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Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing

Echoplanar MRI is associated with significant acoustic noise, which can interfere with the presentation of auditory stimuli, create a more challenging listening environment, and increase discomfort felt by participants. Here we investigate a scanning sequence that significantly reduces the amplitude...

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Detalles Bibliográficos
Autores principales: Peelle, Jonathan E., Eason, Rowena J., Schmitter, Sebastian, Schwarzbauer, Christian, Davis, Matthew H.
Formato: Texto
Lenguaje:English
Publicado: Academic Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946564/
https://www.ncbi.nlm.nih.gov/pubmed/20483377
http://dx.doi.org/10.1016/j.neuroimage.2010.05.015
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author Peelle, Jonathan E.
Eason, Rowena J.
Schmitter, Sebastian
Schwarzbauer, Christian
Davis, Matthew H.
author_facet Peelle, Jonathan E.
Eason, Rowena J.
Schmitter, Sebastian
Schwarzbauer, Christian
Davis, Matthew H.
author_sort Peelle, Jonathan E.
collection PubMed
description Echoplanar MRI is associated with significant acoustic noise, which can interfere with the presentation of auditory stimuli, create a more challenging listening environment, and increase discomfort felt by participants. Here we investigate a scanning sequence that significantly reduces the amplitude of acoustic noise associated with echoplanar imaging (EPI). This is accomplished using a constant phase encoding gradient and a sinusoidal readout echo train to produce a narrow-band acoustic frequency spectrum, which is adapted to the scanner's frequency response function by choosing an optimum gradient switching frequency. To evaluate the effect of these nonstandard parameters we conducted a speech experiment comparing four different EPI sequences: Quiet, Sparse, Standard, and Matched Standard (using the same readout duration as Quiet). For each sequence participants listened to sentences and signal-correlated noise (SCN), which provides an unintelligible amplitude-matched control condition. We used BOLD sensitivity maps to quantify sensitivity loss caused by the longer EPI readout duration used in the Quiet and Matched Standard EPI sequences. We found that the Quiet sequence provided more robust activation for SCN in primary auditory areas and comparable activation in frontal and temporal regions for Sentences > SCN, but less sentence-related activity in inferotemporal cortex. The increased listening effort associated with the louder Standard sequence relative to the Quiet sequence resulted in increased activation in the left temporal and inferior parietal cortices. Together, these results suggest that the Quiet sequence is suitable, and perhaps preferable, for many auditory studies. However, its applicability depends on the specific brain regions of interest.
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spelling pubmed-29465642010-10-21 Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing Peelle, Jonathan E. Eason, Rowena J. Schmitter, Sebastian Schwarzbauer, Christian Davis, Matthew H. Neuroimage Article Echoplanar MRI is associated with significant acoustic noise, which can interfere with the presentation of auditory stimuli, create a more challenging listening environment, and increase discomfort felt by participants. Here we investigate a scanning sequence that significantly reduces the amplitude of acoustic noise associated with echoplanar imaging (EPI). This is accomplished using a constant phase encoding gradient and a sinusoidal readout echo train to produce a narrow-band acoustic frequency spectrum, which is adapted to the scanner's frequency response function by choosing an optimum gradient switching frequency. To evaluate the effect of these nonstandard parameters we conducted a speech experiment comparing four different EPI sequences: Quiet, Sparse, Standard, and Matched Standard (using the same readout duration as Quiet). For each sequence participants listened to sentences and signal-correlated noise (SCN), which provides an unintelligible amplitude-matched control condition. We used BOLD sensitivity maps to quantify sensitivity loss caused by the longer EPI readout duration used in the Quiet and Matched Standard EPI sequences. We found that the Quiet sequence provided more robust activation for SCN in primary auditory areas and comparable activation in frontal and temporal regions for Sentences > SCN, but less sentence-related activity in inferotemporal cortex. The increased listening effort associated with the louder Standard sequence relative to the Quiet sequence resulted in increased activation in the left temporal and inferior parietal cortices. Together, these results suggest that the Quiet sequence is suitable, and perhaps preferable, for many auditory studies. However, its applicability depends on the specific brain regions of interest. Academic Press 2010-10-01 /pmc/articles/PMC2946564/ /pubmed/20483377 http://dx.doi.org/10.1016/j.neuroimage.2010.05.015 Text en © 2010 Elsevier Inc. https://creativecommons.org/licenses/by/4.0/ Open Access under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) license
spellingShingle Article
Peelle, Jonathan E.
Eason, Rowena J.
Schmitter, Sebastian
Schwarzbauer, Christian
Davis, Matthew H.
Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title_full Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title_fullStr Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title_full_unstemmed Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title_short Evaluating an acoustically quiet EPI sequence for use in fMRI studies of speech and auditory processing
title_sort evaluating an acoustically quiet epi sequence for use in fmri studies of speech and auditory processing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946564/
https://www.ncbi.nlm.nih.gov/pubmed/20483377
http://dx.doi.org/10.1016/j.neuroimage.2010.05.015
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