Understanding psychophysiological interaction and its relations to beta series correlation

Psychophysiological interaction (PPI) was proposed 20 years ago for study of task modulated connectivity on functional MRI (fMRI) data. A few modifications have since been made, but there remain misunderstandings on the method, as well as on its relations to a similar method named beta series correlation (BSC). Here, we explain what PPI measures and its relations to BSC. We first clarify that the interpretation of a regressor in a general linear model depends on not only itself but also on how other effects are modeled. In terms of PPI, it always reflects differences in connectivity between conditions, when the physiological variable is included as a covariate. Secondly, when there are multiple conditions, we explain how PPI models calculated from direct contrast between conditions could generate identical results as contrasting separate PPIs of each condition (a.k.a. “generalized” PPI). Thirdly, we explicit the deconvolution process that is used for PPI calculation, and how is it related to the trial-by-trial modeling for BSC, and illustrate the relations between PPI and those based upon BSC. In particular, when context sensitive changes in effective connectivity are present, they manifest as changes in correlations of observed trial-by-trial activations or functional connectivity. Therefore, BSC and PPI can detect similar connectivity differences. Lastly, we report empirical analyses using PPI and BSC on fMRI data of an event-related stop signal task to illustrate our points.

[1]  Xin Di,et al.  Toward Task Connectomics: Examining Whole-Brain Task Modulated Connectivity in Different Task Domains , 2018, Cerebral cortex.

[2]  Sterling C. Johnson,et al.  A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches , 2012, NeuroImage.

[3]  Krzysztof J. Gorgolewski,et al.  A phenome-wide examination of neural and cognitive function , 2016, Scientific Data.

[4]  Hans-Jochen Heinze,et al.  Richness in Functional Connectivity Depends on the Neuronal Integrity within the Posterior Cingulate Cortex , 2017, Front. Neurosci..

[5]  Jonathan D. Power,et al.  Intrinsic and Task-Evoked Network Architectures of the Human Brain , 2014, Neuron.

[6]  Yong He,et al.  BrainNet Viewer: A Network Visualization Tool for Human Brain Connectomics , 2013, PloS one.

[7]  Merel Kindt,et al.  Quantifying learning-dependent changes in the brain: Single-trial multivoxel pattern analysis requires slow event-related fMRI. , 2016, Psychophysiology.

[8]  R. Turner,et al.  Event-Related fMRI: Characterizing Differential Responses , 1998, NeuroImage.

[9]  Christian Windischberger,et al.  Toward discovery science of human brain function , 2010, Proceedings of the National Academy of Sciences.

[10]  Karl J. Friston,et al.  Modeling regional and psychophysiologic interactions in fMRI: the importance of hemodynamic deconvolution , 2003, NeuroImage.

[11]  Karl J. Friston,et al.  Structural and Functional Brain Networks: From Connections to Cognition , 2013, Science.

[12]  Michael Eickenberg,et al.  Data-driven HRF estimation for encoding and decoding models , 2014, NeuroImage.

[13]  Rupert Lanzenberger,et al.  Correlations and anticorrelations in resting-state functional connectivity MRI: A quantitative comparison of preprocessing strategies , 2009, NeuroImage.

[14]  Karl J. Friston Functional and Effective Connectivity: A Review , 2011, Brain Connect..

[15]  Keith Bush,et al.  A comparison of statistical methods for detecting context-modulated functional connectivity in fMRI , 2014, NeuroImage.

[16]  Karl J. Friston Functional and effective connectivity in neuroimaging: A synthesis , 1994 .

[17]  O Sporns,et al.  Predicting human resting-state functional connectivity from structural connectivity , 2009, Proceedings of the National Academy of Sciences.

[18]  Mark W. Woolrich,et al.  Disambiguating brain functional connectivity , 2017, NeuroImage.

[19]  Karl J. Friston,et al.  The prefrontal cortex shows context-specific changes in effective connectivity to motor or visual cortex during the selection of action or colour. , 2004, Cerebral cortex.

[20]  Richard N. A. Henson,et al.  Effect of trial-to-trial variability on optimal event-related fMRI design: Implications for Beta-series correlation and multi-voxel pattern analysis , 2016, NeuroImage.

[21]  Xin Di,et al.  Imperfect (de)convolution may introduce spurious psychophysiological interactions and how to avoid it , 2017, Human brain mapping.

[22]  Karl J. Friston,et al.  Psychophysiological and Modulatory Interactions in Neuroimaging , 1997, NeuroImage.

[23]  Bharat B. Biswal,et al.  Psychophysiological Interactions in a Visual Checkerboard Task: Reproducibility, Reliability, and the Effects of Deconvolution , 2017, bioRxiv.

[24]  Russell A. Poldrack,et al.  The impact of study design on pattern estimation for single-trial multivariate pattern analysis , 2014, NeuroImage.

[25]  A M Dale,et al.  Optimal experimental design for event‐related fMRI , 1999, Human brain mapping.

[26]  B. Biswal,et al.  Functional connectivity in the motor cortex of resting human brain using echo‐planar mri , 1995, Magnetic resonance in medicine.

[27]  Vince D. Calhoun,et al.  Dynamic modeling of neuronal responses in fMRI using cubature Kalman filtering , 2011, NeuroImage.

[28]  E. Hillman Coupling mechanism and significance of the BOLD signal: a status report. , 2014, Annual review of neuroscience.

[29]  Bharat B. Biswal,et al.  Competition between functional brain networks mediates behavioral variability , 2008, NeuroImage.

[30]  Bharat B. Biswal,et al.  Identifying the default mode network structure using dynamic causal modeling on resting-state functional magnetic resonance imaging , 2014, NeuroImage.

[31]  Timothy E. J. Behrens,et al.  Tools of the trade: psychophysiological interactions and functional connectivity. , 2012, Social cognitive and affective neuroscience.

[32]  Adam Gazzaley,et al.  Measuring functional connectivity during distinct stages of a cognitive task , 2004, NeuroImage.

[33]  Mark D'Esposito,et al.  Variation of BOLD hemodynamic responses across subjects and brain regions and their effects on statistical analyses , 2004, NeuroImage.

[34]  Russell A. Poldrack,et al.  Deconvolving BOLD activation in event-related designs for multivoxel pattern classification analyses , 2012, NeuroImage.

[35]  Mert R. Sabuncu,et al.  The influence of head motion on intrinsic functional connectivity MRI , 2012, NeuroImage.

[36]  Dinesh K. Sivakolundu,et al.  Reduced arterial compliance along the cerebrovascular tree predicts cognitive slowing in multiple sclerosis: Evidence for a neurovascular uncoupling hypothesis , 2019, Multiple sclerosis.

[37]  Abraham Z. Snyder,et al.  Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion , 2012, NeuroImage.