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慢性肾脏病中的肠道微生物群

Gut Microbiome in Chronic Kidney Disease.

作者信息

Armani R G, Ramezani A, Yasir A, Sharama S, Canziani M E F, Raj D S

机构信息

Nephrology Division, Department of Medicine, Federal University of São Paulo, São Paulo, Brazil.

Division of Renal Diseases and Hypertension, The George Washington University School of Medicine, 2150 Pennsylvania Avenue NW, Washington, DC, 20037, USA.

出版信息

Curr Hypertens Rep. 2017 Apr;19(4):29. doi: 10.1007/s11906-017-0727-0.

DOI:10.1007/s11906-017-0727-0
PMID:28343357
Abstract

With over 100 trillion microbial cells, the gut microbiome plays important roles in both the maintenance of health and the pathogenesis of disease. Gut microbiome dysbiosis, resulted from alteration of composition and function of the gut microbiome and disruption of gut barrier function, is commonly seen in patients with chronic kidney disease (CKD). The dysbiotic gut microbiome generates excessive amounts of uremic toxins, and the impaired intestinal barrier permits translocation of these toxins into the systemic circulation. Many of these uremic toxins have been implicated in the progression of CKD and increased cardiovascular risk. Various therapeutic interventions have been proposed that aim to restore gut microbiome symbiosis. If proven effective, these interventions will have a significant impact on the management of CKD patients. In this review, we discuss the consequences of gut microbiome dysbiosis in the context of CKD, discuss the consequences of gut dysbiosis, and highlight some of the recent interventions targeting the gut microbiome for therapeutic purposes.

摘要

肠道微生物群含有超过100万亿个微生物细胞,在维持健康和疾病发病机制中都发挥着重要作用。肠道微生物群失调是慢性肾脏病(CKD)患者常见的情况,它是由肠道微生物群的组成和功能改变以及肠道屏障功能破坏引起的。失调的肠道微生物群会产生过量的尿毒症毒素,而受损的肠道屏障会使这些毒素进入体循环。许多这些尿毒症毒素与CKD的进展和心血管风险增加有关。已经提出了各种旨在恢复肠道微生物群共生的治疗干预措施。如果被证明有效,这些干预措施将对CKD患者的管理产生重大影响。在这篇综述中,我们讨论了在CKD背景下肠道微生物群失调的后果,讨论了肠道失调的后果,并重点介绍了一些最近针对肠道微生物群的治疗性干预措施。

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本文引用的文献

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2
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Transl Res. 2017 Jan;179:24-37. doi: 10.1016/j.trsl.2016.04.007. Epub 2016 Apr 30.
3
Intestinal Dysbiosis, Barrier Dysfunction, and Bacterial Translocation Account for CKD-Related Systemic Inflammation.肠道微生物群失调、屏障功能障碍和细菌易位是慢性肾脏病相关全身炎症的原因。
蛋白结合型尿毒症毒素清除作为糖尿病肾病肾小管功能的生物标志物
Sci Rep. 2025 Jul 2;15(1):23406. doi: 10.1038/s41598-025-07248-3.
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Pathological Alterations in Human Blood Microbiome-An Updated Review.人类血液微生物组的病理改变——最新综述
Int J Mol Sci. 2025 Jun 17;26(12):5807. doi: 10.3390/ijms26125807.
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Administration of Trichinella spiralis Antigens Alleviated Diabetic Nephropathy in Diabetic Mice.旋毛虫抗原给药减轻糖尿病小鼠的糖尿病肾病
Acta Parasitol. 2025 Apr 3;70(2):83. doi: 10.1007/s11686-025-01016-z.
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Dietary Phosphorus Levels Influence Protein-Derived Uremic Toxin Production in Nephrectomized Male Rats.饮食磷水平影响肾切除雄性大鼠的蛋白源性尿毒症毒素的产生。
Nutrients. 2024 Jun 8;16(12):1807. doi: 10.3390/nu16121807.
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Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7951-7962. doi: 10.1007/s00210-023-02888-6. Epub 2024 May 17.
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Design and rationale for an open-label, randomized, controlled pilot trial to evaluate the changes in blood uremic toxins in patients with chronic kidney disease by dietary therapy with sake lees.一项开放标签、随机、对照的试点试验的设计与原理,该试验旨在通过酒糟饮食疗法评估慢性肾病患者血液中尿毒症毒素的变化。
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Animal Models for Studying Protein-Bound Uremic Toxin Removal-A Systematic Review.研究蛋白结合型尿毒症毒素清除的动物模型:系统评价。
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