微生物群
代谢组学
拟杆菌
粪便
肠道菌群
体重不足
代谢组
医学
生理学
组学
厚壁菌
神经性厌食
生物
内科学
细菌
肥胖
生物信息学
微生物学
饮食失调
免疫学
遗传学
精神科
超重
16S核糖体RNA
作者
Alessio Maria Monteleone,Jacopo Troisi,Alessio Fasano,Riccardo Dalle Grave,Francesca Marciello,Gloria Serena,Simona Calugi,Giovanni Scala,Giulio Corrivetti,Giammarco Cascino,Palmiero Monteleone,Mario Maj
标识
DOI:10.1016/j.clnu.2020.07.021
摘要
Background & aims We have recently reported specific fecal metabolomic changes in acute and short-term weight restored patients with anorexia nervosa (AN). In this study we explored the association between those metabolomic changes and patients’ gut microbiome composition. Methods The gut microbiome of AN women was sequenced in both the underweight phase (n = 21) and after short-term weight restoration (n = 16) and compared to that of 20 healthy women. According to a multi-omics approach, microbiome data were correlated with 49 relevant fecal metabolites previously characterized in our participants by an untargeted metabolomic procedure. Results Compared to healthy women, AN patients showed a decreased intra-individual bacterial richness, an increased Bacteroidetes-to-Firmicutes abundance ratio and significant changes in the relative abundances of several bacteria at phylum, class, order, family and genus levels. These changes were observed in both the underweight and weight-restored condition. Moreover, the relationships among the 49 previously selected fecal metabolites and bacteria genera showed structures of different complexity among the 3 groups. In particular, a quarter of those relationships showed a divergent direction in the acutely ill patients with respect to the weight-restored ones or normal controls. Finally, in acutely ill patients 70% of those correlations showed a negative sign suggesting a prevalent metabolites consummation by gut microbiome. Conclusions These data confirm a profound perturbation in the gut microbiome composition of AN patients. Moreover, for the first time, they provide the evidence that in AN gut bacteria are connected with several fecal metabolites in a different way from normal controls and with divergent directions in the acute phase with respect to the weight-restored phase.
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