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Updated: Oct 13, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Global and Regional White Matter Fractional Anisotropy in Children with Chronic Kidney Disease
Ellen van der Plas1, Matthew A Solomon2, Lauren Hopkins1
1Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA.
Insights
Children with chronic kidney disease (CKD) show reduced white matter integrity, impacting brain development even before dialysis or transplantation. This study highlights the vulnerability of white matter in pediatric CKD patients.
Area of Science:
- Pediatric Nephrology
- Neuroimaging
- Developmental Neuroscience
Background:
- Chronic kidney disease (CKD) in children can affect neurological development.
- Congenital anomalies of the kidney and urinary tract are a common cause of pediatric CKD.
- Understanding white matter integrity is crucial for assessing neurodevelopmental outcomes in children with CKD.
Purpose of the Study:
- To investigate the relationship between neurocognition and white matter integrity in children with CKD.
- To compare white matter integrity in children with CKD to typically developing controls.
- To identify specific white matter regions affected by CKD in pediatric patients.
Main Methods:
- Cross-sectional study of 17 boys with mild to moderate CKD (stages 1-3) and 20 typically developing controls (ages 6-16).
- Utilized 3T neuroimaging and diffusion-weighted magnetic resonance imaging to assess white matter fractional anisotropy (FA).
- Employed multivariable linear regression and false discovery rate for statistical analysis, adjusting for age.
Main Results:
- Children with CKD exhibited significantly reduced global white matter FA compared to controls.
- Reductions in FA were observed in specific brain regions, including the corpus callosum, cerebral peduncle, cingulum, and internal capsule.
- No significant associations were found between medical variables or neurocognitive abilities and white matter FA within the CKD group.
Conclusions:
- White matter development is vulnerable in children with congenital CKD, even in early stages.
- Early-stage pediatric CKD impacts white matter integrity, suggesting potential long-term neurodevelopmental consequences.
- Findings underscore the need for monitoring brain health in children with CKD, irrespective of disease severity or treatment modality.
Objective:
To investigate the associations between neurocognition and white matter integrity in children with chronic kidney disease (CKD).
Study Design:
This cross-sectional study included 17 boys (age 6-16 years) with a diagnosis of mild to moderate (stages 1-3, nondialysis/nontransplant) CKD because of congenital anomalies of the kidney and urinary tract and 20 typically developing community controls. Participants underwent 3T neuroimaging and diffusion-weighted magnetic resonance imaging to assess white matter fractional anisotropy. Multivariable linear regression models were used to evaluate the impact of each group (controls vs CKD) on white matter fractional anisotropy, adjusting for age. Associations between white matter fractional anisotropy and neurocognitive abilities within the CKD group were also evaluated using regression models that were adjusted for age. The false discovery rate was used to account for multiple comparisons; wherein false discovery values <0.10 were considered significant.
Results:
Global white matter fractional anisotropy was reduced in patients with CKD relative to controls (standardized estimate = -0.38, 95% CI -0.69:-0.07), driven by reductions within the body of the corpus callosum (standardized estimate = -0.44, 95% CI -0.75:-0.13), cerebral peduncle (SE = -0.37, 95% CI -0.67:-0.07), cingulum (hippocampus) (standardized estimate = -0.45, 95% CI -0.75:-0.14), and posterior limb of the internal capsule (standardized estimate = -0.46, 95% CI -0.76:-0.15). Medical variables and neurocognitive abilities were not significantly associated with white matter fractional anisotropy.
Conclusions:
White matter development is vulnerable in children with CKD because of congenital causes, even prior to the need for dialysis or transplantation.
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