[The gastrointestinal microbiome - vision and mission].

IF 0.7 Deutsche medizinische Wochenschrift (1946) Pub Date : 2025-02-01 Epub Date: 2025-01-29 DOI:10.1055/a-2303-3368
Andreas Stallmach
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Abstract

The gastrointestinal microbiome influences physiological functions and is altered in a variety of diseases. The causality of "dysbiosis" in the pathogenesis is not always proven; association studies are often involved. Patients with IBD, bacteria, fungi, bacteriophages, and archaea show disease-typical patterns associated with metabolome disturbances. Fecal microbiome transfer (FMT) for treating various diseases is the subject of numerous clinical studies. Currently, recurrent Clostridioides difficile infection (rCDI) is the only confirmed indication recommended in medical guidelines. In Germany, the FMT is subject to the Medicines Act and may only be carried out as part of individual healing attempts or clinical studies. For patient safety, repeated donor screening, ideally with the construction of a chair bench, is necessary. This significantly limits the nationwide availability of the FMT in Germany. Microbiota-based therapeutics prepared from the stool of tested donors have recently been approved by the US Food and Drug Administration (FDA) for the prevention of rCDI. More microbiome-based medicines can be expected in the future.

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胃肠道微生物群——愿景与使命。
胃肠道微生物群影响生理功能,并在多种疾病中发生改变。致病机制中“生态失调”的因果关系并不总是得到证实;经常涉及关联研究。IBD患者、细菌、真菌、噬菌体和古细菌表现出与代谢组紊乱相关的疾病典型模式。粪便微生物组转移(FMT)治疗各种疾病是众多临床研究的主题。目前,复发性难辨梭菌感染(rCDI)是医学指南中推荐的唯一确认适应症。在德国,FMT受《药品法》的约束,只能作为个人治疗尝试或临床研究的一部分进行。为了病人的安全,反复的供体筛选是必要的,理想的情况是要有一个椅子凳。这极大地限制了FMT在德国全国范围内的可用性。最近,美国食品和药物管理局(FDA)批准了从供体粪便中制备的基于微生物群的疗法,用于预防rCDI。未来可以期待更多基于微生物组的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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