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Published on: September 5, 2025
Cardiorenal syndrome: Multi-organ dysfunction involving the heart, kidney and vasculature
Feby Savira1,2, Ruth Magaye1,2, Danny Liew2
1Biomarker Discovery Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Insights
Cardiorenal syndrome (CRS) involves complex heart, kidney, and vascular dysfunction. Current therapies are inadequate, prompting research into novel treatments targeting gut dysbiosis and metabolic imbalances for better patient outcomes.
Area of Science:
- Cardiology
- Nephrology
- Vascular Biology
Background:
- Cardiorenal syndrome (CRS) is a complex multi-organ disease affecting the heart, kidneys, and vasculature.
- It presents significant global health challenges, characterized by high morbidity and mortality.
- Existing therapies are often symptomatic and limited in efficacy.
Purpose of the Study:
- To review the complex pathophysiology of cardiorenal syndrome.
- To discuss the limitations of current therapeutic strategies.
- To explore emerging unconventional contributors and novel therapeutic avenues.
Main Methods:
- Literature review of cardiorenal syndrome pathophysiology and treatment.
- Analysis of neurohormonal, inflammatory, oxidative stress, and metabolic interactions.
- Examination of novel therapeutic strategies and emerging contributors like gut dysbiosis.
Main Results:
- CRS pathophysiology involves intricate interactions between multiple systems.
- Current treatments are insufficient, facing challenges with drug interactions and volume management.
- Preclinical studies suggest novel pathways, including gut microbiome and metabolic factors, show promise.
Conclusions:
- Novel therapeutic strategies are needed to address the complexity of cardiorenal syndrome.
- Emerging research into gut dysbiosis, toxins, and metabolic imbalances offers new paradigms for CRS treatment.
- Further clinical validation of pharmaceuticals targeting alternative pathways is warranted.
Abstract:
Cardiorenal syndrome (CRS) is a multi-organ disease, encompassing heart, kidney and vascular system dysfunction. CRS is a worldwide problem, with high morbidity, mortality, and inflicts a significant burden on the health care system. The pathophysiology is complex, involving interactions between neurohormones, inflammatory processes, oxidative stress and metabolic derangements. Therapies remain inadequate, mainly comprising symptomatic care with minimal prospect of full recovery. Challenges include limiting the contradictory effects of multi-organ targeted drug prescriptions and continuous monitoring of volume overload. Novel strategies such as multi-organ transplantation and innovative dialysis modalities have been considered but lack evidence in the CRS context. The adjunct use of pharmaceuticals targeting alternative pathways showing positive results in preclinical models also warrants further validation in the clinic. In recent years, studies have identified the involvement of gut dysbiosis, uraemic toxin accumulation, sphingolipid imbalance and other unconventional contributors, which has encouraged a shift in the paradigm of CRS therapy.
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