Department of Health Management, Henan Key Laboratory of Chronic Disease Health Management, Henan Provincial People's Hospital, Henan University People's Hospital, Zhengzhou, China.
Department of Nuclear Medicine, Henan Key Laboratory of Chronic Disease Health Management, Henan Provincial People's Hospital, Zhengzhou, China.
Front Cell Infect Microbiol. 2022 Feb 17;12:722662. doi: 10.3389/fcimb.2022.722662. eCollection 2022.
This study aimed to investigate insomnia-related alterations in gut microbiota and their association with serum metabolites. A total of 24 patients with insomnia disorder and 22 healthy controls were recruited. The fecal and serum samples were collected. The 16s rRNA sequencing and bioinformatics analysis were conducted to explore insomnia-related changes in the diversity, structure, and composition of the gut microbiota. UPLC-MS was performed to identify insomnia-related serum metabolites. Spearman correlation analysis was used to investigate the correlations between insomnia-related gut bacteria and the serum metabolites. Despite the nonsignificant changes in the diversity and structure of gut microbiota, insomnia disorder patients had significantly decreased family , family , and genus , along with significantly increased family and genus , compared with healthy controls. Genus and genus were dominant in patients with insomnia disorder, whereas genus , genus , genus , and family were dominant in healthy controls. The UPLC-MS analysis identified 97 significantly decreased metabolites and 74 significantly increased metabolites in the serum samples of patients with insomnia disorder, compared with those of healthy controls. KEGG enrichment analysis revealed 1 significantly upregulated metabolic pathway and 16 downregulated metabolic pathways in patients with insomnia disorder. Furthermore, Spearman correlation analysis unveiled significant correlations among the altered bacteria genus and serum metabolites. Patients with insomnia disorder have differential gut microbiota and serum metabolic profiles compared with healthy controls. The alterations in gut microbiota were correlated with specific serum metabolites, suggesting that some serum metabolites might mediate gut microbiota-brain communication in the pathogenesis of insomnia disorder.
本研究旨在探究与失眠相关的肠道微生物群变化及其与血清代谢物的关联。共招募了 24 名失眠障碍患者和 22 名健康对照者。收集粪便和血清样本。通过 16s rRNA 测序和生物信息学分析,探索了与失眠相关的肠道微生物多样性、结构和组成的变化。采用 UPLC-MS 鉴定与失眠相关的血清代谢物。采用 Spearman 相关分析探究与失眠相关的肠道细菌与血清代谢物之间的相关性。尽管肠道微生物多样性和结构没有显著变化,但与健康对照组相比,失眠障碍患者的科、科和属显著减少,而科和属显著增加。在失眠障碍患者中,属和属占优势,而属、属、属和科在健康对照组中占优势。与健康对照组相比,失眠障碍患者的血清样本中鉴定出 97 种显著减少的代谢物和 74 种显著增加的代谢物。KEGG 富集分析显示,失眠障碍患者中有 1 个上调代谢途径和 16 个下调代谢途径。此外,Spearman 相关分析揭示了改变的细菌属与血清代谢物之间存在显著相关性。与健康对照组相比,失眠障碍患者的肠道微生物群和血清代谢谱存在差异。肠道微生物群的改变与特定的血清代谢物相关,提示一些血清代谢物可能在失眠障碍的发病机制中介导肠道微生物群-脑通讯。