High b-value apparent diffusion-weighted images from CURVE-ball DTI

14Citations
Citations of this article
48Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Purpose: To investigate the utility of a proposed clinical diffusion imaging scheme for rapidly generating multiple b-value diffusion contrast in brain magnetic resonance imaging (MRI) with high signal-to-noise ratio (SNR). Materials and Methods: Our strategy for efficient image acquisition relies on the invariance property of the diffusion tensor eigenvectors to b-value. A simple addition to the conventional diffusion tensor MR imaging (DTI) data acquisition scheme used for tractography yields diffusionweighted images at twice and three times the conventional b-value. An example from a neurosurgical brain tumor is shown. Apparent diffusion-weighted (ADW) images were calculated for b-values 800, 1600, and 2400 s/mm2, and a map of excess diffusive kurtosis was computed from the three ADWs. Results: High b-value ADW images demonstrated decreased contrast between normal gray and white matter, while the heterogeneity and contrast of the lesion was emphasized relative to conventional b-value data. Kurtosis maps indicated the deviation from Gaussian diffusive behavior. Conclusion: DTI data with multiple b-values and good SNR can be acquired in clinically reasonable times. High b-value ADW images show increased contrast and add information to conventional DWI. Ambiguity in conventional b-value images over whether hyperintense signal results from abnormally low diffusion, or abnormally long T2, is better resolved in high b-value images. © 2009 Wiley-Liss, Inc.

Cite

CITATION STYLE

APA

Peled, S., Whalen, S., Jolesz, F. A., & Golby, A. J. (2009). High b-value apparent diffusion-weighted images from CURVE-ball DTI. Journal of Magnetic Resonance Imaging, 30(1), 243–248. https://doi.org/10.1002/jmri.21808

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free