Knussmann Graham N, Anderson Jeffrey S, Prigge Molly B D, Dean Douglas C, Lange Nicholas, Bigler Erin D, Alexander Andrew L, Lainhart Janet E, Zielinski Brandon A, King Jace B
Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, UT, USA.
Waisman Center, University of Wisconsin-Madison, Madison, WI, USA.
Neuroimage Rep. 2022 Jun;2(2). doi: 10.1016/j.ynirp.2022.100086. Epub 2022 Feb 24.
Large MRI studies often pool data gathered from widely varying imaging sequences. Pooled data creates a potential source of variation in structural analyses which may cause misinterpretation of findings. The purpose of this study is to determine if data acquired using different scan sequences, head coils and scanners offers consistent structural measurements.
Participants (163 right-handed males: 82 typically developing controls, 81 participants with autism spectrum disorder) were scanned on the same day using an MPRAGE sequence with a 12-channel headcoil on a Siemens 3T Trio scanner and an MP2RAGE sequence with a 64-channel headcoil on a Siemens 3T Prisma scanner. Segmentation was performed using FreeSurfer to identify regions exhibiting variation between sequences on measures of volume, surface area, and cortical thickness. Intraclass correlation coefficient (ICC) and mean percent difference (MPD) were used as test-retest reproducibility measures.
ICC for total brain segmented volume yielded a 0.99 intraclass correlation, demonstrating high overall volumetric reproducibility. Comparison of individual regions of interest resulted in greater variation. Volumetric variability, although low overall, was greatest in the entorhinal cortex (ICC = 0.71), frontal (ICC = 0.60) and temporal (ICC = 0.60) poles. Surface area variability was greatest in the insula (ICC = 0.65), temporal (ICC = 0.64) and frontal (ICC = 0.68) poles. Cortical thickness was most variable in the frontal (ICC = 0.41) and temporal (ICC = 0.35) poles.
Data collected on different scanners and head coils using MPRAGE and MP2RAGE are generally consistent for surface area and volume estimates. However, regional variability may constrain accuracy in some regions and cortical thickness measurements exhibit higher generalized variability.
大型MRI研究通常会汇总从广泛不同的成像序列收集的数据。汇总数据会在结构分析中产生潜在的变异源,这可能导致对研究结果的误解。本研究的目的是确定使用不同扫描序列、头部线圈和扫描仪获取的数据是否能提供一致的结构测量结果。
参与者(163名右利手男性:82名发育正常的对照组,81名自闭症谱系障碍参与者)于同一天使用西门子3T Trio扫描仪上的12通道头部线圈进行MPRAGE序列扫描,并使用西门子3T Prisma扫描仪上的64通道头部线圈进行MP2RAGE序列扫描。使用FreeSurfer进行分割,以识别在体积、表面积和皮质厚度测量方面序列之间存在差异的区域。组内相关系数(ICC)和平均百分比差异(MPD)用作重测信度指标。
全脑分割体积的ICC产生了0.99的组内相关性,表明总体积具有较高的可重复性。对各个感兴趣区域的比较导致了更大的差异。体积变异性虽然总体较低,但在内嗅皮质(ICC = 0.71)、额叶(ICC = 0.60)和颞叶(ICC = 0.60)极最大。表面积变异性在岛叶(ICC = 0.65)、颞叶(ICC = 0.64)和额叶(ICC = 0.68)极最大。皮质厚度在额叶(ICC = 0.41)和颞叶(ICC = 0.35)极变化最大。
使用MPRAGE和MP2RAGE在不同扫描仪和头部线圈上收集的数据在表面积和体积估计方面总体上是一致的。然而,区域变异性可能会限制某些区域的准确性,并且皮质厚度测量显示出更高的普遍变异性。