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The Brain Structural-Functional Vulnerability in Drug-Naive Children With Juvenile Idiopathic Arthritis: Insights
Yifei Weng1, Cuili Yi2, Hongyan Liang1
1Department of Radiology, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Insights
Juvenile idiopathic arthritis (JIA) in children shows hippocampal atrophy and altered brain connectivity. These changes correlate with disability, inflammation, and anxiety, offering insights into central nervous system (CNS) comorbidities.
Area of Science:
- Neuroscience
- Pediatric Rheumatology
- Medical Imaging
Background:
- Juvenile idiopathic arthritis (JIA) is a chronic inflammatory disease affecting children and adolescents.
- Central nervous system (CNS) involvement and neurodevelopmental changes are increasingly recognized in JIA.
- Understanding the brain-hippocampus relationship in JIA is crucial for managing associated comorbidities.
Purpose of the Study:
- To investigate structural and functional brain changes in the hippocampus of children and adolescents with JIA.
- To explore correlations between brain alterations and the "joint-inflammation-brain" axis during CNS development.
- To identify potential neuroimaging biomarkers for early detection of neuropathological changes in JIA.
Main Methods:
- Utilized an integrative multimodal MRI paradigm in 21 JIA patients and 23 controls.
- Employed spherical harmonics with a point distribution model (SPHARM-PDM) for hippocampal shape analysis.
- Assessed hippocampo-cortical functional connectivity (FC) using ROI-to-voxel analysis and correlated findings with clinical/laboratory data.
Main Results:
- JIA patients exhibited hippocampal atrophy, particularly in the posterior regions.
- Significant differences in hippocampo-cortical FC were observed in pain, striatal, and temporal regions.
- Altered FC correlated with disability index, inflammation markers (ESR), and anxiety levels.
Conclusions:
- Hippocampal functional connectome alterations may serve as sensitive indicators of early neuropathological changes in JIA.
- Functional brain disturbances are linked to physical disability, inflammation, and emotional status in JIA patients.
- Findings contribute to understanding the neuropathological mechanisms underlying CNS comorbidities in JIA.
Objective:
Leveraging an integrative multimodal MRI paradigm to elaborate on the hippocampus-derived structural and functional changes in children and adolescents with juvenile idiopathic arthritis (JIA) and to explore potential correlations within the "joint-inflammation-brain" axis during the period of central neural system (CNS) development.
Methods:
Twenty-one patients with JIA all completed the multimodal MRI scanning, laboratory tests, and neuropsychological assessments; meanwhile, 23 matched controls were recruited. We then harnessed the spherical harmonics with a point distribution model (SPHARM-PDM) and the ROI-to-voxel functional connectivity (FC) to measure the hippocampal shape and hippocampo-cortical FC patterns. Correlation analysis was performed to explore the potential links in neuroimaging features with disease-related indices.
Results:
Compared to controls, JIA patients only presented an atrophic tendency in the posterior part of the bilateral hippocampus. The hippocampo-cortical FC revealed the between-group divergences mainly located at the pain matrix, striatum, and temporal lobe. Remarkably, the enhanced FC between the right hippocampus and postcentral cortex is positively correlated with the disability index, while the weakened FC of right anterior hippocampus with right insula and that of left posterior hippocampus with left superior temporal gyrus was inversely related to the erythrocyte sedimentation rate and anxiety status, separately.
Conclusion:
As with macroscopic damages, the altered functional-connectome patterns of the hippocampus in JIA patients might be more sensitive to detect the early neuropathological changes. Moreover, the functional disturbances were demonstrated associated with the physical disability, inflammation, and emotional status. These findings may enlighten us on the underlying neuropathological mechanism of CNS comorbidities in JIA.
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