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2
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3
AGA Clinical Practice Guidelines on the Management of Moderate to Severe Ulcerative Colitis.美国胃肠病学会关于中重度溃疡性结肠炎管理的临床实践指南。
Gastroenterology. 2020 Apr;158(5):1450-1461. doi: 10.1053/j.gastro.2020.01.006. Epub 2020 Jan 13.
4
Changes in the rate of and trends in colectomy for ulcerative colitis during the era of biologics and calcineurin inhibitors based on a Japanese nationwide cohort study.基于一项日本全国性队列研究的生物制剂和钙调神经磷酸酶抑制剂时代溃疡性结肠炎结肠切除术率的变化和趋势。
Surg Today. 2019 Dec;49(12):1066-1073. doi: 10.1007/s00595-019-01845-2. Epub 2019 Jul 15.
5
AGA Clinical Practice Guidelines on the Management of Mild-to-Moderate Ulcerative Colitis.美国胃肠病学会关于轻至中度溃疡性结肠炎管理的临床实践指南。
Gastroenterology. 2019 Feb;156(3):748-764. doi: 10.1053/j.gastro.2018.12.009. Epub 2018 Dec 18.
6
AGA Technical Review on the Management of Mild-to-Moderate Ulcerative Colitis.AGA 技术评论:轻度至中度溃疡性结肠炎的治疗。
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7
Evidence-based clinical practice guidelines for inflammatory bowel disease.炎症性肠病的循证临床实践指南。
J Gastroenterol. 2018 Mar;53(3):305-353. doi: 10.1007/s00535-018-1439-1. Epub 2018 Feb 10.
8
Tofacitinib as Induction and Maintenance Therapy for Ulcerative Colitis.托法替布治疗溃疡性结肠炎的诱导缓解和维持治疗。
N Engl J Med. 2017 May 4;376(18):1723-1736. doi: 10.1056/NEJMoa1606910.
9
Higher Surgical Morbidity for Ulcerative Colitis Patients in the Era of Biologics.生物制剂时代溃疡性结肠炎患者的更高手术发病率。
Ann Surg. 2018 Aug;268(2):311-317. doi: 10.1097/SLA.0000000000002275.
10
Update on medical and surgical options for patients with acute severe ulcerative colitis: What is new?急性重症溃疡性结肠炎患者的医学和手术治疗选择最新进展:有哪些新内容?
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日本溃疡性结肠炎患者使用新型治疗药物的长期预后分析及预后与疾病易感基因座的相关性

Analysis of the Long-Term Prognosis in Japanese Patients with Ulcerative Colitis Treated with New Therapeutic Agents and the Correlation between Prognosis and Disease Susceptibility Loci.

作者信息

Hishinuma Kasumi, Moroi Rintaro, Okamoto Daisuke, Shimoyama Yusuke, Kuroha Masatake, Shiga Hisashi, Kakuta Yoichi, Kinouchi Yoshitaka, Masamune Atsushi

机构信息

Division of Gastroenterology, Tohoku University Hospital, Sendai, Japan.

出版信息

Inflamm Intest Dis. 2021 Sep 2;6(3):154-164. doi: 10.1159/000518371. eCollection 2021 Sep.

DOI:10.1159/000518371
PMID:34722645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8527903/
Abstract

BACKGROUND

New therapeutic agents, including biologics and small-molecule drugs, are widely used to treat ulcerative colitis (UC). This study evaluates long-term prognosis in Japanese patients treated with these agents and the association between prognosis and genetic susceptibility to UC.

METHODS

We evaluated surgery-free rates using the Kaplan-Meier method in the total cohort and in patients treated with prednisolone and new therapeutic agents. Multivariate analysis was performed to identify clinical factors affecting surgical rates using Cox's proportional hazard model. The rate of use of new therapeutic agents was compared using the Kaplan-Meier method, and multivariate analysis was conducted to investigate the correlation between the single-nucleotide polymorphism (SNP) rs117506082 and long-term prognosis.

RESULTS

Surgery-free survival decreased over time. There was no significant difference in this parameter between patients who were administered prednisolone and those who were administered new therapeutic agents. Poor response to prednisolone and treatment without topical 5-aminosalicylic acid were poor prognostic factors. Shorter time from diagnosis to initiation of treatment with new therapeutic agents was a risk factor for colectomy. The AA genotype of SNP rs117506082 was associated with a shorter time to surgery and increased use of new therapeutic agents.

CONCLUSIONS

The use of new therapeutic agents might improve long-term prognosis in patients with more severe UC. Previously identified genetic risk factors were not significantly associated with a higher rate of colectomy.

摘要

背景

包括生物制剂和小分子药物在内的新型治疗药物被广泛用于治疗溃疡性结肠炎(UC)。本研究评估了接受这些药物治疗的日本患者的长期预后以及预后与UC遗传易感性之间的关联。

方法

我们使用Kaplan-Meier方法评估了整个队列以及接受泼尼松龙和新型治疗药物治疗的患者的无手术率。使用Cox比例风险模型进行多变量分析,以确定影响手术率的临床因素。使用Kaplan-Meier方法比较新型治疗药物的使用率,并进行多变量分析以研究单核苷酸多态性(SNP)rs117506082与长期预后之间的相关性。

结果

无手术生存率随时间下降。接受泼尼松龙治疗的患者与接受新型治疗药物治疗的患者在该参数上无显著差异。对泼尼松龙反应不佳以及未使用局部5-氨基水杨酸进行治疗是不良预后因素。从诊断到开始使用新型治疗药物的时间较短是结肠切除术的一个危险因素。SNP rs117506082的AA基因型与手术时间缩短和新型治疗药物使用增加有关。

结论

使用新型治疗药物可能会改善重度UC患者的长期预后。先前确定的遗传风险因素与较高的结肠切除率无显著关联。