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A Baseline for the Multivariate Comparison of Resting-State Networks
Open accessAbstract
As the size of functional and structural MRI datasets expands, it becomes increasingly important to establish a baseline from which diagnostic relevance may be determined, a processing strategy that efficiently prepares data for analysis, and a statistical approach that identifies important effects in a manner that is both robust and reproducible. In this paper, we introduce a multivariate analytic approach that optimizes sensitivity and reduces unnecessary testing. We demonstrate the utility of this mega-analytic approach by identifying the effects of age and gender on the resting-state networks (RSNs) of 603 healthy adolescents and adults (mean age: 23.4 years, range: 12-71 years). Data were collected on the same scanner, preprocessed using an automated analysis pipeline based in SPM, and studied using group independent component analysis. RSNs were identified and evaluated in terms of three primary outcome measures: time course spectral power, spatial map intensity, and functional network connectivity. Results revealed robust effects of age on all three outcome measures, largely indicating decreases in network coherence and connectivity with increasing age. Gender effects were of smaller magnitude but suggested stronger intra-network connectivity in females and more inter-network connectivity in males, particularly with regard to sensorimotor networks. These findings, along with the analysis approach and statistical framework described here, provide a useful baseline for future investigations of brain networks in health and disease.
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Analysis of Variance, Design, and Regression: Applied Statistical Methods
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Maturing thalamocortical functional connectivity across development
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Pooling fMRI data: meta-analysis, mega-analysis and multi-center studies
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A resting state network in the motor control circuit of the basal ganglia
Robinson, S., Basso, G., Soldati, N., Sailer, U., Jovicich, J., Bruzzone, L., Kryspin‐Exner, I., Bauer, H., & Moser, E. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-137 · Cited by 154
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Interrater and intermethod reliability of default mode network selection
Franco, A. R., Pritchard, A., Calhoun, V. D., & Mayer, A. R. (2009) · Human Brain Mapping · doi:10.1002/hbm.20668 · Cited by 142
Self-citationSchmithorst, V. J., & Holland, S. K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.11.046 · Cited by 140
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Self-citationData analysis a model comparison approach
Judd, C. M., McClelland, G. H., & Ryan, C. S. (2009) · Cited by 135
Age-related connectivity changes in fMRI data from children listening to stories
Karunanayaka, P., Holland, S. K., Schmithorst, V. J., Solodkin, A., Chen, E. E., Szaflarski, J. P., & Plante, E. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.08.028 · Cited by 126
Meda, S. A., Giuliani, N. R., Calhoun, V. D., Jagannathan, K., Schretlen, D. J., Pulver, A. E., Cascella, N. G., Keshavan, M. S., Kates, W. R., Buchanan, R., et al. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.02.007 · Cited by 119
Self-citationA method for making group inferences from functional MRI data using independent component analysis
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Self-citationJing Sui (Beijing Normal University), my correct affiliation is beijing normal university, N. Q. U. O. S. A. T., Adalı, T., Pearlson, G. D., & Calhoun, V. D. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.01.026 · Cited by 117
Self-citationIidaka, T., Matsumoto, A., Nogawa, J., Yamamoto, Y., & Sadato, N. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl040 · Cited by 115
van der Veen, W., & Jong, B. M. (2004) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 111
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Xiong, J., Ma, L., Wang, B., Narayana, S., Duff, E. P., Egan, G. F., & Fox, P. T. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.11.016 · Cited by 99
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The non-separability of physiologic noise in functional connectivity MRI with spatial ICA at 3 T
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Decreased Default Mode Neural Modulation With Age in Schizophrenia
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Self-citationFunctional segmentation of the brain cortex using high model order group-PICA.
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Tracking whole-brain connectivity dynamics in the resting state
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Self-citationThe Chronnectome: Time-Varying Connectivity Networks as the Next Frontier in fMRI Data Discovery
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Self-citationThe cognitive neuroscience of ageing
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Behavioral interpretations of intrinsic connectivity networks
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Self-citationResting-state functional connectivity in normal brain aging
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Metadata
- Authors
- Allen, E. A., Erhardt, E. B., Damaraju, E., Gruner, W., Segall, J. M., Silva, R. F., Havlicek, M., Rachakonda, S., Fries, J., Kalyanam, R., Michael, A. M., Caprihan, A., Turner, J. A., Eichele, T., Adelsheim, S., Bryan, A. D., Bustillo, J., Clark, V. P., Feldstein Ewing, S. W., Filbey, F., Ford, C. C., Hutchison, K., Jung, R. E., Kiehl, K. A., Kodituwakku, P., Komesu, Y. M., Mayer, A. R., Pearlson, G. D., Phillips, J. P., Sadek, J. R., Stevens, M., Teuscher, U., Thoma, R. J., & Calhoun, V. D.
- Venue
- Frontiers in Systems Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2011
- Volume
- 5
- Pages
- 2-2
- ISSN
- 1662-5137 (ISSN-L)
- OpenAlex
- W1973741448
- Cited by
- 1,293
- References
- 126
- FWCI
- 28.04
- Type
- journal article
- Language
- en
- Open access
- gold
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.