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Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging

Functional magnetic resonance imaging (fMRI) acquisitions include a great deal of individual variability. This individuality often generates obstacles to the efficient use of databanks from multiple subjects. Although recent studies have suggested that inter-regional connectivity reflects individual...

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Autores principales: Fuchigami, Takuya, Shikauchi, Yumi, Nakae, Ken, Shikauchi, Manabu, Ogawa, Takeshi, Ishii, Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098116/
https://www.ncbi.nlm.nih.gov/pubmed/30120378
http://dx.doi.org/10.1038/s41598-018-30676-3
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author Fuchigami, Takuya
Shikauchi, Yumi
Nakae, Ken
Shikauchi, Manabu
Ogawa, Takeshi
Ishii, Shin
author_facet Fuchigami, Takuya
Shikauchi, Yumi
Nakae, Ken
Shikauchi, Manabu
Ogawa, Takeshi
Ishii, Shin
author_sort Fuchigami, Takuya
collection PubMed
description Functional magnetic resonance imaging (fMRI) acquisitions include a great deal of individual variability. This individuality often generates obstacles to the efficient use of databanks from multiple subjects. Although recent studies have suggested that inter-regional connectivity reflects individuality, conventional three-dimensional (3D) registration methods that calibrate inter-subject variability are based on anatomical information about the gray matter shape (e.g., T1-weighted). Here, we present a new registration method focusing more on the white matter structure, which is directly related to the connectivity in the brain, and apply it to subject-transfer brain decoding. Our registration method based on diffusion tensor imaging (DTI) transferred functional maps of each individual to a common anatomical space, where a decoding analysis of multi-voxel patterns was performed. The decoder trained on functional maps from other individuals in the common space showed a transfer decoding accuracy comparable to that of an individual decoder trained on single-subject functional maps. The DTI-based registration allowed more precise transformation of gray matter boundaries than a well-established T1-based method. These results suggest that the DTI-based registration is a promising tool for standardization of the brain functions, and moreover, will allow us to perform ‘zero-shot’ learning of decoders which is profitable in brain machine interface scenes.
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spelling pubmed-60981162018-08-23 Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging Fuchigami, Takuya Shikauchi, Yumi Nakae, Ken Shikauchi, Manabu Ogawa, Takeshi Ishii, Shin Sci Rep Article Functional magnetic resonance imaging (fMRI) acquisitions include a great deal of individual variability. This individuality often generates obstacles to the efficient use of databanks from multiple subjects. Although recent studies have suggested that inter-regional connectivity reflects individuality, conventional three-dimensional (3D) registration methods that calibrate inter-subject variability are based on anatomical information about the gray matter shape (e.g., T1-weighted). Here, we present a new registration method focusing more on the white matter structure, which is directly related to the connectivity in the brain, and apply it to subject-transfer brain decoding. Our registration method based on diffusion tensor imaging (DTI) transferred functional maps of each individual to a common anatomical space, where a decoding analysis of multi-voxel patterns was performed. The decoder trained on functional maps from other individuals in the common space showed a transfer decoding accuracy comparable to that of an individual decoder trained on single-subject functional maps. The DTI-based registration allowed more precise transformation of gray matter boundaries than a well-established T1-based method. These results suggest that the DTI-based registration is a promising tool for standardization of the brain functions, and moreover, will allow us to perform ‘zero-shot’ learning of decoders which is profitable in brain machine interface scenes. Nature Publishing Group UK 2018-08-17 /pmc/articles/PMC6098116/ /pubmed/30120378 http://dx.doi.org/10.1038/s41598-018-30676-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fuchigami, Takuya
Shikauchi, Yumi
Nakae, Ken
Shikauchi, Manabu
Ogawa, Takeshi
Ishii, Shin
Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title_full Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title_fullStr Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title_full_unstemmed Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title_short Zero-shot fMRI decoding with three-dimensional registration based on diffusion tensor imaging
title_sort zero-shot fmri decoding with three-dimensional registration based on diffusion tensor imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098116/
https://www.ncbi.nlm.nih.gov/pubmed/30120378
http://dx.doi.org/10.1038/s41598-018-30676-3
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