Abstract

Spatial patterns of radiotracer binding in positron emission tomography (PET) images may convey information related to the disease topology. However, this information is not captured by the standard PET image analysis that quantifies the mean radiotracer uptake within a region of interest (ROI). On the other hand, spatial analyses that use more advanced radiomic features may be difficult to interpret. Here we propose an alternative data-driven, voxel-based approach to spatial pattern analysis in brain PET, which can be easily interpreted. We apply principal component analysis (PCA) to identify voxel covariance patterns, and optimally combine several patterns using the least absolute shrinkage and selection operator (LASSO). The resulting models predict clinical disease metrics from raw voxel values, allowing for inclusion of clinical covariates. The analysis is performed on high-resolution PET images from healthy controls and subjects affected by Parkinson’s disease (PD), acquired with a pre-synaptic and a post-synaptic dopaminergic PET tracer. We demonstrate that PCA identifies robust and tracer-specific binding patterns in sub-cortical brain structures; the patterns evolve as a function of disease progression. Principal component LASSO (PC-LASSO) models of clinical disease metrics achieve higher predictive accuracy compared to the mean tracer binding ratio (BR) alone: the cross-validated test mean squared error of adjusted disease duration (motor impairment score) was 16.3 ± 0.17 years2 (9.7 ± 0.15) with mean BR, versus 14.4 ± 0.18 years2 (8.9 ± 0.16) with PC-LASSO. We interpret the best-performing PC-LASSO models in the spatial sense and discuss them with reference to the PD pathology and somatotopic organization of the striatum. PC-LASSO is thus shown to be a useful method to analyze clinically-relevant tracer binding patterns, and to construct interpretable, imaging-based predictive models of clinical metrics.

Highlights

  • Pathological processes associated with neurological disorders often develop in distinct spatiotemporal patterns

  • We examined in detail three fitted DTBZ principal components (PCs)-least absolute shrinkage and selection operator (LASSO) models with lower MSEtest compared to that of the mean binding ratio (BR) and constant models: 1. adjusted DD (aDD) predicted from the better-side PC 1, 3, and 4 scores in the putamen

  • We applied PC-LASSO to the analysis of dopaminergic positron emission tomography (PET) tracer binding in the striatum of Parkinson’s disease (PD) subjects

Read more

Summary

Introduction

Pathological processes associated with neurological disorders often develop in distinct spatiotemporal patterns. Traditional quantitative PET and SPECT image analysis metrics, such as the standardized uptake value (SUV) and non-displaceable binding potential (BPND), are often evaluated as averages over a specific region of interest (ROI). This approach neglects the spatial distribution of radiotracer binding, which may be affected by disease within the ROIs. There is a growing realization that better methods of spatial image analysis are needed to achieve a more complete disease characterization and to improve prediction and tracking of disease progression [1,2,3]. The features are used as inputs to one of the established machine learning models (neural nets, decision forests, etc.) to predict clinical measures of interest [12,13,14]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call