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肝移植后原发性硬化性胆管炎的复发与移植前肠道微生物组的特定变化相关 - 一项初步研究。

Recurrence of primary sclerosing cholangitis after liver transplantation is associated with specific changes in the gut microbiome pretransplant - a pilot study.

机构信息

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

Department of Surgery, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Transpl Int. 2020 Nov;33(11):1424-1436. doi: 10.1111/tri.13692. Epub 2020 Jul 26.

Abstract

Primary sclerosing cholangitis (PSC) is a common indication for liver transplantation (LT). Up to 25% of patients experience recurrence of PSC (rPSC) after LT, which is associated with significant morbidity and mortality. To date, it is not possible to predict which patients are at risk for rPSC. The aetiology of PSC is complex and is speculated to involve translocation of intestinal bacteria to the liver, because of its frequent co-occurrence with inflammatory bowel diseases (IBD). Here, we investigate whether the mucosal intestinal microbiome of PSC patients (n = 97) at time of first LT can identify those patients who will develop rPSC. 16S gene sequencing of bacterial DNA isolated from formalin-fixed paraffin-embedded biopsies showed that PSC patients with Crohn's disease (n = 15) have a reduced microbial diversity and that inflammation of the mucosa is associated with beta-diversity changes and feature differences. No differences in alpha- or beta diversity were observed between patients with rPSC (n = 14) and without rPSC (n = 83). However, many over-represented bacterial features were detected in patients with rPSC, while surprisingly, those without recurrence of disease were characterized by an increased presence of the Gammaproteobacteria Shigella. This pilot study warrants further investigation into bacterial differences between rPSC and non-rPSC patients.

摘要

原发性硬化性胆管炎(PSC)是肝移植(LT)的常见适应证。多达 25%的患者在 LT 后会出现 PSC 的复发(rPSC),这与显著的发病率和死亡率相关。迄今为止,尚无法预测哪些患者存在 rPSC 的风险。PSC 的病因复杂,据推测与肠道细菌易位到肝脏有关,因为它常与炎症性肠病(IBD)同时发生。在这里,我们研究了在首次 LT 时,PSC 患者(n=97)的黏膜肠道微生物组是否可以识别出那些将发展为 rPSC 的患者。从福尔马林固定石蜡包埋活检中分离的细菌 DNA 的 16S 基因测序表明,患有克罗恩病的 PSC 患者(n=15)的微生物多样性降低,并且黏膜炎症与 beta 多样性变化和特征差异相关。rPSC 患者(n=14)和无 rPSC 患者(n=83)之间未观察到 alpha 或 beta 多样性的差异。然而,在 rPSC 患者中检测到许多过度表达的细菌特征,而令人惊讶的是,那些没有疾病复发的患者则以 gammaproteobacteria Shigella 的存在增加为特征。这项初步研究值得进一步研究 rPSC 和非 rPSC 患者之间的细菌差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b5/7689804/aaeb256bed89/TRI-33-1424-g001.jpg

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