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成人短肠综合征的粪便微生物组和胆汁酸代谢组。

Fecal microbiome and bile acid metabolome in adult short bowel syndrome.

机构信息

Division of Gastroenterology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2022 Jan 1;322(1):G154-G168. doi: 10.1152/ajpgi.00091.2021. Epub 2021 Nov 24.

Abstract

Loss of functional small bowel surface area causes short bowel syndrome (SBS), intestinal failure, and parenteral nutrition (PN) dependence. The gut adaptive response following resection may be difficult to predict, and it may take up to 2 yr to determine which patients will wean from PN. Here, we examined features of gut microbiota and bile acid (BA) metabolism in determining adaptation and ability to wean from PN. Stool and sera were collected from healthy controls and from patients with SBS ( = 52) with ileostomy, jejunostomy, ileocolonic, and jejunocolonic anastomoses fed with PN plus enteral nutrition or who were exclusively enterally fed. We undertook 16S rRNA gene sequencing, BA profiling, and 7α-hydroxy-4-cholesten-3-one (C4) quantitation with LC-MS/MS and serum amino acid analyses. Patients with SBS exhibited altered gut microbiota with reduced gut microbial diversity compared with healthy controls. We observed differences in the microbiomes of patients with SBS with ileostomy versus jejunostomy, jejunocolonic versus ileocolonic anastomoses, and PN dependence compared with those who weaned from PN. Stool and serum BA composition and C4 concentrations were also altered in patients with SBS, reflecting adaptive changes in enterohepatic BA cycling. Stools from patients who were weaned from PN were enriched in secondary BAs including deoxycholic acid and lithocholic aicd. Shifts in gut microbiota and BA metabolites may generate a favorable luminal environment in select patients with SBS, promoting the ability to wean from PN. Proadaptive microbial species and select BA may provide novel targets for patient-specific therapies for SBS. Loss of intestinal surface area causes short bowel syndrome, intestinal failure, and parenteral nutrition dependence. We analyzed the gut microbiota and bile acid metabolome of a large cohort of short bowel syndrome adult patients with different postsurgical anatomies. We report a novel analysis of the microbiome of patients with ileostomy and jejunostomy. Enrichment of specific microbial and bile acid species may be associated with the ability to wean from parenteral nutrition.

摘要

功能性小肠表面积的丧失会导致短肠综合征(SBS)、肠衰竭和肠外营养(PN)依赖。切除后肠道的适应性反应可能难以预测,可能需要长达 2 年的时间才能确定哪些患者可以脱离 PN。在这里,我们研究了肠道微生物群和胆汁酸(BA)代谢的特征,以确定适应和脱离 PN 的能力。从健康对照者和 SBS 患者(n = 52)收集粪便和血清,SBS 患者有回肠造口术、空肠造口术、回结肠吻合术和空肠结肠吻合术,给予 PN 加肠内营养或仅肠内喂养。我们进行了 16S rRNA 基因测序、BA 谱分析和 LC-MS/MS 定量分析 7α-羟基-4-胆甾烯-3-酮(C4)和血清氨基酸分析。与健康对照者相比,SBS 患者的肠道微生物群发生了改变,肠道微生物多样性降低。我们观察到回肠造口术与空肠造口术、空肠结肠吻合术与回结肠吻合术以及与脱离 PN 的患者相比,SBS 患者的微生物组存在差异。SBS 患者的粪便和血清 BA 组成和 C4 浓度也发生了改变,反映了肠肝 BA 循环的适应性变化。从脱离 PN 的患者的粪便中富含次级 BA,包括脱氧胆酸和石胆酸。肠道微生物群和 BA 代谢物的变化可能会在选择的 SBS 患者中产生有利的腔环境,促进脱离 PN 的能力。前适应性微生物种类和特定 BA 可能为 SBS 的患者特异性治疗提供新的目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b43d/8793869/e11656736841/gi-00091-2021r01.jpg

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