毒感染患者的安全性和长期疗效。

Safety and long-term effect of the probiotic FK-23 in patients with hepatitis C virus infection.

机构信息

Department of Medical Research (Lower Myanmar), No. 5 Ziwaka Road, 11191 Yangon, Republic of the Union of Myanmar.

Central Research Laboratories, Nichinichi Pharmaceutical Corporation Ltd., 239-1 Tominaga, Iga City, Mie 518-1417, Japan.

出版信息

Biosci Microbiota Food Health. 2016;35(3):123-8. doi: 10.12938/bmfh.2015-024. Epub 2016 May 2.

DOI:10.12938/bmfh.2015-024
PMID:27508113
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4965516/
Abstract

A clinical trial was conducted on 39 adult HCV-positive subjects to determine the safety and long-term effect of the probiotic FK-23 (heat-treated Enterococcus faecalis strain FK-23). Asymptomatic anti-HCV positive adults who fulfilled the selection criteria and gave voluntary consent were recruited from attendees of the Hepatitis Carrier Clinic, Department of Medical Research (Lower Myanmar). Each subject was given 2,700 mg of FK-23 per day by oral route. Blood samples were taken at enrollment and every 3 months and tested for alanine aminotransferase (ALT) and aspartate transaminase (AST). Viral load, urea, total protein, hemoglobin and platelet count were determined every 6 months. Among the subjects, 23 completed 36 months, 31 completed 24 months, 35 completed 12 months and 37 completed 6 months of probiotic therapy. Significant decreases in mean ALT levels were observed at 3 months (34. 9 ± 15.1 IU/l) as compared with the initial level (64.8 ± 17.5 IU/l) and persisted up to 36 months (43.7 ± 25.2 IU/l). Decrease of AST was detected after 9 months (46.2 ± 21.7 IU/l) of probiotic therapy as compared with the initial level (64.3 ± 28.7 IU/l). FK-23 was safe based on the stable levels of biochemical and hematological parameters and the absence of untoward side effects. The FK-23 preparation was well tolerated and accepted by the subjects.

摘要

一项临床试验在 39 名成年 HCV 阳性受试者中进行,以确定益生菌 FK-23(热处理粪肠球菌 FK-23 株)的安全性和长期效果。从缅甸下缅甸医学研究所肝炎携带者诊所的参与者中招募符合入选标准并自愿同意的无症状抗 HCV 阳性成年人。每位受试者每天口服 2700 毫克 FK-23。在入组时和每 3 个月采集血样,检测丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)。每 6 个月测定病毒载量、尿素、总蛋白、血红蛋白和血小板计数。在这些受试者中,23 人完成了 36 个月,31 人完成了 24 个月,35 人完成了 12 个月,37 人完成了 6 个月的益生菌治疗。与初始水平(64.8 ± 17.5IU/l)相比,3 个月时(34.9 ± 15.1IU/l)观察到平均 ALT 水平显著下降,并持续至 36 个月(43.7 ± 25.2IU/l)。与初始水平(64.3 ± 28.7IU/l)相比,在益生菌治疗 9 个月后检测到 AST 下降。基于生化和血液学参数的稳定水平以及无不良反应,FK-23 是安全的。FK-23 制剂耐受性良好,被受试者接受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f8f/4965516/a7a81d56dd82/bmfh-35-123-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f8f/4965516/a7a81d56dd82/bmfh-35-123-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f8f/4965516/a7a81d56dd82/bmfh-35-123-g001.jpg

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