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一种基于简单置换的模态对应性检验方法。

A simple permutation-based test of intermodal correspondence.

机构信息

Penn Statistics in Imaging and Visualization Center, Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania.

Department of Biostatistics, Vanderbilt University, Nashville, Tennessee.

出版信息

Hum Brain Mapp. 2021 Nov;42(16):5175-5187. doi: 10.1002/hbm.25577. Epub 2021 Sep 14.

DOI:10.1002/hbm.25577
PMID:34519385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8519855/
Abstract

Many key findings in neuroimaging studies involve similarities between brain maps, but statistical methods used to measure these findings have varied. Current state-of-the-art methods involve comparing observed group-level brain maps (after averaging intensities at each image location across multiple subjects) against spatial null models of these group-level maps. However, these methods typically make strong and potentially unrealistic statistical assumptions, such as covariance stationarity. To address these issues, in this article we propose using subject-level data and a classical permutation testing framework to test and assess similarities between brain maps. Our method is comparable to traditional permutation tests in that it involves randomly permuting subjects to generate a null distribution of intermodal correspondence statistics, which we compare to an observed statistic to estimate a p-value. We apply and compare our method in simulated and real neuroimaging data from the Philadelphia Neurodevelopmental Cohort. We show that our method performs well for detecting relationships between modalities known to be strongly related (cortical thickness and sulcal depth), and it is conservative when an association would not be expected (cortical thickness and activation on the n-back working memory task). Notably, our method is the most flexible and reliable for localizing intermodal relationships within subregions of the brain and allows for generalizable statistical inference.

摘要

许多神经影像学研究中的重要发现都涉及脑图谱之间的相似性,但用于测量这些发现的统计方法却有所不同。目前最先进的方法涉及将观察到的组水平脑图谱(在对多个被试的每个图像位置的强度进行平均之后)与这些组水平图谱的空间零模型进行比较。然而,这些方法通常会做出很强且可能不切实际的统计假设,例如协方差平稳性。为了解决这些问题,本文提出使用个体水平数据和经典的置换检验框架来检验和评估脑图谱之间的相似性。我们的方法与传统的置换检验相当,它涉及随机置换被试以生成模态对应统计量的零分布,然后将其与观察到的统计量进行比较,以估计 p 值。我们在费城神经发育队列的模拟和真实神经影像学数据中应用和比较了我们的方法。我们表明,我们的方法在检测已知具有强相关性的模态之间的关系时表现良好(皮质厚度和脑沟深度),并且在不期望存在关联时具有保守性(皮质厚度和 n 回工作记忆任务中的激活)。值得注意的是,我们的方法在定位大脑子区域内的模态关系方面最为灵活和可靠,并允许进行可推广的统计推断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/f0f1bbe97c24/HBM-42-5175-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/f1c1940820b5/HBM-42-5175-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/27f5cc9b6436/HBM-42-5175-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/39b0e454f227/HBM-42-5175-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/964c11a3f946/HBM-42-5175-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/f0f1bbe97c24/HBM-42-5175-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/f1c1940820b5/HBM-42-5175-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/27f5cc9b6436/HBM-42-5175-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/39b0e454f227/HBM-42-5175-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/964c11a3f946/HBM-42-5175-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb46/8519855/f0f1bbe97c24/HBM-42-5175-g005.jpg

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3
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4
Generative models of MRI-derived neuroimaging features and associated dataset of 18,000 samples.基于MRI的神经影像特征生成模型及包含18000个样本的相关数据集。
Sci Data. 2024 Dec 5;11(1):1330. doi: 10.1038/s41597-024-04157-4.
5
Converging cortical axes.汇聚的皮质轴。
Nat Neurosci. 2025 Jan;28(1):8-10. doi: 10.1038/s41593-024-01722-3.
6
Psychiatric neuroimaging at a crossroads: Insights from psychiatric genetics.精神神经影像学的十字路口:精神遗传学的启示。
Dev Cogn Neurosci. 2024 Dec;70:101443. doi: 10.1016/j.dcn.2024.101443. Epub 2024 Sep 23.
7
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8
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9
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bioRxiv. 2024 Jun 28:2024.06.26.600817. doi: 10.1101/2024.06.26.600817.
10
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4
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5
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Commun Biol. 2020 May 22;3(1):261. doi: 10.1038/s42003-020-0961-x.
6
BrainSpace: a toolbox for the analysis of macroscale gradients in neuroimaging and connectomics datasets.脑空间:用于分析神经影像学和连接组学数据集的宏观梯度的工具包。
Commun Biol. 2020 Mar 5;3(1):103. doi: 10.1038/s42003-020-0794-7.
7
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Neuron. 2020 Apr 22;106(2):340-353.e8. doi: 10.1016/j.neuron.2020.01.029. Epub 2020 Feb 19.
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