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肠球菌定植于胆管与原发性硬化性胆管炎的疾病进展相关。

Bile Duct Colonization With Enterococcus sp. Associates With Disease Progression in Primary Sclerosing Cholangitis.

机构信息

Center for Autoimmune Liver Diseases, Department of Gastroenterology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

First Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Clin Gastroenterol Hepatol. 2023 May;21(5):1223-1232.e3. doi: 10.1016/j.cgh.2022.09.006. Epub 2022 Sep 16.

Abstract

BACKGROUND & AIMS: Primary sclerosing cholangitis (PSC) is characterized by chronic inflammation of the biliary mucosa. Bile ducts in PSC are often colonized with bacteria. Although accumulating evidence demonstrates the importance of microbiota for mucosal immunity, little is known about the impact of bile duct colonization with bacteria on the clinical course of PSC.

METHODS

Bile samples were sent to culture during endoscopic retrograde cholangio-pancreatography before the administration of peri-interventional antibiotics. Procedures during overt bacterial cholangitis or with prior antibiotic treatment were excluded. The primary endpoint was defined as a composite clinical endpoint of decompensated cirrhosis and/or liver transplantation or death.

RESULTS

A cohort of 189 patients with 591 bile fluid cultures was included. In multivariable Cox regression analysis, the presence of Enterococci (present in 28% of the patients), but not of other bacterial species, conferred risk of disease progression with a hazard ratio of 3.61 (95% confidence interval, 1.6-8.11; P = .002) to reach the composite clinical endpoint. Fungobilia, present in 19.6% of patients, was confirmed to associate with disease progression with a hazard ratio of 3.25 (95% confidence interval, 1.87-5.66; P < .001) to reach the composite clinical endpoint.

CONCLUSIONS

The novel association of biliary colonization by Enterococci with disease progression underlines the importance of microbiota-mucosal interplay for the pathogenesis of PSC. These results should stimulate further mechanistic studies on the role of microbiota in PSC and highlight potential new therapeutic targets for a disease without effective treatment options.

摘要

背景与目的

原发性硬化性胆管炎(PSC)的特征为胆道黏膜的慢性炎症。PSC 患者的胆管常被细菌定植。尽管越来越多的证据表明微生物群对黏膜免疫很重要,但对于胆管细菌定植对 PSC 临床病程的影响知之甚少。

方法

在给予介入围手术期抗生素之前,通过内镜逆行胰胆管造影术采集胆汁样本进行培养。排除明显细菌性胆管炎或有先前抗生素治疗的病例。主要终点定义为失代偿性肝硬化和/或肝移植或死亡的复合临床终点。

结果

共纳入了 189 例患者的 591 份胆汁液培养结果。多变量 Cox 回归分析显示,肠球菌定植(见于 28%的患者)而不是其他细菌定植与疾病进展风险相关,其风险比为 3.61(95%置信区间,1.6-8.11;P =.002),达到复合临床终点。19.6%的患者存在真菌性胆汁,与疾病进展相关,其风险比为 3.25(95%置信区间,1.87-5.66;P <.001),达到复合临床终点。

结论

胆道中肠球菌定植与疾病进展的新关联突显了微生物群-黏膜相互作用在 PSC 发病机制中的重要性。这些结果应激发进一步研究微生物群在 PSC 中的作用,并强调针对尚无有效治疗方法的疾病的潜在新治疗靶点。

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