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Nissle 1917 在临床缓解溃疡性结肠炎患者中的治疗潜力:一项基于医院的队列研究。

Therapeutic Potential of Nissle 1917 in Clinically Remission-attained Ulcerative Colitis Patients: A Hospital-based Cohort Study.

机构信息

Department of Internal Medicine, Kosin University College of Medicine, Busan, Korea.

出版信息

Korean J Gastroenterol. 2021 Jan 25;77(1):12-21. doi: 10.4166/kjg.2020.0119.

DOI:10.4166/kjg.2020.0119
PMID:33361702
Abstract

BACKGROUND/AIMS: Nissle 1917 (EcN) alone therapy is as effective as mesalamine in inducing and maintaining remission in ulcerative colitis (UC). The efficacy and safety of EcN in combination with standard therapies have not been studied. This study examined the changes in the inflammation markers and symptoms following the additional administration of EcN to patients showing the clinical remission of UC.

METHODS

UC patients who received EcN after being in clinical remission for more than 3 months at Kosin University Gospel Hospital between 2013 and 2018 were evaluated through the retrospective medical-record-based review. The partial Mayo score, fecal calprotectin (FC), BMI, hemoglobin, serum cholesterol, serum albumin levels, and the safety profiles were examined at 3rd and 6th months after initiating EcN.

RESULTS

Ninety-four patients were included. After 3 months of treatment, there was no significant change in FC (156.3 μg/g to 141.1 μg/g) (p=0.653). On the other hand, partial Mayo score decreased significantly from 0.085 to 0.014 (p=0.025), and the bodyweight (p=0.001), BMI (p<0.001), hemoglobin (p=0.009), and cholesterol level increased (p=0.148). One patient (1.1%) experienced a serious adverse event with UC flare-up, and 14 patients (14.9%) discontinued EcN due to adverse events; all developed within 3 months.

CONCLUSIONS

Additional administration of EcN to clinically remission-attained UC patients may improve the UC symptoms without changing the FC levels. EcN-associated adverse events develop within the early few weeks.

摘要

背景/目的:Nissle 1917(EcN)单独治疗与美沙拉嗪在诱导和维持溃疡性结肠炎(UC)缓解方面同样有效。尚未研究 EcN 与标准疗法联合使用的疗效和安全性。本研究通过回顾性病历审查,评估了在临床缓解期超过 3 个月的 UC 患者接受 EcN 额外治疗后的炎症标志物和症状变化。

方法

2013 年至 2018 年期间,在 Kosin 大学福音医院接受 EcN 治疗后达到临床缓解期超过 3 个月的 UC 患者接受了评估。在开始使用 EcN 后的第 3 个月和第 6 个月,评估了部分 Mayo 评分、粪便钙卫蛋白(FC)、BMI、血红蛋白、血清胆固醇、血清白蛋白水平以及安全性概况。

结果

共纳入 94 例患者。治疗 3 个月后,FC 无显著变化(156.3 μg/g 至 141.1 μg/g)(p=0.653)。另一方面,部分 Mayo 评分从 0.085 显著下降至 0.014(p=0.025),体重(p=0.001)、BMI(p<0.001)、血红蛋白(p=0.009)和胆固醇水平升高(p=0.148)。1 例(1.1%)患者发生 UC 复发的严重不良事件,14 例(14.9%)因不良事件停用 EcN;所有不良事件均发生在治疗后 3 个月内。

结论

对达到临床缓解的 UC 患者额外给予 EcN 治疗可能会改善 UC 症状,而不会改变 FC 水平。EcN 相关不良事件发生在最初的几周内。

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