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A new virtue of phantom MRI data: explaining variance in human participant data

Background: Magnetic resonance imaging (MRI) is an important yet complex data acquisition technology for studying the brain. MRI signals can be affected by many factors and many sources of variance are often simply attributed to “noise”. Unexplained variance in MRI data hinders the statistical power...

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Autores principales: Cheng, Christopher P., Halchenko, Yaroslav O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783534/
https://www.ncbi.nlm.nih.gov/pubmed/33447378
http://dx.doi.org/10.12688/f1000research.24544.1
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author Cheng, Christopher P.
Halchenko, Yaroslav O.
author_facet Cheng, Christopher P.
Halchenko, Yaroslav O.
author_sort Cheng, Christopher P.
collection PubMed
description Background: Magnetic resonance imaging (MRI) is an important yet complex data acquisition technology for studying the brain. MRI signals can be affected by many factors and many sources of variance are often simply attributed to “noise”. Unexplained variance in MRI data hinders the statistical power of MRI studies and affects their reproducibility. We hypothesized that it would be possible to use phantom data as a proxy of scanner characteristics with a simplistic model of seasonal variation to explain some variance in human MRI data. Methods: We used MRI data from human participants collected in several studies, as well as phantom data collected weekly for scanner quality assurance (QA) purposes. From phantom data we identified the variables most likely to explain variance in acquired data and assessed their statistical significance by using them to model signal-to-noise ratio (SNR), a fundamental MRI QA metric. We then included phantom data SNR in the models of morphometric measures obtained from human anatomical MRI data from the same scanner. Results: Phantom SNR and seasonal variation, after multiple comparisons correction, were statistically significant predictors of the volume of gray brain matter. However, a sweep over 16 other brain matter areas and types revealed no statistically significant predictors among phantom SNR or seasonal variables after multiple comparison correction. Conclusions: Seasonal variation and phantom SNR may be important factors to account for in MRI studies. Our results show weak support that seasonal variations are primarily caused by biological human factors instead of scanner performance variation. The phantom QA metric and scanning parameters are useful for more than just QA. Using QA metrics, scanning parameters, and seasonal variation data can help account for some variance in MRI studies, thus making them more powerful and reproducible.
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spelling pubmed-77835342021-01-13 A new virtue of phantom MRI data: explaining variance in human participant data Cheng, Christopher P. Halchenko, Yaroslav O. F1000Res Research Article Background: Magnetic resonance imaging (MRI) is an important yet complex data acquisition technology for studying the brain. MRI signals can be affected by many factors and many sources of variance are often simply attributed to “noise”. Unexplained variance in MRI data hinders the statistical power of MRI studies and affects their reproducibility. We hypothesized that it would be possible to use phantom data as a proxy of scanner characteristics with a simplistic model of seasonal variation to explain some variance in human MRI data. Methods: We used MRI data from human participants collected in several studies, as well as phantom data collected weekly for scanner quality assurance (QA) purposes. From phantom data we identified the variables most likely to explain variance in acquired data and assessed their statistical significance by using them to model signal-to-noise ratio (SNR), a fundamental MRI QA metric. We then included phantom data SNR in the models of morphometric measures obtained from human anatomical MRI data from the same scanner. Results: Phantom SNR and seasonal variation, after multiple comparisons correction, were statistically significant predictors of the volume of gray brain matter. However, a sweep over 16 other brain matter areas and types revealed no statistically significant predictors among phantom SNR or seasonal variables after multiple comparison correction. Conclusions: Seasonal variation and phantom SNR may be important factors to account for in MRI studies. Our results show weak support that seasonal variations are primarily caused by biological human factors instead of scanner performance variation. The phantom QA metric and scanning parameters are useful for more than just QA. Using QA metrics, scanning parameters, and seasonal variation data can help account for some variance in MRI studies, thus making them more powerful and reproducible. F1000 Research Limited 2020-09-14 /pmc/articles/PMC7783534/ /pubmed/33447378 http://dx.doi.org/10.12688/f1000research.24544.1 Text en Copyright: © 2020 Cheng CP and Halchenko YO http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cheng, Christopher P.
Halchenko, Yaroslav O.
A new virtue of phantom MRI data: explaining variance in human participant data
title A new virtue of phantom MRI data: explaining variance in human participant data
title_full A new virtue of phantom MRI data: explaining variance in human participant data
title_fullStr A new virtue of phantom MRI data: explaining variance in human participant data
title_full_unstemmed A new virtue of phantom MRI data: explaining variance in human participant data
title_short A new virtue of phantom MRI data: explaining variance in human participant data
title_sort new virtue of phantom mri data: explaining variance in human participant data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783534/
https://www.ncbi.nlm.nih.gov/pubmed/33447378
http://dx.doi.org/10.12688/f1000research.24544.1
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