Microbiome and Metabolome Profiles Associated With Different Types of Short Bowel Syndrome: Implications for Treatment

代谢组 微生物群 脱氧胆酸 鹅去氧胆酸 失调 代谢组学 粪便 肠道菌群 钙蛋白酶 新陈代谢 化学 胆汁酸 生物 食品科学 微生物学 生物化学 内科学 医学 生物信息学 色谱法 炎症性肠病 疾病
作者
Eva Budínská,Jan Gojda,Marie Heczková,Miriam Brátová,Helena Daňková,Petr Wohl,Hana Bastova,Vĕra Lánska,Martin Kostovčík,Milan Dastych,Michal Šenkyřík,Jarmila Křížová,Miloš Mráz,Jaromír Hradecký,Jana Hajšlová,Martin Leníček,Kateřina Podzimkova,Karel Chalupský,Radislav Sedláček,Monika Cahová
出处
期刊:Journal of Parenteral and Enteral Nutrition [Wiley]
卷期号:44 (1): 105-118 被引量:29
标识
DOI:10.1002/jpen.1595
摘要

The gut microbiome and metabolome may significantly influence clinical outcomes in patients with short bowel syndrome (SBS). The study aimed to describe specific metagenomic/metabolomics profiles of different SBS types and to identify possible therapeutic targets.Fecal microbiome (FM), volatile organic compounds (VOCs), and bile acid (BA) spectrum were analyzed in parenteral nutrition (PN)-dependent SBS I, SBS II, and PN-independent (non-PN) SBS patients.FM in SBS I, SBS II, and non-PN SBS shared characteristic features (depletion of beneficial anaerobes, high abundance of Lactobacilaceae and Enterobacteriaceae). SBS I patients were characterized by the abundance of oxygen-tolerant microrganisms and depletion of strict anaerobes. Non-PN SBS subjects showed markers of partial FM normalization. FM dysbiosis was translated into VOC and BA profiles characteristic for each SBS cohort. A typical signature of all SBS patients comprised high saturated aldehydes and medium-chain fatty acids and reduced short-chain fatty acid (SCFA) content. Particularly, SBS I and II exhibited low protein metabolism intermediate (indole, p-cresol) content despite the hypothetical presence of relevant metabolism pathways. Distinctive non-PN SBS marker was high phenol content. SBS patients' BA fecal spectrum was enriched by chenodeoxycholic and deoxycholic acids and depleted of lithocholic acid.Environmental conditions in SBS gut significantly affect FM composition and metabolic activity. The common feature of diverse SBS subjects is the altered VOC/BA profile and the lack of important products of microbial metabolism. Strategies oriented on the microbiome/metabolome reconstitution and targeted delivery of key compounds may represent a promising therapeutic strategy in SBS patients.

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