Incorporating non-linear alignment and multi-compartmental modeling for improved human optic nerve diffusion imaging

被引:5
|
作者
Kim, Joo-won [1 ,2 ,3 ]
Andersson, Jesper L. R. [4 ]
Seifert, Alan C. [1 ,2 ,3 ]
Sun, Peng [5 ]
Song, Sheng-Kwei [5 ]
Dula, Courtney [6 ]
Naismith, Robert T. [6 ,7 ]
Xu, Junqian [1 ,2 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Translat & Mol Imaging Inst, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Radiol, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, New York, NY 10029 USA
[4] Univ Oxford, Wellcome Ctr Integrat Neuroimaging, Oxford, England
[5] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[7] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
关键词
Optic nerve; Non-linear registration; Motion correction; Diffusion MRI; Multi-compartmental modeling; SPINAL-CORD; COHERENCE TOMOGRAPHY; MULTIPLE-SCLEROSIS; INDUCED DISTORTION; TENSOR; NEURITIS; MRI; NEUROPROTECTION; DEGENERATION; RESOLUTION;
D O I
10.1016/j.neuroimage.2019.03.058
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In vivo human optic nerve diffusion magnetic resonance imaging (dMRI) is technically challenging with two outstanding issues not yet well addressed: (i) non-linear optic nerve movement, independent of head motion, and (ii) effect from partial-volumed cerebrospinal fluid or interstitial fluid such as in edema. In this work, we developed a non-linear optic nerve registration algorithm for improved volume alignment in axial high resolution optic nerve dMRI. During eyes-closed dMRI data acquisition, optic nerve dMRI measurements by diffusion tensor imaging (DTI) with and without free water elimination (FWE), and by diffusion basis spectrum imaging (DBSI), as well as optic nerve motion, were characterized in healthy adults at various locations along the posterior-to-anterior dimension. Optic nerve DTI results showed consistent trends in microstructural parametric measurements along the posterior-to-anterior direction of the entire intraorbital optic nerve, while the anterior portion of the intraorbital optic nerve exhibited the largest spatial displacement. Multi-compartmental dMRI modeling, such as DTI with FWE or DBSI, was less subject to spatially dependent biases in diffusivity and anisotropy measurements in the optic nerve which corresponded to similar spatial distributions of the estimated fraction of isotropic diffusion components. DBSI results derived from our clinically feasible (similar to 10 min) optic nerve dMRI protocol in this study are consistent with those from small animal studies, which provides the basis for evaluating the utility of multi-compartmental dMRI modeling in characterizing coexisting pathophysiology in human optic neuropathies.
引用
收藏
页码:102 / 113
页数:12
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