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Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints

Quantifying differences or similarities in connectomes has been a challenge due to the immense complexity of global brain networks. Here we introduce a noninvasive method that uses diffusion MRI to characterize whole-brain white matter architecture as a single local connectome fingerprint that allow...

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Autores principales: Yeh, Fang-Cheng, Vettel, Jean M., Singh, Aarti, Poczos, Barnabas, Grafton, Scott T., Erickson, Kirk I., Tseng, Wen-Yih I., Verstynen, Timothy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112901/
https://www.ncbi.nlm.nih.gov/pubmed/27846212
http://dx.doi.org/10.1371/journal.pcbi.1005203
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author Yeh, Fang-Cheng
Vettel, Jean M.
Singh, Aarti
Poczos, Barnabas
Grafton, Scott T.
Erickson, Kirk I.
Tseng, Wen-Yih I.
Verstynen, Timothy D.
author_facet Yeh, Fang-Cheng
Vettel, Jean M.
Singh, Aarti
Poczos, Barnabas
Grafton, Scott T.
Erickson, Kirk I.
Tseng, Wen-Yih I.
Verstynen, Timothy D.
author_sort Yeh, Fang-Cheng
collection PubMed
description Quantifying differences or similarities in connectomes has been a challenge due to the immense complexity of global brain networks. Here we introduce a noninvasive method that uses diffusion MRI to characterize whole-brain white matter architecture as a single local connectome fingerprint that allows for a direct comparison between structural connectomes. In four independently acquired data sets with repeated scans (total N = 213), we show that the local connectome fingerprint is highly specific to an individual, allowing for an accurate self-versus-others classification that achieved 100% accuracy across 17,398 identification tests. The estimated classification error was approximately one thousand times smaller than fingerprints derived from diffusivity-based measures or region-to-region connectivity patterns for repeat scans acquired within 3 months. The local connectome fingerprint also revealed neuroplasticity within an individual reflected as a decreasing trend in self-similarity across time, whereas this change was not observed in the diffusivity measures. Moreover, the local connectome fingerprint can be used as a phenotypic marker, revealing 12.51% similarity between monozygotic twins, 5.14% between dizygotic twins, and 4.51% between none-twin siblings, relative to differences between unrelated subjects. This novel approach opens a new door for probing the influence of pathological, genetic, social, or environmental factors on the unique configuration of the human connectome.
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spelling pubmed-51129012016-12-08 Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints Yeh, Fang-Cheng Vettel, Jean M. Singh, Aarti Poczos, Barnabas Grafton, Scott T. Erickson, Kirk I. Tseng, Wen-Yih I. Verstynen, Timothy D. PLoS Comput Biol Research Article Quantifying differences or similarities in connectomes has been a challenge due to the immense complexity of global brain networks. Here we introduce a noninvasive method that uses diffusion MRI to characterize whole-brain white matter architecture as a single local connectome fingerprint that allows for a direct comparison between structural connectomes. In four independently acquired data sets with repeated scans (total N = 213), we show that the local connectome fingerprint is highly specific to an individual, allowing for an accurate self-versus-others classification that achieved 100% accuracy across 17,398 identification tests. The estimated classification error was approximately one thousand times smaller than fingerprints derived from diffusivity-based measures or region-to-region connectivity patterns for repeat scans acquired within 3 months. The local connectome fingerprint also revealed neuroplasticity within an individual reflected as a decreasing trend in self-similarity across time, whereas this change was not observed in the diffusivity measures. Moreover, the local connectome fingerprint can be used as a phenotypic marker, revealing 12.51% similarity between monozygotic twins, 5.14% between dizygotic twins, and 4.51% between none-twin siblings, relative to differences between unrelated subjects. This novel approach opens a new door for probing the influence of pathological, genetic, social, or environmental factors on the unique configuration of the human connectome. Public Library of Science 2016-11-15 /pmc/articles/PMC5112901/ /pubmed/27846212 http://dx.doi.org/10.1371/journal.pcbi.1005203 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Yeh, Fang-Cheng
Vettel, Jean M.
Singh, Aarti
Poczos, Barnabas
Grafton, Scott T.
Erickson, Kirk I.
Tseng, Wen-Yih I.
Verstynen, Timothy D.
Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title_full Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title_fullStr Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title_full_unstemmed Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title_short Quantifying Differences and Similarities in Whole-Brain White Matter Architecture Using Local Connectome Fingerprints
title_sort quantifying differences and similarities in whole-brain white matter architecture using local connectome fingerprints
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112901/
https://www.ncbi.nlm.nih.gov/pubmed/27846212
http://dx.doi.org/10.1371/journal.pcbi.1005203
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