Huang Wei, Chai Yinghui, Li Xiang, Zhang Qiuyue, Yan Zengkui, Wang Yan, Tao Xiaoyong, Zhang Jiatang, Qiu Feng
Department of Neurology, the 8Th Medical Center of PLA General Hospital, Beijing, China.
Department of Clinical Laboratory, the 8Th Medical Center of PLA General Hospital, Beijing, China.
BMC Microbiol. 2025 Aug 30;25(1):567. doi: 10.1186/s12866-025-04259-y.
Cerebral infarction, a cerebrovascular disorder, is characterized by the sudden onset of neurological deficits and clinical symptoms. It ranks among the leading causes of death and severe disability worldwide. The etiology of cerebral infarction is multifaceted, with common risk factors including dietary patterns, smoking, hypertension, and diabetes mellitus. In recent years, the role of the gut microbiota in systemic immunity and tumorigenesis has been intensively explored, thrusting the research on the gut-brain axis into the spotlight. However, there is a lack of literature investigating the relationship between the gut microbiota and blood metabolites in cerebral infarction. In this study, we employed 16S rRNA analysis and ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) for a comprehensive metagenomic and metabolomic analysis of fecal samples from cerebral infarction patients and the general population. Our results revealed a significant correlation between the gut microbiome and serum metabolites, highlighting the impact of the microbiome on metabolic pathways. Specifically, we found that 35 gut microbiome taxa, such as Actinobacteriota and Peptostreptococcales-Tissierellales, were significantly enriched in the control group (N group). Through Linear Discriminant Analysis Effect Size (LEfSe) analysis, 72 taxa showed significant differences between cerebral infarction patients and healthy individuals. Among them, 22 key taxa were identified as microbial biomarkers for differentiating patients from healthy controls. These findings suggest that variations in the microbiome and metabolites could potentially serve as biomarkers for future diagnostic and therapeutic strategies in cerebral infarction.
脑梗死是一种脑血管疾病,其特征为突然出现神经功能缺损和临床症状。它是全球主要的死亡和严重残疾原因之一。脑梗死的病因是多方面的,常见危险因素包括饮食模式、吸烟、高血压和糖尿病。近年来,肠道微生物群在全身免疫和肿瘤发生中的作用得到了深入研究,使肠道-脑轴的研究成为焦点。然而,缺乏关于脑梗死中肠道微生物群与血液代谢物之间关系的文献。在本研究中,我们采用16S rRNA分析和超高效液相色谱-串联质谱(UHPLC-MS/MS)对脑梗死患者和普通人群的粪便样本进行了全面的宏基因组和代谢组分析。我们的结果揭示了肠道微生物群与血清代谢物之间存在显著相关性,突出了微生物群对代谢途径的影响。具体而言,我们发现35种肠道微生物分类群,如放线菌门和消化链球菌-八叠球菌目,在对照组(N组)中显著富集。通过线性判别分析效应大小(LEfSe)分析,72个分类群在脑梗死患者和健康个体之间存在显著差异。其中,22个关键分类群被确定为区分患者与健康对照的微生物生物标志物。这些发现表明,微生物群和代谢物的变化可能作为未来脑梗死诊断和治疗策略的生物标志物。
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