Abstract
An increasing number of neuroimaging studies are based on either combining more than one data modality (inter-modal) or combining more than one measurement from the same modality (intra-modal). To date, most intra-modal studies using multivariate statistics have focused on differences between datasets, for instance relying on classifiers to differentiate between effects in the data. However, to fully characterize these effects, multivariate methods able to measure similarities between datasets are needed. One classical technique for estimating the relationship between two datasets is canonical correlation analysis (CCA). However, in the context of high-dimensional data the application of CCA is extremely challenging. A recent extension of CCA, sparse CCA (SCCA), overcomes this limitation, by regularizing the model parameters while yielding a sparse solution. In this work, we modify SCCA with the aim of facilitating its application to high-dimensional neuroimaging data and finding meaningful multivariate image-to-image correspondences in intra-modal studies. In particular, we show how the optimal subset of variables can be estimated independently and we look at the information encoded in more than one set of SCCA transformations. We illustrate our framework using Arterial Spin Labeling data to investigate multivariate similarities between the effects of two antipsychotic drugs on cerebral blood flow.
Highlights
Acquiring multiple neuroimaging datasets from the same subject is becoming common practice (Sui et al, 2012)
Several studies have employed Blood Oxygen-Level Dependent (BOLD)-fMRI for this purpose based on brain activity patterns derived from participants performing a working memory task (Marquand et al, 2011), on functional connectivity based on resting fMRI (Sripada et al, 2013) or in response to drug infusion (Doyle et al, 2013a)
This study focused on univariate differences between the effects of two antipsychotic drugs on resting cerebral blood flow in the human brain
Summary
Acquiring multiple neuroimaging datasets from the same subject is becoming common practice (Sui et al, 2012). In the context of pharmacological studies using functional Magnetic Resonance Imaging (phMRI), which commonly employ repeated-measures (i.e., intra-modal) designs, multivariate analyses have exclusively focused on discriminating the distributed effects of different drug interventions. Other studies have used Arterial Spin Labeling (ASL) to discriminate the effects of different drugs on regional cerebral blood flow (rCBF) (Chen et al, 2011; Marquand et al, 2012; Doyle et al, 2013b; Paloyelis et al, 2014). This approach offers the advantage over BOLD that the derived measures are quantitative and can be readily compared between scanning sessions
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