Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy

Diffusion MRI tractography has emerged as a useful and popular tool for mapping connections between brain regions. In this study, we examined the performance of quantitative anisotropy (QA) in facilitating deterministic fiber tracking. Two phantom studies were conducted. The first phantom study exam...

Full description

Bibliographic Details
Main Authors: Yeh, Fang-Cheng, Verstynen, Timothy D., Wang, Yibao, Fernández-Miranda, Juan C., Tseng, Wen-Yih Isaac
Format: Online
Language:English
Published: Public Library of Science 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858183/
id pubmed-3858183
recordtype oai_dc
spelling pubmed-38581832013-12-12 Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy Yeh, Fang-Cheng Verstynen, Timothy D. Wang, Yibao Fernández-Miranda, Juan C. Tseng, Wen-Yih Isaac Research Article Diffusion MRI tractography has emerged as a useful and popular tool for mapping connections between brain regions. In this study, we examined the performance of quantitative anisotropy (QA) in facilitating deterministic fiber tracking. Two phantom studies were conducted. The first phantom study examined the susceptibility of fractional anisotropy (FA), generalized factional anisotropy (GFA), and QA to various partial volume effects. The second phantom study examined the spatial resolution of the FA-aided, GFA-aided, and QA-aided tractographies. An in vivo study was conducted to track the arcuate fasciculus, and two neurosurgeons blind to the acquisition and analysis settings were invited to identify false tracks. The performance of QA in assisting fiber tracking was compared with FA, GFA, and anatomical information from T1-weighted images. Our first phantom study showed that QA is less sensitive to the partial volume effects of crossing fibers and free water, suggesting that it is a robust index. The second phantom study showed that the QA-aided tractography has better resolution than the FA-aided and GFA-aided tractography. Our in vivo study further showed that the QA-aided tractography outperforms the FA-aided, GFA-aided, and anatomy-aided tractographies. In the shell scheme (HARDI), the FA-aided, GFA-aided, and anatomy-aided tractographies have 30.7%, 32.6%, and 24.45% of the false tracks, respectively, while the QA-aided tractography has 16.2%. In the grid scheme (DSI), the FA-aided, GFA-aided, and anatomy-aided tractographies have 12.3%, 9.0%, and 10.93% of the false tracks, respectively, while the QA-aided tractography has 4.43%. The QA-aided deterministic fiber tracking may assist fiber tracking studies and facilitate the advancement of human connectomics. Public Library of Science 2013-11-15 /pmc/articles/PMC3858183/ /pubmed/24348913 http://dx.doi.org/10.1371/journal.pone.0080713 Text en © 2013 Yeh et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Yeh, Fang-Cheng
Verstynen, Timothy D.
Wang, Yibao
Fernández-Miranda, Juan C.
Tseng, Wen-Yih Isaac
spellingShingle Yeh, Fang-Cheng
Verstynen, Timothy D.
Wang, Yibao
Fernández-Miranda, Juan C.
Tseng, Wen-Yih Isaac
Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
author_facet Yeh, Fang-Cheng
Verstynen, Timothy D.
Wang, Yibao
Fernández-Miranda, Juan C.
Tseng, Wen-Yih Isaac
author_sort Yeh, Fang-Cheng
title Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
title_short Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
title_full Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
title_fullStr Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
title_full_unstemmed Deterministic Diffusion Fiber Tracking Improved by Quantitative Anisotropy
title_sort deterministic diffusion fiber tracking improved by quantitative anisotropy
description Diffusion MRI tractography has emerged as a useful and popular tool for mapping connections between brain regions. In this study, we examined the performance of quantitative anisotropy (QA) in facilitating deterministic fiber tracking. Two phantom studies were conducted. The first phantom study examined the susceptibility of fractional anisotropy (FA), generalized factional anisotropy (GFA), and QA to various partial volume effects. The second phantom study examined the spatial resolution of the FA-aided, GFA-aided, and QA-aided tractographies. An in vivo study was conducted to track the arcuate fasciculus, and two neurosurgeons blind to the acquisition and analysis settings were invited to identify false tracks. The performance of QA in assisting fiber tracking was compared with FA, GFA, and anatomical information from T1-weighted images. Our first phantom study showed that QA is less sensitive to the partial volume effects of crossing fibers and free water, suggesting that it is a robust index. The second phantom study showed that the QA-aided tractography has better resolution than the FA-aided and GFA-aided tractography. Our in vivo study further showed that the QA-aided tractography outperforms the FA-aided, GFA-aided, and anatomy-aided tractographies. In the shell scheme (HARDI), the FA-aided, GFA-aided, and anatomy-aided tractographies have 30.7%, 32.6%, and 24.45% of the false tracks, respectively, while the QA-aided tractography has 16.2%. In the grid scheme (DSI), the FA-aided, GFA-aided, and anatomy-aided tractographies have 12.3%, 9.0%, and 10.93% of the false tracks, respectively, while the QA-aided tractography has 4.43%. The QA-aided deterministic fiber tracking may assist fiber tracking studies and facilitate the advancement of human connectomics.
publisher Public Library of Science
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858183/
_version_ 1612037007162212352