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Updated: May 28, 2025

A Mouse 5/6th Nephrectomy Model That Induces Experimental Uremic Cardiomyopathy
Published on: November 7, 2017
Protein-bound uremic toxins as therapeutic targets for cardiovascular, kidney, and metabolic disorders
Shihan Zhang1, Shasha Tang1, Yalei Liu1
1Department of Endocrinology, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, Henan Provincial Key Medicine Laboratory of Intestinal Microecology and Diabetes, Zhengzhou, China.
Abstract:
Cardiovascular-kidney-metabolic (CKM) syndrome is a systemic clinical condition characterized by pathological and physiological interactions among metabolic abnormalities, chronic kidney disease, and cardiovascular diseases, leading to multi-organ dysfunction and a higher incidence of cardiovascular endpoints. Traditional approaches to managing CKM syndrome risk are inadequate in these patients, necessitating strategies targeting specific CKM syndrome risk factors. Increasing evidence suggests that addressing uremic toxins and/or pathways induced by uremic toxins may reduce CKM syndrome risk and treat the disease. This review explores the interactions among heart, kidney, and metabolic pathways in the context of uremic toxins and underscores the significant role of uremic toxins as potential therapeutic targets in the pathophysiology of these diseases. Strategies aimed at regulating these uremic toxins offer potential avenues for reversing and managing CKM syndrome, providing new insights for its clinical diagnosis and treatment.
Insights
Cardiovascular-kidney-metabolic (CKM) syndrome involves complex interactions between heart, kidney, and metabolic issues. Targeting uremic toxins offers a promising strategy for managing CKM syndrome and improving patient outcomes.
Area of Science:
- Nephrology
- Cardiology
- Metabolic Diseases
Background:
- Cardiovascular-kidney-metabolic (CKM) syndrome is a complex condition involving interactions between metabolic abnormalities, chronic kidney disease, and cardiovascular diseases.
- This syndrome leads to multi-organ dysfunction and increased cardiovascular events.
- Current management strategies for CKM syndrome risk are insufficient.
Purpose of the Study:
- To explore the intricate interactions among cardiac, renal, and metabolic pathways within the context of uremic toxins.
- To highlight the critical role of uremic toxins as potential therapeutic targets in CKM syndrome pathophysiology.
- To review strategies for regulating uremic toxins for CKM syndrome management.
Main Methods:
- Literature review focusing on the interplay of uremic toxins with cardiovascular, kidney, and metabolic systems.
- Analysis of evidence supporting the role of uremic toxins in CKM syndrome development and progression.
- Exploration of therapeutic strategies targeting uremic toxins.
Main Results:
- Uremic toxins significantly contribute to the pathophysiology of CKM syndrome.
- Addressing uremic toxins and their pathways shows potential in reducing CKM syndrome risk.
- Regulation of uremic toxins may offer avenues for disease reversal and management.
Conclusions:
- Uremic toxins are key players in CKM syndrome and represent viable therapeutic targets.
- Targeting uremic toxins may provide novel approaches for clinical diagnosis and treatment of CKM syndrome.
- Further research into uremic toxin regulation is warranted for effective CKM syndrome management.
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