Clinical DT-MRI Estimation, Smoothing, and Fiber Tracking With Log-Euclidean Metrics | IEEE Journals & Magazine | IEEE Xplore

Clinical DT-MRI Estimation, Smoothing, and Fiber Tracking With Log-Euclidean Metrics


Abstract:

Diffusion tensor magnetic resonance imaging (DT-MRI or DTI) is an imaging modality that is gaining importance in clinical applications. However, in a clinical environment...Show More

Abstract:

Diffusion tensor magnetic resonance imaging (DT-MRI or DTI) is an imaging modality that is gaining importance in clinical applications. However, in a clinical environment, data have to be acquired rapidly, often at the expense of the image quality. This often results in DTI datasets that are not suitable for complex postprocessing like fiber tracking. We propose a new variational framework to improve the estimation of DT-MRI in this clinical context. Most of the existing estimation methods rely on a log-Gaussian noise (Gaussian noise on the image logarithms), or a Gaussian noise, that do not reflect the Rician nature of the noise in MR images with a low signal-to-noise ratio (SNR). With these methods, the Rician noise induces a shrinking effect: the tensor volume is underestimated when other noise models are used for the estimation. In this paper, we propose a maximum likelihood strategy that fully exploits the assumption of a Rician noise. To further reduce the influence of the noise, we optimally exploit the spatial correlation by coupling the estimation with an anisotropic prior previously proposed on the spatial regularity of the tensor field itself, which results in a maximum a posteriori estimation. Optimizing such a nonlinear criterion requires adapted tools for tensor computing. We show that Riemannian metrics for tensors, and more specifically the log-Euclidean metrics, are a good candidate and that this criterion can be efficiently optimized. Experiments on synthetic data show that our method correctly handles the shrinking effect even with very low SNR, and that the positive definiteness of tensors is always ensured. Results on real clinical data demonstrate the truthfulness of the proposed approach and show promising improvements of fiber tracking in the brain and the spinal cord.
Published in: IEEE Transactions on Medical Imaging ( Volume: 26, Issue: 11, November 2007)
Page(s): 1472 - 1482
Date of Publication: 29 October 2007

ISSN Information:

PubMed ID: 18041263
Citations are not available for this document.

I. Introduction

Diffusion tensor magnetic resonance imaging (DT-MRI or DTI) [1] is a unique tool to assess in vivo oriented structures within tissues via the measure of water diffusion. However, using such an imaging modality in a clinical environment is difficult and acquisitions generally have a limited number of encoding gradients and low signal-to-noise ratios (SNRs). Indeed, pathologies often prevent the patient from staying too long in the same position in the scanner. This short scanning time prevents from acquiring and averaging the large number of gradient directions that is necessary for enhancing the SNR. Moreover, the devices that are commonly available for clinical purposes (at least in France) offer only low-quality diffusion weighted images (DWI) datasets (generally 6 gradient directions with four repeated scans). It is known that the estimation of the diffusion tensor field from DWI is noise-sensitive. Consequently, clinical DTI is very often not suitable for complex post processing, like fiber tracking. For these reasons, there has been a growing interest in the regularization of tensor images. In the following, we quickly summarize the state of the art in diffusion tensor estimation and regularization. Available methods generally perform each of theses two steps independently. We propose in this paper to couple them in a single maximum a posteriori (MAP) estimation that better captures the information in these intrinsically noisy clinical images. Note that a preliminary version of this work was previously presented in [2].

Getting results...

Contact IEEE to Subscribe

References

References is not available for this document.