Heart Center of Henan Provincial People's Hospital, Department of Cardiology of Central China Fuwai Hospital, Henan Key Laboratory for Coronary Heart Disease Prevention and Control, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, China.
Department of Medicine Huddinge, Karolinska Institute, Huddinge, Sweden.
Front Endocrinol (Lausanne). 2024 Jul 15;15:1410295. doi: 10.3389/fendo.2024.1410295. eCollection 2024.
The gut microbiota plays a pivotal role in the development of diabetes and kidney disease. However, it is not clear how the intestinal microecological imbalance is involved in the context of diabetic kidney disease (DKD), the leading cause of renal failure.
To elucidate the gut microbial signatures associated with DKD progression towards end-stage renal disease (ESRD) and explore whether they could reflect renal dysfunction and psychological distress.
A cross-sectional study was conducted to explore the gut microbial signatures of 29 DKD non-ESRD patients and 19 DKD ESRD patients compared to 20 healthy controls. Differential analysis was performed to detect distinct gut microbial alterations in diversities and taxon abundance of DKD with and without ESRD. Renal dysfunction was estimated by urea, creatinine, and estimated glomerular filtration rate. Psychological distress was assessed using the Self-Rating Anxiety Scale, Self-Rating Depression Scale, Hamilton Anxiety Rating Scale, and Hamilton Depression Rating Scale.
Alpha diversity indexes were reduced in DKD patients, particularly those with ESRD. Beta diversity analysis revealed that the gut microbial compositions of DKD patients were different with healthy individuals whereas similar compositions were observed in DKD patients. Taxon differential analysis showed that when compared with the controls, DKD patients exhibit distinct microbial profiles including reduced abundances of butyrate-produced, anti-inflammatory bacteria , , , and increased abundances of pro-inflammatory bacteria , etc. These distinctive genera presented consistent associations with renal dysfunction, as well as psychological distress, especially in DKD patients.
DKD patients, especially those who have progressed to ESRD, exhibit unique characteristics in their gut microbiota that are associated with both renal dysfunction and psychological distress. The gut microbiota may be a significant factor in the deterioration of DKD and its eventual progression to ESRD.
肠道微生物群在糖尿病和肾脏疾病的发展中起着关键作用。然而,目前尚不清楚肠道微生态失衡如何参与糖尿病肾病(DKD),这是肾衰竭的主要原因。
阐明与 DKD 向终末期肾病(ESRD)进展相关的肠道微生物特征,并探讨它们是否能反映肾功能障碍和心理困扰。
进行了一项横断面研究,以比较 29 名 DKD 非 ESRD 患者和 19 名 DKD ESRD 患者与 20 名健康对照者的肠道微生物特征。通过差异分析,检测了 DKD 患者中具有和不具有 ESRD 的肠道微生物多样性和分类群丰度的明显变化。肾功能障碍通过尿素、肌酐和估计肾小球滤过率来评估。使用自评焦虑量表、自评抑郁量表、汉密尔顿焦虑量表和汉密尔顿抑郁量表评估心理困扰。
DKD 患者的 alpha 多样性指数降低,尤其是那些有 ESRD 的患者。β多样性分析显示,与健康个体相比,DKD 患者的肠道微生物组成不同,而 DKD 患者之间的肠道微生物组成相似。分类群差异分析表明,与对照组相比,DKD 患者表现出独特的微生物特征,包括丁酸产生菌、抗炎菌 、 、 的丰度降低,促炎菌 、 等的丰度增加。这些独特的属与肾功能障碍以及心理困扰呈一致关联,尤其是在 DKD 患者中。
DKD 患者,尤其是进展为 ESRD 的患者,其肠道微生物群具有独特的特征,与肾功能障碍和心理困扰都有关。肠道微生物群可能是 DKD 恶化及其最终进展为 ESRD 的重要因素。