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Published on: November 7, 2017
Cardiovascular burden associated with uremic toxins in patients with chronic kidney disease
Hamid Moradi1, Domenic A Sica, Kamyar Kalantar-Zadeh
1University of California Irvine School of Medicine, Orange, Calif., USA.
Insights
Uremic toxins contribute to cardiovascular disease in chronic kidney disease (CKD) patients, increasing risks. Emerging treatments show promise, but large trials are needed to confirm their effectiveness in managing these toxic effects.
Area of Science:
- Nephrology
- Cardiology
- Toxicology
Background:
- Uremic toxins accumulate in chronic kidney disease (CKD), adversely impacting multiple organs, particularly the cardiovascular system.
- This accumulation leads to significant patient morbidity and mortality, making toxin alleviation a key management priority.
Purpose of the Study:
- To review the evidence linking uremic toxins to cardiovascular morbidity and mortality in CKD patients with slowly developing uremia.
- To summarize data on potential treatments for mitigating the adverse cardiovascular effects of uremic toxins.
Main Methods:
- Literature review focusing on uremic toxins and cardiovascular outcomes in CKD.
- Exclusion of cardiovascular effects related to acute kidney injury and rapid azotemia.
Main Results:
- Uremic toxins are strongly associated with increased cardiovascular morbidity and mortality in CKD.
- While preclinical data are extensive, clinical studies on cardiovascular outcomes are recent.
Conclusions:
- Uremic toxins significantly contribute to cardiovascular disease progression in CKD patients.
- Further research is essential to fully understand the impact of uremic toxins on cardiovascular health.
- Preliminary evidence suggests beneficial treatments exist, but large randomized trials are required to validate their utility.
Background:
Retention of uremic toxins in patients with chronic kidney disease (CKD) negatively affects multiple organ systems, including the cardiovascular system, resulting in significant morbidity and mortality. Alleviation of the adverse effects of uremic toxins is an important priority in the management of CKD.
Scope:
This review focuses on the evidence for the influence of uremic toxins on cardiovascular morbidity and mortality among patients with CKD and slowly developing uremia. The cardiovascular effects of acute kidney injury and rapidly developing azotemia are beyond the scope of this review and will not be discussed. Data on potential treatment options aimed at ameliorating the toxic effects of uremic toxins are summarized.
Findings:
Uremic toxins are associated with significant cardiovascular morbidity and mortality in patients with CKD. While a number of preclinical studies have detailed these effects, clinical studies directly evaluating cardiovascular outcomes consequent to the presence of uremic toxins have only recently become available.
Conclusion:
Uremic toxins play an important role in the progression of cardiovascular disease in patients with CKD. Further studies are needed to better characterize the impact of these compounds on cardiovascular outcomes. Beneficial treatments are currently available that, in preliminary studies, appear to neutralize some of the adverse effects of uremic toxins. Large randomized clinical trials are needed to further determine the utility of these varied therapeutic agents.
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