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磷酸盐、微生物群与慢性肾脏病。

Phosphate, Microbiota and CKD.

机构信息

Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz, Universidad Autonoma de Madrid, Av Reyes Católicos 2, 28040 Madrid, Spain.

Red de Investigacion Renal (REDINREN), Av Reyes Católicos 2, 28040 Madrid, Spain.

出版信息

Nutrients. 2021 Apr 13;13(4):1273. doi: 10.3390/nu13041273.

DOI:10.3390/nu13041273
PMID:33924419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8070653/
Abstract

Phosphate is a key uremic toxin associated with adverse outcomes. As chronic kidney disease (CKD) progresses, the kidney capacity to excrete excess dietary phosphate decreases, triggering compensatory endocrine responses that drive CKD-mineral and bone disorder (CKD-MBD). Eventually, hyperphosphatemia develops, and low phosphate diet and phosphate binders are prescribed. Recent data have identified a potential role of the gut microbiota in mineral bone disorders. Thus, parathyroid hormone (PTH) only caused bone loss in mice whose microbiota was enriched in the Th17 cell-inducing taxa segmented filamentous bacteria. Furthermore, the microbiota was required for PTH to stimulate bone formation and increase bone mass, and this was dependent on bacterial production of the short-chain fatty acid butyrate. We review current knowledge on the relationship between phosphate, microbiota and CKD-MBD. Topics include microbial bioactive compounds of special interest in CKD, the impact of dietary phosphate and phosphate binders on the gut microbiota, the modulation of CKD-MBD by the microbiota and the potential therapeutic use of microbiota to treat CKD-MBD through the clinical translation of concepts from other fields of science such as the optimization of phosphorus utilization and the use of phosphate-accumulating organisms.

摘要

磷酸盐是一种与不良结局相关的重要尿毒症毒素。随着慢性肾脏病(CKD)的进展,肾脏排泄过多膳食磷酸盐的能力下降,引发代偿性内分泌反应,导致 CKD 矿物质和骨代谢紊乱(CKD-MBD)。最终,高磷血症发展,低磷饮食和磷酸盐结合剂被开处方。最近的数据表明,肠道微生物群在矿物质骨疾病中可能发挥作用。因此,甲状旁腺激素(PTH)仅在其微生物群中富含诱导 Th17 细胞的分类丝状细菌的小鼠中引起骨丢失。此外,微生物群是 PTH 刺激骨形成和增加骨量所必需的,这依赖于细菌产生短链脂肪酸丁酸。我们综述了目前关于磷酸盐、微生物群和 CKD-MBD 之间关系的知识。主题包括 CKD 中特别感兴趣的微生物生物活性化合物、饮食磷酸盐和磷酸盐结合剂对肠道微生物群的影响、微生物群对 CKD-MBD 的调节以及通过将其他科学领域的概念(如优化磷利用和使用聚磷生物体)转化为临床实践,利用微生物群治疗 CKD-MBD 的潜在治疗用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/3177ad40279b/nutrients-13-01273-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/4cea9fa16348/nutrients-13-01273-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/83bacbaaf54c/nutrients-13-01273-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/3177ad40279b/nutrients-13-01273-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/4cea9fa16348/nutrients-13-01273-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/83bacbaaf54c/nutrients-13-01273-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/8070653/3177ad40279b/nutrients-13-01273-g003.jpg

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Water Res. 2021 Apr 1;193:116884. doi: 10.1016/j.watres.2021.116884. Epub 2021 Jan 29.
2
A microbial metabolite remodels the gut-liver axis following bariatric surgery.减重手术后,一种微生物代谢产物重塑了肠道-肝脏轴。
Cell Host Microbe. 2021 Mar 10;29(3):408-424.e7. doi: 10.1016/j.chom.2020.12.004. Epub 2021 Jan 11.
3
Comparative Gut Microbiome Differences between Ferric Citrate and Calcium Carbonate Phosphate Binders in Patients with End-Stage Kidney Disease.
慢性肾病患者摄入活微生物与全因、心血管疾病及癌症相关死亡率的关联
Ren Fail. 2025 Dec;47(1):2449196. doi: 10.1080/0886022X.2024.2449196. Epub 2025 Jan 6.
4
Association between dietary intake of selenium and chronic kidney disease in US adults: a cross-sectional study of NHANES 2015-2018.美国成年人饮食中硒摄入量与慢性肾脏病之间的关联:一项基于2015 - 2018年美国国家健康与营养检查调查(NHANES)的横断面研究
Front Nutr. 2024 Aug 13;11:1396470. doi: 10.3389/fnut.2024.1396470. eCollection 2024.
5
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Heliyon. 2024 Jun 11;10(12):e32828. doi: 10.1016/j.heliyon.2024.e32828. eCollection 2024 Jun 30.
6
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7
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Microorganisms. 2020 Dec 20;8(12):2040. doi: 10.3390/microorganisms8122040.
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8
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9
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10
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