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 in | NeuroImage (Orlando, Fla.) Vol. 39; no. 4; pp. 1693 - 1705 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.02.2008
Elsevier Limited Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 1053-8119 1095-9572 |
DOI | 10.1016/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. |
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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 |
AuthorAffiliation_xml | – name: b Center for Molecular and Functional Imaging, San Francisco, CA – name: e Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA – name: d Department of Neurology, University of California San Francisco, San Francisco, CA – name: c Department of Radiology, University of California San Francisco, San Francisco, CA – name: a UCSF / UC Berkeley Joint Graduate Group in Bioengineering |
Author_xml | – sequence: 1 givenname: SungWon surname: Chung fullname: Chung, SungWon organization: UCSF/UC Berkeley Joint Graduate Group in Bioengineering, USA – sequence: 2 givenname: Daniel surname: Pelletier fullname: Pelletier, Daniel organization: Center for Molecular and Functional Imaging, San Francisco, CA, USA – sequence: 3 givenname: Michael surname: Sdika fullname: Sdika, Michael organization: Center for Molecular and Functional Imaging, San Francisco, CA, USA – sequence: 4 givenname: Ying surname: Lu fullname: Lu, Ying organization: UCSF/UC Berkeley Joint Graduate Group in Bioengineering, USA – sequence: 5 givenname: Jeffrey I. surname: Berman fullname: Berman, Jeffrey I. organization: Center for Molecular and Functional Imaging, San Francisco, CA, USA – sequence: 6 givenname: Roland G. surname: Henry fullname: Henry, Roland G. email: roland.henry@radiology.ucsf.edu organization: UCSF/UC Berkeley Joint Graduate Group in Bioengineering, USA |
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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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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 PMCID: PMC2276665 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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