首页> 外文OA文献 >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
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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

机译:多模式方法在临床评分,形态学MRI和生化T2映射以及弥散加权成像中的应用,以评估微骨折治疗和基质相关自体软骨细胞移植后软骨修复组织之间的差异:一项试点研究

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摘要

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.
机译:目的:本实验研究的目的是展示一种使用临床评分,形态磁共振成像(MRI)以及生化T2松弛和弥散加权成像(DWI)的多峰方法评估软骨之间差异的能力的初步结果微骨折治疗(MFX)和基质相关自体软骨细胞移植(MACT)后修复组织。方法:20例患者在MFX术后12至63个月和MACT术后12-59个月的不同术后间隔进行横断面评估。两组按年龄(MFX:36.0 +/- 10.4岁; MACT:35.1 +/- 7.7岁)和术后间隔时间(MFX:32.6 +/- 16.7个月; MACT:31.7 +/- 18.3个月)进行匹配。使用Lysholm评分进行临床评估后,进行3T-MRI,以获得软骨修复组织(MOCART)评分的MR观察,以及多参数MRI的T2-mapping和DWI。使用多回旋自旋回波序列实现了定量的T2松弛;半定量扩散商(不具有扩散权重的信号强度除以具有扩散权重的信号强度)是通过部分平衡的稳态梯度回波脉冲序列制备的。结果:MFX和MACT在Lysholm(P = 0.420)或MOCART(P = 0.209)评分上没有差异。与MACT相比,MFX之后的T2映射显示出较低的T2值(P = 0.039)。在两种手术中,DWI在健康软骨和软骨修复组织之间进行了区分(MFX:P = 0.001; MATT:P = 0.007)。 Lysholm评分与MOCART评分之间的相关性(Pearson:0.484; P = 0.031),Lysholm评分与DWI之间的相关性(Pearson:-0.557; P = 0.011)和Lysholm评分与T2之间的相关性(人:0.304; P = 0.193)。结论:与临床评分或形态学MRI相比,使用T2映射和DWI,可以获得更多信息。在临床结合中,MR形态学和MR生化参数可以看作是软骨修复随访中有希望的多峰工具。

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