Department of Nephrology, The First Hospital of Jilin University, Changchun, Jilin Province, China.
Department of Thyroid Surgery, General surgery center, The First Hospital of Jilin University, Changchun, Jilin Province, China.
Microbiol Spectr. 2023 Aug 17;11(4):e0038223. doi: 10.1128/spectrum.00382-23. Epub 2023 Jun 21.
Many studies have suggested that gut microbiota dysbiosis may be one of the pathogenesis factors of diabetes mellitus (DM), while it is not clear whether it is involved in the development of diabetic kidney diseases (DKD). The objective of this study was to determine bacterial taxa biomarkers during the progression of DKD by investigating bacterial compositional changes in early and late DKD. 16S rRNA gene sequencing was performed on fecal samples, including the diabetes mellitus (DM), DNa (early DKD), and DNb (late DKD) groups. Taxonomic annotation of microbial composition was performed. Samples were sequenced on the Illumina NovaSeq platform. At the genus level, we found counts of , , and were significantly elevated both in the DNa group (0.0001, 0.0007, and 0.0174, respectively) and the DNb group (0.0001, 0.0012, and 0.0003, respectively) compared with those in the DM group. Only the level of was significantly decreased in the DNa group than the DM group and in the DNb group than the DNa group. Counts of , were significantly decreased in the DNa group compared with those in the DM group (0.001 and 0.006, respectively) and in the DNb group compared with those in the DM group (0.0001 and 0.003, respectively). Levels of , and were positively correlated with an estimated glomerular filtration rate (eGFR), but negatively correlated with microalbuminuria (MAU), 24 h urinary protein quantity (24hUP), and serum creatinine (Scr). Moreover, the areas under the curve (AUCs) of and were 83.33% and 80.77%, respectively, for the DM and DNa cohorts, respectively. Notably, the largest AUC for DNa and DNb cohorts was also that of at 83.60%. Gut microbiota dysbiosis was found in the early and late stages of DKD, especially in the early stage. may be the most promising intestinal bacteria biomarker that can help distinguish different stages of DKD. It is not clear as to whether gut microbiota dysbiosis is involved in the progression of DKD. This study may be the first to explore gut microbiota compositional changes in diabetes, early-DKD, and late DKD. We identify different gut microbial characteristics during different stages of DKD. Gut microbiota dysbiosis is found in the early and late stages of DKD. may be the most promising intestinal bacteria biomarker that can help distinguish different stages of DKD, although further studies are warranted to illustrate these mechanisms.
许多研究表明,肠道微生物群落失调可能是糖尿病(DM)发病机制的因素之一,但尚不清楚其是否参与糖尿病肾病(DKD)的发生发展。本研究旨在通过研究早期和晚期 DKD 中细菌组成的变化,确定 DKD 进展过程中的细菌分类群生物标志物。对粪便样本进行了 16S rRNA 基因测序,包括糖尿病组(DM)、DNa(早期 DKD)和 DNb(晚期 DKD)组。对微生物组成进行了分类注释。样本在 Illumina NovaSeq 平台上进行测序。在属水平上,我们发现 DNa 组(0.0001、0.0007 和 0.0174)和 DNb 组(0.0001、0.0012 和 0.0003)的计数均显著高于 DM 组。仅 DNa 组与 DM 组相比,DNb 组与 DNa 组相比,属水平的计数显著降低。与 DM 组相比,DNa 组的计数显著降低(0.001 和 0.006),与 DM 组相比,DNb 组的计数显著降低(0.0001 和 0.003)。与估计肾小球滤过率(eGFR)呈正相关,但与微量白蛋白尿(MAU)、24 小时尿蛋白量(24hUP)和血清肌酐(Scr)呈负相关。此外,DM 和 DNa 队列的 和 的 AUC 分别为 83.33%和 80.77%。值得注意的是,DNa 和 DNb 队列中最大的 AUC 也是 ,为 83.60%。在 DKD 的早期和晚期都发现了肠道微生物群失调,尤其是在早期。 可能是最有前途的肠道细菌生物标志物,可以帮助区分 DKD 的不同阶段。目前尚不清楚肠道微生物群失调是否参与 DKD 的进展。本研究可能是首次探索糖尿病、早期-DKD 和晚期 DKD 中肠道微生物组成的变化。我们确定了 DKD 不同阶段的不同肠道微生物特征。在 DKD 的早期和晚期都发现了肠道微生物群失调。 可能是最有前途的肠道细菌生物标志物,可以帮助区分 DKD 的不同阶段,尽管还需要进一步的研究来阐明这些机制。