voxel based morphometry with unified segmentation n.
Skip this Video
Loading SlideShow in 5 Seconds..
Voxel-Based Morphometry with Unified Segmentation PowerPoint Presentation
Download Presentation
Voxel-Based Morphometry with Unified Segmentation

Voxel-Based Morphometry with Unified Segmentation

510 Vues Download Presentation
Télécharger la présentation

Voxel-Based Morphometry with Unified Segmentation

- - - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript

  1. Voxel-Based Morphometry with Unified Segmentation Ged Ridgway Centre for Medical Image ComputingUniversity College London Thanks to: John Ashburner and the FIL Methods Group.

  2. Preprocessing in SPM • Realignment • With non-linear unwarping for EPI fMRI • Slice-time correction • Coregistration • Normalisation • Segmentation • Smoothing SPM8b’s unified tissue segmentation and spatial normalisation procedure But first, an introduction toComputational Neuroanatomy

  3. Aims of computational neuroanatomy • Many interesting and clinically important questions might relate to the shape or local size of regions of the brain • For example, whether (and where) local patterns of brain morphometry help to: • Distinguish schizophrenics from healthy controls • Understand plasticity, e.g. when learning new skills • Explain the changes seen in development and aging • Differentiate degenerative disease from healthy aging • Evaluate subjects on drug treatments versus placebo

  4. Alzheimer’s Disease example Baseline Image Standard clinical MRI 1.5T T1 SPGR 1x1x1.5mm voxels Repeat image 12 month follow-uprigidly registered Subtraction image

  5. SPM for group fMRI fMRI time-series Preprocessing Stat. modelling Results query “Contrast”Image fMRI time-series Preprocessing Stat. modelling Results query “Contrast”Image Group-wisestatistics fMRI time-series Preprocessing Stat. modelling Results query spm TImage “Contrast”Image

  6. SPM for structural MRI Group-wisestatistics ? High-res T1 MRI ? High-res T1 MRI ? High-res T1 MRI ?

  7. The need for tissue segmentation • High-resolution MRI reveals fine structural detail in the brain, but not all of it reliable or interesting • Noise, intensity-inhomogeneity, vasculature, … • MR Intensity is usually not quantitatively meaningful (in the same way that e.g. CT is) • fMRI time-series allow signal changes to be analysed statistically, compared to baseline or global values • Regional volumes of the three main tissue types: gray matter, white matter and CSF, are well-defined and potentially very interesting

  8. Examples ofsegmentation GM and WM segmentations overlaid on original images Structural image, GM and WM segments, and brain-mask (sum of GM and WM)

  9. Segmentation – basic approach • Intensities are modelled by a Gaussian Mixture Model (AKA Mixture Of Gaussians) • With a specified number of components • Parameterised by means, variances and mixing proportions (prior probabilities for components)

  10. Non-Gaussian Intensity Distributions • Multiple MoG components per tissue class allow non-Gaussian distributions to be modelled • E.g. accounting for partial volume effects • Or possibility of deep GM differing from cortical GM

  11. Tissue Probability Maps • Tissue probability maps (TPMs) can be used to provide a spatially varying prior distribution, which is tuned by the mixing proportions • These TPMs come from the segmented images of many subjects, done by the ICBM project

  12. Class priors • The probability of class k at voxel i, given weights γ is then: • Where bij is the value of the jth TPM at voxel i.

  13. Aligning the tissue probability maps • Initially affine-registered using a multi-dimensional form of mutual information • Iteratively warped to improve the fit of theunified segmentationmodel to the data • Familiar DCT-basisfunction concept, asused in normalisation

  14. MRI Bias Correction • MR Images are corupted by smoothly varying intensity inhomogeneity caused by magnetic field imperfections and subject-field interactions • Would make intensity distribution spatially variable • A smooth intensity correction can be modelled by a linear combination of DCT basis functions

  15. Summary of the unified model • SPM8b implements a generative model • Principled Bayesian probabilistic formulation • Combines deformable tissue probability maps with Gaussian mixture model segmentation • The inverse of the transformation that aligns the TPMs can be used to normalise the original image • Bias correction is included within the model

  16. Segmentation clean-up • Results may contain some non-brain tissue (dura, scalp, etc.) • This can be removedautomatically usingsimple morphologicalfiltering operations • Erosion • Conditional dilation Lower segmentationshave been cleaned up

  17. Limitations of the current model • Assumes that the brain consists of only GM and WM, with some CSF around it. • No model for lesions (stroke, tumours, etc) • Prior probability model is based on relatively young and healthy brains • Less appropriate for subjects outside this population • Needs reasonable quality images to work with • No severe artefacts • Good separation of intensities • Good initial alignment with TPMs...

  18. Extensions (possible or prototype) • Multispectral modelling • (New Segment Toolbox) • Deeper Bayesian philosophy • E.g. priors over means and variances • Marginalisation of nuisance variables • Model comparison • Groupwise model (enormous!) • Combination with DARTEL (see later and new seg tbx) • More tissue priors e.g. deep grey, meninges, etc. • Imaging physics • See Fischl et al. 2004, as cited in A&F introduction

  19. Voxel-Based Morphometry • In essence VBM is Statistical Parametric Mapping of segmented tissue density • The exact interpretation of gray matter concentration or density is complicated, and depends on the preprocessing steps used • It is not interpretable as neuronal packing density or other cytoarchitectonic tissue properties, though changes in these microscopic properties may lead to macro- or mesoscopic VBM-detectable differences

  20. A brief history of VBM • A Voxel-Based Method for the Statistical Analysis of Gray and White Matter Density… Wright, McGuire, Poline, Travere, Murrary, Frith, Frackowiak and Friston. NeuroImage 2(4), 1995 (!) • Rigid reorientation (by eye), semi-automatic scalp editing and segmentation, 8mm smoothing, SPM statistics, global covars. • Voxel-Based Morphometry – The Methods. Ashburner and Friston. NeuroImage 11(6 pt.1), 2000 • Non-linear spatial normalisation, automatic segmentation • Thorough consideration of assumptions and confounds

  21. A brief history of VBM • A Voxel-Based Morphometric Study of Ageing… Good, Johnsrude, Ashburner, Henson and Friston. NeuroImage 14(1), 2001 • Optimised GM-normalisation (“a half-baked procedure”), modulation of segments with Jacobian determinants • Unified Segmentation. Ashburner and Friston. NeuroImage 26(3), 2005 • Principled generative model for segmentation usingdeformable priors • A Fast Diffeomorphic Image Registration Algorithm. Ashburner. Neuroimage 38(1), 2007 • Large deformation normalisation to average shape templates • …

  22. VBM overview • Unified segmentation and spatial normalisation • Optional modulation with Jacobian determinant • Optional computation of tissue totals/globals • Gaussian smoothing • Voxel-wise statistical analysis

  23. VBM in pictures Segment Normalise

  24. VBM in pictures Segment Normalise Modulate (?) Smooth

  25. VBM in pictures Segment Normalise Modulate (?) Smooth Voxel-wise statistics

  26. VBM in pictures Segment Normalise Modulate (?) Smooth Voxel-wise statistics

  27. VBM Subtleties • Whether to modulate • Adjusting for total GM or Intracranial Volume • How much to smooth • Limitations of linear correlation • Statistical validity

  28. Modulation Native intensity = tissue density • Multiplication of the warped (normalised) tissue intensities so that their regional or global volume is preserved • Can detect differences in completely registered areas • Otherwise, we preserve concentrations, and are detecting mesoscopic effects that remain after approximate registration has removed the macroscopic effects • Flexible (not necessarily “perfect”) registration may not leave any such differences Modulated Unmodulated

  29. “Globals” for VBM • Shape is really a multivariate concept • Dependencies among volumes in different regions • SPM is mass univariate • Combining voxel-wise information with “global” integrated tissue volume provides a compromise • Using either ANCOVA or proportional scaling Above: (ii) is globally thicker, but locally thinner than (i) – either of these effects may be of interest to us. Below: The two “cortices” on the right both have equal volume… Figures from: Voxel-based morphometry of the human brain… Mechelli, Price, Friston and Ashburner. Current Medical Imaging Reviews 1(2), 2005.

  30. Total Intracranial Volume (TIV/ICV) • “Global” integrated tissue volume may be correlated with interesting regional effects • Correcting for globals in this case may overly reduce sensitivity to local differences • Total intracranial volume integrates GM, WM and CSF, or attempts to measure the skull-volume directly • Not sensitive to global reduction of GM+WM (cancelled out by CSF expansion – skull is fixed!) • Correcting for TIV in VBM statistics may give more powerful and/or more interpretable results

  31. Smoothing • The analysis will be most sensitive to effects that match the shape and size of the kernel • The data will be more Gaussian and closer to a continuous random field for larger kernels • Results will be rough and noise-like if too little smoothing is used • Too much will lead to distributed, indistinct blobs

  32. Smoothing • Between 7 and 14mm is probably best • (lower is okay with better registration, e.g. DARTEL) • The results below show two fairly extreme choices, 5mm on the left, and 16mm, right

  33. Nonlinearity Caution may be needed when looking for linear relationships between grey matter concentrations and some covariate of interest. Circles of uniformly increasing area. Plot of intensity at circle centres versus area Smoothed

  34. VBM’s statistical validity • Residuals are not normally distributed • Little impact on uncorrected statistics for experiments comparing reasonably sized groups • Probably invalid for experiments that compare single subjects or tiny groups with a larger control group • Need to use nonparametric tests that make less assumptions, e.g. permutation testing with SnPM

  35. VBM’s statistical validity • Correction for multiple comparisons • RFT correction based on peak heights should be OK • Correction using cluster extents is problematic • SPM usually assumes that the smoothness of the residuals is spatially stationary • VBM residuals have spatially varying smoothness • Bigger blobs expected in smoother regions • Toolboxes are now available for non-stationary cluster-based correction •

  36. VBM’s statistical validity • False discovery rate • Less conservative than FWE • Popular in morphometric work • (almost universal for cortical thickness in FS) • Recently questioned… • Topological FDR in SPM8 • See release notes for details and paper

  37. Variations on VBM • “All modulation, no gray matter” • Jacobian determinant “Tensor” Based Morphometry • Davatzikos et al. (1996) JCAT 20:88-97 • Deformation field morphometry • Cao and Worsley (1999) Ann Stat 27:925-942 • Ashburner et al (1998) Hum Brain Mapp 6:348-357 • Other variations on TBM • Chung et al (2001) NeuroImage 14:595-606

  38. Deformation and shape change Figures from Ashburner and Friston, “Morphometry”, Ch.6of Human Brain Function, 2nd Edition, Academic Press

  39. Deformation fields and Jacobians Deformation vector field Original Warped Template Determinant of Jacobian Matrixencodes voxel’s volume change Jacobian Matrix

  40. Longitudinal VBM • Intra-subject registration over time much more accurate than inter-subject normalisation • Imprecise inter-subject normalisation • Spatial smoothing required • Different methods have been developed to reduce the danger of expansion and contraction cancelling out…

  41. Longitudinal VBM variations • Voxel Compression mapping separates expansion and contraction before smoothing • Scahill et al (2002) PNAS 99:4703-4707 • Longitudinal VBM multiplies longitudinal volume change with baseline or average grey matter density • Chételat et al (2005) NeuroImage 27:934-946

  42. Longitudinal VBM variations Late Early Late CSF Early CSF Late CSF - Early CSF Late CSF - modulated CSF Smoothed CSF “modulated” by relative volume Warped early Difference Relative volumes

  43. Nonrigid registration developments • Large deformation concept • Regularise velocity not displacement • (syrup instead of elastic) • Leads to concept of geodesic • Provides a metric for distance between shapes • Geodesic or Riemannian average = mean shape • If velocity assumed constant computation is fast • Ashburner (2007) NeuroImage 38:95-113 • DARTEL toolbox in SPM8b • Currently initialised from unified seg_sn.mat files

  44. DARTEL exponentiates a velocity flow field to get a deformation field Velocity flow field

  45. Example geodesic shape average Average on Riemannian manifold Linear Average (Not on Riemannian manifold)

  46. DARTEL averagetemplate evolution Grey matter average of 452 subjects – affine Iterations 471 subjects– DARTEL

  47. Questioning Intersubject normalisation • Registration algorithms might find very different correspondences to human experts • Crum et al. (2003) NeuroImage 20:1425-1437 • Higher dimensional warping improves image similarity but not necessarily landmark correspondence • Hellier et al. (2003) IEEE TMI 22:1120-1130

  48. Questioning Intersubject normalisation • Subjects can have fundamentally different sulcal/gyral morphological variants • Caulo et al. (2007) Am. J. Neuroradiol. 28:1480-85 • Sulcal landmarks don’t always match underlying cytoarchitectonics • Amunts, et al. (2007) NeuroImage37(4):1061-5

  49. Intersubject normalisation opportunities • High-field high-resolution MR may have potential to image cytoarchitecture • Will registration be better or worse at higher resolution? • More information to use • More severe discrepancies? • Need rougher deformations • Non-diffeomorphic? 4.7T FSE De Vita et al (2003) Br J Radiol 76:631-7

  50. Intersubject normalisation opportunities • Regions of interest for fMRI can be defined from functional localisers or orthogonal SPM contrasts • No obvious equivalent for single-subject structural MR • Potential to include diffusion-weighted MRI information in registration ? • Zhang et al. (2006) Med. Image Analysis 10:764-785