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Published on: May 2, 2025
Gut microbiome in chronic kidney disease
Maria R Wing1, Samir S Patel1, Ali Ramezani1
1Division of Renal Diseases and Hypertension, The George Washington University, Washington, DC, USA.
Altered gut microbiomes in chronic kidney disease (CKD) produce toxins that worsen uraemic syndrome. Restoring gut symbiosis may reduce inflammation and slow CKD progression.
Area of Science:
- Microbiology
- Nephrology
- Gastroenterology
Background:
- The human intestine is a metabolic organ influenced by gut microbiota.
- Chronic kidney disease (CKD) is associated with significant alterations in the gut microbiome.
- These alterations contribute to the development of uraemic syndrome.
Purpose of the Study:
- To review the role of the gut microbiome in uraemic syndrome.
- To discuss gut microbiome-derived uraemic toxins and their impact on CKD.
- To explore potential therapeutic strategies for normalizing the gut microbiome in CKD.
Main Methods:
- Literature review focusing on the gut-kidney axis in CKD.
- Analysis of the contribution of specific gut microbiome-derived toxins (e.g., p-cresol sulfate, indoxyl sulfate, trimethylamine N-oxide) to CKD progression.
- Examination of the link between gut dysbiosis, inflammation, and cardiovascular disease in CKD patients.
Main Results:
- Altered gut microbiota in CKD patients produces key uraemic toxins.
- These toxins accelerate CKD progression, cardiovascular disease, and mortality.
- Gut-derived endotoxin translocation contributes to systemic inflammation in CKD.
Conclusions:
- The gut microbiome plays a critical role in CKD pathogenesis.
- Targeting the gut microbiome to restore symbiosis is a promising therapeutic strategy.
- Reducing uraemic toxin production and inflammation may improve outcomes for CKD patients.
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