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Published on: November 7, 2017
Cardiorenal syndrome
Claudio Ronco1, Mikko Haapio, Andrew A House
1Department of Nephrology, St. Bortolo Hospital, Vicenza, Italy. cronco@goldnet.it
Insights
A new classification for cardiorenal syndrome (CRS) defines 5 subtypes based on heart and kidney dysfunction. This framework aids in understanding the bidirectional relationship and guides diagnosis and treatment for CRS patients.
Area of Science:
- Cardiology
- Nephrology
- Pathophysiology
Background:
- The term cardiorenal syndrome (CRS) lacks a consistent definition, hindering understanding of heart-kidney interactions.
- Existing knowledge does not fully capture the complex, bidirectional relationship between cardiac and renal dysfunction.
Purpose of the Study:
- To introduce a novel 5-subtype classification for cardiorenal syndrome (CRS).
- To provide a framework reflecting the pathophysiology, timeframe, and nature of heart and kidney dysfunction in CRS.
- To improve the characterization, management, and clinical trial design for CRS.
Main Methods:
- Defined CRS as a disorder where dysfunction of one organ induces dysfunction in the other.
- Developed 5 subtypes based on the directionality and acuity of cardiac and renal involvement.
- Highlighted the role of biomarkers in early diagnosis and intervention.
Main Results:
- Introduced 5 subtypes of CRS: Type 1 (cardiac to kidney, acute), Type 2 (cardiac to kidney, chronic), Type 3 (kidney to cardiac, acute), Type 4 (kidney to cardiac, chronic), and Type 5 (systemic).
- Emphasized the bidirectional nature of heart and kidney interactions in CRS pathophysiology.
- Proposed that this classification aids in patient stratification and clinical trial design.
Conclusions:
- The proposed 5-subtype classification offers a standardized approach to understanding cardiorenal syndrome.
- This classification facilitates targeted management strategies and enhances the precision of clinical research in CRS.
- Biomarkers are crucial for early CRS detection and timely therapeutic interventions.
Abstract:
The term cardiorenal syndrome (CRS) increasingly has been used without a consistent or well-accepted definition. To include the vast array of interrelated derangements, and to stress the bidirectional nature of heart-kidney interactions, we present a new classification of the CRS with 5 subtypes that reflect the pathophysiology, the time-frame, and the nature of concomitant cardiac and renal dysfunction. CRS can be generally defined as a pathophysiologic disorder of the heart and kidneys whereby acute or chronic dysfunction of 1 organ may induce acute or chronic dysfunction of the other. Type 1 CRS reflects an abrupt worsening of cardiac function (e.g., acute cardiogenic shock or decompensated congestive heart failure) leading to acute kidney injury. Type 2 CRS comprises chronic abnormalities in cardiac function (e.g., chronic congestive heart failure) causing progressive chronic kidney disease. Type 3 CRS consists of an abrupt worsening of renal function (e.g., acute kidney ischemia or glomerulonephritis) causing acute cardiac dysfunction (e.g., heart failure, arrhythmia, ischemia). Type 4 CRS describes a state of chronic kidney disease (e.g., chronic glomerular disease) contributing to decreased cardiac function, cardiac hypertrophy, and/or increased risk of adverse cardiovascular events. Type 5 CRS reflects a systemic condition (e.g., sepsis) causing both cardiac and renal dysfunction. Biomarkers can contribute to an early diagnosis of CRS and to a timely therapeutic intervention. The use of this classification can help physicians characterize groups of patients, provides the rationale for specific management strategies, and allows the design of future clinical trials with more accurate selection and stratification of the population under investigation.
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