Prados Ferran, Cardoso Manuel Jorge, Leung Kelvin K, Cash David M, Modat Marc, Fox Nick C, Wheeler-Kingshott Claudia A M, Ourselin Sebastien
Centre for Medical Image Computing (CMIC), Department of Medical Physics and Bioengineering, University College London, London, UK; NMR Research Unit, Queen Square MS Centre, Department of Neuroinflammation, UCL Institute of Neurology, London, UK.
Centre for Medical Image Computing (CMIC), Department of Medical Physics and Bioengineering, University College London, London, UK.
Neurobiol Aging. 2015 Jan;36 Suppl 1(Suppl 1):S81-90. doi: 10.1016/j.neurobiolaging.2014.04.035. Epub 2014 Aug 29.
Brain atrophy measured using structural magnetic resonance imaging (MRI) has been widely used as an imaging biomarker for disease diagnosis and tracking of pathologic progression in neurodegenerative diseases. In this work, we present a generalized and extended formulation of the boundary shift integral (gBSI) using probabilistic segmentations to estimate anatomic changes between 2 time points. This method adaptively estimates a non-binary exclusive OR region of interest from probabilistic brain segmentations of the baseline and repeat scans to better localize and capture the brain atrophy. We evaluate the proposed method by comparing the sample size requirements for a hypothetical clinical trial of Alzheimer's disease to that needed for the current implementation of BSI as well as a fuzzy implementation of BSI. The gBSI method results in a modest but reduced sample size, providing increased sensitivity to disease changes through the use of the probabilistic exclusive OR region.
使用结构磁共振成像(MRI)测量的脑萎缩已被广泛用作疾病诊断的成像生物标志物以及神经退行性疾病病理进展的跟踪指标。在这项工作中,我们提出了一种广义且扩展的边界位移积分(gBSI)公式,使用概率分割来估计两个时间点之间的解剖学变化。该方法从基线和重复扫描的概率性脑部分割中自适应地估计一个非二元异或感兴趣区域,以更好地定位和捕捉脑萎缩。我们通过比较阿尔茨海默病假设临床试验的样本量要求与当前BSI实施以及模糊BSI实施所需的样本量要求,来评估所提出的方法。gBSI方法导致样本量适度减少,但通过使用概率异或区域提高了对疾病变化的敏感性。