Brain connectivity fingerprinting and behavioural prediction rest on distinct functional systems of the human connectome.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
24 03 2022
Historique:
received: 17 03 2021
accepted: 08 02 2022
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 13 4 2022
Statut: epublish

Résumé

The prediction of inter-individual behavioural differences from neuroimaging data is a rapidly evolving field of research focusing on individualised methods to describe human brain organisation on the single-subject level. One method that harnesses such individual signatures is functional connectome fingerprinting, which can reliably identify individuals from large study populations. However, the precise relationship between functional signatures underlying fingerprinting and behavioural prediction remains unclear. Expanding on previous reports, here we systematically investigate the link between discrimination and prediction on different levels of brain network organisation (individual connections, network interactions, topographical organisation, and connection variability). Our analysis revealed a substantial divergence between discriminatory and predictive connectivity signatures on all levels of network organisation. Across different brain parcellations, thresholds, and prediction algorithms, we find discriminatory connections in higher-order multimodal association cortices, while neural correlates of behaviour display more variable distributions. Furthermore, we find the standard deviation of connections between participants to be significantly higher in fingerprinting than in prediction, making inter-individual connection variability a possible separating marker. These results demonstrate that participant identification and behavioural prediction involve highly distinct functional systems of the human connectome. The present study thus calls into question the direct functional relevance of connectome fingerprints.

Identifiants

pubmed: 35332230
doi: 10.1038/s42003-022-03185-3
pii: 10.1038/s42003-022-03185-3
pmc: PMC8948277
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

261

Informations de copyright

© 2022. The Author(s).

Références

Castellanos, F. X., Di Martino, A., Craddock, R. C., Mehta, A. D. & Milham, M. P. Clinical applications of the functional connectome. NeuroImage 80, 527–540 (2013).
pubmed: 23631991 doi: 10.1016/j.neuroimage.2013.04.083
Woo, C.-W., Chang, L. J., Lindquist, M. A. & Wager, T. D. Building better biomarkers: brain models in translational neuroimaging. Nat. Neurosci. 20, 365–377 (2017).
pubmed: 28230847 pmcid: 5988350 doi: 10.1038/nn.4478
Gabrieli, J. D. E., Ghosh, S. S. & Whitfield-Gabrieli, S. Prediction as a humanitarian and pragmatic contribution from human cognitive neuroscience. Neuron 85, 11–26 (2015).
pubmed: 25569345 pmcid: 4287988 doi: 10.1016/j.neuron.2014.10.047
Eickhoff, S. B. & Langner, R. Neuroimaging-based prediction of mental traits: poad to utopia or Orwell? PLoS Biol. 17, e3000497 (2019).
pubmed: 31725713 pmcid: 6879158 doi: 10.1371/journal.pbio.3000497
Finn, E. S. et al. Can brain state be manipulated to emphasize individual differences in functional connectivity? NeuroImage 160, 140–151 (2017).
pubmed: 28373122 doi: 10.1016/j.neuroimage.2017.03.064
Miranda-Dominguez, O. et al. Connectotyping: model based fingerprinting of the functional connectome. PLoS ONE 9, e111048 (2014).
pubmed: 25386919 pmcid: 4227655 doi: 10.1371/journal.pone.0111048
Finn, E. S. et al. Functional connectome fingerprinting: identifying individuals using patterns of brain connectivity. Nat. Neurosci. 18, 1664–1671 (2015).
pubmed: 26457551 pmcid: 5008686 doi: 10.1038/nn.4135
Amico, E. & Goñi, J. The quest for identifiability in human functional connectomes. Sci. Rep. 8, 1–14 (2018).
doi: 10.1038/s41598-018-25089-1
Horien, C., Shen, X., Scheinost, D. & Constable, R. T. The individual functional connectome is unique and stable over months to years. NeuroImage 189, 676–687 (2019).
pubmed: 30721751 doi: 10.1016/j.neuroimage.2019.02.002
Milham, M. P., Vogelstein, J. & Xu, T. Removing the reliability bottleneck in functional magnetic resonance imaging research to achieve clinical utility. JAMA Psychiatry 78, 587–588 (2021).
Byrge, L. & Kennedy, D. P. Accurate prediction of individual subject identity and task, but not autism diagnosis, from functional connectomes. Hum. Brain Mapp. 41, 2249–2262 (2020).
pubmed: 32150312 pmcid: 7268028 doi: 10.1002/hbm.24943
Mansour, S., Tian, Y., Yeo, B. T. T., Cropley, V. & Zalesky, A. High-resolution connectomic fingerprints: mapping neural identity and behavior. NeuroImage 229, 117695 (2021).
doi: 10.1016/j.neuroimage.2020.117695
Liu, J., Liao, X., Xia, M. & He, Y. Chronnectome fingerprinting: identifying individuals and predicting higher cognitive functions using dynamic brain connectivity patterns. Hum. Brain Mapp. 39, 902–915 (2018).
pubmed: 29143409 doi: 10.1002/hbm.23890
Lin, Y.-C., Baete, S. H., Wang, X. & Boada, F. E. Mapping brain–behavior networks using functional and structural connectome fingerprinting in the HCP dataset. Brain Behav. 10, e01647 (2020).
pubmed: 32351025 pmcid: 7303390 doi: 10.1002/brb3.1647
Mueller, S. et al. Individual variability in functional connectivity architecture of the human brain. Neuron 77, 586–595 (2013).
pubmed: 23395382 pmcid: 3746075 doi: 10.1016/j.neuron.2012.12.028
Laumann, T. O. et al. Functional system and areal organization of a highly sampled individual human brain. Neuron 87, 657–670 (2015).
pubmed: 26212711 pmcid: 4642864 doi: 10.1016/j.neuron.2015.06.037
Gordon, E. M., Laumann, T. O., Adeyemo, B. & Petersen, S. E. Individual variability of the system-level organization of the human brain. Cereb. Cortex 27, 386–399 (2017).
pubmed: 26464473
Miranda-Dominguez, O. et al. Heritability of the human connectome: a connectotyping study. Netw. Neurosci. 2, 175–199 (2017).
doi: 10.1162/netn_a_00029
Menon, S. S. & Krishnamurthy, K. A comparison of static and dynamic functional connectivities for identifying subjects and biological sex using intrinsic individual brain connectivity. Sci. Rep. 9, 5729 (2019).
pubmed: 30952913 pmcid: 6450922 doi: 10.1038/s41598-019-42090-4
Demeter, D. V. et al. Functional connectivity fingerprints at rest are similar across youths and adults and vary with genetic similarity. iScience 23, 100801 (2020).
pubmed: 31958758 doi: 10.1016/j.isci.2019.100801
Corbetta, M. & Shulman, G. L. Control of goal-directed and stimulus-driven attention in the brain. Nat. Rev. Neurosci. 3, 201–215 (2002).
pubmed: 11994752 doi: 10.1038/nrn755
Cole, M. W. et al. Multi-task connectivity reveals flexible hubs for adaptive task control. Nat. Neurosci. 16, 1348–1355 (2013).
pubmed: 23892552 pmcid: 3758404 doi: 10.1038/nn.3470
Marek, S. & Dosenbach, N. U. F. The frontoparietal network: function, electrophysiology, and importance of individual precision mapping. Dialogues Clin. Neurosci. 20, 133–140 (2018).
pubmed: 30250390 pmcid: 6136121 doi: 10.31887/DCNS.2018.20.2/smarek
Xu, T. et al. Assessing variations in areal organization for the intrinsic brain: from fingerprints to reliability. Cereb. Cortex 26, 4192–4211 (2016).
pubmed: 27600846 pmcid: 5066830 doi: 10.1093/cercor/bhw241
Jalbrzikowski, M. et al. Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5-years apart. Hum. Brain Mapp. 41, 4187–4199 (2020).
pubmed: 32652852 pmcid: 7502841 doi: 10.1002/hbm.25118
Cai, H., Chen, J., Liu, S., Zhu, J. & Yu, Y. Brain functional connectome-based prediction of individual decision impulsivity. Cortex 125, 288–298 (2020).
pubmed: 32113043 doi: 10.1016/j.cortex.2020.01.022
Shen, X. et al. Using connectome-based predictive modeling to predict individual behavior from brain connectivity. Nat. Protoc. 12, 506–518 (2017).
pubmed: 28182017 pmcid: 5526681 doi: 10.1038/nprot.2016.178
Noble, S., Scheinost, D. & Constable, R. T. A decade of test-retest reliability of functional connectivity: a systematic review and meta-analysis. NeuroImage 203, 116157 (2019).
pubmed: 31494250 doi: 10.1016/j.neuroimage.2019.116157
Duan, D. et al. Cortical Foldingprints for Infant Identification. in 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019) 396–399 (2019).
Paquola, C. et al. Microstructural and functional gradients are increasingly dissociated in transmodal cortices. PLoS Biol. 17, e3000284 (2019).
pubmed: 31107870 pmcid: 6544318 doi: 10.1371/journal.pbio.3000284
Seitzman, B. A. et al. Trait-like variants in human functional brain networks. Proc. Natl Acad. Sci. USA 116, 22851–22861 (2019).
pubmed: 31611415 pmcid: 6842602 doi: 10.1073/pnas.1902932116
Ferguson, M. A., Anderson, J. S. & Spreng, R. N. Fluid and flexible minds: Intelligence reflects synchrony in the brain’s intrinsic network architecture. Netw. Neurosci. 1, 192–207 (2017).
pubmed: 29911673 pmcid: 5988392 doi: 10.1162/NETN_a_00010
Greene, A. S., Gao, S., Scheinost, D. & Constable, R. T. Task-induced brain state manipulation improves prediction of individual traits. Nat. Commun. 9, 2807 (2018).
pubmed: 30022026 pmcid: 6052101 doi: 10.1038/s41467-018-04920-3
Poldrack, R. A., Huckins, G. & Varoquaux, G. Establishment of best practices for evidence for prediction: a review. JAMA Psychiatry 77, 534–540 (2020).
pubmed: 31774490 pmcid: 7250718 doi: 10.1001/jamapsychiatry.2019.3671
Varoquaux, G. et al. Assessing and tuning brain decoders: cross-validation, caveats, and guidelines. NeuroImage 145, 166–179 (2017).
pubmed: 27989847 doi: 10.1016/j.neuroimage.2016.10.038
Van Essen, D. C. et al. The WU-Minn human connectome project: an overview. NeuroImage 80, 62–79 (2013).
pubmed: 23684880 doi: 10.1016/j.neuroimage.2013.05.041
Glasser, M. F. et al. The minimal preprocessing pipelines for the Human Connectome Project. NeuroImage 80, 105–124 (2013).
pubmed: 23668970 doi: 10.1016/j.neuroimage.2013.04.127
Whitfield-Gabrieli, S. & Nieto-Castanon, A. Conn: a functional connectivity toolbox for correlated and anticorrelated brain networks. Brain Connect 2, 125–141 (2012).
pubmed: 22642651 doi: 10.1089/brain.2012.0073
Fan, L. et al. The Human Brainnetome Atlas: a new brain atlas based on connectional architecture. Cereb. Cortex 26, 3508–3526 (2016).
pubmed: 27230218 pmcid: 4961028 doi: 10.1093/cercor/bhw157
Glasser, M. F. et al. A multi-modal parcellation of human cerebral cortex. Nature 536, 171–178 (2016).
pubmed: 27437579 pmcid: 4990127 doi: 10.1038/nature18933
Tzourio-Mazoyer, N. et al. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. NeuroImage 15, 273–289 (2002).
pubmed: 11771995 doi: 10.1006/nimg.2001.0978
Shen, X., Tokoglu, F., Papademetris, X. & Constable, R. T. Groupwise whole-brain parcellation from resting-state fMRI data for network node identification. NeuroImage 82, 403–415 (2013).
pubmed: 23747961 doi: 10.1016/j.neuroimage.2013.05.081
Yeo, B. T. et al. The organization of the human cerebral cortex estimated by intrinsic functional connectivity. J. Neurophysiol. 106, 1125–1165 (2011).
pubmed: 21653723 doi: 10.1152/jn.00338.2011
Ji, J. L. et al. Mapping the human brain’s cortical-subcortical functional network organization. NeuroImage 185, 35–57 (2019).
pubmed: 30291974 doi: 10.1016/j.neuroimage.2018.10.006
He, Y. et al. Uncovering intrinsic modular organization of spontaneous brain activity in humans. PLoS ONE 4, e5226 (2009).
pubmed: 19381298 pmcid: 2668183 doi: 10.1371/journal.pone.0005226
Rubinov, M. & Sporns, O. Complex network measures of brain connectivity: uses and interpretations. NeuroImage 52, 1059–1069 (2010).
pubmed: 19819337 doi: 10.1016/j.neuroimage.2009.10.003
Sui, J., Jiang, R., Bustillo, J. & Calhoun, V. Neuroimaging-based individualized prediction of cognition and behavior for mental disorders and health: methods and promises. Biol. Psychiatry 88, 818–828 (2020).
Nostro, A. D. et al. Predicting personality from network-based resting-state functional connectivity. Brain Struct. Funct. 223, 2699–2719 (2018).
pubmed: 29572625 pmcid: 5997535 doi: 10.1007/s00429-018-1651-z
Alexander-Bloch, A. F. et al. On testing for spatial correspondence between maps of human brain structure and function. NeuroImage 178, 540–551 (2018).
pubmed: 29860082 doi: 10.1016/j.neuroimage.2018.05.070
Váša, F. et al. Adolescent tuning of association cortex in human structural brain. Netw. Cereb. Cortex 28, 281–294 (2018).
doi: 10.1093/cercor/bhx249

Auteurs

Maron Mantwill (M)

Charité-Universitätsmedizin Berlin, Department of Neurology, Berlin, Germany. maron.mantwill@charite.de.
Humboldt-Universität zu Berlin, Faculty of Philosophy, Berlin School of Mind and Brain, Berlin, Germany. maron.mantwill@charite.de.

Martin Gell (M)

Humboldt-Universität zu Berlin, Faculty of Philosophy, Berlin School of Mind and Brain, Berlin, Germany.
Institute of Neuroscience and Medicine (INM-7: Brain & Behaviour), Research Centre Jülich, Jülich, Germany.
Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Stephan Krohn (S)

Charité-Universitätsmedizin Berlin, Department of Neurology, Berlin, Germany.
Humboldt-Universität zu Berlin, Faculty of Philosophy, Berlin School of Mind and Brain, Berlin, Germany.

Carsten Finke (C)

Charité-Universitätsmedizin Berlin, Department of Neurology, Berlin, Germany.
Humboldt-Universität zu Berlin, Faculty of Philosophy, Berlin School of Mind and Brain, Berlin, Germany.

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