4.7 Article

Exploring MEG brain fingerprints: Evaluation, pitfalls, and interpretations

期刊

NEUROIMAGE
卷 240, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2021.118331

关键词

Brain fingerprinting; MEG connectivity; Functional connectomes; Brain networks

资金

  1. NIH Institutes and Centers [1U54MH091657]
  2. NIH Blueprint for Neuroscience Research
  3. McDonnell Center for Systems Neuroscience at Washington University
  4. SNSF Ambizione [PZ00P2_185716]
  5. centre of Excellence in Healthcare, IIIT-Delhi, India
  6. Swiss National Science Foundation (SNF) [PZ00P2_185716] Funding Source: Swiss National Science Foundation (SNF)

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The performance of MEG fingerprinting heavily depends on functional connectivity measures, frequency bands, identification scoring methods, and spatial leakage correction. Phase-coupling methods, central frequency bands (alpha and beta), and specific networks such as visual, frontoparietal, dorsal-attention, and default-mode networks show higher MEG fingerprinting performances. Cross-modality comparisons reveal spatial concordance in fingerprinting patterns between MEG and fMRI data, especially in the visual system. Additionally, multivariate correlation analyses indicate strong behavioral significance of MEG connectomes, with dependency on connectivity measures and temporal scales.
Individual characterization of subjects based on their functional connectome (FC), termed FC fingerprinting , has become a highly sought-after goal in contemporary neuroscience research. Recent functional magnetic resonance imaging (fMRI) studies have demonstrated unique characterization and accurate identification of individuals as an accomplished task. However, FC fingerprinting in magnetoencephalography (MEG) data is still widely un-explored. Here, we study resting-state MEG data from the Human Connectome Project to assess the MEG FC fingerprinting and its relationship with several factors including amplitude-and phase-coupling functional con-nectivity measures, spatial leakage correction, frequency bands, and behavioral significance. To this end, we first employ two identification scoring methods, differential identifiability and success rate, to provide quantitative fingerprint scores for each FC measurement. Secondly, we explore the edgewise and nodal MEG fingerprinting patterns across the different frequency bands (delta, theta, alpha, beta, and gamma). Finally, we investigate the cross-modality fingerprinting patterns obtained from MEG and fMRI recordings from the same subjects. We assess the behavioral significance of FC across connectivity measures and imaging modalities using partial least square correlation analyses. Our results suggest that fingerprinting performance is heavily dependent on the functional connectivity measure, frequency band, identification scoring method, and spatial leakage correction. We report higher MEG fingerprinting performances in phase-coupling methods, central frequency bands (alpha and beta), and in the visual, frontoparietal, dorsal-attention, and default-mode networks. Furthermore, cross-modality com-parisons reveal a certain degree of spatial concordance in fingerprinting patterns between the MEG and fMRI data, especially in the visual system. Finally, the multivariate correlation analyses show that MEG connectomes have strong behavioral significance, which however depends on the considered connectivity measure and temporal scale. This comprehensive, albeit preliminary investigation of MEG connectome test-retest identifiability offers a first characterization of MEG fingerprinting in relation to different methodological and electrophysiological factors and contributes to the understanding of fingerprinting cross-modal relationships. We hope that this first investigation will contribute to setting the grounds for MEG connectome identification.

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