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Updated: Jun 11, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cardiac magnetic resonance assessment of cardiac function across chronic kidney disease stages
Shutian An1, Hao Qian2, Jinxiu Yang1
1Department of Radiology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Insights
Chronic kidney disease (CKD) patients show impaired right ventricular (RV) and left atrial (LA) function, even with preserved left ventricular ejection fraction. Cardiac magnetic resonance imaging (CMR) can identify these dysfunctions, aiding early detection.
Area of Science:
- Cardiology
- Nephrology
- Medical Imaging
Background:
- Cardiovascular disease is highly prevalent in chronic kidney disease (CKD) patients.
- Left ventricular function is well-studied in CKD, but left atrial and right heart function are less understood.
- Cardiac magnetic resonance imaging (CMR) is crucial for evaluating myocardial structure and function.
Purpose of the Study:
- To assess the interplay of left atrial and right ventricular function in CKD patients using CMR.
- To identify imaging biomarkers for cardiac dysfunction in CKD.
- To compare cardiac function between CKD stages and healthy controls.
Main Methods:
- A cross-sectional study of 58 CKD patients (Stages 2-5) and 26 healthy controls.
- Comprehensive CMR protocols including cine imaging, T1/T2 mapping, and strain analysis.
- Assessment of left ventricular (LV), right ventricular (RV), and left atrial (LA) structure, function, and strain parameters.
Main Results:
- Both CKD groups exhibited impaired RV and LA function compared to controls.
- Significant increases in RV volumes (end-diastolic and end-systolic) were observed in CKD patients.
- Reduced LV, RV, and LA strain parameters were found in CKD patients.
- RV global longitudinal strain (GLS) and LA strain were independent predictors of CKD.
Conclusions:
- RV size, LA strain, and volume by CMR are markers of RV and LA cardiac dysfunction in CKD patients with preserved LVEF.
- RV and LA dysfunction require greater attention for early identification in CKD.
- CMR provides valuable insights into subclinical cardiac abnormalities in CKD.
Background:
Cardiovascular disease prevalence remains high among chronic kidney disease (CKD) patients. Mechanisms and treatments to improve prognosis remain of paramount importance, and imaging biomarkers of left ventricular myocardial structure and function have better defined the phenotype of renal cardiomyopathy. The left atrial function and right heart remain are less well reported in CKD. This study used cardiac magnetic resonance imaging (CMR) to assess the interplay of left atrial and right ventricular function.
Methods:
In a cross-sectional study, we examined 58 CKD patients (Group I: stages 2-3, n = 25; Group II: stages 4-5, n = 33). Additionally, 26 age-matched healthy controls were included. Comprehensive CMR protocols (1.5T) were employed, encompassing cine imaging, native T1 and T2 mapping, and tissue tracking strain analysis. Left ventricular (LV), right ventricular (RV) and left atrial (LA) structure, function and strain parameters were assessed.
Results:
Compared with healthy controls, both Groups I and II exhibited impaired RV and LA function. right ventricular end-diastolic volume index and right ventricular end-systolic volume index showed significant increases in both Groups I and II (P < .001). All LV, RV and LA strain parameters were reduced in the patient groups (all P < .001). In the univariate binary logistic regression, several parameters, including age, blood pressure, RV volumes and LV/RV strain, were found to have a statistically significant association with CKD. In a multivariable model adjusted for other confounders, RV GLS and left atrial strain remained as independent significant predictors.
Conclusions:
RV size, LA strain and volume assessed by CMR serve as markers of RV and LA cardiac dysfunction in CKD patients with preserved LVEF. Greater attention should be given to RV and LA dysfunction for early identification of cardiac dysfunction in CKD patients.
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