Chen Tso-Hsiao, Liu Chao-Wei, Ho Yi-Hsien, Huang Chun-Kai, Hung Ching-Sheng, Smith Barry H, Lin Jung-Chun
Division of Nephrology, Wan Fang Hospital, Taipei Medical University, Taipei 116, Taiwan.
Department of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
J Clin Med. 2021 Aug 29;10(17):3881. doi: 10.3390/jcm10173881.
A growing body of study have documented the association of gut dysbiosis or fecal metabolites with chronic kidney disease (CKD). However, it is not clear whether the phenomenon simply reflects the microenvironment changes correlated with the CKD severity or contributes to the progression of CKD. In this study, we identified the gut microbiota and metabolite in feces samples correlated with CKD severity using the Nanopore long-read sequencing platform and UPLC-coupled MS/MS approach. A cross-sectional cohort study was performed from 1 June 2020 to 31 December 2020. One hundred and fifty-six clinical participants, including 60 healthy enrollees and 96 Stage 1-5 CKD patients, were enrolled in this study. The ROC curve generated with the relative abundance of Klebsiella pneumonia or S-Adenosylhomocysteine showed a gradual increase with the CKD severity. Our results further revealed the positive correlation of increased K. pneumonia and S-Adenosylhomocysteine in gut environment, which may be of etiological importance to the deterioration of a CKD patient. In that sense, the microbiota or metabolite changes constitute potential candidates for evaluating the progression of CKD.
越来越多的研究记录了肠道菌群失调或粪便代谢产物与慢性肾脏病(CKD)之间的关联。然而,尚不清楚这种现象仅仅是反映了与CKD严重程度相关的微环境变化,还是对CKD的进展有促进作用。在本研究中,我们使用纳米孔长读长测序平台和超高效液相色谱-串联质谱联用方法,确定了与CKD严重程度相关的粪便样本中的肠道微生物群和代谢产物。于2020年6月1日至2020年12月31日进行了一项横断面队列研究。本研究纳入了156名临床参与者,包括60名健康受试者和96名1-5期CKD患者。根据肺炎克雷伯菌或S-腺苷同型半胱氨酸的相对丰度生成的ROC曲线显示,其随着CKD严重程度的增加而逐渐上升。我们的结果进一步揭示了肠道环境中肺炎克雷伯菌增加与S-腺苷同型半胱氨酸之间的正相关,这可能对CKD患者的病情恶化具有病因学意义。从这个意义上说,微生物群或代谢产物的变化构成了评估CKD进展的潜在指标。