Altered Callosal Morphology and Connectivity in Asymptomatic Carotid Stenosis
Background Carotid stenosis, even in the clinically asymptomatic stage, causes cognitive impairment, silent lesions, and hemispheric changes. The corpus callosum (CC) is crucial for hemispheric cortical integration and specialization. Purpose To examine if CC morphology and connectivity relate to co...
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Veröffentlicht in: | Journal of magnetic resonance imaging 2024-03, Vol.59 (3), p.998-1007 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Carotid stenosis, even in the clinically asymptomatic stage, causes cognitive impairment, silent lesions, and hemispheric changes. The corpus callosum (CC) is crucial for hemispheric cortical integration and specialization.
Purpose
To examine if CC morphology and connectivity relate to cognitive decline and lesion burden in asymptomatic carotid stenosis (ACS).
Study Type
Retrospective, cross‐sectional.
Population
33 patients with unilaterally severe (70%) ACS and 28 demographically and comorbidity‐matched controls. A publicly available healthy adult lifespan (ages between 18 and 80; n = 483) MRI dataset was also included.
Field Strength/Sequence
A 3.0 T; T1 MPRAGE and diffusion weighted gradient echo‐planar imaging sequences.
Assessment
Structural MRI and multidomain cognitive data were obtained. Midsagittal CC area, circularity, thickness, integrity, and probabilistic tractography were calculated and correlated with cognitive tests and white matter hyperintensity. Fractional anisotropy, mean diffusivity (MD), and radial diffusivity were determined from DTI.
Statistical Tests
Independent two‐sample t‐tests, χ2 tests, Mann–Whitney U, locally weighted scatterplot smoothing (LOWESS) curve fit, and Pearson correlation. A P value < 0.05 was considered statistically significant.
Results
Patients with ACS demonstrated significant reductions in callosal area, circularity, and thickness compared to controls. The callosal atrophy was significantly correlated with white matter hyperintensity size (r = −0.629, P |
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ISSN: | 1053-1807 1522-2586 1522-2586 |
DOI: | 10.1002/jmri.28872 |