Whole brain voxel-wise analysis of single-subject serial DTI by permutation testing

Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and aging. In particular, longitudinal changes are vital to the understanding of progression but these studies are typically designed for specific...

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Published inNeuroImage (Orlando, Fla.) Vol. 39; no. 4; pp. 1693 - 1705
Main Authors Chung, SungWon, Pelletier, Daniel, Sdika, Michael, Lu, Ying, Berman, Jeffrey I., Henry, Roland G.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.02.2008
Elsevier Limited
Elsevier
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Online AccessGet full text
ISSN1053-8119
1095-9572
DOI10.1016/j.neuroimage.2007.10.039

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Abstract Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and aging. In particular, longitudinal changes are vital to the understanding of progression but these studies are typically designed for specific regions of interest. To analyze changes in these regions traditional statistical methods are often employed to elucidate group differences which are measured against the variability found in a control cohort. However, in some cases, rather than collecting multiple subjects into two groups, it is necessary and more informative to analyze the data for individual subjects. There is also a need for understanding changes in a single subject without prior information regarding the spatial distribution of the pathology, but no formal statistical framework exists for these voxel-wise analyses of DTI. In this study, we present PERVADE (permutation voxel-wise analysis of diffusion estimates), a whole brain analysis method for detecting localized FA changes between two separate points in time of any given subject, without any prior hypothesis about where changes might occur. Exploiting the nature of DTI that it is calculated from multiple diffusion-weighted images of each region, permutation testing, a non-parametric hypothesis testing technique, was modified for the analysis of serial DTI data and implemented for voxel-wise hypothesis tests of diffusion metric changes, as well as for suprathreshold cluster analysis to correct for multiple comparisons. We describe PERVADE in detail and present results from Monte Carlo simulation supporting the validity of the technique as well as illustrative examples from a healthy subject and patients in the early stages of multiple sclerosis.
AbstractList Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and aging. In particular, longitudinal changes are vital to the understanding of progression but these studies are typically designed for specific regions of interest. To analyze changes in these regions traditional statistical methods are often employed to elucidate group differences which are measured against the variability found in a control cohort. However, in some cases, rather than collecting multiple subjects into two groups, it is necessary and more informative to analyze the data for individual subjects. There is also a need for understanding changes in a single subject without prior information regarding the spatial distribution of the pathology, but no formal statistical framework exists for these voxel-wise analyses of DTI. In this study, we present PERVADE (permutation voxel-wise analysis of diffusion estimates), a whole brain analysis method for detecting localized FA changes between two separate points in time of any given subject, without any prior hypothesis about where changes might occur. Exploiting the nature of DTI that it is calculated from multiple diffusion-weighted images of each region, permutation testing, a non-parametric hypothesis testing technique, was modified for the analysis of serial DTI data and implemented for voxel-wise hypothesis tests of diffusion metric changes, as well as for suprathreshold cluster analysis to correct for multiple comparisons. We describe PERVADE in detail and present results from Monte Carlo simulation supporting the validity of the technique as well as illustrative examples from a healthy subject and patients in the early stages of multiple sclerosis.
Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and aging. In particular, longitudinal changes are vital to the understanding of progression but these studies are typically designed for specific regions of interest. To analyze changes in these regions traditional statistical methods are often employed to elucidate group differences which are measured against the variability found in a control cohort. However, in some cases, rather than collecting multiple subjects into two groups, it is necessary and more informative to analyze the data for individual subjects. There is also a need for understanding changes in a single subject without prior information regarding the spatial distribution of the pathology, but no formal statistical framework exists for these voxel-wise analyses of DTI. In this study, we present PERVADE (permutation voxel-wise analysis of diffusion estimates), a whole brain analysis method for detecting localized FA changes between two separate points in time of any given subject, without any prior hypothesis about where changes might occur. Exploiting the nature of DTI that it is calculated from multiple diffusion-weighted images of each region, permutation testing, a non-parametric hypothesis testing technique, was modified for the analysis of serial DTI data and implemented for voxel-wise hypothesis tests of diffusion metric changes, as well as for suprathreshold cluster analysis to correct for multiple comparisons. We describe PERVADE in detail and present results from Monte Carlo simulation supporting the validity of the technique as well as illustrative examples from a healthy subject and patients in the early stages of multiple sclerosis.Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and aging. In particular, longitudinal changes are vital to the understanding of progression but these studies are typically designed for specific regions of interest. To analyze changes in these regions traditional statistical methods are often employed to elucidate group differences which are measured against the variability found in a control cohort. However, in some cases, rather than collecting multiple subjects into two groups, it is necessary and more informative to analyze the data for individual subjects. There is also a need for understanding changes in a single subject without prior information regarding the spatial distribution of the pathology, but no formal statistical framework exists for these voxel-wise analyses of DTI. In this study, we present PERVADE (permutation voxel-wise analysis of diffusion estimates), a whole brain analysis method for detecting localized FA changes between two separate points in time of any given subject, without any prior hypothesis about where changes might occur. Exploiting the nature of DTI that it is calculated from multiple diffusion-weighted images of each region, permutation testing, a non-parametric hypothesis testing technique, was modified for the analysis of serial DTI data and implemented for voxel-wise hypothesis tests of diffusion metric changes, as well as for suprathreshold cluster analysis to correct for multiple comparisons. We describe PERVADE in detail and present results from Monte Carlo simulation supporting the validity of the technique as well as illustrative examples from a healthy subject and patients in the early stages of multiple sclerosis.
Author Henry, Roland G.
Sdika, Michael
Lu, Ying
Chung, SungWon
Berman, Jeffrey I.
Pelletier, Daniel
AuthorAffiliation a UCSF / UC Berkeley Joint Graduate Group in Bioengineering
c Department of Radiology, University of California San Francisco, San Francisco, CA
d Department of Neurology, University of California San Francisco, San Francisco, CA
e Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA
b Center for Molecular and Functional Imaging, San Francisco, CA
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Issue 4
Keywords Fiber tracking
Serial
Multiple sclerosis
Longitudinal
Permutation
Voxel
Diffusion tensor MRI
Cluster
White matter
Brain
USA
Corpus Callosum
Humans
Cerebral Cortex
Reference Values
reseau_international
Central Nervous System Diseases
Computer-Assisted
Multiple Sclerosis
Pyramidal Tracts
Algorithms
categₘixte
Image Processing
Diffusion Magnetic Resonance Imaging
Adult
Images et Modèles
Nonlinear Dynamics
Monte Carlo Method
Cluster Analysis
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Address Correspondence to: Roland G. Henry, Ph.D., Center for Molecular and Functional Imaging, University of California, San Francisco, 185 Berry Street, Suite 350, Rm 339, Box 0946, San Francisco, CA 94107-0946, Email: roland.henry@radiology.ucsf.edu, Phone: 415-353-9406
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Snippet Diffusion tensor MRI (DTI) has been widely used to investigate brain microstructural changes in pathological conditions as well as for normal development and...
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SubjectTerms Adult
Algorithms
Brain - anatomy & histology
Brain - pathology
Central Nervous System Diseases - diagnosis
Central Nervous System Diseases - pathology
Cerebral Cortex - anatomy & histology
Cerebral Cortex - pathology
Cluster
Cluster Analysis
Computer Science
Corpus Callosum - pathology
Diffusion Magnetic Resonance Imaging - statistics & numerical data
Diffusion tensor MRI
Engineering Sciences
Fiber tracking
Humans
Image Processing
Image Processing, Computer-Assisted - methods
Longitudinal
Medical Imaging
Monte Carlo Method
Multiple sclerosis
Multiple Sclerosis - pathology
NMR
Nonlinear Dynamics
Nuclear magnetic resonance
Permutation
Pyramidal Tracts - pathology
Reference Values
Serial
Signal and Image Processing
Statistical analysis
Statistics
Studies
Voxel
White matter
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Title Whole brain voxel-wise analysis of single-subject serial DTI by permutation testing
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