Detection of functional networks within white matter using independent component analysis
•Functional BOLD signals evoked by finger movements were detected in white matter using ICA.•Symmetrical functional structures were delineated from correlated BOLD signals in white matter in a resting state.•Resting-state correlations in BOLD signals across white matter were quantified by ICA to rev...
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Published in | NeuroImage (Orlando, Fla.) Vol. 222; p. 117278 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
15.11.2020
Elsevier Limited Elsevier |
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ISSN | 1053-8119 1095-9572 1095-9572 |
DOI | 10.1016/j.neuroimage.2020.117278 |
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Abstract | •Functional BOLD signals evoked by finger movements were detected in white matter using ICA.•Symmetrical functional structures were delineated from correlated BOLD signals in white matter in a resting state.•Resting-state correlations in BOLD signals across white matter were quantified by ICA to reveal functional connectivity.
Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their inter-regional correlations may be analyzed to reveal functional connectivity. However, most studies of intrinsic neuronal activity have ignored the spontaneous fluctuations that also arise in white matter (WM). In this work, we explore spontaneous fluctuations in resting state MRI signals in WM based on spatial independent component analyses (ICA), a data-driven approach that separates signals into independent sources without making specific modeling assumptions. ICA has become widely accepted as a valuable approach for identifying functional connectivity within cortex but has been rarely applied to derive equivalent structures within WM. Here, BOLD signal changes in WM of a group of subjects performing motor tasks were first detected using ICA, and a spatial component whose time course was consistent with the task was found, demonstrating the analysis is sensitive to evoked BOLD signals in WM. Secondly, multiple spatial components were derived by applying ICA to identify those voxels in WM whose MRI signals showed similar temporal behaviors in a resting state. These functionally-related structures are grossly symmetric and coincide with corresponding tracts identified from diffusion MRI. Finally, functional connectivity was quantified by calculating correlations between pairs of structures to explore the synchronicity of resting state BOLD signals across WM regions, and the experimental results revealed that there exist two distinct groupings of functional correlations in WM tracts at rest. Our study provides further insights into the nature of activation patterns, functional responses and connectivity in WM, and support previous suggestions that BOLD signals in WM show similarities with cortical activations and are characterized by distinct underlying structures in tasks and at rest. |
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AbstractList | Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their inter-regional correlations may be analyzed to reveal functional connectivity. However, most studies of intrinsic neuronal activity have ignored the spontaneous fluctuations that also arise in white matter (WM). In this work, we explore spontaneous fluctuations in resting state MRI signals in WM based on spatial independent component analyses (ICA), a data-driven approach that separates signals into independent sources without making specific modeling assumptions. ICA has become widely accepted as a valuable approach for identifying functional connectivity within cortex but has been rarely applied to derive equivalent structures within WM. Here, BOLD signal changes in WM of a group of subjects performing motor tasks were first detected using ICA, and a spatial component whose time course was consistent with the task was found, demonstrating the analysis is sensitive to evoked BOLD signals in WM. Secondly, multiple spatial components were derived by applying ICA to identify those voxels in WM whose MRI signals showed similar temporal behaviors in a resting state. These functionally-related structures are grossly symmetric and coincide with corresponding tracts identified from diffusion MRI. Finally, functional connectivity was quantified by calculating correlations between pairs of structures to explore the synchronicity of resting state BOLD signals across WM regions, and the experimental results revealed that there exist two distinct groupings of functional correlations in WM tracts at rest. Our study provides further insights into the nature of activation patterns, functional responses and connectivity in WM, and support previous suggestions that BOLD signals in WM show similarities with cortical activations and are characterized by distinct underlying structures in tasks and at rest. •Functional BOLD signals evoked by finger movements were detected in white matter using ICA.•Symmetrical functional structures were delineated from correlated BOLD signals in white matter in a resting state.•Resting-state correlations in BOLD signals across white matter were quantified by ICA to reveal functional connectivity. Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their inter-regional correlations may be analyzed to reveal functional connectivity. However, most studies of intrinsic neuronal activity have ignored the spontaneous fluctuations that also arise in white matter (WM). In this work, we explore spontaneous fluctuations in resting state MRI signals in WM based on spatial independent component analyses (ICA), a data-driven approach that separates signals into independent sources without making specific modeling assumptions. ICA has become widely accepted as a valuable approach for identifying functional connectivity within cortex but has been rarely applied to derive equivalent structures within WM. Here, BOLD signal changes in WM of a group of subjects performing motor tasks were first detected using ICA, and a spatial component whose time course was consistent with the task was found, demonstrating the analysis is sensitive to evoked BOLD signals in WM. Secondly, multiple spatial components were derived by applying ICA to identify those voxels in WM whose MRI signals showed similar temporal behaviors in a resting state. These functionally-related structures are grossly symmetric and coincide with corresponding tracts identified from diffusion MRI. Finally, functional connectivity was quantified by calculating correlations between pairs of structures to explore the synchronicity of resting state BOLD signals across WM regions, and the experimental results revealed that there exist two distinct groupings of functional correlations in WM tracts at rest. Our study provides further insights into the nature of activation patterns, functional responses and connectivity in WM, and support previous suggestions that BOLD signals in WM show similarities with cortical activations and are characterized by distinct underlying structures in tasks and at rest. Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their inter-regional correlations may be analyzed to reveal functional connectivity. However, most studies of intrinsic neuronal activity have ignored the spontaneous fluctuations that also arise in white matter (WM). In this work, we explore spontaneous fluctuations in resting state MRI signals in WM based on spatial independent component analyses (ICA), a data-driven approach that separates signals into independent sources without making specific modeling assumptions. ICA has become widely accepted as a valuable approach for identifying functional connectivity within cortex but has been rarely applied to derive equivalent structures within WM. Here, BOLD signal changes in WM of a group of subjects performing motor tasks were first detected using ICA, and a spatial component whose time course was consistent with the task was found, demonstrating the analysis is sensitive to evoked BOLD signals in WM. Secondly, multiple spatial components were derived by applying ICA to identify those voxels in WM whose MRI signals showed similar temporal behaviors in a resting state. These functionally-related structures are grossly symmetric and coincide with corresponding tracts identified from diffusion MRI. Finally, functional connectivity was quantified by calculating correlations between pairs of structures to explore the synchronicity of resting state BOLD signals across WM regions, and the experimental results revealed that there exist two distinct groupings of functional correlations in WM tracts at rest. Our study provides further insights into the nature of activation patterns, functional responses and connectivity in WM, and support previous suggestions that BOLD signals in WM show similarities with cortical activations and are characterized by distinct underlying structures in tasks and at rest.Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their inter-regional correlations may be analyzed to reveal functional connectivity. However, most studies of intrinsic neuronal activity have ignored the spontaneous fluctuations that also arise in white matter (WM). In this work, we explore spontaneous fluctuations in resting state MRI signals in WM based on spatial independent component analyses (ICA), a data-driven approach that separates signals into independent sources without making specific modeling assumptions. ICA has become widely accepted as a valuable approach for identifying functional connectivity within cortex but has been rarely applied to derive equivalent structures within WM. Here, BOLD signal changes in WM of a group of subjects performing motor tasks were first detected using ICA, and a spatial component whose time course was consistent with the task was found, demonstrating the analysis is sensitive to evoked BOLD signals in WM. Secondly, multiple spatial components were derived by applying ICA to identify those voxels in WM whose MRI signals showed similar temporal behaviors in a resting state. These functionally-related structures are grossly symmetric and coincide with corresponding tracts identified from diffusion MRI. Finally, functional connectivity was quantified by calculating correlations between pairs of structures to explore the synchronicity of resting state BOLD signals across WM regions, and the experimental results revealed that there exist two distinct groupings of functional correlations in WM tracts at rest. Our study provides further insights into the nature of activation patterns, functional responses and connectivity in WM, and support previous suggestions that BOLD signals in WM show similarities with cortical activations and are characterized by distinct underlying structures in tasks and at rest. |
ArticleNumber | 117278 |
Author | Huang, Yali Hao, Lei Gao, Jia-Hong Wang, Peiguang Gore, John C. Yang, Yang Hu, Xuefang Ding, Zhaohua |
AuthorAffiliation | e Department of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, TN 37232, United States g McGovern Institute for Brain Research, Peking University, Beijing 100871, China h Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, United States a College of Electronics and Information Engineering, Hebei University, Baoding 071002, China k Department of Physics and Astronomy, Vanderbilt University, Nashville, TN 37232, United States j Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN 37232, United States b Center for MRI Research, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China i Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, United States c College of Mathematics and Information Science, Hebei University, Baoding 071002, China d Vanderbilt University Institute of Imaging Science, Vanderbilt University, |
AuthorAffiliation_xml | – name: e Department of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, TN 37232, United States – name: j Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN 37232, United States – name: d Vanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37232, United States – name: k Department of Physics and Astronomy, Vanderbilt University, Nashville, TN 37232, United States – name: b Center for MRI Research, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China – name: h Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, United States – name: g McGovern Institute for Brain Research, Peking University, Beijing 100871, China – name: i Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, United States – name: a College of Electronics and Information Engineering, Hebei University, Baoding 071002, China – name: c College of Mathematics and Information Science, Hebei University, Baoding 071002, China – name: f Beijing City Key Lab for Medical Physics and Engineering, Institute of Heavy Ion Physics, School of Physics, Peking University, Beijing 100871, China |
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Cites_doi | 10.1016/j.neuroimage.2008.10.057 10.1073/pnas.87.24.9868 10.1186/1471-2202-9-84 10.3389/fnins.2019.01024 10.1038/nrn2201 10.1016/S0006-3495(94)80775-1 10.1097/WCO.0b013e328306f2c5 10.1523/JNEUROSCI.3872-16.2017 10.1038/nrneurol.2009.198 10.1016/j.neuroimage.2017.02.074 10.1016/j.neuroimage.2016.10.005 10.1073/pnas.0905267106 10.1162/neco.1995.7.6.1129 10.1016/j.neuroimage.2013.05.041 10.3389/fnsys.2011.00002 10.1016/j.neuroimage.2018.08.049 10.1002/hbm.1048 10.1097/00004728-199903000-00016 10.1073/pnas.98.2.676 10.1016/j.neuroimage.2012.10.002 10.1098/rstb.2005.1634 10.1038/s41593-018-0312-0 10.1016/j.mri.2019.07.017 10.1016/j.neuroimage.2007.12.035 10.1073/pnas.1121329109 10.1016/j.neuroimage.2008.11.005 10.1073/pnas.1711567115 10.1016/j.neuron.2018.05.019 10.1002/hbm.1024 10.1002/mrm.1910340409 10.1196/annals.1440.011 10.1073/pnas.95.3.803 10.3389/fnins.2014.00138 10.1016/j.mri.2015.10.003 10.1155/2013/251308 10.1371/journal.pone.0082107 10.3174/ajnr.A3263 10.1038/s41467-019-09076-2 10.1016/j.neuroimage.2005.08.040 |
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Keywords | Functional connectivity White matter fMRI Functional structure Functional activation Independent component analysis |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Yali Huang: Methodology, Software, Formal analysis, Writing - original draft. Yang Yang: Data curation. Lei Hao: Software, Visualization. Xuefang Hu: Software, Visualization. Peiguang Wang: Project administration. Zhaohua Ding: Project administration, Writing - review & editing. Jia-Hong Gao: Project administration. John C. Gore: Project administration, Writing - review & editing. CRediT authorship contribution statement |
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References | Zhang, Raichle (bib0005) 2010; 6 Wu, Yang, Bailey (bib0023) 2017; 152 Greicius (bib0010) 2008; 21 Huang, Bailey, Wang (bib0024) 2018; 183 Basser, Mattiello, LeBihan (bib0015) 1994; 66 Mori, Oishi, Jiang (bib0035) 2008; 40 Fox, Raichle (bib0003) 2007; 8 Marussich, Lu, Wen, Liu (bib0013) 2017; 146 Petersen, Hansen, Kolenda, Rostrup, Strother (bib0038) 2000 Zhang, Watrous, Patel, Jacobs (bib0041) 2018; 98 Bell, Sejnowski (bib0037) 1995; 7 Lee, Smyser, Shimony (bib0006) 2013; 34 Grajauskas, Frizzell, Song, D'Arcy (bib0018) 2019; 13 Smith, Miller, Moeller (bib0033) 2012; 109 Ogawa, Lee, Kay, Tank (bib0001) 1990; 87 Takahashi, Ohki, Kim (bib0040) 2013; 65 Gore, Li, Gao (bib0017) 2019; 63 Smith, Fox, Miller (bib0032) 2009; 106 Bürgel, Amunts, Hoemke (bib0039) 2006; 29 Beckmann, DeLuca, Devlin, Smith (bib0031) 2005; 360 Gonzalez-Castillo, Handwerker, Robinson (bib0004) 2014; 8 Ding, Newton, Xu (bib0011) 2013; 8 Mazerolle, D'Arcy, Beyea (bib0019) 2008; 9 Allen, Erhardt, Damaraju (bib0042) 2011; 5 Van Essen, Smith, Barch (bib0034) 2013; 80 Gawryluk, Brewer, Beyea, D'arcy (bib0020) 2009; 45 Raichle, MacLeod, Snyder (bib0008) 2001; 98 Calhoun, Adali, Pearlson, Pekar (bib0028) 2001; 13 McKeown, Jung, Makeig (bib0029) 1998; 95 Calhoun, Adali, Pearlson, Pekar (bib0026) 2001; 14 Shine, Breakspear, Bell (bib0036) 2019; 22 Buckner, Andrews‐Hanna, Schacter (bib0009) 2008; 1124 Peer, Nitzan, Bick, Levin, Arzy (bib0014) 2017; 37 Biswal, Zerrin Yetkin, Haughton, Hyde (bib0002) 1995; 34 Ding, Xu, Bailey (bib0016) 2016; 34 Li, Newton, Anderson, Ding, Gore (bib0025) 2019; 10 Calhoun, Liu, Adalı (bib0027) 2009; 45 Fabri, Polonara (bib0022) 2013; 2013 Gawryluk, Mazerolle, Brewer, Beyea, D'Arcy (bib0021) 2011; 12 Fox, Greicius (bib0007) 2010; 4 Ding, Huang, Bailey (bib0012) 2018; 115 Biswal, Ulmer (bib0030) 1999; 23 Lee (10.1016/j.neuroimage.2020.117278_bib0006) 2013; 34 Calhoun (10.1016/j.neuroimage.2020.117278_bib0027) 2009; 45 Buckner (10.1016/j.neuroimage.2020.117278_bib0009) 2008; 1124 Van Essen (10.1016/j.neuroimage.2020.117278_bib0034) 2013; 80 Wu (10.1016/j.neuroimage.2020.117278_bib0023) 2017; 152 Ding (10.1016/j.neuroimage.2020.117278_bib0011) 2013; 8 Ding (10.1016/j.neuroimage.2020.117278_bib0012) 2018; 115 Greicius (10.1016/j.neuroimage.2020.117278_bib0010) 2008; 21 Huang (10.1016/j.neuroimage.2020.117278_bib0024) 2018; 183 Basser (10.1016/j.neuroimage.2020.117278_bib0015) 1994; 66 Raichle (10.1016/j.neuroimage.2020.117278_bib0008) 2001; 98 Li (10.1016/j.neuroimage.2020.117278_bib0025) 2019; 10 Allen (10.1016/j.neuroimage.2020.117278_bib0042) 2011; 5 Fox (10.1016/j.neuroimage.2020.117278_bib0003) 2007; 8 Ogawa (10.1016/j.neuroimage.2020.117278_bib0001) 1990; 87 Fabri (10.1016/j.neuroimage.2020.117278_bib0022) 2013; 2013 Gonzalez-Castillo (10.1016/j.neuroimage.2020.117278_bib0004) 2014; 8 McKeown (10.1016/j.neuroimage.2020.117278_bib0029) 1998; 95 Petersen (10.1016/j.neuroimage.2020.117278_bib0038) 2000 Gore (10.1016/j.neuroimage.2020.117278_bib0017) 2019; 63 Gawryluk (10.1016/j.neuroimage.2020.117278_bib0021) 2011; 12 Beckmann (10.1016/j.neuroimage.2020.117278_bib0031) 2005; 360 Shine (10.1016/j.neuroimage.2020.117278_bib0036) 2019; 22 Fox (10.1016/j.neuroimage.2020.117278_bib0007) 2010; 4 Peer (10.1016/j.neuroimage.2020.117278_bib0014) 2017; 37 Grajauskas (10.1016/j.neuroimage.2020.117278_bib0018) 2019; 13 Biswal (10.1016/j.neuroimage.2020.117278_bib0030) 1999; 23 Zhang (10.1016/j.neuroimage.2020.117278_bib0005) 2010; 6 Ding (10.1016/j.neuroimage.2020.117278_bib0016) 2016; 34 Zhang (10.1016/j.neuroimage.2020.117278_bib0041) 2018; 98 Biswal (10.1016/j.neuroimage.2020.117278_bib0002) 1995; 34 Marussich (10.1016/j.neuroimage.2020.117278_bib0013) 2017; 146 Mazerolle (10.1016/j.neuroimage.2020.117278_bib0019) 2008; 9 Bürgel (10.1016/j.neuroimage.2020.117278_bib0039) 2006; 29 Smith (10.1016/j.neuroimage.2020.117278_bib0032) 2009; 106 Takahashi (10.1016/j.neuroimage.2020.117278_bib0040) 2013; 65 Calhoun (10.1016/j.neuroimage.2020.117278_bib0026) 2001; 14 Calhoun (10.1016/j.neuroimage.2020.117278_bib0028) 2001; 13 Smith (10.1016/j.neuroimage.2020.117278_bib0033) 2012; 109 Bell (10.1016/j.neuroimage.2020.117278_bib0037) 1995; 7 Gawryluk (10.1016/j.neuroimage.2020.117278_bib0020) 2009; 45 Mori (10.1016/j.neuroimage.2020.117278_bib0035) 2008; 40 |
References_xml | – volume: 4 start-page: 19 year: 2010 ident: bib0007 article-title: Clinical applications of resting state functional connectivity publication-title: Front. Syst. Neurosci. – volume: 6 start-page: 15 year: 2010 ident: bib0005 article-title: Disease and the brain's dark energy publication-title: Nat. Rev. Neurol. – volume: 14 start-page: 140 year: 2001 end-page: 151 ident: bib0026 article-title: A method for making group inferences from functional MRI data using independent component analysis publication-title: Hum. Brain Mapp. – volume: 106 start-page: 13040 year: 2009 end-page: 13045 ident: bib0032 article-title: Correspondence of the brain's functional architecture during activation and rest publication-title: Proc. Natl. Acad. Sci. USA – start-page: 615 year: 2000 end-page: 620 ident: bib0038 article-title: On the independent components of functional neuroimages publication-title: Proceedings of the Third International Conference on Independent Component Analysis and Blind Source Separation – volume: 21 start-page: 424 year: 2008 end-page: 430 ident: bib0010 article-title: Resting-state functional connectivity in neuropsychiatric disorders publication-title: Curr. Opin. Neurol. – volume: 1124 start-page: 1 year: 2008 end-page: 38 ident: bib0009 article-title: The brain's default network publication-title: Ann. N. Y. Acad. Sci. – volume: 22 start-page: 289 year: 2019 ident: bib0036 article-title: Human cognition involves the dynamic integration of neural activity and neuromodulatory systems publication-title: Nat. Neurosci. – volume: 29 start-page: 1092 year: 2006 end-page: 1105 ident: bib0039 article-title: White matter fiber tracts of the human brain: three-dimensional mapping at microscopic resolution, topography and intersubject variability publication-title: Neuroimage – volume: 5 start-page: 1 year: 2011 end-page: 23 ident: bib0042 article-title: A baseline for the multivariate comparison of resting-state networks publication-title: Front. Syst. Neurosci. – volume: 8 start-page: 138 year: 2014 ident: bib0004 article-title: The spatial structure of resting state connectivity stability on the scale of minutes publication-title: Front. Neurosci. – volume: 360 start-page: 1001 year: 2005 end-page: 1013 ident: bib0031 article-title: Investigations into resting-state connectivity using independent component analysis publication-title: Philos. Trans. R. Soc. B: Biol. Sci. – volume: 23 start-page: 265 year: 1999 end-page: 271 ident: bib0030 article-title: Blind source separation of multiple signal sources of fMRI data sets using independent component analysis publication-title: J. Comput. Assist. Tomogr. – volume: 37 start-page: 6394 year: 2017 end-page: 6407 ident: bib0014 article-title: Evidence for functional networks within the human brain's white matter publication-title: J. Neurosci. – volume: 65 start-page: 488 year: 2013 end-page: 498 ident: bib0040 article-title: Dissociation and convergence of the dorsal and ventral visual working memory streams in the human prefrontal cortex publication-title: Neuroimage – volume: 9 start-page: 84 year: 2008 ident: bib0019 article-title: Detecting functional magnetic resonance imaging activation in white matter: interhemispheric transfer across the corpus callosum publication-title: BMC Neurosci. – volume: 40 start-page: 570 year: 2008 end-page: 582 ident: bib0035 article-title: Stereotaxic white matter atlas based on diffusion tensor imaging in an ICBM template publication-title: Neuroimage – volume: 45 start-page: 83 year: 2009 end-page: 88 ident: bib0020 article-title: Optimizing the detection of white matter fMRI using asymmetric spin echo spiral publication-title: Neuroimage – volume: 66 start-page: 259 year: 1994 end-page: 267 ident: bib0015 article-title: MR diffusion tensor spectroscopy and imaging publication-title: Biophys. J. – volume: 34 start-page: 537 year: 1995 end-page: 541 ident: bib0002 article-title: Functional connectivity in the motor cortex of resting human brain using echo-planar mri publication-title: Magn. Reson. Med. – volume: 8 start-page: 700 year: 2007 end-page: 711 ident: bib0003 article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging publication-title: Nat. Rev. Neurosci. – volume: 13 start-page: 43 year: 2001 end-page: 53 ident: bib0028 article-title: Spatial and temporal independent component analysis of functional MRI data containing a pair of task‐related waveforms publication-title: Hum. Brain Mapp. – volume: 80 start-page: 62 year: 2013 end-page: 79 ident: bib0034 article-title: The WU-Minn human connectome project: an overview publication-title: Neuroimage – volume: 183 start-page: 544 year: 2018 end-page: 552 ident: bib0024 article-title: Voxel-wise detection of functional networks in white matter publication-title: Neuroimage – volume: 109 start-page: 3131 year: 2012 end-page: 3136 ident: bib0033 article-title: Temporally-independent functional modes of spontaneous brain activity publication-title: Proc. Natl. Acad. Sci. USA – volume: 98 start-page: 1269 year: 2018 end-page: 1281 ident: bib0041 article-title: Theta and alpha oscillations are traveling waves in the human neocortex publication-title: Neuron – volume: 8 start-page: e82107 year: 2013 ident: bib0011 article-title: Spatio-temporal correlation tensors reveal functional structure in human brain publication-title: PLoS One – volume: 12 start-page: 1 year: 2011 end-page: 7 ident: bib0021 article-title: Investigation of fMRI activation in the internal capsule publication-title: BMC Neurosci. – volume: 98 start-page: 676 year: 2001 end-page: 682 ident: bib0008 article-title: A default mode of brain function publication-title: Proc. Natl. Acad. Sci. USA – volume: 146 start-page: 1128 year: 2017 end-page: 1141 ident: bib0013 article-title: Mapping white-matter functional organization at rest and during naturalistic visual perception publication-title: Neuroimage – volume: 13 start-page: 1024 year: 2019 ident: bib0018 article-title: White matter fMRI activation cannot be treated as a nuisance regressor: Overcoming a historical blind spot publication-title: Front. Neurosci. – volume: 115 start-page: 595 year: 2018 end-page: 600 ident: bib0012 article-title: Detection of synchronous brain activity in white matter tracts at rest and under functional loading publication-title: Proc. Natl. Acad. Sci. USA – volume: 7 start-page: 1129 year: 1995 end-page: 1159 ident: bib0037 article-title: An information-maximization approach to blind separation and blind deconvolution publication-title: Neural Comput. – volume: 34 start-page: 8 year: 2016 end-page: 17 ident: bib0016 article-title: Visualizing functional pathways in the human brain using correlation tensors and magnetic resonance imaging publication-title: Magn. Reson. Imaging – volume: 2013 start-page: 1 year: 2013 end-page: 15 ident: bib0022 article-title: Functional topography of human corpus callosum: an FMRI mapping study publication-title: Neural Plast. – volume: 34 start-page: 1866 year: 2013 end-page: 1872 ident: bib0006 article-title: Resting-state fMRI: a review of methods and clinical applications publication-title: Am. J. Neuroradiol. – volume: 63 start-page: 1 year: 2019 end-page: 11 ident: bib0017 article-title: Functional MRI and resting state connectivity in white matter-a mini-review publication-title: Magn. Reson. Imaging – volume: 45 start-page: S163 year: 2009 end-page: S172 ident: bib0027 article-title: A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data publication-title: Neuroimage – volume: 10 start-page: 1140 year: 2019 ident: bib0025 article-title: Characterization of the hemodynamic response function in white matter tracts for event-related fMRI publication-title: Nat. Commun. – volume: 87 start-page: 9868 year: 1990 end-page: 9872 ident: bib0001 article-title: Brain magnetic resonance imaging with contrast dependent on blood oxygenation publication-title: Proc. Natl. Acad. Sci. USA – volume: 152 start-page: 371 year: 2017 end-page: 380 ident: bib0023 article-title: Functional connectivity and activity of white matter in somatosensory pathways under tactile stimulations publication-title: Neuroimage – volume: 95 start-page: 803 year: 1998 end-page: 810 ident: bib0029 article-title: Spatially independent activity patterns in functional MRI data during the Stroop color-naming task publication-title: Proc. Natl. Acad. Sci. USA – volume: 12 start-page: 1 issue: 56 year: 2011 ident: 10.1016/j.neuroimage.2020.117278_bib0021 article-title: Investigation of fMRI activation in the internal capsule publication-title: BMC Neurosci. – start-page: 615 year: 2000 ident: 10.1016/j.neuroimage.2020.117278_bib0038 article-title: On the independent components of functional neuroimages – volume: 45 start-page: S163 issue: 1 year: 2009 ident: 10.1016/j.neuroimage.2020.117278_bib0027 article-title: A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data publication-title: Neuroimage doi: 10.1016/j.neuroimage.2008.10.057 – volume: 87 start-page: 9868 issue: 24 year: 1990 ident: 10.1016/j.neuroimage.2020.117278_bib0001 article-title: Brain magnetic resonance imaging with contrast dependent on blood oxygenation publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.87.24.9868 – volume: 9 start-page: 84 issue: 1 year: 2008 ident: 10.1016/j.neuroimage.2020.117278_bib0019 article-title: Detecting functional magnetic resonance imaging activation in white matter: interhemispheric transfer across the corpus callosum publication-title: BMC Neurosci. doi: 10.1186/1471-2202-9-84 – volume: 13 start-page: 1024 year: 2019 ident: 10.1016/j.neuroimage.2020.117278_bib0018 article-title: White matter fMRI activation cannot be treated as a nuisance regressor: Overcoming a historical blind spot publication-title: Front. Neurosci. doi: 10.3389/fnins.2019.01024 – volume: 8 start-page: 700 issue: 9 year: 2007 ident: 10.1016/j.neuroimage.2020.117278_bib0003 article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging publication-title: Nat. Rev. Neurosci. doi: 10.1038/nrn2201 – volume: 66 start-page: 259 issue: 1 year: 1994 ident: 10.1016/j.neuroimage.2020.117278_bib0015 article-title: MR diffusion tensor spectroscopy and imaging publication-title: Biophys. J. doi: 10.1016/S0006-3495(94)80775-1 – volume: 21 start-page: 424 issue: 4 year: 2008 ident: 10.1016/j.neuroimage.2020.117278_bib0010 article-title: Resting-state functional connectivity in neuropsychiatric disorders publication-title: Curr. Opin. Neurol. doi: 10.1097/WCO.0b013e328306f2c5 – volume: 37 start-page: 6394 issue: 27 year: 2017 ident: 10.1016/j.neuroimage.2020.117278_bib0014 article-title: Evidence for functional networks within the human brain's white matter publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.3872-16.2017 – volume: 6 start-page: 15 issue: 1 year: 2010 ident: 10.1016/j.neuroimage.2020.117278_bib0005 article-title: Disease and the brain's dark energy publication-title: Nat. Rev. Neurol. doi: 10.1038/nrneurol.2009.198 – volume: 152 start-page: 371 year: 2017 ident: 10.1016/j.neuroimage.2020.117278_bib0023 article-title: Functional connectivity and activity of white matter in somatosensory pathways under tactile stimulations publication-title: Neuroimage doi: 10.1016/j.neuroimage.2017.02.074 – volume: 146 start-page: 1128 year: 2017 ident: 10.1016/j.neuroimage.2020.117278_bib0013 article-title: Mapping white-matter functional organization at rest and during naturalistic visual perception publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.10.005 – volume: 106 start-page: 13040 issue: 31 year: 2009 ident: 10.1016/j.neuroimage.2020.117278_bib0032 article-title: Correspondence of the brain's functional architecture during activation and rest publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.0905267106 – volume: 7 start-page: 1129 issue: 6 year: 1995 ident: 10.1016/j.neuroimage.2020.117278_bib0037 article-title: An information-maximization approach to blind separation and blind deconvolution publication-title: Neural Comput. doi: 10.1162/neco.1995.7.6.1129 – volume: 80 start-page: 62 year: 2013 ident: 10.1016/j.neuroimage.2020.117278_bib0034 article-title: The WU-Minn human connectome project: an overview publication-title: Neuroimage doi: 10.1016/j.neuroimage.2013.05.041 – volume: 5 start-page: 1 year: 2011 ident: 10.1016/j.neuroimage.2020.117278_bib0042 article-title: A baseline for the multivariate comparison of resting-state networks publication-title: Front. Syst. Neurosci. doi: 10.3389/fnsys.2011.00002 – volume: 183 start-page: 544 year: 2018 ident: 10.1016/j.neuroimage.2020.117278_bib0024 article-title: Voxel-wise detection of functional networks in white matter publication-title: Neuroimage doi: 10.1016/j.neuroimage.2018.08.049 – volume: 14 start-page: 140 issue: 3 year: 2001 ident: 10.1016/j.neuroimage.2020.117278_bib0026 article-title: A method for making group inferences from functional MRI data using independent component analysis publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.1048 – volume: 23 start-page: 265 issue: 2 year: 1999 ident: 10.1016/j.neuroimage.2020.117278_bib0030 article-title: Blind source separation of multiple signal sources of fMRI data sets using independent component analysis publication-title: J. Comput. Assist. Tomogr. doi: 10.1097/00004728-199903000-00016 – volume: 98 start-page: 676 issue: 2 year: 2001 ident: 10.1016/j.neuroimage.2020.117278_bib0008 article-title: A default mode of brain function publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.98.2.676 – volume: 65 start-page: 488 year: 2013 ident: 10.1016/j.neuroimage.2020.117278_bib0040 article-title: Dissociation and convergence of the dorsal and ventral visual working memory streams in the human prefrontal cortex publication-title: Neuroimage doi: 10.1016/j.neuroimage.2012.10.002 – volume: 360 start-page: 1001 issue: 1457 year: 2005 ident: 10.1016/j.neuroimage.2020.117278_bib0031 article-title: Investigations into resting-state connectivity using independent component analysis publication-title: Philos. Trans. R. Soc. B: Biol. Sci. doi: 10.1098/rstb.2005.1634 – volume: 22 start-page: 289 issue: 2 year: 2019 ident: 10.1016/j.neuroimage.2020.117278_bib0036 article-title: Human cognition involves the dynamic integration of neural activity and neuromodulatory systems publication-title: Nat. Neurosci. doi: 10.1038/s41593-018-0312-0 – volume: 63 start-page: 1 year: 2019 ident: 10.1016/j.neuroimage.2020.117278_bib0017 article-title: Functional MRI and resting state connectivity in white matter-a mini-review publication-title: Magn. Reson. Imaging doi: 10.1016/j.mri.2019.07.017 – volume: 40 start-page: 570 year: 2008 ident: 10.1016/j.neuroimage.2020.117278_bib0035 article-title: Stereotaxic white matter atlas based on diffusion tensor imaging in an ICBM template publication-title: Neuroimage doi: 10.1016/j.neuroimage.2007.12.035 – volume: 109 start-page: 3131 issue: 8 year: 2012 ident: 10.1016/j.neuroimage.2020.117278_bib0033 article-title: Temporally-independent functional modes of spontaneous brain activity publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.1121329109 – volume: 45 start-page: 83 year: 2009 ident: 10.1016/j.neuroimage.2020.117278_bib0020 article-title: Optimizing the detection of white matter fMRI using asymmetric spin echo spiral publication-title: Neuroimage doi: 10.1016/j.neuroimage.2008.11.005 – volume: 115 start-page: 595 issue: 3 year: 2018 ident: 10.1016/j.neuroimage.2020.117278_bib0012 article-title: Detection of synchronous brain activity in white matter tracts at rest and under functional loading publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.1711567115 – volume: 98 start-page: 1269 issue: 6 year: 2018 ident: 10.1016/j.neuroimage.2020.117278_bib0041 article-title: Theta and alpha oscillations are traveling waves in the human neocortex publication-title: Neuron doi: 10.1016/j.neuron.2018.05.019 – volume: 13 start-page: 43 issue: 1 year: 2001 ident: 10.1016/j.neuroimage.2020.117278_bib0028 article-title: Spatial and temporal independent component analysis of functional MRI data containing a pair of task‐related waveforms publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.1024 – volume: 34 start-page: 537 issue: 4 year: 1995 ident: 10.1016/j.neuroimage.2020.117278_bib0002 article-title: Functional connectivity in the motor cortex of resting human brain using echo-planar mri publication-title: Magn. Reson. Med. doi: 10.1002/mrm.1910340409 – volume: 1124 start-page: 1 issue: 1 year: 2008 ident: 10.1016/j.neuroimage.2020.117278_bib0009 article-title: The brain's default network publication-title: Ann. N. Y. Acad. Sci. doi: 10.1196/annals.1440.011 – volume: 95 start-page: 803 issue: 3 year: 1998 ident: 10.1016/j.neuroimage.2020.117278_bib0029 article-title: Spatially independent activity patterns in functional MRI data during the Stroop color-naming task publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.95.3.803 – volume: 8 start-page: 138 year: 2014 ident: 10.1016/j.neuroimage.2020.117278_bib0004 article-title: The spatial structure of resting state connectivity stability on the scale of minutes publication-title: Front. Neurosci. doi: 10.3389/fnins.2014.00138 – volume: 34 start-page: 8 issue: 1 year: 2016 ident: 10.1016/j.neuroimage.2020.117278_bib0016 article-title: Visualizing functional pathways in the human brain using correlation tensors and magnetic resonance imaging publication-title: Magn. Reson. Imaging doi: 10.1016/j.mri.2015.10.003 – volume: 2013 start-page: 1 year: 2013 ident: 10.1016/j.neuroimage.2020.117278_bib0022 article-title: Functional topography of human corpus callosum: an FMRI mapping study publication-title: Neural Plast. doi: 10.1155/2013/251308 – volume: 8 start-page: e82107 issue: 12 year: 2013 ident: 10.1016/j.neuroimage.2020.117278_bib0011 article-title: Spatio-temporal correlation tensors reveal functional structure in human brain publication-title: PLoS One doi: 10.1371/journal.pone.0082107 – volume: 34 start-page: 1866 issue: 10 year: 2013 ident: 10.1016/j.neuroimage.2020.117278_bib0006 article-title: Resting-state fMRI: a review of methods and clinical applications publication-title: Am. J. Neuroradiol. doi: 10.3174/ajnr.A3263 – volume: 10 start-page: 1140 issue: 1 year: 2019 ident: 10.1016/j.neuroimage.2020.117278_bib0025 article-title: Characterization of the hemodynamic response function in white matter tracts for event-related fMRI publication-title: Nat. Commun. doi: 10.1038/s41467-019-09076-2 – volume: 4 start-page: 19 year: 2010 ident: 10.1016/j.neuroimage.2020.117278_bib0007 article-title: Clinical applications of resting state functional connectivity publication-title: Front. Syst. Neurosci. – volume: 29 start-page: 1092 year: 2006 ident: 10.1016/j.neuroimage.2020.117278_bib0039 article-title: White matter fiber tracts of the human brain: three-dimensional mapping at microscopic resolution, topography and intersubject variability publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.08.040 |
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Snippet | •Functional BOLD signals evoked by finger movements were detected in white matter using ICA.•Symmetrical functional structures were delineated from correlated... Spontaneous fluctuations in MRI signals from gray matter (GM) in the brain are interpreted as originating from variations in neural activity, and their... |
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SubjectTerms | Adult Brain Brain Mapping - methods Cortex (temporal) Diffusion Tensor Imaging - methods Female Functional activation Functional connectivity Functional magnetic resonance imaging Functional structure Gray Matter - physiology Humans Independent component analysis Magnetic Resonance Imaging - methods Male Neural networks Neural Pathways - physiology Neurons - physiology Substantia alba Substantia grisea White Matter - physiology White matter fMRI Young Adult |
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Title | Detection of functional networks within white matter using independent component analysis |
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