DBP2:MIND:Roadmap

Back to NA-MIC Internal Collaborations, MIND DBP 2

Brain Lesion Analysis in Neuropsychiatric Systemic Lupus Erythematosus

Objective

We would like to create an end-to-end application within NA-MIC Kit allowing individual analysis of white matter lesions. Such a workflow applied to lupus patients is one of goals of the MIND DBP. This page describes the technology roadmap for lesion analysis in the NA-MIC Kit. The basic components necessary for this application are:

• Registration: co-registration of T1-weighted, T2-weighted, and FLAIR images
• Tissue segmentation: Should be multi-modality, correcting for intensity inhomogeneity and work on non-skull-stripped data.
• Lesion Localization: Each unique lesion should be detected and anatomical location summarized
• Lesion Load Measurement: Measure volume of each lesion, summarize lesion load by regions
• Tutorial: Documentation will be written for a tutorial and sample data sets will be provided

Roadmap

We will obtain gray matter, white matter, CSF, and lesion maps for each subject based on T1-weighted, T2-weighted, and FLAIR images. Ultimately, the NA-MIC Kit will provide a workflow for individual and group analysis of lesions. It will be implemented as a set of Slicer3 modules that can be used interactively within the Slicer3 application as well as in batch on a computing cluster using BatchMake.

The current status of the main modules to be used are:

Registration

• ITK has mutual information registration
• BRAINS2 has AIR package wrapped

Lesion segmentation

A number of algorithms for fully or semi-automated lesion analysis will be evaluated. These include:

• Tools developed at UNC known as itkEMS Compare Lesion Analysis Tools (Marcel)
• EM-segment (Sandy Wells)
• BRAINS2 (Magnotta)
• Manual tracing by clinically trained rater

Lesion Localization

• Slicer has tools for labeling white matter lesions and summarizing their anatomical location
• BRAINS2 has tools for creating masks for white matter lesions and summarizing their anatomical location

Lesion Load Measurement

• Slicer has tools for measurement of labelled lesions
• BRAINS2 has tools for measurement of lesions and regional summaries

Performance characterization and validation

• Data will be collected at both 1.5 and 3T. Data at 1.5T will be obtained with the protocol utilized for the current project on lupus at UNM.
• Data at 3T will be obtained with sequences optimized for segmentation by the group at Utah.
• Comparisons will be based on the approach developed by Martin-Fernandez et al.
• The algorithm with the best performance will be incorporated into the NA-MIC kit.

Tutorial

• 5 Publically sharable T1,T2,Flair,Lesion Map data-sets (NIFTI format) will be made available
• A tutorial will be created that will guide end-users through each step needed to complete a lesion analysis in the NA-MIC kit

Schedule

• Sequence Optimization and Data Collection

• 10/15/2007 T1, T2, FLAIR optimized sequences for Siemens 3T Trio Tim scanner (Jeremy, Bruce, Chuck)
  • We will work with Bruce Fischl on using MEMPR, Mugler, and FLAIR sequences that have been optimized for maximum constrast and minimal geometric distortion across sequences
• 11/15/2007 collection of 5 lupus subjects on clinical sequence and optimized 3T sequence (Chuck)

• Registration

• 10/30/2007 optimized mutual information registration for clinical sequences and optimized 3T sequences (Jeremy)

• Lesion segmentation

• 11/30/2007 complete lesion segmentation methods for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Kilian/Brad, Marcel)

• Lesion Localization

• 11/30/2007 complete lesion localizations and maps for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Bruce, Steve)

• Lesion Measurement

• 11/30/2007 complete lesion measurements and regional lesion load summaries for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Bruce, Steve)

• Performance characterization and validation

• 1/6/2008 report to 2008 NA-MIC AHM on performance and validation of lesion segmentation methods for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy)
• 2/15/2008 submit manuscript on reliability and summary of novel NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully)
• 3/15/2008 analyze NIH study clinical sample using NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully)
• 4/15/2008 submit manuscript on clinical application of NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully, Carlos Roldan, Bill Sibbitt)

• Incorporation of approach into NA-MIC kit

• 11/1/2007 Slicer3 Lesion Analysis Module that handles co-registration of T1, T2, and Flair (Mark Scully, Steve)
• 12/1/2008 extend Slicer3 Lesion Analysis Module to handle lesion localization and measurement (Mark Scully, Steve)
• 1/6/2008 extend Slicer3 Lesion Analysis Module to implement the lesion analysis method (EM-segment, BRAINS2, MedX, UNC packages) with the best performance (Mark Scully, Steve)
  • a demonstration will be given at the 2008 NA-MIC AHM--we would consider this version a prototype and would be testing, refining the module through the clinical application phase (Jeremy, Mark Scully)
• 4/1/2008 production version of lesion analysis Slicer3 Module complete (Mark Scully, Steve)

• Tutorial and Data-sharing

• 5/1/2008 make data sets and tutorial publically available (Jeremy, Sonja)

Team and Institute

• Co-PI: H Jeremy Bockholt (jbockholt at mrn.org)
• Co-PI: Charles Gasparovic (chuck at unm.edu)
• Software Engineer: Mark Scully (mscully at mrn .org)
• NA-MIC Engineering Contact: Steve Pieper, Isomics
• NA-MIC Algorithms Contact: Ross Whitaker, Utah
• Kilian Pohl
• Brad Davis
• Consultant: Vincent Magnotta, University of Iowa
• Host Institues: The MIND Institute and The University of New Mexico