Two step Gaussian mixture model approach to characterize white matter disease based on distributional changes

- Analyses focused on mean intensity fail to detect deviation in higher order moments by risk factors.
- A two-step Gaussian mixture model approach was proposed to meet such a limitation in current imaging data analysis.
- Aging-related FA change was found in mean, variance, skewness, and kurtosis.

BackgroundMagnetic resonance imaging reveals macro- and microstructural correlates of neurodegeneration, which are often assessed using voxel-by-voxel t-tests for comparing mean image intensities measured by fractional anisotropy (FA) between cases and controls or regression analysis for associating mean intensity with putative risk factors. This analytic strategy focusing on mean intensity in individual voxels, however, fails to account for change in distribution of image intensities due to disease.New methodWe propose a method that aims to facilitate simple and clear characterization of underlying distribution. Our method consists of two steps: subject-level (Step 1) and group-level or a specific risk-level density function estimation across subjects (Step 2).ResultsThe proposed method was demonstrated with a simulated data set and real FA data sets from two white matter tracts, where the proposed method successfully detected any departure of the FA distribution from the normal state by disease: p < 0.001 for simulated data; p = 0.047 for the posterior limb of internal capsule; p = 0.06 for the posterior thalamic radiation.Comparison with existing method(s)The proposed method found significant disease effect (p < 0.001) while conventional 2-group t-test focused only on mean intensity did not (p = 0.61) in a simulation study. While significant age effects were found for each white matter tract from conventional linear model analysis with real FA data, the proposed method further confirmed that aging also triggers distribution-wide change.ConclusionOur proposed method is powerful for detection of risk factors associated with any type of microstructural neurodegenerations with brain imaging data.