fMRI hemodynamics accurately reflects neuronal timing in the human brain measured by MEG
Neuronal activation sequence information is essential for understanding brain functions. Extracting such timing information from blood oxygenation level dependent (BOLD) fMRI is confounded by interregional neurovascular differences and poorly understood relations between BOLD and electrophysiologica...
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creator | Lin, Fa-Hsuan Witzel, Thomas Raij, Tommi Ahveninen, Jyrki Wen-Kai Tsai, Kevin Chu, Yin-Hua Chang, Wei-Tang Nummenmaa, Aapo Polimeni, Jonathan R. Kuo, Wen-Jui Hsieh, Jen-Chuen Rosen, Bruce R. Belliveau, John W. |
description | Neuronal activation sequence information is essential for understanding brain functions. Extracting such timing information from blood oxygenation level dependent (BOLD) fMRI is confounded by interregional neurovascular differences and poorly understood relations between BOLD and electrophysiological response delays. Here, we recorded whole-head BOLD fMRI at 100ms resolution and magnetoencephalography (MEG) during a visuomotor reaction-time task. Both methods detected the same activation sequence across five regions, from visual towards motor cortices, with linearly correlated interregional BOLD and MEG response delays. The smallest significant interregional BOLD delay was 100ms; all delays ≥400ms were significant. Switching the order of external events reversed the sequence of BOLD activations, indicating that interregional neurovascular differences did not confound the results. This may open new avenues for using fMRI to follow rapid activation sequences in the brain.
•fMRI at 100ms resolution and MEG were recorded in a visuomotor reaction-time task.•Interregional BOLD and MEG response delays are linearly correlated.•The smallest significant interregional BOLD delay was 100ms.•All BOLD delays ≥400ms were significant.•Switching the order of external events reversed the sequence of BOLD activations. |
doi_str_mv | 10.1016/j.neuroimage.2013.04.017 |
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•fMRI at 100ms resolution and MEG were recorded in a visuomotor reaction-time task.•Interregional BOLD and MEG response delays are linearly correlated.•The smallest significant interregional BOLD delay was 100ms.•All BOLD delays ≥400ms were significant.•Switching the order of external events reversed the sequence of BOLD activations.</description><identifier>ISSN: 1053-8119</identifier><identifier>EISSN: 1095-9572</identifier><identifier>DOI: 10.1016/j.neuroimage.2013.04.017</identifier><identifier>PMID: 23591071</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adult ; Biological and medical sciences ; BOLD ; Brain - physiology ; Brain Mapping ; Brain research ; Electroencephalography ; Experiments ; Female ; Fundamental and applied biological sciences. Psychology ; Hemodynamics ; Hemodynamics - physiology ; Humans ; Image Processing, Computer-Assisted ; Inverse imaging ; Latency ; Magnetic Resonance Imaging ; Magnetoencephalography ; Male ; Medical research ; Neuronal timing ; Neurons - physiology ; Neurovascular coupling ; Photic Stimulation ; Reaction Time - physiology ; Studies ; Vertebrates: nervous system and sense organs ; Young Adult</subject><ispartof>NeuroImage (Orlando, Fla.), 2013-09, Vol.78, p.372-384</ispartof><rights>2013 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Sep 1, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-39ca49a2a385c1aa9baf7a39e259dddfdbc30b99d4de638882f2cafbe51316e3</citedby><cites>FETCH-LOGICAL-c581t-39ca49a2a385c1aa9baf7a39e259dddfdbc30b99d4de638882f2cafbe51316e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053811913003443$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27512860$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23591071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Fa-Hsuan</creatorcontrib><creatorcontrib>Witzel, Thomas</creatorcontrib><creatorcontrib>Raij, Tommi</creatorcontrib><creatorcontrib>Ahveninen, Jyrki</creatorcontrib><creatorcontrib>Wen-Kai Tsai, Kevin</creatorcontrib><creatorcontrib>Chu, Yin-Hua</creatorcontrib><creatorcontrib>Chang, Wei-Tang</creatorcontrib><creatorcontrib>Nummenmaa, Aapo</creatorcontrib><creatorcontrib>Polimeni, Jonathan R.</creatorcontrib><creatorcontrib>Kuo, Wen-Jui</creatorcontrib><creatorcontrib>Hsieh, Jen-Chuen</creatorcontrib><creatorcontrib>Rosen, Bruce R.</creatorcontrib><creatorcontrib>Belliveau, John W.</creatorcontrib><title>fMRI hemodynamics accurately reflects neuronal timing in the human brain measured by MEG</title><title>NeuroImage (Orlando, Fla.)</title><addtitle>Neuroimage</addtitle><description>Neuronal activation sequence information is essential for understanding brain functions. Extracting such timing information from blood oxygenation level dependent (BOLD) fMRI is confounded by interregional neurovascular differences and poorly understood relations between BOLD and electrophysiological response delays. Here, we recorded whole-head BOLD fMRI at 100ms resolution and magnetoencephalography (MEG) during a visuomotor reaction-time task. Both methods detected the same activation sequence across five regions, from visual towards motor cortices, with linearly correlated interregional BOLD and MEG response delays. The smallest significant interregional BOLD delay was 100ms; all delays ≥400ms were significant. Switching the order of external events reversed the sequence of BOLD activations, indicating that interregional neurovascular differences did not confound the results. This may open new avenues for using fMRI to follow rapid activation sequences in the brain.
•fMRI at 100ms resolution and MEG were recorded in a visuomotor reaction-time task.•Interregional BOLD and MEG response delays are linearly correlated.•The smallest significant interregional BOLD delay was 100ms.•All BOLD delays ≥400ms were significant.•Switching the order of external events reversed the sequence of BOLD activations.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>BOLD</subject><subject>Brain - physiology</subject><subject>Brain Mapping</subject><subject>Brain research</subject><subject>Electroencephalography</subject><subject>Experiments</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hemodynamics</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Inverse imaging</subject><subject>Latency</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetoencephalography</subject><subject>Male</subject><subject>Medical research</subject><subject>Neuronal timing</subject><subject>Neurons - physiology</subject><subject>Neurovascular coupling</subject><subject>Photic Stimulation</subject><subject>Reaction Time - physiology</subject><subject>Studies</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Young Adult</subject><issn>1053-8119</issn><issn>1095-9572</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkV1rFTEQhhdR7If-BQmI4M0eM8lmN7nUUmuhRZBeeBdmk9meHPajJrvC-fdme44WvOlVEnhmJvM-RcGAb4BD_Wm3GWmJUxjwnjaCg9zwasOheVGcAjeqNKoRL9e7kqUGMCfFWUo7zrmBSr8uToRUBngDp8XP7vbHNdvSMPn9iENwiaFzS8SZ-j2L1PXk5sQex43YszkMYbxnYWTzlth2GXBkbcT8HgjTEsmzds9uL6_eFK867BO9PZ7nxd3Xy7uLb-XN96vri883pVMa5lIah5VBgVIrB4imxa5BaUgo473vfOskb43xladaaq1FJxx2LSmQUJM8Lz4e2j7E6ddCabZDSI76HkealmRBcd7UIDh_HpV11eRUKpnR9_-hu2mJef-1oaiNzjFCpvSBcnFKKWdlH2JWEvcWuF092Z198mRXT5ZXNnvKpe-OA5Z2IP-v8K-YDHw4Apgc9l3E0YX0xDUKhK7Xpb4cOMoZ_w4UbXKBRkc-xGzO-ik8_5s_loy1zQ</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Lin, Fa-Hsuan</creator><creator>Witzel, Thomas</creator><creator>Raij, Tommi</creator><creator>Ahveninen, Jyrki</creator><creator>Wen-Kai Tsai, Kevin</creator><creator>Chu, Yin-Hua</creator><creator>Chang, Wei-Tang</creator><creator>Nummenmaa, Aapo</creator><creator>Polimeni, Jonathan R.</creator><creator>Kuo, Wen-Jui</creator><creator>Hsieh, Jen-Chuen</creator><creator>Rosen, Bruce R.</creator><creator>Belliveau, John W.</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20130901</creationdate><title>fMRI hemodynamics accurately reflects neuronal timing in the human brain measured by MEG</title><author>Lin, Fa-Hsuan ; Witzel, Thomas ; Raij, Tommi ; Ahveninen, Jyrki ; Wen-Kai Tsai, Kevin ; Chu, Yin-Hua ; Chang, Wei-Tang ; Nummenmaa, Aapo ; Polimeni, Jonathan R. ; Kuo, Wen-Jui ; Hsieh, Jen-Chuen ; Rosen, Bruce R. ; Belliveau, John W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-39ca49a2a385c1aa9baf7a39e259dddfdbc30b99d4de638882f2cafbe51316e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>BOLD</topic><topic>Brain - physiology</topic><topic>Brain Mapping</topic><topic>Brain research</topic><topic>Electroencephalography</topic><topic>Experiments</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hemodynamics</topic><topic>Hemodynamics - physiology</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Inverse imaging</topic><topic>Latency</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetoencephalography</topic><topic>Male</topic><topic>Medical research</topic><topic>Neuronal timing</topic><topic>Neurons - physiology</topic><topic>Neurovascular coupling</topic><topic>Photic Stimulation</topic><topic>Reaction Time - physiology</topic><topic>Studies</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Fa-Hsuan</creatorcontrib><creatorcontrib>Witzel, Thomas</creatorcontrib><creatorcontrib>Raij, Tommi</creatorcontrib><creatorcontrib>Ahveninen, Jyrki</creatorcontrib><creatorcontrib>Wen-Kai Tsai, Kevin</creatorcontrib><creatorcontrib>Chu, Yin-Hua</creatorcontrib><creatorcontrib>Chang, Wei-Tang</creatorcontrib><creatorcontrib>Nummenmaa, Aapo</creatorcontrib><creatorcontrib>Polimeni, Jonathan R.</creatorcontrib><creatorcontrib>Kuo, Wen-Jui</creatorcontrib><creatorcontrib>Hsieh, Jen-Chuen</creatorcontrib><creatorcontrib>Rosen, Bruce R.</creatorcontrib><creatorcontrib>Belliveau, John W.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>NeuroImage (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Fa-Hsuan</au><au>Witzel, Thomas</au><au>Raij, Tommi</au><au>Ahveninen, Jyrki</au><au>Wen-Kai Tsai, Kevin</au><au>Chu, Yin-Hua</au><au>Chang, Wei-Tang</au><au>Nummenmaa, Aapo</au><au>Polimeni, Jonathan R.</au><au>Kuo, Wen-Jui</au><au>Hsieh, Jen-Chuen</au><au>Rosen, Bruce R.</au><au>Belliveau, John W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>fMRI hemodynamics accurately reflects neuronal timing in the human brain measured by MEG</atitle><jtitle>NeuroImage (Orlando, Fla.)</jtitle><addtitle>Neuroimage</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>78</volume><spage>372</spage><epage>384</epage><pages>372-384</pages><issn>1053-8119</issn><eissn>1095-9572</eissn><abstract>Neuronal activation sequence information is essential for understanding brain functions. Extracting such timing information from blood oxygenation level dependent (BOLD) fMRI is confounded by interregional neurovascular differences and poorly understood relations between BOLD and electrophysiological response delays. Here, we recorded whole-head BOLD fMRI at 100ms resolution and magnetoencephalography (MEG) during a visuomotor reaction-time task. Both methods detected the same activation sequence across five regions, from visual towards motor cortices, with linearly correlated interregional BOLD and MEG response delays. The smallest significant interregional BOLD delay was 100ms; all delays ≥400ms were significant. Switching the order of external events reversed the sequence of BOLD activations, indicating that interregional neurovascular differences did not confound the results. This may open new avenues for using fMRI to follow rapid activation sequences in the brain.
•fMRI at 100ms resolution and MEG were recorded in a visuomotor reaction-time task.•Interregional BOLD and MEG response delays are linearly correlated.•The smallest significant interregional BOLD delay was 100ms.•All BOLD delays ≥400ms were significant.•Switching the order of external events reversed the sequence of BOLD activations.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>23591071</pmid><doi>10.1016/j.neuroimage.2013.04.017</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences BOLD Brain - physiology Brain Mapping Brain research Electroencephalography Experiments Female Fundamental and applied biological sciences. Psychology Hemodynamics Hemodynamics - physiology Humans Image Processing, Computer-Assisted Inverse imaging Latency Magnetic Resonance Imaging Magnetoencephalography Male Medical research Neuronal timing Neurons - physiology Neurovascular coupling Photic Stimulation Reaction Time - physiology Studies Vertebrates: nervous system and sense organs Young Adult |
title | fMRI hemodynamics accurately reflects neuronal timing in the human brain measured by MEG |
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