Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Neurocure Cluster of Excellence, NeuroCure Clinical Research Center, NCRC Charité, Charitéplatz 1, 10117 Berlin, Germany; Department of Neurology, Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany.
Department of Neurology, The Agnes Ginges Center for Human Neurogenetics, Hadassah-Hebrew-University Medical Center, Kiryat Hadassah Ein kerem, Jerusalem 91120, Israel.
Neuroimage Clin. 2018 May 8;19:538-550. doi: 10.1016/j.nicl.2018.05.004. eCollection 2018.
Diffusion Tensor Imaging (DTI) can evaluate microstructural tissue damage in the optic radiation (OR) of patients with clinically isolated syndrome (CIS), early relapsing-remitting multiple sclerosis and neuromyelitis optica spectrum disorders (NMOSD). Different post-processing techniques, e.g. tract-based spatial statistics (TBSS) and probabilistic tractography, exist to quantify this damage.
To evaluate the capacity of TBSS-based atlas region-of-interest (ROI) combination with 1) posterior thalamic radiation ROIs from the Johns Hopkins University atlas (JHU-TBSS), 2) Juelich Probabilistic ROIs (JUEL-TBSS) and tractography methods using 3) ConTrack (CON-PROB) and 4) constrained spherical deconvolution tractography (CSD-PROB) to detect OR damage in patients with a) NMOSD with prior ON (NMOSD-ON), b) CIS and early RRMS patients with ON (CIS/RRMS-ON) and c) CIS and early RRMS patients without prior ON (CIS/RRMS-NON) against healthy controls (HCs).
Twenty-three NMOSD-ON, 18 CIS/RRMS-ON, 21 CIS/RRMS-NON, and 26 HCs underwent 3 T MRI. DTI data analysis was carried out using JUEL-TBSS, JHU-TBSS, CON-PROB and CSD-PROB. Optical coherence tomography (OCT) and visual acuity testing was performed in the majority of patients and HCs.
Absolute OR fractional anisotropy (FA) values differed between all methods but showed good correlation and agreement in Bland-Altman analysis. OR FA values between NMOSD and HC differed throughout the methodologies (p-values ranging from p < 0.0001 to 0.0043). ROC-analysis and effect size estimation revealed higher AUCs and R for CSD-PROB (AUC = 0.812; R = 0.282) and JHU-TBSS (AUC = 0.756; R = 0.262), compared to CON-PROB (AUC = 0.742; R = 0.179) and JUEL-TBSS (AUC = 0.719; R = 0.161). Differences between CIS/RRMS-NON and HC were only observable in CSD-PROB (AUC = 0.796; R = 0.094). No significant differences between CIS/RRMS-ON and HC were detected by any of the methods.
All DTI post-processing techniques facilitated the detection of OR damage in patient groups with severe microstructural OR degradation. The comparison of distinct disease groups by use of different methods may lead to different - either false-positive or false-negative - results. Since different DTI post-processing approaches seem to provide complementary information on OR damage, application of distinct methods may depend on the relevant research question.
弥散张量成像(DTI)可评估临床孤立综合征(CIS)、早期复发缓解型多发性硬化症和视神经脊髓炎谱系疾病(NMOSD)患者视神经辐射(OR)的微观结构组织损伤。存在不同的后处理技术,例如基于束的空间统计学(TBSS)和概率追踪,用于量化这种损伤。
评估基于 TBSS 的图谱区域感兴趣区(ROI)组合的能力,这些 ROI 组合 1)来自约翰霍普金斯大学图谱(JHU-TBSS)的后丘脑辐射 ROI,2)Juelich 概率 ROI(JUEL-TBSS)和 3)ConTrack(CON-PROB)和 4)约束球谐反卷积追踪(CSD-PROB)方法,用于检测 a)有先前视神经炎(NMOSD-ON)的 NMOSD 患者、b)有视神经炎(CIS/RRMS-ON)的 CIS 和早期 RRMS 患者和 c)无先前视神经炎(CIS/RRMS-NON)的 CIS 和早期 RRMS 患者的 OR 损伤,与健康对照组(HC)进行比较。
23 名 NMOSD-ON、18 名 CIS/RRMS-ON、21 名 CIS/RRMS-NON 和 26 名 HC 接受了 3T MRI 检查。使用 JUEL-TBSS、JHU-TBSS、CON-PROB 和 CSD-PROB 进行 DTI 数据分析。大多数患者和 HC 都进行了光学相干断层扫描(OCT)和视力测试。
所有方法之间的 OR 绝对各向异性分数(FA)值均存在差异,但在 Bland-Altman 分析中显示出良好的相关性和一致性。NMOSD 和 HC 之间的 OR FA 值在所有方法中均存在差异(p 值范围从 p<0.0001 到 0.0043)。ROC 分析和效应量估计显示,CSD-PROB(AUC=0.812;R=0.282)和 JHU-TBSS(AUC=0.756;R=0.262)的 AUC 和 R 更高,而 CON-PROB(AUC=0.742;R=0.179)和 JUEL-TBSS(AUC=0.719;R=0.161)则较低。CSD-PROB 检测到 CIS/RRMS-NON 和 HC 之间的差异(AUC=0.796;R=0.094),而 CON-PROB 和 JUEL-TBSS 则没有。在任何方法中均未检测到 CIS/RRMS-ON 和 HC 之间的显著差异。
所有 DTI 后处理技术都有助于检测严重微观 OR 降解的患者组中的 OR 损伤。使用不同方法比较不同疾病组可能会导致不同的结果-要么是假阳性,要么是假阴性。由于不同的 DTI 后处理方法似乎提供了关于 OR 损伤的互补信息,因此应用不同的方法可能取决于相关的研究问题。