Multiscale heterogeneity of white matter morphometry in psychiatric disorders.

Ashlea Segal, Robert E Smith, Sidhant Chopra, Stuart Oldham, Linden Parkes, Kevin Aquino, Seyed Mostafa Kia, Thomas Wolfers, Barbara Franke, Martine Hoogman, Christian F Beckmann, Lars T Westlye, Ole A Andreassen, Andrew Zalesky, Ben J Harrison, Christopher G Davey, Carles Soriano-Mas, Narcís Cardoner, Jeggan Tiego, Murat Yücel, Leah Braganza, Chao Suo, Michael Berk, Sue Cotton, Mark A Bellgrove, Andre F Marquand, Alex Fornito
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Abstract

Background: Inter-individual variability in the neurobiological and clinical characteristics of mental illnesses are often overlooked by classical group-mean case-control studies. Studies using normative modelling to infer person-specific deviations of grey matter volume have indicated that group means are not representative of most individuals. The extent to which this variability is present in white matter morphometry, which is integral to brain function, remains unclear.

Methods: We applied Warped Bayesian Linear Regression normative models to T1-weighted magnetic resonance imaging data and mapped inter-individual variability in person-specific white matter volume deviations in 1,294 cases (58% male) diagnosed with one of six disorders (attention-deficit/hyperactivity, autism, bipolar, major depressive, obsessive-compulsive and schizophrenia) and 1,465 matched controls (54% male) recruited across 25 scan sites. We developed a framework to characterize deviation heterogeneity at multiple spatial scales, from individual voxels, through inter-regional connections, specific brain regions, and spatially extended brain networks.

Results: The specific locations of white matter volume deviations were highly heterogeneous across participants, affecting the same voxel in fewer than 8% of individuals with the same diagnosis. For autism and schizophrenia, negative deviations (i.e., areas where volume is lower than normative expectations) aggregated into common tracts, regions, and large-scale networks in up to 69% of individuals.

Conclusions: The prevalence of white matter volume deviations was lower than previously observed in grey matter, and the specific location of these deviations was highly heterogeneous when considering voxel-wise spatial resolution. Evidence of aggregation within common pathways and networks was apparent in schizophrenia and autism, but not other disorders.

精神疾病中白质形态测量的多尺度异质性。
背景:精神疾病的神经生物学和临床特征的个体间变异性常常被经典的组平均病例对照研究所忽视。使用规范模型来推断灰质体积的个体特异性偏差的研究表明,群体均值不能代表大多数个体。这种可变性在脑功能不可或缺的白质形态测量中存在的程度尚不清楚。方法:我们将扭曲贝叶斯线性回归规范模型应用于t1加权磁共振成像数据,并绘制了1294例(58%男性)被诊断为6种疾病之一(注意缺陷/多动、自闭症、双相情感障碍、重度抑郁症、强迫症和精神分裂症)和1465例匹配对照(54%男性)在25个扫描点的个人特异性白质体积偏差的个体间变异。我们开发了一个框架来描述多个空间尺度上的偏差异质性,从个体体素,通过区域间连接,特定的大脑区域和空间扩展的大脑网络。结果:白质体积偏差的具体位置在参与者中是高度异质性的,在相同诊断的个体中影响相同体素的不到8%。对于自闭症和精神分裂症,负偏差(即,容量低于规范预期的区域)在高达69%的个体中聚集成共同的区域、区域和大规模网络。结论:白质体积偏差的患病率低于先前在灰质中观察到的,并且当考虑到体素方向的空间分辨率时,这些偏差的具体位置是高度异质性的。在精神分裂症和自闭症中,在共同途径和网络中聚集的证据很明显,但在其他疾病中没有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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