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Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease

Resting state fMRI (rfMRI) is gaining in popularity, being easy to acquire and with promising clinical applications. However, rfMRI studies, especially those involving clinical groups, still lack reproducibility, largely due to the different analysis settings. This is particularly important for the...

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Autores principales: Griffanti, Ludovica, Rolinski, Michal, Szewczyk-Krolikowski, Konrad, Menke, Ricarda A., Filippini, Nicola, Zamboni, Giovanna, Jenkinson, Mark, Hu, Michele T.M., Mackay, Clare E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655939/
https://www.ncbi.nlm.nih.gov/pubmed/26386348
http://dx.doi.org/10.1016/j.neuroimage.2015.09.021
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author Griffanti, Ludovica
Rolinski, Michal
Szewczyk-Krolikowski, Konrad
Menke, Ricarda A.
Filippini, Nicola
Zamboni, Giovanna
Jenkinson, Mark
Hu, Michele T.M.
Mackay, Clare E.
author_facet Griffanti, Ludovica
Rolinski, Michal
Szewczyk-Krolikowski, Konrad
Menke, Ricarda A.
Filippini, Nicola
Zamboni, Giovanna
Jenkinson, Mark
Hu, Michele T.M.
Mackay, Clare E.
author_sort Griffanti, Ludovica
collection PubMed
description Resting state fMRI (rfMRI) is gaining in popularity, being easy to acquire and with promising clinical applications. However, rfMRI studies, especially those involving clinical groups, still lack reproducibility, largely due to the different analysis settings. This is particularly important for the development of imaging biomarkers. The aim of this work was to evaluate the reproducibility of our recent study regarding the functional connectivity of the basal ganglia network in early Parkinson's disease (PD) (Szewczyk-Krolikowski et al., 2014). In particular, we systematically analysed the influence of two rfMRI analysis steps on the results: the individual cleaning (artefact removal) of fMRI data and the choice of the set of independent components (template) used for dual regression. Our experience suggests that the use of a cleaning approach based on single-subject independent component analysis, which removes non neural-related sources of inter-individual variability, can help to increase the reproducibility of clinical findings. A template generated using an independent set of healthy controls is recommended for studies where the aim is to detect differences from a “healthy” brain, rather than an “average” template, derived from an equal number of patients and controls. While, exploratory analyses (e.g. testing multiple resting state networks) should be used to formulate new hypotheses, careful validation is necessary before promising findings can be translated into useful biomarkers.
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spelling pubmed-46559392016-01-01 Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease Griffanti, Ludovica Rolinski, Michal Szewczyk-Krolikowski, Konrad Menke, Ricarda A. Filippini, Nicola Zamboni, Giovanna Jenkinson, Mark Hu, Michele T.M. Mackay, Clare E. Neuroimage Article Resting state fMRI (rfMRI) is gaining in popularity, being easy to acquire and with promising clinical applications. However, rfMRI studies, especially those involving clinical groups, still lack reproducibility, largely due to the different analysis settings. This is particularly important for the development of imaging biomarkers. The aim of this work was to evaluate the reproducibility of our recent study regarding the functional connectivity of the basal ganglia network in early Parkinson's disease (PD) (Szewczyk-Krolikowski et al., 2014). In particular, we systematically analysed the influence of two rfMRI analysis steps on the results: the individual cleaning (artefact removal) of fMRI data and the choice of the set of independent components (template) used for dual regression. Our experience suggests that the use of a cleaning approach based on single-subject independent component analysis, which removes non neural-related sources of inter-individual variability, can help to increase the reproducibility of clinical findings. A template generated using an independent set of healthy controls is recommended for studies where the aim is to detect differences from a “healthy” brain, rather than an “average” template, derived from an equal number of patients and controls. While, exploratory analyses (e.g. testing multiple resting state networks) should be used to formulate new hypotheses, careful validation is necessary before promising findings can be translated into useful biomarkers. Academic Press 2016-01-01 /pmc/articles/PMC4655939/ /pubmed/26386348 http://dx.doi.org/10.1016/j.neuroimage.2015.09.021 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Griffanti, Ludovica
Rolinski, Michal
Szewczyk-Krolikowski, Konrad
Menke, Ricarda A.
Filippini, Nicola
Zamboni, Giovanna
Jenkinson, Mark
Hu, Michele T.M.
Mackay, Clare E.
Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title_full Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title_fullStr Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title_full_unstemmed Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title_short Challenges in the reproducibility of clinical studies with resting state fMRI: An example in early Parkinson's disease
title_sort challenges in the reproducibility of clinical studies with resting state fmri: an example in early parkinson's disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655939/
https://www.ncbi.nlm.nih.gov/pubmed/26386348
http://dx.doi.org/10.1016/j.neuroimage.2015.09.021
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