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Power calculations for multicenter imaging studies controlled by the false discovery rate

机译:由错误发现率控制的多中心成像研究的功效计算

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摘要

Magnetic resonance imaging (MRI) is widely used in brain imaging research (neuroimaging) to explore structural and functional changes across dispersed neural networks visible only via multisubject experiments. Multicenter investigations are an effective way to increase recruitment rates. This article describes image‐based power calculations for a two‐group, cross‐sectional design specified by the mean effect size and its standard error, sample size, false discovery rate (FDR), and size of the network (i.e., proportion of image locations) that truly demonstrates an effect. Minimum sample size (for fixed effect size) and the minimum effect size (for fixed sample size) are calculated by specifying the acceptable power threshold. Within‐center variance was estimated in five participating centers by repeat MRI scanning of 12 healthy participants from whom distributions of gray matter were estimated. The effect on outcome measures when varying FDR and the proportion of true positives is presented. Their spatial patterns reflect within‐center variance, which is consistent across centers. Sample sizes 3–6 times larger are needed when detecting effects in subcortical regions compared to the neocortex. Hypothesized multicenter studies of patients with first episode psychosis and control participants were simulated with varying proportions of the cohort recruited at each center. There is little penalty to sample size for recruitment at five centers compared to the center with the lowest variance alone. At 80% power 80 participants per group are required to observe differences in gray matter in high variance regions. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc.
机译:磁共振成像(MRI)在脑成像研究(神经成像)中被广泛使用,以探索仅通过多对象实验才能看到的分散神经网络中的结构和功能变化。多中心调查是提高招聘率的有效方法。本文介绍了由平均效果大小及其标准误差,样本大小,错误发现率(FDR)和网络大小(即图像比例)指定的两组横截面设计的基于图像的功率计算位置)才能真正展示出效果。通过指定可接受的功率阈值,可以计算出最小样本量(用于固定效应量)和最小效应量(用于固定样本量)。通过对12名健康参与者进行重复MRI扫描,估计了五个灰质分布,从而估计了五个参与中心的中心内差异。提出了改变FDR和真实阳性比例对结果衡量的影响。它们的空间格局反映了中心内的方差,这在中心之间是一致的。与新皮层相比,在皮层下区域检测效果时需要3至6倍的样本量。针对首发性精神病患者和对照组参与者进行的假设性多中心研究,采用在每个中心招募的不同比例的队列进行了模拟。与仅具有最小方差的中心相比,五个中心的招募样本量几乎没有损失。在功率为80%的情况下,每组80位参与者需要观察高方差区域中灰质的差异。嗡嗡的脑图,2010年。©2010 Wiley-Liss,Inc.

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