Intersite brain MRI volumetric biases persist even in a harmonized multisubject study of multiple sclerosis

被引:5
作者
Clark, Kelly M. [1 ,2 ,11 ]
O'Donnell, Carly A. [1 ,2 ]
Elliott, Mark [3 ]
Tauhid, Shahamat E. [4 ]
Dewey, Blake [5 ]
Chu, Renxin [4 ]
Khalil, Samar [4 ]
Nair, Govind [6 ]
Sati, Pascal [7 ]
DuVal, Anna [5 ]
Pellegrini, Nicole [5 ]
Bar-Or, Amit [8 ,9 ]
Markowitz, Clyde K. [8 ,9 ]
Schindler, Matthew [8 ,9 ]
Zurawski, Jonathan A.
Calabresi, Peter S. [5 ]
Reich, Daniel [10 ]
Bakshi, Rohit T. [1 ,4 ]
Shinohara, Russell [1 ,2 ,8 ]
NAIMS Cooperative
机构
[1] Univ Penn, Perelman Sch Med, Penn Stat Imaging & Visualizat Endeavor, Philadelphia, PA USA
[2] Univ Penn, Perelman Sch Med, Dept Biostat Epidemiol & Informat, Philadelphia, PA USA
[3] Univ Penn, Dept Radiol, Philadelphia, PA USA
[4] Harvard Med Sch, Brigham & Womens Hosp, Dept Neurol, Boston, MA USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD USA
[6] NINDS, Quantitat MRI Core Facil, NIH, Bethesda, MD USA
[7] Cedars Sinai Med Ctr, Dept Neurol, Neuroimaging Program, Los Angeles, CA USA
[8] Univ Penn, Ctr Neuroinflammat & Neurotherapeut, Perelman Sch Med, Philadelphia, PA USA
[9] Univ Penn, Perelman Sch Med, Dept Neurol, Philadelphia, PA USA
[10] NINDS, Translat Neuroradiol Sect, NIH, Bethesda, MD USA
[11] Univ Penn, Perelman Sch Med, Dept Biostat Epidemiol & Informat, Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA
关键词
MRI; multiple sclerosis; white matter lesions; BLACK-HOLES; RELIABILITY; ATROPHY; DEHYDRATION; DISABILITY; EVOLUTION; GRAY;
D O I
10.1111/jon.13147
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and PurposeMulticenter study designs involving a variety of MRI scanners have become increasingly common. However, these present the issue of biases in image-based measures due to scanner or site differences. To assess these biases, we imaged 11 volunteers with multiple sclerosis (MS) with scan and rescan data at four sites. MethodsImages were acquired on Siemens or Philips scanners at 3 Tesla. Automated white matter lesion detection and whole-brain, gray and white matter, and thalamic volumetry were performed, as well as expert manual delineations of T1 magnetization-prepared rapid acquisition gradient echo and T2 fluid-attenuated inversion recovery lesions. Random-effect and permutation-based nonparametric modeling was performed to assess differences in estimated volumes within and across sites. ResultsRandom-effect modeling demonstrated model assumption violations for most comparisons of interest. Nonparametric modeling indicated that site explained >50% of the variation for most estimated volumes. This expanded to >75% when data from both Siemens and Philips scanners were included. Permutation tests revealed significant differences between average inter- and intrasite differences in most estimated brain volumes (P < .05). The automatic activation of spine coil elements during some acquisitions resulted in a shading artifact in these images. Permutation tests revealed significant differences between thalamic volume measurements from acquisitions with and without this artifact. ConclusionDifferences in brain volumetry persisted across MR scanners despite protocol harmonization. These differences were not well explained by variance component modeling; however, statistical innovations for mitigating intersite differences show promise in reducing biases in multicenter studies of MS.
引用
收藏
页码:941 / 952
页数:12
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