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Gray Matter Features of Reading Disability: A Combined Meta-Analytic and Direct Analysis Approach

机译:阅读障碍的灰质特征:荟萃分析和直接分析相结合的方法

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摘要

Meta-analysis of voxel-based morphometry dyslexia studies and direct analysis of 293 reading disability and control cases from six different research sites were performed to characterize defining gray matter features of reading disability. These analyses demonstrated consistently lower gray matter volume in left posterior superior temporal sulcus/middle temporal gyrus regions and left orbitofrontal gyrus/pars orbitalis regions. Gray matter volume within both of these regions significantly predicted individual variation in reading comprehension after correcting for multiple comparisons. These regional gray matter differences were observed across published studies and in the multisite dataset after controlling for potential age and gender effects, and despite increased anatomical variance in the reading disability group, but were not significant after controlling for total gray matter volume. Thus, the orbitofrontal and posterior superior temporal sulcus gray matter findings are relatively reliable effects that appear to be dependent on cases with low total gray matter volume. The results are considered in the context of genetics studies linking orbitofrontal and superior temporal sulcus regions to alleles that confer risk for reading disability.
机译:进行了基于体素的形态计量学阅读障碍研究的荟萃分析,以及对来自六个不同研究地点的293名阅读障碍者和对照病例的直接分析,以表征阅读障碍者的灰质特征。这些分析表明左后上颞沟/中颞回和左眶额回/ pars眶区的灰质体积始终较低。在校正多个比较之后,这两个区域内的灰质体积显着预测了阅读理解中的个体差异。在控制潜在的年龄和性别影响后,在已发表的研究中和多站点数据集中观察到了这些区域灰质差异,尽管阅读障碍组的解剖差异有所增加,但在控制总灰质体积后,这些差异并不显着。因此,眶额和后颞上颞沟灰质发现是相对可靠的效果,似乎取决于总灰质量低的病例。在遗传研究的背景下考虑了结果,该研究将眶额和上颞沟区域与赋予阅读障碍风险的等位基因联系起来。

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