Jian J. Lin1, Mark J. Lowe1, Robert J. Fox2, and Ken Sakaie1
1Imaging Institute, The Cleveland Clinic, Cleveland, OH, United States, 2Neurological Institute, The Cleveland Clinic, Cleveland, OH, United States
Synopsis
Deciding from among the many available tractography
algorithms can be challenging. We demonstrate that track-based measures can be
compared using standard statistical approaches to compare the performance of two
probablistic tractography algoirthms to determine the conditions under which
one algorithm can replace another.
Introduction
Comparison of tractography algorithms is an important step
when deciding among the many algorithms available, but it can be difficult to
define a well-behaved statistic for individual fiber tracks. Track-based
measures—values of tissue microstructure parameters averaged across a white
matter pathway— are readily analyzed with standard statistical approaches. We
compare two probabilistic tractography approaches—a stochastic algorithm that
uses Monte Carlo (MC) sampling of fiber orientation distributions1 and a partial differential
equation (PDE)-based approach2 that was formulated to mimic
the MC approach. One motivation for the comparison is that the MC approach,
while robust against the presence of lesions and crossing fibers, is
computationally intensive. The PDE approach requires minmal computational
resources. In order to understand the impact of the algorithm used, we study two
aspects of the tracking methods: 1) reproducibility, which directly affects the
ability to detect a significant change in diffusivity for longitudinal studies
or a significant difference between groups for cross sectional studies and 2)
the difference in mean value of track-based measures, as this will determine if
the tracking methods are interchangeable, or have systematic differences.
Methods
Under an IRB-approved protocol, five healthy controls were
scanned, repositioned and scanned again on a Siemens Trio with standard 12-channel head coil (Siemens Medical Solutions, Erlangen). DTI was acquired at
2.5 mm isotropic spatial resolution with 64 b=700sec/mm2
diffusion-weighting gradients and 8 b=0. After motion correction with TORTOISE3, tissue microstructure
parameters (fractional anisotropy (FA), mean diffusivity (MD), radial
diffusivity (RD) and axial diffusivity (AD))4 and fiber orientation
distributions5,6
were calculated. Hand-drawn ROIs were used to define endpoints of corticospinal
tract (CST) and transcallosal motor pathway (TMP), followed by MC- and
PDE-based tractography. Means of tissue microstructure parameters, calculated within
each track1 , were used for statistical
comparison.Results
Figure 1 shows track density maps from MC and PDE
tractography in the TMP. The spatial location of tracks is qualitatively
consistent, but there are systematic differences in the values of track
density. Figures 2 and 3 show these differences quantitively. Figure 4 shows
measures of reproducibility, intra-class correlation coefficient (ICC) and
coefficient of variation (CV). All values meet conventions for high
reproducibility (ICC > 0.70 and CV < 10)7, but measures of
reproducibility are slightly worse for PDE than for MC. The implications of
this difference can be illustrated with a power analysis. Assuming a value of
0.5x10-3 mm2/sec for RD, a 3% change per year over two
years, and a type I error of 0.05 results in power of 0.8 for the MC algorithm
and 0.48 for the PDE algorithm.Discussion and Conclusion
There are clear systematic differences between the algorithms.
The same underlying data, voxel-wise derived quantities and ROIs were used for
each tractography algorithm, eliminating the possibility of these as sources of
the differences. Although the PDE approach was formulated to replicate the
results of the MC algorithm, these results suggest that it would be unwise to
mix track-based measures from different algorithms in a group analysis. The
reproducibility results show comparable and high values for both algorithms. However,
the difference in reproducibility
results in a reduction in statistical power. In conclusion, the PDE algorithm
can be used a replacement for the MC algorithm if used for all scans used in the
study and only if the loss of sensitivity can be compensated for with a
sufficiently large sample sizeAcknowledgements
We acknowledge support from the National Institute of
Neurological Disorders and Stroke (U01NS082329), National Multiple Sclerosis
Society (RG 4778-A-6) and from MediciNova through a contract with the National
Institutes of Health.References
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