Difference between revisions of "Projects:PathologyAnalysis"

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= Analysis of Brain Images with Pathological Changes =
  
 
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Quantification, analysis and display of brain pathology such as white matter lesions as observed in MRI is important for diagnosis, monitoring of disease progression, improved understanding of pathological processes and for developing new therapies. Utah Center for Neuroimage Analysis develops new methodology for extraction of brain lesions from volumetric MRI scans and for characterization of lesion patterns over time. The images show white matter lesions (yellow) displayed with ventricles (blue) and transparent brain surface in a patient with an autoimmune disease (lupus). Lesions in white matter and possible correlations with cognitive deficits are also studied in patients with multiple sclerosis (MS), chronic depression, Alzheimer’s disease (AD) and in older persons.
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Traumatic brain injury (TBI) occurs when an external force traumatically injures the brain. TBI is a major cause of death and disability worldwide, especially in children and young adults. TBI affects 1.4 million Americans annually. The UCLA medical school has been working on this topic for years.
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On anatomical MRI scans, to quantitatively analyze the cortical thickness, white matter changes, we need to have a good segmentation on TBI images. However, for TBI data, standard automated image analysis methods are not robust with respect to the TBI-related changes in image contrast, changes in brain shape, cranial fractures, white matter fiber alterations, and other signatures of head injury.
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We will work on an extension of ABC for TBI datasets with the clinical goal to investigate alterations in cortical thickness, subsequent ventricular, and white matter changes in patients with TBI.
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Revision as of 14:24, 23 March 2011

Home < Projects:PathologyAnalysis

Back to Utah 2 Algorithms


Analysis of Brain Images with Pathological Changes

Description

Traumatic brain injury (TBI) occurs when an external force traumatically injures the brain. TBI is a major cause of death and disability worldwide, especially in children and young adults. TBI affects 1.4 million Americans annually. The UCLA medical school has been working on this topic for years.

On anatomical MRI scans, to quantitatively analyze the cortical thickness, white matter changes, we need to have a good segmentation on TBI images. However, for TBI data, standard automated image analysis methods are not robust with respect to the TBI-related changes in image contrast, changes in brain shape, cranial fractures, white matter fiber alterations, and other signatures of head injury.

We will work on an extension of ABC for TBI datasets with the clinical goal to investigate alterations in cortical thickness, subsequent ventricular, and white matter changes in patients with TBI.


Segmentation of a lupus case with large lesions.
Segmentation of a 3T lupus case with small lesions.

In addition to the identification of the location and shape of lesions in 3D, we are interested in analyzing the longitudinal series of brain MRI showing lesions. For this purpose, we have developed a method for estimating a physical model for lesion formation. The model that we use is an approximation using a reaction-diffusion process that is based on expected diffusion properties (as observed through DTI). This approach gives a richer parametrization of lesion changes in addition to volume and location, as the model estimation provides descriptions of growth and spread for individual lesions. In the future, we plan to incorporate this approach for analyzing lesion MRI of a subject over time by characterizing the change patterns through the physical model parameters.

An example of the lesion model formation estimation result. Starting from an initial guess of the reaction-diffusion process, the method estimates a model that best fits the observed data. Left: initial guess. Center: final estimate. Right: observed patient data. Top row: the T2 intensities, bottom row: lesion probabilities

Key Investigators

  • Utah Algorithms: Marcel Prastawa, Guido Gerig
  • Clinical Collaborators
    • MIND: Jeremy Bockholt, Mark Scully

Publications

In Print