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关节软骨体内扩散成像的技术与应用

Techniques and applications of in vivo diffusion imaging of articular cartilage.

作者信息

Raya José G

机构信息

Department Radiology, New York University Langone Medical Center, New York, New York, USA.

出版信息

J Magn Reson Imaging. 2015 Jun;41(6):1487-504. doi: 10.1002/jmri.24767. Epub 2015 Apr 10.

Abstract

Early in the process of osteoarthritis (OA) the composition (water, proteoglycan [PG], and collagen) and structure of articular cartilage is altered leading to changes in its mechanical properties. A technique that can assess the composition and structure of the cartilage in vivo can provide insight in the mechanical integrity of articular cartilage and become a powerful tool for the early diagnosis of OA. Diffusion tensor imaging (DTI) has been proposed as a biomarker for cartilage composition and structure. DTI is sensitive to the PG content through the mean diffusivity and to the collagen architecture through the fractional anisotropy. However, the acquisition of DTI of articular cartilage in vivo is challenging due to the short T2 of articular cartilage (∼40 ms at 3 Tesla) and the high resolution needed (0.5-0.7 mm in plane) to depict the cartilage anatomy. We describe the pulse sequences used for in vivo DTI of articular cartilage and discus general strategies for protocol optimization. We provide a comprehensive review of measurements of DTI of articular cartilage from ex vivo validation experiments to its recent clinical applications.

摘要

在骨关节炎(OA)病程早期,关节软骨的组成(水、蛋白聚糖[PG]和胶原蛋白)及结构会发生改变,进而导致其力学性能变化。一种能够在体内评估软骨组成和结构的技术,可深入了解关节软骨的力学完整性,并成为OA早期诊断的有力工具。扩散张量成像(DTI)已被提议作为软骨组成和结构的生物标志物。DTI通过平均扩散率对PG含量敏感,通过分数各向异性对胶原蛋白结构敏感。然而,由于关节软骨的T2较短(在3特斯拉时约为40毫秒)以及描绘软骨解剖结构所需的高分辨率(平面内0.5 - 0.7毫米),在体内获取关节软骨的DTI具有挑战性。我们描述了用于关节软骨体内DTI的脉冲序列,并讨论了方案优化的一般策略。我们提供了从体外验证实验到其近期临床应用的关节软骨DTI测量的全面综述。

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