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本文引用的文献

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Machine learning and dyslexia: Classification of individual structural neuro-imaging scans of students with and without dyslexia.机器学习与诵读困难:有诵读困难和无诵读困难学生个体结构性神经影像扫描的分类
Neuroimage Clin. 2016 Mar 29;11:508-514. doi: 10.1016/j.nicl.2016.03.014. eCollection 2016.
2
Disrupted white matter connectivity underlying developmental dyslexia: A machine learning approach.发育性阅读障碍背后的白质连接中断:一种机器学习方法。
Hum Brain Mapp. 2016 Apr;37(4):1443-58. doi: 10.1002/hbm.23112. Epub 2016 Jan 20.
3
Cortical thickness abnormalities associated with dyslexia, independent of remediation status.与阅读障碍相关的皮质厚度异常,与矫正状态无关。
Neuroimage Clin. 2014 Nov 18;7:177-86. doi: 10.1016/j.nicl.2014.11.005. eCollection 2015.
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How reliable are gray matter disruptions in specific reading disability across multiple countries and languages? Insights from a large-scale voxel-based morphometry study.跨多个国家和语言,特定阅读障碍中灰质破坏的可靠性如何?一项基于体素的大规模形态学研究的见解。
Hum Brain Mapp. 2015 May;36(5):1741-54. doi: 10.1002/hbm.22734. Epub 2015 Jan 17.
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Atypical Sulcal Pattern in Children with Developmental Dyslexia and At-Risk Kindergarteners.发育性阅读障碍儿童及高危幼儿园儿童的非典型脑沟模式
Cereb Cortex. 2016 Mar;26(3):1138-1148. doi: 10.1093/cercor/bhu305. Epub 2015 Jan 9.
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Anatomical Abnormalities in Autism?自闭症中的解剖学异常?
Cereb Cortex. 2016 Apr;26(4):1440-52. doi: 10.1093/cercor/bhu242. Epub 2014 Oct 14.
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Structural imaging biomarkers of Alzheimer's disease: predicting disease progression.阿尔茨海默病的结构成像生物标志物:预测疾病进展
Neurobiol Aging. 2015 Jan;36 Suppl 1:S23-31. doi: 10.1016/j.neurobiolaging.2014.04.034. Epub 2014 Aug 28.
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Neuroanatomical precursors of dyslexia identified from pre-reading through to age 11.从阅读前到 11 岁识别阅读障碍的神经解剖学前兆。
Brain. 2014 Dec;137(Pt 12):3136-41. doi: 10.1093/brain/awu229. Epub 2014 Aug 14.
9
Planum temporale asymmetry in developmental dyslexia: Revisiting an old question.发育性阅读障碍中的颞平面不对称性:重新审视一个老问题。
Hum Brain Mapp. 2014 Dec;35(12):5717-35. doi: 10.1002/hbm.22579. Epub 2014 Jul 10.
10
Spatial distribution and longitudinal development of deep cortical sulcal landmarks in infants.婴儿大脑深部皮质沟回标志的空间分布及纵向发育
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发育性阅读障碍神经解剖学基础的多参数机器学习方法。

Multi-parameter machine learning approach to the neuroanatomical basis of developmental dyslexia.

作者信息

Płoński Piotr, Gradkowski Wojciech, Altarelli Irene, Monzalvo Karla, van Ermingen-Marbach Muna, Grande Marion, Heim Stefan, Marchewka Artur, Bogorodzki Piotr, Ramus Franck, Jednoróg Katarzyna

机构信息

Institute of Radioelectronics, Warsaw University of Technology, Poland.

Imagilys SPRL, Brussels, Belgium.

出版信息

Hum Brain Mapp. 2017 Feb;38(2):900-908. doi: 10.1002/hbm.23426. Epub 2016 Oct 6.

DOI:10.1002/hbm.23426
PMID:27712002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6867128/
Abstract

Despite decades of research, the anatomical abnormalities associated with developmental dyslexia are still not fully described. Studies have focused on between-group comparisons in which different neuroanatomical measures were generally explored in isolation, disregarding potential interactions between regions and measures. Here, for the first time a multivariate classification approach was used to investigate grey matter disruptions in children with dyslexia in a large (N = 236) multisite sample. A variety of cortical morphological features, including volumetric (volume, thickness and area) and geometric (folding index and mean curvature) measures were taken into account and generalizability of classification was assessed with both 10-fold and leave-one-out cross validation (LOOCV) techniques. Classification into control vs. dyslexic subjects achieved above chance accuracy (AUC = 0.66 and ACC = 0.65 in the case of 10-fold CV, and AUC = 0.65 and ACC = 0.64 using LOOCV) after principled feature selection. Features that discriminated between dyslexic and control children were exclusively situated in the left hemisphere including superior and middle temporal gyri, subparietal sulcus and prefrontal areas. They were related to geometric properties of the cortex, with generally higher mean curvature and a greater folding index characterizing the dyslexic group. Our results support the hypothesis that an atypical curvature pattern with extra folds in left hemispheric perisylvian regions characterizes dyslexia. Hum Brain Mapp 38:900-908, 2017. © 2016 Wiley Periodicals, Inc.

摘要

尽管经过了数十年的研究,但与发育性阅读障碍相关的解剖学异常仍未得到充分描述。以往的研究主要集中在组间比较上,通常是孤立地探究不同的神经解剖学测量指标,而忽略了不同脑区和测量指标之间潜在的相互作用。在此,我们首次采用多变量分类方法,对一个大型(N = 236)多中心样本中的阅读障碍儿童的灰质破坏情况进行研究。我们考虑了多种皮质形态学特征,包括体积(容积、厚度和面积)和几何(折叠指数和平均曲率)测量指标,并使用10倍交叉验证和留一法交叉验证(LOOCV)技术评估分类的可推广性。在进行了有原则的特征选择后,将对照组与阅读障碍组受试者进行分类,其准确率高于随机水平(在10倍交叉验证中,AUC = 0.66,ACC = 0.65;使用留一法交叉验证时,AUC = 0.65,ACC = 0.64)。区分阅读障碍儿童和对照组儿童的特征仅位于左半球,包括颞上回和颞中回、顶下沟和前额叶区域。这些特征与皮质的几何特性有关,阅读障碍组的平均曲率通常更高,折叠指数更大。我们的研究结果支持以下假设:左侧半球颞周区域出现额外褶皱的非典型曲率模式是阅读障碍的特征。《人类大脑图谱》38:900 - 908, 2017。© 2016威利期刊公司。