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Effects of phase encoding direction on test-retest reliability of human functional connectome
The majority of human connectome studies in the literature based on functional magnetic resonance imaging (fMRI) data use either an anterior-to-posterior (AP) or a posterior-to-anterior (PA) phase encoding direction (PED). However, whether and how PED would affect test-retest reliability of function...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529794/ https://www.ncbi.nlm.nih.gov/pubmed/37364743 http://dx.doi.org/10.1016/j.neuroimage.2023.120238 |
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author | Cao, Hengyi Barber, Anita D. Rubio, Jose M. Argyelan, Miklos Gallego, Juan A. Lencz, Todd Malhotra, Anil K. |
author_facet | Cao, Hengyi Barber, Anita D. Rubio, Jose M. Argyelan, Miklos Gallego, Juan A. Lencz, Todd Malhotra, Anil K. |
author_sort | Cao, Hengyi |
collection | PubMed |
description | The majority of human connectome studies in the literature based on functional magnetic resonance imaging (fMRI) data use either an anterior-to-posterior (AP) or a posterior-to-anterior (PA) phase encoding direction (PED). However, whether and how PED would affect test-retest reliability of functional connectome is unclear. Here, in a sample of healthy subjects with two sessions of fMRI scans separated by 12 weeks (two runs per session, one with AP, the other with PA), we tested the influence of PED on global, nodal, and edge connectivity in the constructed brain networks. All data underwent the state-of-the-art Human Connectome Project (HCP) pipeline to correct for phase-encoding-related distortions before entering analysis. We found that at the global level, the PA scans showed significantly higher intraclass correlation coefficients (ICCs) for global connectivity compared with AP scans, which was particularly prominent when using the Seitzman-300 atlas (versus the CAB-NP-718 atlas). At the nodal level, regions most strongly affected by PED were consistently mapped to the cingulate cortex, temporal lobe, sensorimotor areas, and visual areas, with significantly higher ICCs during PA scans compared with AP scans, regardless of atlas. Better ICCs were also observed during PA scans at the edge level, in particular when global signal regression (GSR) was not performed. Further, we demonstrated that the observed reliability differences between PEDs may relate to a similar effect on the reliability of temporal signal-to-noise ratio (tSNR) in the same regions (that PA scans were associated with higher reliability of tSNR than AP scans). Averaging the connectivity outcome from the AP and PA scans could increase median ICCs, especially at the nodal and edge levels. Similar results at the global and nodal levels were replicated in an independent, public dataset from the HCP-Early Psychosis (HCP-EP) study with a similar design but a much shorter scan session interval. Our findings suggest that PED has significant effects on the reliability of connectomic estimates in fMRI studies. We urge that these effects need to be carefully considered in future neuroimaging designs, especially in longitudinal studies such as those related to neurodevelopment or clinical intervention. |
format | Online Article Text |
id | pubmed-10529794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105297942023-09-27 Effects of phase encoding direction on test-retest reliability of human functional connectome Cao, Hengyi Barber, Anita D. Rubio, Jose M. Argyelan, Miklos Gallego, Juan A. Lencz, Todd Malhotra, Anil K. Neuroimage Article The majority of human connectome studies in the literature based on functional magnetic resonance imaging (fMRI) data use either an anterior-to-posterior (AP) or a posterior-to-anterior (PA) phase encoding direction (PED). However, whether and how PED would affect test-retest reliability of functional connectome is unclear. Here, in a sample of healthy subjects with two sessions of fMRI scans separated by 12 weeks (two runs per session, one with AP, the other with PA), we tested the influence of PED on global, nodal, and edge connectivity in the constructed brain networks. All data underwent the state-of-the-art Human Connectome Project (HCP) pipeline to correct for phase-encoding-related distortions before entering analysis. We found that at the global level, the PA scans showed significantly higher intraclass correlation coefficients (ICCs) for global connectivity compared with AP scans, which was particularly prominent when using the Seitzman-300 atlas (versus the CAB-NP-718 atlas). At the nodal level, regions most strongly affected by PED were consistently mapped to the cingulate cortex, temporal lobe, sensorimotor areas, and visual areas, with significantly higher ICCs during PA scans compared with AP scans, regardless of atlas. Better ICCs were also observed during PA scans at the edge level, in particular when global signal regression (GSR) was not performed. Further, we demonstrated that the observed reliability differences between PEDs may relate to a similar effect on the reliability of temporal signal-to-noise ratio (tSNR) in the same regions (that PA scans were associated with higher reliability of tSNR than AP scans). Averaging the connectivity outcome from the AP and PA scans could increase median ICCs, especially at the nodal and edge levels. Similar results at the global and nodal levels were replicated in an independent, public dataset from the HCP-Early Psychosis (HCP-EP) study with a similar design but a much shorter scan session interval. Our findings suggest that PED has significant effects on the reliability of connectomic estimates in fMRI studies. We urge that these effects need to be carefully considered in future neuroimaging designs, especially in longitudinal studies such as those related to neurodevelopment or clinical intervention. 2023-08-15 2023-06-24 /pmc/articles/PMC10529794/ /pubmed/37364743 http://dx.doi.org/10.1016/j.neuroimage.2023.120238 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Article Cao, Hengyi Barber, Anita D. Rubio, Jose M. Argyelan, Miklos Gallego, Juan A. Lencz, Todd Malhotra, Anil K. Effects of phase encoding direction on test-retest reliability of human functional connectome |
title | Effects of phase encoding direction on test-retest reliability of human functional connectome |
title_full | Effects of phase encoding direction on test-retest reliability of human functional connectome |
title_fullStr | Effects of phase encoding direction on test-retest reliability of human functional connectome |
title_full_unstemmed | Effects of phase encoding direction on test-retest reliability of human functional connectome |
title_short | Effects of phase encoding direction on test-retest reliability of human functional connectome |
title_sort | effects of phase encoding direction on test-retest reliability of human functional connectome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529794/ https://www.ncbi.nlm.nih.gov/pubmed/37364743 http://dx.doi.org/10.1016/j.neuroimage.2023.120238 |
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