Abstract
Large diffusion MRI datasets provide the statistical power necessary to model complex effects in the white matter. They also motivate the need for fully automatic algorithms for finding white matter bundles. One popular algorithm, Automated Fiber Quantification (AFQ), has been shown to be reliable for analyzing a suite of large bundles. Here, we demonstrate that this approach can be extended to a relatively small white matter bundle, the optic tract. We develop an automated method that finds a portion of this bundle automatically. We compare the automatically found optic tract to optic tracts previously found using an algorithm that requires expert intervention, and find high degree of overlap. While previous methods work well in high-quality data, we demonstrate that the novel method proposed here generalizes broadly in subjects from three different datasets with differing data quality and a broad age range. Finally, we describe how this approach could be easily extended to other small bundles.
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References
Jernigan, T.L., Brown, S.A., Dowling, G.J.: The adolescent brain cognitive development study. J. Res. Adolesc. 28(1), 154–156 (2018)
Sudlow, C.: UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age. PLoS Med. 12(3), e1001779 (2015)
Yeatman, J.D., Dougherty, R.F., Myall, N.J., Wandell, B.A., Feldman, H.M.: Tract profiles of white matter properties: automating fiber-tract quantification. PloS One 7(11), e49790 (2012)
Jones, D.K., Travis, A.R., Eden, G., Pierpaoli, C., Basser, P.J.: PASTA: pointwise assessment of streamline tractography attributes. Magn. Reson. Med. 53(6), 1462–1467 (2005)
Kruper, J., et al.: Evaluating the reliability of human brain white matter tractometry. Apert. Neuro 1(1) (2021)
Miyata, T., Benson, N.C., Winawer, J., Takemura, H.: Structural covariance and heritability of the optic tract and primary visual cortex in living human brains. J. Neurosci. 42(35), 6761–6769 (2022)
Ogawa, S., et al.: Multi-contrast magnetic resonance imaging of visual white matter pathways in patients with glaucoma. Invest. Ophthalmol. Vis. Sci. 63(2), 29 (2022)
He, J., et al.: Comparison of multiple tractography methods for reconstruction of the retinogeniculate visual pathway using diffusion MRI. Hum. Brain Mapp. 42(12), 3887–3904 (2021)
Lerma-Usabiaga, G., Liu, M., Paz-Alonso, P.M., Wandell, B.A.: Reproducible tract profiles 2 (RTP2) suite, from diffusion MRI acquisition to clinical practice and research. Sci. Rep. 13(1), 6010 (2023)
Liu, M., Lerma-Usabiaga, G., Clascá, F., Paz-Alonso, P.M.: Reproducible protocol to obtain and measure first-order relay human thalamic white-matter tracts. Neuroimage 262, 119558 (2022)
Van Essen, D. C., Smith, S. M., Barch, D. M., Behrens, T. E., Yacoub, E., Ugurbil, K., Wu-Minn HCP Consortium: The WU-Minn human connectome project: an overview. Neuroimage 80, 62–79 (2013)
Alexander, L.M., et al.: An open resource for transdiagnostic research in pediatric mental health and learning disorders. Sci. Data 4, 170181 (2017)
Richie-Halford, A., et al.: An analysis-ready and quality controlled resource for pediatric brain white-matter research. Sci. Data 9(1), 616 (2022)
Fonov, V., Evans, A.C., Botteron, K., Almli, C.R., McKinstry, R.C., Collins, D.L., Brain Development Cooperative Group: Unbiased average age-appropriate atlases for pediatric studies. Neuroimage 54(1), 313–327 (2011)
Yeh, F.C., Wedeen, V.J., Tseng, W.Y.I.: Generalized q-sampling imaging. IEEE Trans. Med. Imaging 29(9), 1626–1635 (2010)
Dell’Acqua, F., Lacerda, L., Catani, M., Simmons, A.: Anisotropic power maps: a diffusion contrast to reveal low anisotropy tissues from HARDI data. Proc. Intl. Soc. Mag. Reson. Med. 22, 29960–29967 (2014)
Rokem, A., et al. GPU-accelerated diffusion MRI tractography in DIPY. Proc. Intl. Soc. Mag. Reson. Med. 21 (2021)
Tournier, J.D., Calamante, F., Connelly, A.: Robust determination of the fibre orientation distribution in diffusion MRI: non-negativity constrained super-resolved spherical deconvolution. Neuroimage 35(4), 1459–1472 (2007)
Garyfallidis, E., Brett, M., Correia, M.M., Williams, G.B., Nimmo-Smith, I.: Quickbundles, a method for tractography simplification. Front. Neurosci. 6, 175 (2012)
Garyfallidis, E., et al.: Dipy, a library for the analysis of diffusion MRI data. Front. Neuroinf. 8, 8 (2014)
Cousineau, M., et al.: A test-retest study on parkinson’s PPMI dataset yields statistically significant white matter fascicles. NeuroImage Clin. 16, 222–233 (2017)
Garyfallidis, E.: Recognition of white matter bundles using local and global streamline-based registration and clustering. Neuroimage 170, 283–295 (2018)
Acknowledgements
Data were provided in part by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University. This research has been conducted using the UK Biobank Resource under Application Number 28541. Work on this project was funded by NSF grant 1934292, and NIH grants RF1 MH121868, NIA/NIH U19AG066567. We would like to thank the Child Mind Institute Biobank for access to the Healthy Brain Network dataset. We are also grateful to Fan Zhang and Lauren O’Donnell for sharing data from [8].
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Kruper, J., Rokem, A. (2023). Automatic Fast and Reliable Recognition of a Small Brain White Matter Bundle. In: Karaman, M., Mito, R., Powell, E., Rheault, F., Winzeck, S. (eds) Computational Diffusion MRI. CDMRI 2023. Lecture Notes in Computer Science, vol 14328. Springer, Cham. https://doi.org/10.1007/978-3-031-47292-3_7
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