Automatic magnetic resonance spinal cord segmentation with topology constraints for variable fields of view

被引:53
作者
Chen, Min [1 ,3 ]
Carass, Aaron [1 ]
Oh, Jiwon [2 ]
Nair, Govind [3 ]
Pham, Dzung L. [4 ]
Reich, Daniel S. [2 ,3 ]
Prince, Jerry L. [1 ]
机构
[1] Johns Hopkins Univ, Dept Elect & Comp Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Sch Med, Dept Neurol, Baltimore, MD USA
[3] NINDS, Translat Neuroradiol Unit, Bethesda, MD 20892 USA
[4] Ctr Neurosci & Regenerat Med, Image Proc Core, Bethesda, MD USA
关键词
Atlas construction; Topology-preserving segmentation; Digital homeomorphism; Spinal cord segmentation; Magnetic resonance imaging; MULTIPLE-SCLEROSIS; MR-IMAGES; SEMIAUTOMATIC SEGMENTATION; ATROPHY; DISABILITY; ARTIFACTS; BRAIN; ALGORITHM; MODEL;
D O I
10.1016/j.neuroimage.2013.07.060
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Spinal cord segmentation is an important step in the analysis of neurological diseases such as multiple sclerosis. Several studies have shown correlations between disease progression and metrics relating to spinal cord atrophy and shape changes. Current practices primarily involve segmenting the spinal cord manually or semiautomatically, which can be inconsistent and time-consuming for large datasets. An automatic method that segments the spinal cord and cerebrospinal fluid from magnetic resonance images is presented. The method uses a deformable atlas and topology constraints to produce results that are robust to noise and artifacts. The method is designed to be easily extended to new data with different modalities, resolutions, and fields of view. Validation was performed on two distinct datasets. The first consists of magnetization transfer-prepared T2*-weighted gradient-echo MRI centered only on the cervical vertebrae (CI-CS). The second consists of TI-weighted MRI that covers both the cervical and portions of the thoracic vertebrae (C1-T4). Results were found to be highly accurate in comparison to manual segmentations. A pilot study was carried out to demonstrate the potential utility of this new method for research and clinical studies of multiple sclerosis. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1051 / 1062
页数:12
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