Clustering the Brain With “CluB”: A New Toolbox for Quantitative Meta-Analysis of Neuroimaging Data

In this paper we describe and validate a new coordinate-based method for meta-analysis of neuroimaging data based on an optimized hierarchical clustering algorithm: CluB (Clustering the Brain). The CluB toolbox permits both to extract a set of spatially coherent clusters of activations from a database of stereotactic coordinates, and to explore each single cluster of activation for its composition according to the cognitive dimensions of interest. This last step, called “cluster composition analysis,” permits to explore neurocognitive effects by adopting a factorial-design logic and by testing the working hypotheses using either asymptotic tests, or exact tests either in a classic inference, or in a Bayesian-like context. To perform our validation study, we selected the fMRI data from 24 normal controls involved in a reading task. We run a standard random-effects second level group analysis to obtain a “Gold Standard” of reference. In a second step, the subject-specific reading effects (i.e., the linear t-contrast “reading > baseline”) were extracted to obtain a coordinates-based database that was used to run a meta-analysis using both CluB and the popular Activation Likelihood Estimation method implemented in the software GingerALE. The results of the two meta-analyses were compared against the “Gold Standard” to compute performance measures, i.e., sensitivity, specificity, and accuracy. The GingerALE method obtained a high level of accuracy (0.967) associated with a high sensitivity (0.728) and specificity (0.971). The CluB method obtained a similar level of accuracy (0.956) and specificity (0.969), notwithstanding a lower level of sensitivity (0.14) due to the lack of prior Gaussian transformation of the data. Finally, the two methods obtained a good-level of concordance (AC1 = 0.93). These results suggested that methods based on hierarchical clustering (and post-hoc statistics) and methods requiring prior Gaussian transformation of the data can be used as complementary tools, with the GingerALE method being optimal for neurofunctional mapping of pooled data according to simpler designs, and the CluB method being preferable to test more specific, and localized, neurocognitive hypotheses according to factorial designs.

[1]  Anil K. Jain,et al.  Data clustering: a review , 1999, CSUR.

[2]  Mark W. Woolrich,et al.  Using Gaussian-Process Regression for Meta-Analytic Neuroimaging Inference Based on Sparse Observations , 2011, IEEE Transactions on Medical Imaging.

[3]  R. Cabeza,et al.  Neural bases of learning and memory: functional neuroimaging evidence , 2000, Current opinion in neurology.

[4]  M A Just,et al.  Modeling the mind: very-high-field functional magnetic resonance imaging activation during cognition. , 1999, Topics in magnetic resonance imaging : TMRI.

[5]  I. Johnsrude,et al.  The problem of functional localization in the human brain , 2002, Nature Reviews Neuroscience.

[6]  J. H. Ward Hierarchical Grouping to Optimize an Objective Function , 1963 .

[7]  R. Seitz,et al.  Diversity of the inferior frontal gyrus—A meta-analysis of neuroimaging studies , 2011, Behavioural Brain Research.

[8]  Ronald L. Graham,et al.  On the History of the Minimum Spanning Tree Problem , 1985, Annals of the History of Computing.

[9]  B. Biswal,et al.  The resting brain: unconstrained yet reliable. , 2009, Cerebral cortex.

[10]  Michael Peacock,et al.  Hierarchical Clustering Analysis of Tissue Microarray Immunostaining Data Identifies Prognostically Significant Groups of Breast Carcinoma , 2004, Clinical Cancer Research.

[11]  Simon B Eickhoff,et al.  Minimizing within‐experiment and within‐group effects in activation likelihood estimation meta‐analyses , 2012, Human brain mapping.

[12]  R. J. Zatorre,et al.  PET Studies of Phonological Processing: A Critical Reply to Poeppel , 1996, Brain and Language.

[13]  John Quackenbush,et al.  Genesis: cluster analysis of microarray data , 2002, Bioinform..

[14]  Dietmar Cordes,et al.  Hierarchical clustering to measure connectivity in fMRI resting-state data. , 2002, Magnetic resonance imaging.

[15]  Kevin Murphy,et al.  An empirical investigation into the number of subjects required for an event-related fMRI study , 2004, NeuroImage.

[16]  G. Fornara,et al.  A neuroanatomical account of mental time travelling in schizophrenia: A meta-analysis of functional and structural neuroimaging data , 2017, Neuroscience & Biobehavioral Reviews.

[17]  Thomas E. Nichols,et al.  Minimal Data Needed for Valid & Accurate Image-Based fMRI Meta-Analysis , 2016, bioRxiv.

[18]  Giorgio Valentini,et al.  A Novel Approach to the Problem of Non-uniqueness of the Solution in Hierarchical Clustering , 2013, IEEE Transactions on Neural Networks and Learning Systems.

[19]  R. Baumgartner,et al.  Ranking fMRI Time Courses by Minimum Spanning Trees: Assessing Coactivation in fMRI , 2001, NeuroImage.

[20]  Angela R. Laird,et al.  Ten simple rules for neuroimaging meta-analysis , 2018, Neuroscience & Biobehavioral Reviews.

[21]  G Jobard,et al.  Evaluation of the dual route theory of reading: a metanalysis of 35 neuroimaging studies , 2003, NeuroImage.

[22]  P. Scheltens,et al.  Research criteria for the diagnosis of Alzheimer's disease: revising the NINCDS–ADRDA criteria , 2007, The Lancet Neurology.

[23]  E. Paulesu,et al.  Reading the dyslexic brain: multiple dysfunctional routes revealed by a new meta-analysis of PET and fMRI activation studies , 2014, Front. Hum. Neurosci..

[24]  N. A. Borghese,et al.  How many deficits in the same dyslexic brains? A behavioural and fMRI assessment of comorbidity in adult dyslexics , 2017, Cortex.

[25]  N. A. Borghese,et al.  Clustering the lexicon in the brain: a meta-analysis of the neurofunctional evidence on noun and verb processing , 2013, Front. Hum. Neurosci..

[26]  A. Meyer-Lindenberg,et al.  Multimodal meta-analysis of structural and functional brain changes in first episode psychosis and the effects of antipsychotic medication , 2012, Neuroscience & Biobehavioral Reviews.

[27]  E. Paulesu,et al.  Hungry brains: A meta-analytical review of brain activation imaging studies on food perception and appetite in obese individuals , 2018, Neuroscience & Biobehavioral Reviews.

[28]  Stephen M. Smith,et al.  Meta-analysis of neuroimaging data: A comparison of image-based and coordinate-based pooling of studies , 2009, NeuroImage.

[29]  Guinevere F. Eden,et al.  Meta-Analysis of the Functional Neuroanatomy of Single-Word Reading: Method and Validation , 2002, NeuroImage.

[30]  William A. Cunningham,et al.  Type I and Type II error concerns in fMRI research: re-balancing the scale. , 2009, Social cognitive and affective neuroscience.

[31]  Sergi G. Costafreda,et al.  Pooling fMRI Data: Meta-Analysis, Mega-Analysis and Multi-Center Studies , 2009, Front. Neuroinform..

[32]  Fatos T. Yarman-Vural,et al.  Cognitive process representation with minimum spanning tree of local meshes , 2013, 2013 21st Signal Processing and Communications Applications Conference (SIU).

[33]  L. K. Hansen,et al.  Feature‐space clustering for fMRI meta‐analysis , 2001, Human brain mapping.

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

[35]  Fatos T. Yarman-Vural,et al.  Representation of cognitive processes using the minimum spanning tree of local meshes , 2013, 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC).

[36]  Kilem Gwet Computing Inter-Rater Reliability With the SAS System Kilem Gwet , Ph . D . Sr , 2002 .

[37]  J. Morris,et al.  The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer's disease , 2011, Alzheimer's & Dementia.

[38]  W. Heiser,et al.  Instability of hierarchical cluster analysis due to input order of the data: the PermuCLUSTER solution. , 2005, Psychological methods.

[39]  Eraldo Paulesu,et al.  Reading the reading brain: A new meta-analysis of functional imaging data on reading , 2013, Journal of Neurolinguistics.

[40]  Matthew L Senjem,et al.  Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study. , 2009, Brain : a journal of neurology.

[41]  C. Rorden,et al.  Stereotaxic display of brain lesions. , 2000, Behavioural neurology.

[42]  Giuseppe Scialfa,et al.  Nouns and verbs in the brain: Grammatical class and task specific effects as revealed by fMRI , 2008, Cognitive neuropsychology.

[43]  Rui Xu,et al.  Survey of clustering algorithms , 2005, IEEE Transactions on Neural Networks.

[44]  J. Ioannidis,et al.  Potential Reporting Bias in fMRI Studies of the Brain , 2013, PloS one.

[45]  M. Lindquist,et al.  Meta-analysis of functional neuroimaging data: current and future directions. , 2007, Social cognitive and affective neuroscience.

[46]  E. Paulesu,et al.  The What, the When, and the Whether of Intentional Action in the Brain: A Meta-Analytical Review , 2017, Front. Hum. Neurosci..

[47]  Karimnagar Salim Jiwani,et al.  A Survey on clustering , 2010 .

[48]  K. Zilles,et al.  Coordinate‐based activation likelihood estimation meta‐analysis of neuroimaging data: A random‐effects approach based on empirical estimates of spatial uncertainty , 2009, Human brain mapping.

[49]  E. Bullmore,et al.  Neurophysiological architecture of functional magnetic resonance images of human brain. , 2005, Cerebral cortex.