Challenges in measuring individual differences in functional connectivity using fMRI: The case of healthy aging

Many studies report individual differences in functional connectivity, such as those related to age. However, estimates of connectivity from fMRI are confounded by other factors, such as vascular health, head motion and changes in the location of functional regions. Here, we investigate the impact of these confounds, and pre‐processing strategies that can mitigate them, using data from the Cambridge Centre for Ageing & Neuroscience (www.cam-can.com). This dataset contained two sessions of resting‐state fMRI from 214 adults aged 18–88. Functional connectivity between all regions was strongly related to vascular health, most likely reflecting respiratory and cardiac signals. These variations in mean connectivity limit the validity of between‐participant comparisons of connectivity estimates, and were best mitigated by regression of mean connectivity over participants. We also showed that high‐pass filtering, instead of band‐pass filtering, produced stronger and more reliable age‐effects. Head motion was correlated with gray‐matter volume in selected brain regions, and with various cognitive measures, suggesting that it has a biological (trait) component, and warning against regressing out motion over participants. Finally, we showed that the location of functional regions was more variable in older adults, which was alleviated by smoothing the data, or using a multivariate measure of connectivity. These results demonstrate that analysis choices have a dramatic impact on connectivity differences between individuals, ultimately affecting the associations found between connectivity and cognition. It is important that fMRI connectivity studies address these issues, and we suggest a number of ways to optimize analysis choices. Hum Brain Mapp 38:4125–4156, 2017. © 2017 Wiley Periodicals, Inc.

[1]  Catie Chang,et al.  Corrigendum to “Mapping the end-tidal CO2 response function in the resting-state BOLD fMRI signal: Spatial specificity, test-retest reliability and effect of fMRI sampling rate.” , 2018, NeuroImage.

[2]  Timothy O. Laumann,et al.  Sources and implications of whole-brain fMRI signals in humans , 2017, NeuroImage.

[3]  Cam-CAN Group,et al.  The Cambridge Centre for Ageing and Neuroscience (Cam-CAN) data repository: Structural and functional MRI, MEG, and cognitive data from a cross-sectional adult lifespan sample , 2017, NeuroImage.

[4]  Simon B. Eickhoff,et al.  Resting-state test–retest reliability of a priori defined canonical networks over different preprocessing steps , 2017, Brain Structure and Function.

[5]  A. McIntosh,et al.  Aging Effects on Whole-Brain Functional Connectivity in Adults Free of Cognitive and Psychiatric Disorders. , 2016, Cerebral cortex.

[6]  Linda Geerligs,et al.  Functional connectivity and structural covariance between regions of interest can be measured more accurately using multivariate distance correlation , 2016, NeuroImage.

[7]  Stephen C. Strother,et al.  The association between cerebrovascular reactivity and resting-state fMRI functional connectivity in healthy adults: The influence of basal carbon dioxide , 2016, NeuroImage.

[8]  Timothy O. Laumann,et al.  Generation and Evaluation of a Cortical Area Parcellation from Resting-State Correlations. , 2016, Cerebral cortex.

[9]  Darren Price,et al.  Idiosyncratic responding during movie-watching predicted by age differences in attentional control , 2015, Neurobiology of Aging.

[10]  R. Buckner,et al.  Parcellating Cortical Functional Networks in Individuals , 2015, Nature Neuroscience.

[11]  Linda Geerligs,et al.  State and Trait Components of Functional Connectivity: Individual Differences Vary with Mental State , 2015, The Journal of Neuroscience.

[12]  Yong He,et al.  Identifying and Mapping Connectivity Patterns of Brain Network Hubs in Alzheimer's Disease. , 2015, Cerebral cortex.

[13]  Bernard Ng,et al.  Optimization of rs-fMRI Pre-processing for Enhanced Signal-Noise Separation, Test-Retest Reliability, and Group Discrimination , 2015, NeuroImage.

[14]  Y. Jeong,et al.  Influence of ROI selection on resting state functional connectivity: an individualized approach for resting state fMRI analysis , 2015, Front. Neurosci..

[15]  Erin L. Mazerolle,et al.  Metabolic and vascular origins of the BOLD effect: Implications for imaging pathology and resting‐state brain function , 2015, Journal of magnetic resonance imaging : JMRI.

[16]  N. Maurits,et al.  A Brain-Wide Study of Age-Related Changes in Functional Connectivity. , 2015, Cerebral cortex.

[17]  Kevin Murphy,et al.  Is fMRI “noise” really noise? Resting state nuisance regressors remove variance with network structure , 2015, NeuroImage.

[18]  Alberto Llera,et al.  ICA-AROMA: A robust ICA-based strategy for removing motion artifacts from fMRI data , 2015, NeuroImage.

[19]  James B. Rowe,et al.  The effect of ageing on fMRI: Correction for the confounding effects of vascular reactivity evaluated by joint fMRI and MEG in 335 adults , 2015, Human brain mapping.

[20]  M. Dylan Tisdall,et al.  Head motion during MRI acquisition reduces gray matter volume and thickness estimates , 2015, NeuroImage.

[21]  Gary H. Glover,et al.  BOLD fractional contribution to resting-state functional connectivity above 0.1Hz , 2015, NeuroImage.

[22]  Catie Chang,et al.  Mapping the end-tidal CO2 response function in the resting-state BOLD fMRI signal: Spatial specificity, test–retest reliability and effect of fMRI sampling rate , 2015, NeuroImage.

[23]  Leslie M. Loew,et al.  Computational neurobiology is a useful tool in translational neurology: the example of ataxia , 2014, Frontiers in Neuroscience.

[24]  Joaquín Goñi,et al.  Changes in structural and functional connectivity among resting-state networks across the human lifespan , 2014, NeuroImage.

[25]  Vince D. Calhoun,et al.  Impact of autocorrelation on functional connectivity , 2014, NeuroImage.

[26]  Denise C. Park,et al.  Decreased segregation of brain systems across the healthy adult lifespan , 2014, Proceedings of the National Academy of Sciences.

[27]  William D. Marslen-Wilson,et al.  The Cambridge Centre for Ageing and Neuroscience (Cam-CAN) study protocol: a cross-sectional, lifespan, multidisciplinary examination of healthy cognitive ageing , 2014, BMC Neurology.

[28]  Mary Beth Nebel,et al.  Reduction of motion-related artifacts in resting state fMRI using aCompCor , 2014, NeuroImage.

[29]  John Suckling,et al.  A wavelet method for modeling and despiking motion artifacts from resting-state fMRI time series , 2014, NeuroImage.

[30]  Timothy O. Laumann,et al.  An approach for parcellating human cortical areas using resting-state correlations , 2014, NeuroImage.

[31]  Ludovica Griffanti,et al.  Automatic denoising of functional MRI data: Combining independent component analysis and hierarchical fusion of classifiers , 2014, NeuroImage.

[32]  Roland N. Boubela,et al.  The Spectral Diversity of Resting-State Fluctuations in the Human Brain , 2014, PloS one.

[33]  D. Hu,et al.  Neurobiological basis of head motion in brain imaging , 2014, Proceedings of the National Academy of Sciences.

[34]  Linda Geerligs,et al.  Reduced specificity of functional connectivity in the aging brain during task performance , 2014, Human brain mapping.

[35]  John DeLuca,et al.  Functional magnetic resonance imaging movers and shakers: Does subject‐movement cause sampling bias? , 2014, Human brain mapping.

[36]  Timothy O. Laumann,et al.  Methods to detect, characterize, and remove motion artifact in resting state fMRI , 2014, NeuroImage.

[37]  Yong He,et al.  Topological organization of the human brain functional connectome across the lifespan , 2013, Developmental Cognitive Neuroscience.

[38]  R. Buckner The Cerebellum and Cognitive Function: 25 Years of Insight from Anatomy and Neuroimaging , 2013, Neuron.

[39]  Yufeng Zang,et al.  Standardizing the intrinsic brain: Towards robust measurement of inter-individual variation in 1000 functional connectomes , 2013, NeuroImage.

[40]  Kevin Murphy,et al.  Resting-state fMRI confounds and cleanup , 2013, NeuroImage.

[41]  Thomas T. Liu,et al.  Neurovascular factors in resting-state functional MRI , 2013, NeuroImage.

[42]  Hang Joon Jo,et al.  Correcting Brain-Wide Correlation Differences in Resting-State FMRI , 2013, Brain Connect..

[43]  David J. Madden,et al.  Functional brain connectivity and cognition: effects of adult age and task demands , 2013, Neurobiology of Aging.

[44]  R. Cameron Craddock,et al.  A comprehensive assessment of regional variation in the impact of head micromovements on functional connectomics , 2013, NeuroImage.

[45]  Roland N. Boubela,et al.  Beyond Noise: Using Temporal ICA to Extract Meaningful Information from High-Frequency fMRI Signal Fluctuations during Rest , 2013, Front. Hum. Neurosci..

[46]  Gábor J. Székely,et al.  The distance correlation t-test of independence in high dimension , 2013, J. Multivar. Anal..

[47]  P. Grant,et al.  Dopaminergic foundations of schizotypy as measured by the German version of the Oxford-Liverpool Inventory of Feelings and Experiences (O-LIFE)—a suitable endophenotype of schizophrenia , 2013, Front. Hum. Neurosci..

[48]  Simon B. Eickhoff,et al.  An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data , 2013, NeuroImage.

[49]  Shannon L Risacher,et al.  Altered default mode network connectivity in older adults with cognitive complaints and amnestic mild cognitive impairment. , 2013, Journal of Alzheimer's disease : JAD.

[50]  Wenjun Li,et al.  A method to determine the necessity for global signal regression in resting‐state fMRI studies , 2012, Magnetic resonance in medicine.

[51]  Masaki Ishihara,et al.  Decreased Functional Connectivity by Aging Is Associated with Cognitive Decline , 2012, Journal of Cognitive Neuroscience.

[52]  R Cameron Craddock,et al.  A whole brain fMRI atlas generated via spatially constrained spectral clustering , 2012, Human brain mapping.

[53]  Hans Knutsson,et al.  Does Parametric Fmri Analysis with Spm Yield Valid Results? -an Empirical Study of 1484 Rest Datasets Does Parametric Fmri Analysis with Spm Yield Valid Results? - an Empirical Study of 1484 Rest Datasets , 2022 .

[54]  Hang Joon Jo,et al.  Trouble at Rest: How Correlation Patterns and Group Differences Become Distorted After Global Signal Regression , 2012, Brain Connect..

[55]  Wen-Ming Luh,et al.  Differentiating BOLD and non-BOLD signals in fMRI time series using multi-echo EPI , 2012, NeuroImage.

[56]  Jeroen van der Grond,et al.  Imaging the default mode network in aging and dementia. , 2012, Biochimica et biophysica acta.

[57]  Mary E. Meyerand,et al.  Support vector machine classification and characterization of age-related reorganization of functional brain networks , 2012, NeuroImage.

[58]  Stephen M. Smith,et al.  Temporally-independent functional modes of spontaneous brain activity , 2012, Proceedings of the National Academy of Sciences.

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

[60]  Dost Öngür,et al.  Anticorrelations in resting state networks without global signal regression , 2012, NeuroImage.

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

[62]  Timothy O. Laumann,et al.  Functional Network Organization of the Human Brain , 2011, Neuron.

[63]  J. Pekar,et al.  On the relationship between seed‐based and ICA‐based measures of functional connectivity , 2011, Magnetic resonance in medicine.

[64]  Marisa O. Hollinshead,et al.  The organization of the human cerebral cortex estimated by intrinsic functional connectivity. , 2011, Journal of neurophysiology.

[65]  Christopher L. Asplund,et al.  The organization of the human cerebellum estimated by intrinsic functional connectivity. , 2011, Journal of neurophysiology.

[66]  Hang Joon Jo,et al.  Mapping sources of correlation in resting state FMRI, with artifact detection and removal , 2010, NeuroImage.

[67]  J. Callicott,et al.  Age-related alterations in default mode network: Impact on working memory performance , 2010, Neurobiology of Aging.

[68]  Usman Zulfiqar,et al.  Relation of high heart rate variability to healthy longevity. , 2010, The American journal of cardiology.

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

[70]  Raj N Kalarianure,et al.  Vascular basis for brain degeneration : faltering controls and risk factors for dementia , 2010 .

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

[72]  R. Varadhan,et al.  Frailty and impaired cardiac autonomic control: new insights from principal components aggregation of traditional heart rate variability indices. , 2009, The journals of gerontology. Series A, Biological sciences and medical sciences.

[73]  Sébastien Ourselin,et al.  Issues with threshold masking in voxel-based morphometry of atrophied brains , 2009, NeuroImage.

[74]  S. Rombouts,et al.  Reduced resting-state brain activity in the "default network" in normal aging. , 2008, Cerebral cortex.

[75]  N. Logothetis What we can do and what we cannot do with fMRI , 2008, Nature.

[76]  Justin L. Vincent,et al.  Disruption of Large-Scale Brain Systems in Advanced Aging , 2007, Neuron.

[77]  Maria L. Rizzo,et al.  Measuring and testing dependence by correlation of distances , 2007, 0803.4101.

[78]  Jeff H. Duyn,et al.  Low-frequency fluctuations in the cardiac rate as a source of variance in the resting-state fMRI BOLD signal , 2007, NeuroImage.

[79]  Thomas T. Liu,et al.  A component based noise correction method (CompCor) for BOLD and perfusion based fMRI , 2007, NeuroImage.

[80]  Naoki Tanaka,et al.  Quantitative evaluation of interrelations between spontaneous low-frequency oscillations in cerebral hemodynamics and systemic cardiovascular dynamics , 2006, NeuroImage.

[81]  Joydeep Ghosh,et al.  Cluster Ensembles --- A Knowledge Reuse Framework for Combining Multiple Partitions , 2002, J. Mach. Learn. Res..

[82]  Michael Brady,et al.  Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images , 2002, NeuroImage.

[83]  Karl J. Friston,et al.  Classical and Bayesian Inference in Neuroimaging: Applications , 2002, NeuroImage.

[84]  G H Glover,et al.  Image‐based method for retrospective correction of physiological motion effects in fMRI: RETROICOR , 2000, Magnetic resonance in medicine.

[85]  Karl J. Friston,et al.  Voxel-Based Morphometry—The Methods , 2000, NeuroImage.

[86]  M. D’Esposito,et al.  The Effect of Normal Aging on the Coupling of Neural Activity to the Bold Hemodynamic Response , 1999, NeuroImage.

[87]  M Malik,et al.  Changes in Heart Rate Variability with Age , 1996, Pacing and clinical electrophysiology : PACE.

[88]  A. Baddeley,et al.  The Spot-the-Word test: a robust estimate of verbal intelligence based on lexical decision. , 1993, The British journal of clinical psychology.

[89]  J. H. Steiger Tests for comparing elements of a correlation matrix. , 1980 .

[90]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.