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Updated: Feb 11, 2026

Diffusion Tensor Magnetic Resonance Imaging in Chronic Spinal Cord Compression
Published on: May 7, 2019
Equilibrio entre Precisión y Exactitud: Valores b Óptimos para la Imagen por Tensor de Difusión a lo Largo del
Nelly Vuong1, Samo Lasič2, Sara Hall2
1From the Department of Clinical Sciences (N.V., S.L., D.vW., M.N. C.G.), Diagnostic Radiology, Clinical Memory Research Unit (S.H., N.S., O.H.), Department of Clinical Sciences Malmo, Faculty of Medicine, Lund University; Image and Function (N.V., D. vW., C.G.), Skane University Hospital; Memory Clinic (S.H.), Skane University Hospital nelly.vuong@med.lu.se.
Background And Purpose:
The glymphatic system facilitates perivascular clearance, and its dysfunction has been implicated in neurodegenerative diseases. Diffusion Tensor Imaging Along the Perivascular Space (DTI-ALPS) has been proposed as an indirect approach to assess glymphatic function, but its reliability is debated. The choice of b-value is an aspect of possible improvement. While a b-value of 1000 s/mm2 is commonly used, the optimal b-value for DTI-ALPS remains unknown. This study aims to determine the optimal b-value for DTI-ALPS.
Methods:
Simulations were conducted to examine how the choice of maximum b-value influences bias, precision, and effect size of the ALPS index. DTI-ALPS was applied in a cohort of 194 participants divided into four groups: healthy controls (n=42), Parkinson's disease patients (n=119), Parkinson's disease dementia patients (n=16), and progressive supranuclear palsy patients (n=17). ALPS indices were calculated by manually placing regions of interest on projection and association fibers in each hemisphere. Group differences in ALPS indices across b-values were analyzed using mixed models.
Results:
In vivo, ALPS indices were higher at a b-value of 500 and 250 s/mm2 compared to a b-value of 1000 s/mm2 in both hemispheres. Simulations indicated a bias-variance trade-off: very low b-values reduced sensitivity and compromised precision, while high b-values improved precision but reduced accuracy. The simulated effect size of the ALPS index peaked at intermediate b-values (≈700 s/mm2). In vivo, ALPS indices were lower in Parkinson's disease dementia and Progressive supranuclear palsy patients compared to healthy controls, though differences varied across b-values.
Conclusions:
Both simulations and in vivo results suggest that the commonly used b-value of 1000 s/mm2 is not optimal for assessing diffusion in the perivascular spaces. Intermediate b-values at approximately 700 s/mm2 appear more suitable. However, further optimization of acquisition parameters is needed.
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