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Diffusional Kurtosis along the Corticospinal Tract in Adult Normal Pressure Hydrocephalus
B Ades-Aron1, S Yeager2, N Miskin3
1From the Center for Biomedical Imaging (B.A.-A., S.Y., E.F., A.G.), Department of Radiology benjamin.ades-aron@nyumc.org.
Diffusion MRI can detect microstructural damage in the corticospinal tract of Normal Pressure Hydrocephalus patients. Specific diffusion and kurtosis parameters reveal differences compared to Alzheimer disease and healthy controls.
Area of Science:
- Neuroimaging
- White Matter Integrity
- Diffusion MRI
Background:
- Normal Pressure Hydrocephalus (NPH) is a reversible dementia linked to enlarged ventricles.
- Ventricular enlargement can distort white matter fibers, particularly the corticospinal tract.
- Understanding white matter changes is crucial for diagnosing and managing NPH.
Purpose of the Study:
- To investigate diffusion and kurtosis parameter variations along the corticospinal tract in NPH patients.
- To pinpoint the location of microstructural compromise within the corticospinal tract.
- To assess if diffusion MRI can differentiate NPH from Alzheimer disease and healthy controls.
Main Methods:
- Developed a novel method for analyzing diffusion parameters at discrete points along neural tracts.
- Utilized diffusion MRI data from NPH patients, Alzheimer disease patients, and healthy controls.
- Compared diffusion parameters of the corticospinal tract across the three groups.
Main Results:
- Diffusion parameters successfully differentiated NPH patients from Alzheimer disease patients and healthy controls.
- Significant differences in axial diffusion, axial kurtosis, and axonal water fraction were observed (P < .05).
- These differences were localized to the superior internal capsule and corona radiata region, near the ventricles.
Conclusions:
- Diffusion MRI parameters can serve as biomarkers for NPH.
- Axial kurtosis and axonal water fraction changes suggest axonal compression and reduced density in NPH.
- Findings highlight the potential of diffusion MRI for early detection and understanding of NPH pathophysiology.
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