肠道微生物群与糖尿病肾病:微生物群及其衍生代谢物在调节肾脏炎症和疾病进展中的作用。

Intestinal microbiota and diabetic kidney diseases: the Role of microbiota and derived metabolites inmodulation of renal inflammation and disease progression.

机构信息

Department of Internal and Vascular Medicine, Amsterdam UMC, Location VUmc, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.

Department of Medicine, Division of Nephrology, Koc University School of Medicine, Istanbul, Turkey.

出版信息

Best Pract Res Clin Endocrinol Metab. 2021 May;35(3):101484. doi: 10.1016/j.beem.2021.101484. Epub 2021 Jan 13.

Abstract

Diabetic kidney disease (DKD) represents a growing public health burden and is the leading cause of end-stage kidney diseases. In recent years, host-gut microbiota interactions have emerged as an integral part for host homeostasis. In the context of nephropathies, mounting evidence supports a bidirectional microbiota-kidney crosstalk, which becomes particularly manifest during progressive kidney dysfunction. Indeed, in chronic kidney disease (CKD), the "healthy" microbiota structure is disrupted and intestinal microbes produce large quantities of uremic solutes responsible for renal damage; on the other hand, the uremic state, fueled by reduced renal clearance, causes shifts in microbial metabolism and composition, hence creating a vicious cycle in which dysbiosis and renal dysfunction are progressively worsened. In this review, we will summarize the evidence from clinical/experimental studies concerning the occurrence of gut dysbiosis in diabetic and non-diabetic CKD, discuss the functional consequences of dysbiosis for CKD progression and debate putative therapeutic interventions targeting the intestinal microbiome.

摘要

糖尿病肾病(DKD)是一个日益严重的公共卫生负担,也是终末期肾病的主要原因。近年来,宿主-肠道微生物群相互作用已成为宿主内环境稳定的一个组成部分。在肾脏病的背景下,越来越多的证据支持微生物群-肾脏的双向相互作用,这种相互作用在进行性肾功能障碍时表现得尤为明显。事实上,在慢性肾脏病(CKD)中,“健康”的微生物群结构被破坏,肠道微生物产生大量尿毒症溶质,导致肾脏损伤;另一方面,由于肾脏清除率降低导致的尿毒症状态会引起微生物代谢和组成的变化,从而形成一个恶性循环,其中肠道菌群失调和肾功能障碍逐渐恶化。在这篇综述中,我们将总结临床/实验研究中关于糖尿病和非糖尿病 CKD 中肠道菌群失调发生的证据,讨论菌群失调对 CKD 进展的功能后果,并探讨针对肠道微生物组的潜在治疗干预措施。

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