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多模态方法在临床评分、形态 MRI 及生化 T2 映射和弥散加权成像中的应用,评估微骨折治疗后软骨修复组织与基质内自体软骨细胞移植之间的差异:一项初步研究。

Multimodal approach in the use of clinical scoring, morphological MRI and biochemical T2-mapping and diffusion-weighted imaging in their ability to assess differences between cartilage repair tissue after microfracture therapy and matrix-associated autologous chondrocyte transplantation: a pilot study.

机构信息

MR Center, Department of Radiology, Medical University of Vienna, Vienna, Austria.

出版信息

Osteoarthritis Cartilage. 2009 Sep;17(9):1219-27. doi: 10.1016/j.joca.2009.03.018. Epub 2009 Apr 17.

Abstract

OBJECTIVE

The aim of the present pilot study is to show initial results of a multimodal approach using clinical scoring, morphological magnetic resonance imaging (MRI) and biochemical T2-relaxation and diffusion-weighted imaging (DWI) in their ability to assess differences between cartilage repair tissue after microfracture therapy (MFX) and matrix-associated autologous chondrocyte transplantation (MACT).

METHOD

Twenty patients were cross-sectionally evaluated at different post-operative intervals from 12 to 63 months after MFX and 12-59 months after MACT. The two groups were matched by age (MFX: 36.0+/-10.4 years; MACT: 35.1+/-7.7 years) and post-operative interval (MFX: 32.6+/-16.7 months; MACT: 31.7+/-18.3 months). After clinical evaluation using the Lysholm score, 3T-MRI was performed obtaining the MR observation of cartilage repair tissue (MOCART) score as well as T2-mapping and DWI for multi-parametric MRI. Quantitative T2-relaxation was achieved using a multi-echo spin-echo sequence; semi-quantitative diffusion-quotient (signal intensity without diffusion-weighting divided by signal intensity with diffusion weighting) was prepared by a partially balanced, steady-state gradient-echo pulse sequence.

RESULTS

No differences in Lysholm (P=0.420) or MOCART (P=0.209) score were observed between MFX and MACT. T2-mapping showed lower T2 values after MFX compared to MACT (P=0.039). DWI distinguished between healthy cartilage and cartilage repair tissue in both procedures (MFX: P=0.001; MACT: P=0.007). Correlations were found between the Lysholm and the MOCART score (Pearson: 0.484; P=0.031), between the Lysholm score and DWI (Pearson:-0.557; P=0.011) and a trend between the Lysholm score and T2 (Person: 0.304; P=0.193).

CONCLUSION

Using T2-mapping and DWI, additional information could be gained compared to clinical scoring or morphological MRI. In combination clinical, MR-morphological and MR-biochemical parameters can be seen as a promising multimodal tool in the follow-up of cartilage repair.

摘要

目的

本初步研究旨在展示一种多模态方法的初步结果,该方法使用临床评分、形态磁共振成像(MRI)以及生化 T2 弛豫和扩散加权成像(DWI)来评估微骨折治疗(MFX)和基质相关自体软骨细胞移植(MACT)后软骨修复组织之间的差异。

方法

20 例患者分别在 MFX 后 12 至 63 个月和 MACT 后 12 至 59 个月进行了横断面评估。两组通过年龄(MFX:36.0+/-10.4 岁;MACT:35.1+/-7.7 岁)和术后间隔(MFX:32.6+/-16.7 个月;MACT:31.7+/-18.3 个月)进行匹配。在使用 Lysholm 评分进行临床评估后,进行 3T-MRI 检查,获得软骨修复组织的磁共振观察评分(MOCART)以及 T2 映射和 DWI 用于多参数 MRI。通过多回波自旋回波序列获得定量 T2 弛豫;通过部分平衡稳态梯度回波脉冲序列制备半定量扩散商(无扩散加权的信号强度除以有扩散加权的信号强度)。

结果

MFX 和 MACT 之间的 Lysholm(P=0.420)或 MOCART(P=0.209)评分无差异。T2 映射显示 MFX 后 T2 值低于 MACT(P=0.039)。DWI 在两种手术中均能区分健康软骨和软骨修复组织(MFX:P=0.001;MACT:P=0.007)。Lysholm 和 MOCART 评分之间存在相关性(Pearson:0.484;P=0.031),Lysholm 评分与 DWI 之间存在相关性(Pearson:-0.557;P=0.011),Lysholm 评分与 T2 之间存在趋势(Person:0.304;P=0.193)。

结论

与临床评分或形态 MRI 相比,使用 T2 映射和 DWI 可以获得更多信息。临床、MR 形态和 MR 生化参数的联合可以作为软骨修复随访的一种很有前途的多模态工具。

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