Loading…
Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment
Direct manipulation of brain activity can be used to investigate causal brain-behavior relationships. Current noninvasive neural stimulation techniques are too coarse to manipulate behaviors that correlate with fine-grained spatial patterns recorded by fMRI. However, these activity patterns can be m...
Saved in:
Published in: | PLoS computational biology 2017-07, Vol.13 (7), p.e1005681-e1005681 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333 |
---|---|
cites | cdi_FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333 |
container_end_page | e1005681 |
container_issue | 7 |
container_start_page | e1005681 |
container_title | PLoS computational biology |
container_volume | 13 |
creator | Oblak, Ethan F Lewis-Peacock, Jarrod A Sulzer, James S |
description | Direct manipulation of brain activity can be used to investigate causal brain-behavior relationships. Current noninvasive neural stimulation techniques are too coarse to manipulate behaviors that correlate with fine-grained spatial patterns recorded by fMRI. However, these activity patterns can be manipulated by having people learn to self-regulate their own recorded neural activity. This technique, known as fMRI neurofeedback, faces challenges as many participants are unable to self-regulate. The causes of this non-responder effect are not well understood due to the cost and complexity of such investigation in the MRI scanner. Here, we investigated the temporal dynamics of the hemodynamic response measured by fMRI as a potential cause of the non-responder effect. Learning to self-regulate the hemodynamic response involves a difficult temporal credit-assignment problem because this signal is both delayed and blurred over time. Two factors critical to this problem are the prescribed self-regulation strategy (cognitive or automatic) and feedback timing (continuous or intermittent). Here, we sought to evaluate how these factors interact with the temporal dynamics of fMRI without using the MRI scanner. We first examined the role of cognitive strategies by having participants learn to regulate a simulated neurofeedback signal using a unidimensional strategy: pressing one of two buttons to rotate a visual grating that stimulates a model of visual cortex. Under these conditions, continuous feedback led to faster regulation compared to intermittent feedback. Yet, since many neurofeedback studies prescribe implicit self-regulation strategies, we created a computational model of automatic reward-based learning to examine whether this result held true for automatic processing. When feedback was delayed and blurred based on the hemodynamics of fMRI, this model learned more reliably from intermittent feedback compared to continuous feedback. These results suggest that different self-regulation mechanisms prefer different feedback timings, and that these factors can be effectively explored and optimized via simulation prior to deployment in the MRI scanner. |
doi_str_mv | 10.1371/journal.pcbi.1005681 |
format | article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1929415030</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A499694482</galeid><doaj_id>oai_doaj_org_article_40e5b328cb6c4e3abaaf8263fbbd6102</doaj_id><sourcerecordid>A499694482</sourcerecordid><originalsourceid>FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333</originalsourceid><addsrcrecordid>eNqVk01v1DAQhiMEoqXwDxBY4gISu9hx7NgXpKriY6UCUtu75TiT1CWxFzup2Ds_HGc3XXVRL8QHW5NnXs87yWTZS4KXhJbkw40fg9Pdcm0quyQYMy7Io-yYMEYXJWXi8b3zUfYsxhuM01Hyp9lRLkpGOZXH2Z9L6JpFgHbs9GC9Q3EIeoB28x41AHWlzU802N66FmlXo2vofb1xurcGrYNfQxgsRJSCUz6gDnRwE2wd0ijafhuuUfPtYoUcjMHvVcHd2uBdD254nj1pdBfhxbyfZFefP12dfV2c__iyOjs9XxjOybAoK8xZgQmtRF7U1JScCiFyXlLKJJOcM1FjIRpZ0ryQIrltDE1PTWQj036Svd7Jrjsf1dy_qIjMZUEYpjgRqx1Re32j1sH2OmyU11ZtAz60SifHpgNVYGAVzYWpuCmA6krrJtVCm6qqOcF50vo43zZWPdQm-Qy6OxA9fOPstWr9rWKMYYzLJPB2Fgj-1whxUL2NBrpOO_Djtu6CY8KITOibf9CH3c1Uq5MB6xqf7jWTqDotpOSyKMRU9_IBKq0a0lf3Dhqb4gcJ7w4SEjPA76HVY4xqdXnxH-z3Q7bYsSb4GAM0-94RrKYRuDOpphFQ8wiktFf3-75Puvvn6V-kmwJR</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1929415030</pqid></control><display><type>article</type><title>Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment</title><source>PubMed Central (Open Access)</source><source>ProQuest Publicly Available Content database</source><creator>Oblak, Ethan F ; Lewis-Peacock, Jarrod A ; Sulzer, James S</creator><contributor>Gershman, Samuel J.</contributor><creatorcontrib>Oblak, Ethan F ; Lewis-Peacock, Jarrod A ; Sulzer, James S ; Gershman, Samuel J.</creatorcontrib><description>Direct manipulation of brain activity can be used to investigate causal brain-behavior relationships. Current noninvasive neural stimulation techniques are too coarse to manipulate behaviors that correlate with fine-grained spatial patterns recorded by fMRI. However, these activity patterns can be manipulated by having people learn to self-regulate their own recorded neural activity. This technique, known as fMRI neurofeedback, faces challenges as many participants are unable to self-regulate. The causes of this non-responder effect are not well understood due to the cost and complexity of such investigation in the MRI scanner. Here, we investigated the temporal dynamics of the hemodynamic response measured by fMRI as a potential cause of the non-responder effect. Learning to self-regulate the hemodynamic response involves a difficult temporal credit-assignment problem because this signal is both delayed and blurred over time. Two factors critical to this problem are the prescribed self-regulation strategy (cognitive or automatic) and feedback timing (continuous or intermittent). Here, we sought to evaluate how these factors interact with the temporal dynamics of fMRI without using the MRI scanner. We first examined the role of cognitive strategies by having participants learn to regulate a simulated neurofeedback signal using a unidimensional strategy: pressing one of two buttons to rotate a visual grating that stimulates a model of visual cortex. Under these conditions, continuous feedback led to faster regulation compared to intermittent feedback. Yet, since many neurofeedback studies prescribe implicit self-regulation strategies, we created a computational model of automatic reward-based learning to examine whether this result held true for automatic processing. When feedback was delayed and blurred based on the hemodynamics of fMRI, this model learned more reliably from intermittent feedback compared to continuous feedback. These results suggest that different self-regulation mechanisms prefer different feedback timings, and that these factors can be effectively explored and optimized via simulation prior to deployment in the MRI scanner.</description><identifier>ISSN: 1553-7358</identifier><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1005681</identifier><identifier>PMID: 28753639</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Activity patterns ; Adolescent ; Adult ; Behavior ; Biofeedback ; Biology and Life Sciences ; Brain ; Brain - physiology ; Brain mapping ; Brain research ; Buttons ; Cognitive ability ; Computational neuroscience ; Computer simulation ; Cortex (temporal) ; Electroencephalography ; Engineering and Technology ; Feedback ; Female ; Functional magnetic resonance imaging ; Funding ; Hemodynamics ; Hemodynamics - physiology ; Humans ; Learning ; Learning - physiology ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Mechanical engineering ; Medical imaging ; Medical research ; Medicine and Health Sciences ; Methods ; Models, Neurological ; Neural circuitry ; Neurofeedback - physiology ; Neuroimaging ; Neurosciences ; NMR ; Nuclear magnetic resonance ; Observations ; Physiological aspects ; Reinforcement ; Research and Analysis Methods ; Roles ; Scanners ; Simulation ; Social Sciences ; Stimulation ; Strategy ; Studies ; Temporal lobe ; Visual cortex ; Visual Cortex - physiology ; Visual perception ; Young Adult</subject><ispartof>PLoS computational biology, 2017-07, Vol.13 (7), p.e1005681-e1005681</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Public Library of Science. 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 credited: Oblak EF, Lewis-Peacock JA, Sulzer JS (2017) Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment. PLoS Comput Biol 13(7): e1005681. https://doi.org/10.1371/journal.pcbi.1005681</rights><rights>2017 Oblak et al 2017 Oblak et al</rights><rights>2017 Public Library of Science. 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 credited: Oblak EF, Lewis-Peacock JA, Sulzer JS (2017) Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment. PLoS Comput Biol 13(7): e1005681. https://doi.org/10.1371/journal.pcbi.1005681</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333</citedby><cites>FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333</cites><orcidid>0000-0002-9918-465X ; 0000-0001-9487-9850</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1929415030/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1929415030?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28753639$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gershman, Samuel J.</contributor><creatorcontrib>Oblak, Ethan F</creatorcontrib><creatorcontrib>Lewis-Peacock, Jarrod A</creatorcontrib><creatorcontrib>Sulzer, James S</creatorcontrib><title>Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment</title><title>PLoS computational biology</title><addtitle>PLoS Comput Biol</addtitle><description>Direct manipulation of brain activity can be used to investigate causal brain-behavior relationships. Current noninvasive neural stimulation techniques are too coarse to manipulate behaviors that correlate with fine-grained spatial patterns recorded by fMRI. However, these activity patterns can be manipulated by having people learn to self-regulate their own recorded neural activity. This technique, known as fMRI neurofeedback, faces challenges as many participants are unable to self-regulate. The causes of this non-responder effect are not well understood due to the cost and complexity of such investigation in the MRI scanner. Here, we investigated the temporal dynamics of the hemodynamic response measured by fMRI as a potential cause of the non-responder effect. Learning to self-regulate the hemodynamic response involves a difficult temporal credit-assignment problem because this signal is both delayed and blurred over time. Two factors critical to this problem are the prescribed self-regulation strategy (cognitive or automatic) and feedback timing (continuous or intermittent). Here, we sought to evaluate how these factors interact with the temporal dynamics of fMRI without using the MRI scanner. We first examined the role of cognitive strategies by having participants learn to regulate a simulated neurofeedback signal using a unidimensional strategy: pressing one of two buttons to rotate a visual grating that stimulates a model of visual cortex. Under these conditions, continuous feedback led to faster regulation compared to intermittent feedback. Yet, since many neurofeedback studies prescribe implicit self-regulation strategies, we created a computational model of automatic reward-based learning to examine whether this result held true for automatic processing. When feedback was delayed and blurred based on the hemodynamics of fMRI, this model learned more reliably from intermittent feedback compared to continuous feedback. These results suggest that different self-regulation mechanisms prefer different feedback timings, and that these factors can be effectively explored and optimized via simulation prior to deployment in the MRI scanner.</description><subject>Activity patterns</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Behavior</subject><subject>Biofeedback</subject><subject>Biology and Life Sciences</subject><subject>Brain</subject><subject>Brain - physiology</subject><subject>Brain mapping</subject><subject>Brain research</subject><subject>Buttons</subject><subject>Cognitive ability</subject><subject>Computational neuroscience</subject><subject>Computer simulation</subject><subject>Cortex (temporal)</subject><subject>Electroencephalography</subject><subject>Engineering and Technology</subject><subject>Feedback</subject><subject>Female</subject><subject>Functional magnetic resonance imaging</subject><subject>Funding</subject><subject>Hemodynamics</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Learning</subject><subject>Learning - physiology</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Mechanical engineering</subject><subject>Medical imaging</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Models, Neurological</subject><subject>Neural circuitry</subject><subject>Neurofeedback - physiology</subject><subject>Neuroimaging</subject><subject>Neurosciences</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Observations</subject><subject>Physiological aspects</subject><subject>Reinforcement</subject><subject>Research and Analysis Methods</subject><subject>Roles</subject><subject>Scanners</subject><subject>Simulation</subject><subject>Social Sciences</subject><subject>Stimulation</subject><subject>Strategy</subject><subject>Studies</subject><subject>Temporal lobe</subject><subject>Visual cortex</subject><subject>Visual Cortex - physiology</subject><subject>Visual perception</subject><subject>Young Adult</subject><issn>1553-7358</issn><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqVk01v1DAQhiMEoqXwDxBY4gISu9hx7NgXpKriY6UCUtu75TiT1CWxFzup2Ds_HGc3XXVRL8QHW5NnXs87yWTZS4KXhJbkw40fg9Pdcm0quyQYMy7Io-yYMEYXJWXi8b3zUfYsxhuM01Hyp9lRLkpGOZXH2Z9L6JpFgHbs9GC9Q3EIeoB28x41AHWlzU802N66FmlXo2vofb1xurcGrYNfQxgsRJSCUz6gDnRwE2wd0ijafhuuUfPtYoUcjMHvVcHd2uBdD254nj1pdBfhxbyfZFefP12dfV2c__iyOjs9XxjOybAoK8xZgQmtRF7U1JScCiFyXlLKJJOcM1FjIRpZ0ryQIrltDE1PTWQj036Svd7Jrjsf1dy_qIjMZUEYpjgRqx1Re32j1sH2OmyU11ZtAz60SifHpgNVYGAVzYWpuCmA6krrJtVCm6qqOcF50vo43zZWPdQm-Qy6OxA9fOPstWr9rWKMYYzLJPB2Fgj-1whxUL2NBrpOO_Djtu6CY8KITOibf9CH3c1Uq5MB6xqf7jWTqDotpOSyKMRU9_IBKq0a0lf3Dhqb4gcJ7w4SEjPA76HVY4xqdXnxH-z3Q7bYsSb4GAM0-94RrKYRuDOpphFQ8wiktFf3-75Puvvn6V-kmwJR</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Oblak, Ethan F</creator><creator>Lewis-Peacock, Jarrod A</creator><creator>Sulzer, James S</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AL</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</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>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0N</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9918-465X</orcidid><orcidid>https://orcid.org/0000-0001-9487-9850</orcidid></search><sort><creationdate>20170701</creationdate><title>Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment</title><author>Oblak, Ethan F ; Lewis-Peacock, Jarrod A ; Sulzer, James S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Activity patterns</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Behavior</topic><topic>Biofeedback</topic><topic>Biology and Life Sciences</topic><topic>Brain</topic><topic>Brain - physiology</topic><topic>Brain mapping</topic><topic>Brain research</topic><topic>Buttons</topic><topic>Cognitive ability</topic><topic>Computational neuroscience</topic><topic>Computer simulation</topic><topic>Cortex (temporal)</topic><topic>Electroencephalography</topic><topic>Engineering and Technology</topic><topic>Feedback</topic><topic>Female</topic><topic>Functional magnetic resonance imaging</topic><topic>Funding</topic><topic>Hemodynamics</topic><topic>Hemodynamics - physiology</topic><topic>Humans</topic><topic>Learning</topic><topic>Learning - physiology</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Mechanical engineering</topic><topic>Medical imaging</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Methods</topic><topic>Models, Neurological</topic><topic>Neural circuitry</topic><topic>Neurofeedback - physiology</topic><topic>Neuroimaging</topic><topic>Neurosciences</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Observations</topic><topic>Physiological aspects</topic><topic>Reinforcement</topic><topic>Research and Analysis Methods</topic><topic>Roles</topic><topic>Scanners</topic><topic>Simulation</topic><topic>Social Sciences</topic><topic>Stimulation</topic><topic>Strategy</topic><topic>Studies</topic><topic>Temporal lobe</topic><topic>Visual cortex</topic><topic>Visual Cortex - physiology</topic><topic>Visual perception</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oblak, Ethan F</creatorcontrib><creatorcontrib>Lewis-Peacock, Jarrod A</creatorcontrib><creatorcontrib>Sulzer, James S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale in Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Computing Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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 (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Computing Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Publicly Available Content database</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 Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PLoS computational biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oblak, Ethan F</au><au>Lewis-Peacock, Jarrod A</au><au>Sulzer, James S</au><au>Gershman, Samuel J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment</atitle><jtitle>PLoS computational biology</jtitle><addtitle>PLoS Comput Biol</addtitle><date>2017-07-01</date><risdate>2017</risdate><volume>13</volume><issue>7</issue><spage>e1005681</spage><epage>e1005681</epage><pages>e1005681-e1005681</pages><issn>1553-7358</issn><issn>1553-734X</issn><eissn>1553-7358</eissn><abstract>Direct manipulation of brain activity can be used to investigate causal brain-behavior relationships. Current noninvasive neural stimulation techniques are too coarse to manipulate behaviors that correlate with fine-grained spatial patterns recorded by fMRI. However, these activity patterns can be manipulated by having people learn to self-regulate their own recorded neural activity. This technique, known as fMRI neurofeedback, faces challenges as many participants are unable to self-regulate. The causes of this non-responder effect are not well understood due to the cost and complexity of such investigation in the MRI scanner. Here, we investigated the temporal dynamics of the hemodynamic response measured by fMRI as a potential cause of the non-responder effect. Learning to self-regulate the hemodynamic response involves a difficult temporal credit-assignment problem because this signal is both delayed and blurred over time. Two factors critical to this problem are the prescribed self-regulation strategy (cognitive or automatic) and feedback timing (continuous or intermittent). Here, we sought to evaluate how these factors interact with the temporal dynamics of fMRI without using the MRI scanner. We first examined the role of cognitive strategies by having participants learn to regulate a simulated neurofeedback signal using a unidimensional strategy: pressing one of two buttons to rotate a visual grating that stimulates a model of visual cortex. Under these conditions, continuous feedback led to faster regulation compared to intermittent feedback. Yet, since many neurofeedback studies prescribe implicit self-regulation strategies, we created a computational model of automatic reward-based learning to examine whether this result held true for automatic processing. When feedback was delayed and blurred based on the hemodynamics of fMRI, this model learned more reliably from intermittent feedback compared to continuous feedback. These results suggest that different self-regulation mechanisms prefer different feedback timings, and that these factors can be effectively explored and optimized via simulation prior to deployment in the MRI scanner.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28753639</pmid><doi>10.1371/journal.pcbi.1005681</doi><orcidid>https://orcid.org/0000-0002-9918-465X</orcidid><orcidid>https://orcid.org/0000-0001-9487-9850</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1553-7358 |
ispartof | PLoS computational biology, 2017-07, Vol.13 (7), p.e1005681-e1005681 |
issn | 1553-7358 1553-734X 1553-7358 |
language | eng |
recordid | cdi_plos_journals_1929415030 |
source | PubMed Central (Open Access); ProQuest Publicly Available Content database |
subjects | Activity patterns Adolescent Adult Behavior Biofeedback Biology and Life Sciences Brain Brain - physiology Brain mapping Brain research Buttons Cognitive ability Computational neuroscience Computer simulation Cortex (temporal) Electroencephalography Engineering and Technology Feedback Female Functional magnetic resonance imaging Funding Hemodynamics Hemodynamics - physiology Humans Learning Learning - physiology Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Mechanical engineering Medical imaging Medical research Medicine and Health Sciences Methods Models, Neurological Neural circuitry Neurofeedback - physiology Neuroimaging Neurosciences NMR Nuclear magnetic resonance Observations Physiological aspects Reinforcement Research and Analysis Methods Roles Scanners Simulation Social Sciences Stimulation Strategy Studies Temporal lobe Visual cortex Visual Cortex - physiology Visual perception Young Adult |
title | Self-regulation strategy, feedback timing and hemodynamic properties modulate learning in a simulated fMRI neurofeedback environment |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T07%3A23%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Self-regulation%20strategy,%20feedback%20timing%20and%20hemodynamic%20properties%20modulate%20learning%20in%20a%20simulated%20fMRI%20neurofeedback%20environment&rft.jtitle=PLoS%20computational%20biology&rft.au=Oblak,%20Ethan%20F&rft.date=2017-07-01&rft.volume=13&rft.issue=7&rft.spage=e1005681&rft.epage=e1005681&rft.pages=e1005681-e1005681&rft.issn=1553-7358&rft.eissn=1553-7358&rft_id=info:doi/10.1371/journal.pcbi.1005681&rft_dat=%3Cgale_plos_%3EA499694482%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c661t-7b0654013b824d3c7638882673359596658d088f9732498035fc3333d19f9333%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1929415030&rft_id=info:pmid/28753639&rft_galeid=A499694482&rfr_iscdi=true |