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Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference

Inference in neuroimaging typically occurs at the level of focal brain areas or circuits. Yet, increasingly, well-powered studies paint a much richer picture of broad-scale effects distributed throughout the brain, suggesting that many focal reports may only reflect the tip of the iceberg of underly...

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Autores principales: Noble, Stephanie, Mejia, Amanda F., Zalesky, Andrew, Scheinost, Dustin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371642/
https://www.ncbi.nlm.nih.gov/pubmed/35925887
http://dx.doi.org/10.1073/pnas.2203020119
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author Noble, Stephanie
Mejia, Amanda F.
Zalesky, Andrew
Scheinost, Dustin
author_facet Noble, Stephanie
Mejia, Amanda F.
Zalesky, Andrew
Scheinost, Dustin
author_sort Noble, Stephanie
collection PubMed
description Inference in neuroimaging typically occurs at the level of focal brain areas or circuits. Yet, increasingly, well-powered studies paint a much richer picture of broad-scale effects distributed throughout the brain, suggesting that many focal reports may only reflect the tip of the iceberg of underlying effects. How focal versus broad-scale perspectives influence the inferences we make has not yet been comprehensively evaluated using real data. Here, we compare sensitivity and specificity across procedures representing multiple levels of inference using an empirical benchmarking procedure that resamples task-based connectomes from the Human Connectome Project dataset (∼1,000 subjects, 7 tasks, 3 resampling group sizes, 7 inferential procedures). Only broad-scale (network and whole brain) procedures obtained the traditional 80% statistical power level to detect an average effect, reflecting >20% more statistical power than focal (edge and cluster) procedures. Power also increased substantially for false discovery rate– compared with familywise error rate–controlling procedures. The downsides are fairly limited; the loss in specificity for broad-scale and FDR procedures was relatively modest compared to the gains in power. Furthermore, the broad-scale methods we introduce are simple, fast, and easy to use, providing a straightforward starting point for researchers. This also points to the promise of more sophisticated broad-scale methods for not only functional connectivity but also related fields, including task-based activation. Altogether, this work demonstrates that shifting the scale of inference and choosing FDR control are both immediately attainable and can help remedy the issues with statistical power plaguing typical studies in the field.
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spelling pubmed-93716422022-08-12 Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference Noble, Stephanie Mejia, Amanda F. Zalesky, Andrew Scheinost, Dustin Proc Natl Acad Sci U S A Biological Sciences Inference in neuroimaging typically occurs at the level of focal brain areas or circuits. Yet, increasingly, well-powered studies paint a much richer picture of broad-scale effects distributed throughout the brain, suggesting that many focal reports may only reflect the tip of the iceberg of underlying effects. How focal versus broad-scale perspectives influence the inferences we make has not yet been comprehensively evaluated using real data. Here, we compare sensitivity and specificity across procedures representing multiple levels of inference using an empirical benchmarking procedure that resamples task-based connectomes from the Human Connectome Project dataset (∼1,000 subjects, 7 tasks, 3 resampling group sizes, 7 inferential procedures). Only broad-scale (network and whole brain) procedures obtained the traditional 80% statistical power level to detect an average effect, reflecting >20% more statistical power than focal (edge and cluster) procedures. Power also increased substantially for false discovery rate– compared with familywise error rate–controlling procedures. The downsides are fairly limited; the loss in specificity for broad-scale and FDR procedures was relatively modest compared to the gains in power. Furthermore, the broad-scale methods we introduce are simple, fast, and easy to use, providing a straightforward starting point for researchers. This also points to the promise of more sophisticated broad-scale methods for not only functional connectivity but also related fields, including task-based activation. Altogether, this work demonstrates that shifting the scale of inference and choosing FDR control are both immediately attainable and can help remedy the issues with statistical power plaguing typical studies in the field. National Academy of Sciences 2022-08-04 2022-08-09 /pmc/articles/PMC9371642/ /pubmed/35925887 http://dx.doi.org/10.1073/pnas.2203020119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Noble, Stephanie
Mejia, Amanda F.
Zalesky, Andrew
Scheinost, Dustin
Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title_full Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title_fullStr Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title_full_unstemmed Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title_short Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
title_sort improving power in functional magnetic resonance imaging by moving beyond cluster-level inference
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371642/
https://www.ncbi.nlm.nih.gov/pubmed/35925887
http://dx.doi.org/10.1073/pnas.2203020119
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