Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data

  • Spetsieris P
  • Ma Y
  • Peng S
 et al. 
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Abstract

The scaled subprofile model (SSM) 1-4 is a multivariate PCA-based algorithm that identifies major sources of variation in patient and control group brain image data while rejecting lesser components (Figure 1). Applied directly to voxel-by-voxel covariance data of steady-state multimodality images, an entire group image set can be reduced to a few significant linearly independent covariance patterns and corresponding subject scores. Each pattern, termed a group invariant subprofile (GIS), is an orthogonal principal component that represents a spatially distributed network of functionally interrelated brain regions. Large global mean scalar effects that can obscure smaller network-specific contributions are removed by the inherent logarithmic conversion and mean centering of the data 2,5,6 . Subjects express each of these patterns to a variable degree represented by a simple scalar score that can correlate with independent clinical or psychometric descriptors 7,8 . Using logistic regression analysis of subject scores (i.e. pattern expression values), linear coefficients can be derived to combine multiple principal components into single disease-related spatial covariance patterns, i.e. composite networks with improved discrimination of patients from healthy control subjects 5,6 . Cross-validation within the derivation set can be performed using bootstrap resampling techniques 9 . Forward validation is easily confirmed by direct score evaluation of the derived patterns in prospective datasets 10 . Once validated, disease-related patterns can be used to score individual patients with respect to a fixed reference sample, often the set of healthy subjects that was used (with the disease group) in the original pattern derivation 11 . These standardized values can in turn be used to assist in differential diagnosis 12,13 and to assess disease progression and treatment effects at the network level 7,14-16 . We present an example of the application of this methodology to FDG PET data of Parkinson's Disease patients and normal controls using our in-house software to derive a characteristic covariance pattern biomarker of disease.

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Authors

  • Phoebe Spetsieris

  • Yilong Ma

  • Shichun Peng

  • Ji Hyun Ko

  • Vijay Dhawan

  • Chris C. Tang

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