Johnson-Martínez Johannes P, Diener Christian, Levine Anne E, Wilmanski Tomasz, Suskind David L, Ralevski Alexandra, Hadlock Jennifer, Magis Andrew T, Hood Leroy, Rappaport Noa, Gibbons Sean M
Institute for Systems Biology, Seattle, WA 98109, USA; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Institute for Systems Biology, Seattle, WA 98109, USA; Diagnostic and Research Institute of Hygiene, Microbiology and Environmental Medicine, Medical University of Graz, Graz, Austria.
Cell Rep Med. 2024 Jul 16;5(7):101646. doi: 10.1016/j.xcrm.2024.101646.
Bowel movement frequency (BMF) directly impacts the gut microbiota and is linked to diseases like chronic kidney disease or dementia. In particular, prior work has shown that constipation is associated with an ecosystem-wide switch from fiber fermentation and short-chain fatty acid production to more detrimental protein fermentation and toxin production. Here, we analyze multi-omic data from generally healthy adults to see how BMF affects their molecular phenotypes, in a pre-disease context. Results show differential abundances of gut microbial genera, blood metabolites, and variation in lifestyle factors across BMF categories. These differences relate to inflammation, heart health, liver function, and kidney function. Causal mediation analysis indicates that the association between lower BMF and reduced kidney function is partially mediated by the microbially derived toxin 3-indoxyl sulfate (3-IS). This result, in a generally healthy context, suggests that the accumulation of microbiota-derived toxins associated with abnormal BMF precede organ damage and may be drivers of chronic, aging-related diseases.
排便频率(BMF)直接影响肠道微生物群,并与慢性肾病或痴呆症等疾病相关。特别是,先前的研究表明,便秘与整个生态系统从纤维发酵和短链脂肪酸产生向更有害的蛋白质发酵和毒素产生的转变有关。在这里,我们分析了一般健康成年人的多组学数据,以了解在疾病前期背景下BMF如何影响他们的分子表型。结果显示,不同BMF类别之间肠道微生物属、血液代谢物的丰度存在差异,生活方式因素也有所不同。这些差异与炎症、心脏健康、肝功能和肾功能有关。因果中介分析表明,较低的BMF与肾功能降低之间的关联部分由微生物衍生的毒素3-吲哚硫酸酯(3-IS)介导。在一般健康的背景下,这一结果表明,与异常BMF相关的微生物衍生毒素的积累先于器官损伤,可能是慢性衰老相关疾病的驱动因素。