A within-subject voxel-wise constant-block partial least squares correlation method to explore MRI-based brain structure–function relationship
Cognitive Neurodynamics - Trang 1-15 - 2023
Tóm tắt
The brain structure–function relationship is crucial to how the human brain works under normal or diseased conditions. Exploring such a relationship is challenging when using the 3-dimensional magnetic resonance imaging (MRI) functional dataset which is temporal dynamic and the structural MRI which is static. Partial Least Squares Correlation (PLSC) is one of the classical methods for exploring the joint spatial and temporal relationship. The goal of PLSC is to identify covarying patterns via linear voxel-wise combinations in each of the structural and functional data sets to maximize the covariance. However, existing PLSC cannot adequately deal with the unmatched temporal dimensions between structural and functional data sets. We proposed a new alternative variant of the PLSC, termed within-subject, voxel-wise, and constant-block PLSC, to address this problem. To validate our method, we used two data sets with weak and strong relationships in simulated data. Additionally, the analysis of real brain data was carried out based on gray matter volume hubs derived from sMRI and whole-brain voxel-wise measures from resting-state fMRI for aging effect based on healthy subjects aged 16–85 years. Our results showed that our constant-block PLSC can detect weak structure–function relationships and has better robustness to noise. In fact, it adequately unearthed the true simulated number of significant and more accurate latent variables for the simulated data and more meaningful LVs for the real data, with covariance improvement from 16.19 to 41.48% (simulated) and 13.29–53.68% (real data), respectively. More interestingly in the real data analysis, our method identified simultaneously the well-known brain networks such as the default mode, sensorimotor, auditory, and dorsal attention networks both functionally and structurally, implying the hubs we derived from gray matter volumes are the basis of brain function, supporting diverse functions. Constant-block PLSC is a feasible tool for analyzing the brain structure–function relationship.
Tài liệu tham khảo
Altan A, Karasu S (2020) Recognition of COVID-19 disease from X-ray images by hybrid model consisting of 2D curvelet transform, chaotic salp swarm algorithm and deep learning technique. Chaos Solitons Fractals 140:1–10
Aydin S (2022) Cross-validated adaboost classification of emotion regulation strategies identified by spectral coherence in resting-state. Neuroinformatics 20(3):627–639
Aydın S, Çetin FH, Uytun MÇ, Babadaği Z, Güven AS, Işık Y (2022) Comparison of domain specific connectivity metrics for estimation brain network indices in boys with ADHD-C. Biomed Signal Process Control 76:1–10
Baecker L, Garcia-Dias R, Vieira S, Scarpazza C, Mechelli A (2021) Machine learning for brain age prediction: Introduction to methods and clinical applications. EBioMedicine 72:1–9
Bajic D, Craig MM, Mongerson CRL, Borsook D, Becerra L (2017) Identifying rodent resting-state brain networks with independent component analysis. Front Neurosci 11:1–24
Breakspear M (2017) Dynamic models of large-scale brain activity. Nat Neurosci 20(3):340–352
Calhoun VD, Sui J (2016) Multimodal fusion of brain imaging data: a key to finding the missing link(s) in complex mental illness. Biol Psychiatry Cogn Neurosci Neuroimag 1(3):230–244
Campbell KL, Grigg O, Saverino C, Churchill N, Grady CL (2013) Age differences in the intrinsic functional connectivity of default network subsystems. Front Aging Neurosci 5:1–12
Cao M, Wang JH, Dai ZJ, Cao XY (2014) Topological organization of the human brain functional connectome across the lifespan. Dev Cogn Neurosci 7:76–93
Chen K, Reiman EM, Huan Z, Caselli RJ, Bandy D, Ayutyanont N et al (2009) Linking functional and structural brain images with multivariate network analyses: a novel application of the partial least square method. Neuroimage 47(2):602–610
Crofts JJ, Higham DJ (2009) A weighted communicability measure applied to complex brain networks. J R Soc Interface 6(33):411–414
Damoiseaux JS (2017) Effects of aging on functional and structural brain connectivity. Neuroimage 160:32–40
Deco G, Jirsa V, McIntoshe AR (2009) Key role of coupling, delay, and noise in resting brain fluctuations. Proc Natl Acad Sci 106(29):12207–12208
Deligianni F, Carmichael DW, Zhang GH, Clark CA, Clayden JD (2016) NODDI and tensor-based microstructural indices as predictors of functional connectivity. PLoS ONE 11(4):1–17
DuPre E, Spreng RN (2017) Structural covariance networks across the lifespan, from 6–94 years of age. Neuroscience 1(3):302–323
Erhardt EB, Allen EA, Wei Y, Eichele T, Calhoun VD (2012) SimTB, a simulation toolbox for fMRI data under a model of spatiotemporal separability. Neuroimage 59(4):4160–4167
Goni J, van den Heuvel MP, Avena-Koenigsberger A (2013) Resting-brain functional connectivity predicted by analytic measures of network communication. Proc Natl Acad Sci 111(2):833–838
Graham D, Rockmore D (2011) The Packet Switching Brain. J Cogn Neurosci 23(2):267–276
Grigg O, Grady CL (2010a) The default network and processing of personally relevant information: converging evidence from task-related modulations and functional connectivity. Neuropsychologia 48(13):3815–3823
Grigg O, Grady CL (2010b) Task-related effects on the temporal and spatial dynamics of resting-state functional connectivity in the default network. PLoS ONE 5(10):1–12
Gudbjartsson H, Patz S (1995) The Rician distribution of noisy MRI data. Magn Reson Med 34(6):1–15
Haimovici A, Tagliazucchi E, Balenzuela P, Chialvo DR (2013) Brain organization into resting state networks emerges at criticality on a model of the human connectome. Phys Rev Lett 110:1–4
Hansen ECA, Battaglia D, Spiegler A (2014) Functional connectivity dynamics: modeling the switching behavior of the resting state. Neuroimage 1:1–11
Hervé Abdi, Williams LJ (2012) Partial least squares methods: partial least squares correlation and partial least square regression. Methods Mol Biol 930(1):549–579
van den Heuvel MP, Sporns O (2011) Rich-club organization of the human connectome. J Neurosci 2:15775–15786
van den Heuvel MP, Sporns O (2013) Network hubs in the human brain. Trends Cogn Sci 17(12):683–696
Honey CJ, Kötter R, Breakspear M (2007) Network structure of cerebral cortex shapes functional connectivity on multiple time scales-PNAS. PNAS 104(24):10240–10245
Keshavamurthy R, Dixon S, Pazdernik KT, Charles LE (2022) Predicting infectious disease for biopreparedness and response: a systematic review of machine learning and deep learning approaches. One Health 15:1–13
Krishnan A, Williams LJ, McIntosh AR, Abdi H (2011) Partial Least Squares (PLS) methods for neuroimaging: a tutorial and review. Neuroimage 56(2):455–475
Levakov G, Rosenthal G, Shelef I, Raviv TR, Avidan G (2020) From a deep learning model back to the brain-Identifying regional predictors and their relation to aging. Hum Brain Mapp 41(12):3235–3252
Liu K, Yao S, Chen K, Zhang J, Yao L, Li K et al (2017) Structural brain network changes across the adult lifespan. Front Aging Neurosci 9:1–10
Marstaller L, Williams M, Rich A, Savage G, Burianova H (2015) Aging and large-scale functional networks: white matter integrity, gray matter volume, and functional connectivity in the resting state. Neuroscience 290(2015):369–378
McIntosh AR, Chau WK, Protzner AB (2004) Spatiotemporal analysis of event-related fMRI data using partial least squares. Neuroimage 23(2):764–775
McIntosh AR, Lobaugh NJ (2004a) Partial least squares analysis of neuroimaging data: applications and advances. Neuroimage 23(2004):250–263
McIntosh AR, Lobaugh NJ (2004b) Partial least squares analysis of neuroimaging data: applications and advances. Neuroimage 23:250–263
Meskaldjia D-E, Pretia MG, Boltona TA (2016) Prediction of long-term memory scores in MCI based on resting-state fMRI. NeuroImage: Clin 12(2016):785–795.
Messe A, Rudrauf D, Benali H (2014) Relating structure and function in the human brain: relative contributions of anatomy, stationary dynamics, and non-stationarities. PLoS Comput Biol 10(3):1–9
Misic B, Betzel RF, Nematzadeh A (2015) Cooperative and competitive spreading dynamics on the human connectome. Neuron 86(6):1518–1529
Misic B, Betzel RF, de Reus MA, van den Heuvel MP, Berman MG, McIntosh AR et al (2016) Network-level structure-function relationships in human neocortex. Cereb Cortex 26(7):3285–3296
Neudorf J, Kress S, Borowsky R (2022) Structure can predict function in the human brain: a graph neural network deep learning model of functional connectivity and centrality based on structural connectivity. Brain Struct Funct 227(1):331–343
Nooner KB, Colcombe SJ, Tobe RH, Mennes M, Benedict MM, Moreno AL et al (2012) The NKI-Rockland sample: a model for accelerating the pace of discovery science in psychiatry. Front Neurosci 6:1–11
Park HJ, Friston K (2013) Structural and functional brain networks: from connections to cognition. Science 342(6158):579–586
Ponce-Alvarez A, Deco G, Hagmann P (2015) Resting-state temporal synchronization networks emerge from connectivity topology and heterogeneity. PLoS Comput Biol 11(2):1–23
Ren C, Kim D-K, Jeong D (2020) A survey of deep learning in agriculture techniques and their applications. J Inform Process Syst 16:1015–1033
Van Roon P, Zakizadeh J, Chartier S (2014) Partial least squares tutorial for analyzing neuroimaging data. Quant Methods Psychol 10(2):200–215
Rosenthal G, Vasa F, Griffa A, Hagmann P, Amico E, Goni J et al (2018) Mapping higher-order relations between brain structure and function with embedded vector representations of connectomes. Nat Commun 9(1):1–12
Sanz-Leon P, Knock SA, Spiegler A, Jirsa VK (2015) Mathematical framework for large-scale brain network modeling in The Virtual Brain. Neuroimage 111(2):385–430
Sarwar T, Tian Y, Yeo BTT, Ramamohanarao K, Zalesky A (2021) Structure-function coupling in the human connectome: a machine learning approach. Neuroimage 226:1–11
Segall JM, Allen EA, Jung RE, Erhardt EB, Arja SK, Kiehl K et al (2012) Correspondence between structure and function in the human brain at rest. Front Neuroinform 6(10):1–17
Shaw DJ, Marecek R, Grosbras MH, Leonard G, Pike GB, Paus T (2016) Co-ordinated structural and functional covariance in the adolescent brain underlies face processing performance. Soc Cogn Affect Neurosci 11(4):556–568
Spreng RN, Turner GR (2013) Structural covariance of the default network in healthy and pathological aging. J Neurosci 33(38):15226–15234
Stephen JM, Coffman BA, Jung RE, Bustillo JR, Aine CJ, Calhoun VD (2013) Using joint ICA to link function and structure using MEG and DTI in schizophrenia. Neuroimage 83:418–430
Straathof M, Sinke MR (2019) A systematic review on the quantitative relationship between structural and functional network connectivity strength in mammalian brains. J Cereb Blood Flow Metab 39(2):189–209
Suarez LE, Markello RD, Betzel RF, Misic B (2020) Linking structure and function in macroscale brain networks. Trends Cogn Sci 24(4):302–315
Sui J, Huster R, Yu Q, Segall JM, Calhoun VD (2014) Function-structure associations of the brain: evidence from multimodal connectivity and covariance studies. Neuroimage 102(2014):11–23
Wang Z, Dai Z, Gong G, Zhou C, He Y (2015) Understanding structural-functional relationships in the human brain: a large-scale network perspective. Neuroscientist 21(3):290–305
Wang X, Lin Q, Xia M, He Y (2018) Differentially categorized structural brain hubs are involved in different microstructural, functional, and cognitive characteristics and contribute to individual identification. Hum Brain Mapp 39(4):1647–1663
Yan CG, Cheung B, Kelly C, Colcombe S, Craddock RC, Di Martino A et al (2013) A comprehensive assessment of regional variation in the impact of head micromovements on functional connectomics. Neuroimage 76(1):183–201
Yağ İ, Altan A (2022) Artificial intelligence-based robust hybrid algorithm design and implementation for real-time detection of plant diseases in agricultural environments. Biology 11(12):1–30
Zhang L, Wang M, Liu M, Zhang D (2020) A survey on deep learning for neuroimaging-based brain disorder analysis. Front Neurosci 14:779
Zhang C, Yao L, Song S, Wen X, Zhao X, Long Z (2018) Euler elastica regularized logistic regression for whole-brain decoding of fMRI data. IEEE Trans Biomed Eng 65(7):1639–1653
Zhao X, Kewei Chen L (2019) Changes in the functional and structural default mode network across the adult lifespan based on partial least squares. IEEE Access 7:82256–82265
Zhao X, Yao LI, Chen K, Li KE, Zhang J, Guo X (2019) Changes in the functional and structural default mode network across the adult lifespan based on partial least squares. IEEE Access 7:82256–82265
Zhuang X, Yang Z, Cordes D (2020) A technical review of canonical correlation analysis for neuroscience applications. Hum Brain Mapp 41(13):3807–3833
Zimmermann J, Ritter P, Shen K (2016) Structural architecture supports functional organization in the human aging brain at a regionwise and network level. Hum Brain Mapp 37:2645–2661