Program on Pediatric Imaging and Tissue Sciences, NICHD, NIH, Bethesda, Maryland; Center for Neuroscience and Regenerative Medicine at the Uniformed Services University of the Health Sciences, Bethesda, Maryland.
Hum Brain Mapp. 2013 Oct;34(10):2439-54. doi: 10.1002/hbm.22081. Epub 2012 Mar 28.
Diffusion tensor imaging (DTI) is commonly used for studies of the human brain due to its inherent sensitivity to the microstructural architecture of white matter. To increase sampling diversity, it is often desirable to perform multicenter studies. However, it is likely that the variability of acquired data will be greater in multicenter studies than in single-center studies due to the added confound of differences between sites. Therefore, careful characterization of the contributions to variance in a multicenter study is extremely important for meaningful pooling of data from multiple sites. We propose a two-step analysis framework for first identifying outlier datasets, followed by a parametric variance analysis for identification of intersite and intrasite contributions to total variance. This framework is then applied to phantom data from the NIH MRI study of normal brain development (PedsMRI). Our results suggest that initial outlier identification is extremely important for accurate assessment of intersite and intrasite variability, as well as for early identification of problems with data acquisition. We recommend the use of the presented framework at frequent intervals during the data acquisition phase of multicenter DTI studies, which will allow investigators to identify and solve problems as they occur.
弥散张量成像(DTI)由于其对白质微观结构的固有敏感性,常用于人类大脑的研究。为了增加采样的多样性,通常希望进行多中心研究。然而,由于站点之间的差异带来的混杂因素,多中心研究中获得的数据的可变性很可能比单中心研究中更大。因此,仔细描述多中心研究中变异的贡献对于从多个站点有意义地汇总数据非常重要。我们提出了一个两步分析框架,首先识别离群数据集,然后进行参数方差分析,以确定站点间和站点内对总方差的贡献。然后将该框架应用于来自 NIH MRI 正常脑发育研究(PedsMRI)的体模数据。我们的结果表明,初始离群值识别对于准确评估站点间和站点内的变异性以及早期识别数据采集问题非常重要。我们建议在多中心 DTI 研究的数据采集阶段频繁使用所提出的框架,这将使研究人员能够在问题发生时识别和解决问题。