Acknowledgement
This work was supported by the National Natural Science Foundation of China (grant number: 61527807, 81800840, 81701644, 61801311, 81871322), Beijing Scholars Program (grant number: [2015] 160), Beijing Municipal Administration of Hospitals (grant number: SML20150101, PX2018001, YYZZ2017A14, YYZZ2017B01), and Fundamental Research Funds for the Central Universities (SWU118065).
References
- Holden BA, Wilson DA, Jong M, Sankaridurg P, Fricke TR, Smith EL III, et al. Myopia: a growing global problem with sight-threatening complications. Community Eye Health 2015;28:35
- Morgan IG, French AN, Ashby RS, Guo X, Ding X, He M, et al. The epidemics of myopia: aetiology and prevention. Prog Retin Eye Res 2018;62:134-149 https://doi.org/10.1016/j.preteyeres.2017.09.004
- Hsu CC, Chen SJ, Li AF, Lee FL. Systolic blood pressure, choroidal thickness, and axial length in patients with myopic maculopathy. J Chin Med Assoc 2014;77:487-491 https://doi.org/10.1016/j.jcma.2014.06.009
- Morgan IG, Ohno-Matsui K, Saw SM. Myopia. Lancet 2012;379:1739-1748 https://doi.org/10.1016/S0140-6736(12)60272-4
- Huang X, Hu Y, Zhou F, Xu X, Wu Y, Jay R, et al. Altered whole-brain gray matter volume in high myopia patients: a voxel-based morphometry study. Neuroreport 2018;29:760-767 https://doi.org/10.1097/WNR.0000000000001028
- Li Q, Guo M, Dong H, Zhang Y, Fu Y, Yin X. Voxel-based analysis of regional gray and white matter concentration in high myopia. Vision Res 2012;58:45-50 https://doi.org/10.1016/j.visres.2012.02.005
- Shu N, Li J, Li K, Yu C, Jiang T. Abnormal diffusion of cerebral white matter in early blindness. Hum Brain Mapp 2009;30:220-227 https://doi.org/10.1002/hbm.20507
- Marcus MW, de Vries MM, Junoy Montolio FG, Jansonius NM. Myopia as a risk factor for open-angle glaucoma: a systematic review and meta-analysis. Ophthalmology 2011;118:1989-1994.e2 https://doi.org/10.1016/j.ophtha.2011.03.012
- Xu ZF, Sun JS, Zhang XH, Feng YY, Pan AZ, Gao MY, et al. Microstructural visual pathway abnormalities in patients with primary glaucoma: 3 T diffusion kurtosis imaging study. Clin Radiol 2018;73:591.e9-591.e15 https://doi.org/10.1016/j.crad.2018.01.010
- Allen B, Schmitt MA, Kushner BJ, Rokers B. Retinothalamic white matter abnormalities in amblyopia. Invest Ophthalmol Vis Sci 2018;59:921-929 https://doi.org/10.1167/iovs.17-22930
- Basser PJ, Jones DK. Diffusion-tensor MRI: theory, experimental design and data analysis - a technical review. NMR Biomed 2002;15:456-467 https://doi.org/10.1002/nbm.783
- Veraart J, Poot DH, Van Hecke W, Blockx I, Van der Linden A, Verhoye M, et al. More accurate estimation of diffusion tensor parameters using diffusion kurtosis imaging. Magn Reson Med 2011;65:138-145 https://doi.org/10.1002/mrm.22603
- Zhu J, Zhuo C, Qin W, Wang D, Ma X, Zhou Y, et al. Performances of diffusion kurtosis imaging and diffusion tensor imaging in detecting white matter abnormality in schizophrenia. Neuroimage Clin 2015;7:170-176 https://doi.org/10.1016/j.nicl.2014.12.008
- Tabesh A, Jensen JH, Ardekani BA, Helpern JA. Estimation of tensors and tensor-derived measures in diffusional kurtosis imaging. Magn Reson Med 2011;65:823-836 https://doi.org/10.1002/mrm.22655
- Wen H, Liu Y, Wang J, Rekik I, Zhang J, Zhang Y, et al. Combining tract-and atlas-based analysis reveals microstructural abnormalities in early tourette syndrome children. Hum Brain Mapp 2016;37:1903-1919 https://doi.org/10.1002/hbm.23146
- Smith SM, Jenkinson M, Johansen-Berg H, Rueckert D, Nichols TE, Mackay CE, et al. Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data. Neuroimage 2006;31:1487-1505 https://doi.org/10.1016/j.neuroimage.2006.02.024
- Wu EX, Cheung MM. MR diffusion kurtosis imaging for neural tissue characterization. NMR Biomed 2010;23:836-848 https://doi.org/10.1002/nbm.1506
- Wang R, Tang Z, Sun X, Wu L, Wang J, Zhong Y, et al. White matter abnormalities and correlation with severity in normal tension glaucoma: a whole brain atlas-based diffusion tensor study. Invest Ophthalmol Vis Sci 2018;59:1313-1322 https://doi.org/10.1167/iovs.17-23597
- Falangola MF, Guilfoyle DN, Tabesh A, Hui ES, Nie X, Jensen JH, et al. Histological correlation of diffusional kurtosis and white matter modeling metrics in cuprizone-induced corpus callosum demyelination. NMR Biomed 2014;27:948-957 https://doi.org/10.1002/nbm.3140
- Song SK, Sun SW, Ju WK, Lin SJ, Cross AH, Neufeld AH. Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia. Neuroimage 2003;20:1714-1722 https://doi.org/10.1016/j.neuroimage.2003.07.005
- van der Valk P, De Groot CJ. Staging of multiple sclerosis (MS) lesions: pathology of the time frame of MS. Neuropathol Appl Neurobiol 2000;26:2-10 https://doi.org/10.1046/j.1365-2990.2000.00217.x
- De Stefano N, Narayanan S, Francis GS, Arnaoutelis R, Tartaglia MC, Antel JP, et al. Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability. Arch Neurol 2001;58:65-70 https://doi.org/10.1001/archneur.58.1.65
- Phillips J. Rethinking multiple sclerosis. Arch Neurol 2001;58:30-32 https://doi.org/10.1001/archneur.58.1.30
- Glenn GR, Helpern JA, Tabesh A, Jensen JH. Quantitative assessment of diffusional kurtosis anisotropy. NMR Biomed 2015;28:448-459 https://doi.org/10.1002/nbm.3271
- Douaud G, Jbabdi S, Behrens TE, Menke RA, Gass A, Monsch AU, et al. DTI measures in crossing-fibre areas: increased diffusion anisotropy reveals early white matter alteration in MCI and mild alzheimer's disease. Neuroimage 2011;55:880-890 https://doi.org/10.1016/j.neuroimage.2010.12.008
- Zhang Y, Du G, Yang Y, Qin W, Li X, Zhang Q. Corrigendum: higher integrity of the motor and visual pathways in long-term video game players. Front Hum Neurosci 2015;9:98
- Wang D, Qin W, Liu Y, Zhang Y, Jiang T, Yu C. Altered white matter integrity in the congenital and late blind people. Neural Plast 2013;2013:128236
- Long M, Wang L, Tian Q, Ding H, Qin W, Shi D, et al. Brain white matter changes in asymptomatic carriers of Leber's hereditary optic neuropathy. J Neurol 2019;266:1474-1480 https://doi.org/10.1007/s00415-019-09284-2
- Lundberg K, Suhr Thykjaer A, Sogaard Hansen R, Vestergaard AH, Jacobsen N, Goldschmidt E, et al. Physical activity and myopia in danish children-the CHAMPS eye study. Acta Ophthalmol 2018;96:134-141 https://doi.org/10.1111/aos.13513
- Parks EL, Madden DJ. Brain connectivity and visual attention. Brain Connect 2013;3:317-338 https://doi.org/10.1089/brain.2012.0139
- Chechlacz M, Rotshtein P, Hansen PC, Riddoch JM, Deb S, Humphreys GW. The Neural underpinings of simultanagnosia: disconnecting the visuospatial attention network. J Cogn Neurosci 2012;24:718-735 https://doi.org/10.1162/jocn_a_00159
- Klarborg B, Skak Madsen K, Vestergaard M, Skimminge A, Jernigan TL, Baare WF. Sustained attention is associated with right superior longitudinal fasciculus and superior parietal white matter microstructure in children. Hum Brain Mapp 2013;34:3216-3232 https://doi.org/10.1002/hbm.22139
- Catani M, Jones DK, Donato R, Ffytche DH. Occipito-temporal connections in the human brain. Brain 2003;126:2093-2107 https://doi.org/10.1093/brain/awg203
- Catani M, Thiebaut de Schotten M. A diffusion tensor imaging tractography atlas for virtual in vivo dissections. Cortex 2008;44:1105-1132 https://doi.org/10.1016/j.cortex.2008.05.004
- Shin J, Rowley J, Chowdhury R, Jolicoeur P, Klein D, Grova C, et al. Inferior longitudinal fasciculus' role in visual processing and language comprehension: a combined MEG-DTI study. Front Neurosci 2019;13:875
- Ross ED. Sensory-specific amnesia and hypoemotionality in humans and monkeys: gateway for developing a hodology of memory. Cortex 2008;44:1010-1022 https://doi.org/10.1016/j.cortex.2008.02.002
- Umarova RM, Saur D, Schnell S, Kaller CP, Vry MS, Glauche V, et al. Structural connectivity for visuospatial attention: significance of ventral pathways. Cereb Cortex 2010;20:121-129 https://doi.org/10.1093/cercor/bhp086
- Fox CJ, Iaria G, Barton JJ. Disconnection in prosopagnosia and face processing. Cortex 2008;44:996-1009 https://doi.org/10.1016/j.cortex.2008.04.003
- Philippi CL, Mehta S, Grabowski T, Adolphs R, Rudrauf D. Damage to association fiber tracts impairs recognition of the facial expression of emotion. J Neurosci 2009;29:15089-15099 https://doi.org/10.1523/JNEUROSCI.0796-09.2009
- Mayer KM, Vuong QC. TBSS and probabilistic tractography reveal white matter connections for attention to object features. Brain Struct Funct 2014;219:2159-2171 https://doi.org/10.1007/s00429-013-0631-6
- Kang DW, Kim D, Chang LH, Kim YH, Takahashi E, Cain MS, et al. Structural and functional connectivity changes beyond visual cortex in a later phase of visual perceptual learning. Sci Rep 2018;8:5186
- Phillips JW, Schulmann A, Hara E, Winnubst J, Liu C, Valakh V, et al. A repeated molecular architecture across thalamic pathways. Nat Neurosci 2019;22:1925-1935 https://doi.org/10.1038/s41593-019-0483-3
- Van Cauter S, Veraart J, Sijbers J, Peeters RR, Himmelreich U, De Keyzer F, et al. Gliomas: diffusion kurtosis MR imaging in grading. Radiology 2012;263:492-501 https://doi.org/10.1148/radiol.12110927
- Lu P, Shi L, Du H, Xie B, Li C, Li S, et al. Reduced white matter integrity in primary open-angle glaucoma: a DTI study using tract-based spatial statistics. J Neuroradiol 2013;40:89-93 https://doi.org/10.1016/j.neurad.2012.04.001