Rosskopf Johannes, Müller Hans-Peter, Dreyhaupt Jens, Gorges Martin, Ludolph Albert C, Kassubek Jan
Department of Neurology, University of Ulm , Germany.
Amyotroph Lateral Scler Frontotemporal Degener. 2015 Mar;16(1-2):92-101. doi: 10.3109/21678421.2014.977297. Epub 2015 Jan 9.
Diffusion tensor imaging (DTI) for assessing ALS-associated white matter alterations has still not reached the level of a neuroimaging biomarker. Since large-scale multicentre DTI studies in ALS may be hampered by differences in scanning protocols, an approach for pooling of DTI data acquired with different protocols was investigated. Three hundred and nine datasets from 170 ALS patients and 139 controls were collected ex post facto from a monocentric database reflecting different scanning protocols. A 3D correction algorithm was introduced for a combined analysis of DTI metrics despite different acquisition protocols, with the focus on the CST as the tract correlate of ALS neuropathological stage 1. A homogenous set of data was obtained by application of 3D correction matrices. Results showed that a fractional anisotropy (FA) threshold of 0.41 could be defined to discriminate ALS patients from controls (sensitivity/specificity, 74%/72%). For the remaining test sample, sensitivity/specificity values of 68%/74% were obtained. In conclusion, the objective was to merge data recorded with different DTI protocols with 3D correction matrices for analyses at group level. These post processing tools might facilitate analysis of large study samples in a multicentre setting for DTI analysis at group level to aid in establishing DTI as a non-invasive biomarker for ALS.
用于评估肌萎缩侧索硬化症(ALS)相关白质改变的扩散张量成像(DTI)尚未达到神经影像学生物标志物的水平。由于ALS的大规模多中心DTI研究可能会受到扫描协议差异的阻碍,因此研究了一种汇总不同协议采集的DTI数据的方法。从反映不同扫描协议的单中心数据库中事后收集了170例ALS患者和139例对照的309个数据集。引入了一种三维校正算法,用于对DTI指标进行联合分析,尽管采集协议不同,重点是将皮质脊髓束(CST)作为ALS神经病理1期的相关束。通过应用三维校正矩阵获得了一组同质数据。结果表明,可以定义0.41的分数各向异性(FA)阈值来区分ALS患者和对照(敏感性/特异性,74%/72%)。对于其余测试样本,获得的敏感性/特异性值为68%/74%。总之,目标是使用三维校正矩阵合并不同DTI协议记录的数据,以便在组水平上进行分析。这些后处理工具可能有助于在多中心环境中对大型研究样本进行分析,以便在组水平上进行DTI分析,从而有助于将DTI确立为ALS的非侵入性生物标志物。