自闭症谱系障碍的 Beery VMI 和脑容量关系。

Pub Date : 2019-09-01 Epub Date: 2019-08-16 DOI:10.1007/s40817-019-00069-z
Ryan R Green, Erin D Bigler, Alyson Froehlich, Molly B D Prigge, Brandon A Zielinski, Brittany G Travers, Jeffrey S Anderson, Andrew Alexander, Nicholas Lange, Janet E Lainhart
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引用次数: 0

摘要

虽然有报道称自闭症谱系障碍(ASD)患者在完成需要视觉-运动整合(VMI)的任务时能力下降,但很少有研究探讨 VMI 表现与涉及运动和感知功能的神经解剖感兴趣区(ROI)之间的关联。为了解决这些问题,本研究选取了 41 名 ASD 患者(3-23 岁)和 27 名发育正常的 TD 患者(5-26 岁)作为全男性样本,他们完成了 Beery-Buktenica 视觉-运动整合发育测试(Beery VMI),该测试是综合神经心理测试的一部分。所有参与者均接受了 3.0 T 磁共振成像(MRI),并进行了图像量化(FreeSurfer 软件 v5.3)。两组的年龄、惯用手和颅内容积(ICV)在统计学上是匹配的。与 TD 组相比,ASD 参与者在 VMI 和 IQ 测量中的表现明显较低。只有 TD 组的 VMI 表现与 FSIQ 和 PIQ 有明显相关性。各组之间预先定义的神经解剖学 ROI 均无明显差异。在 TD 组中,VMI 与中央前回灰质总体积(r = .51,p = .006)和额叶灰质总体积(r = .46,p = .017)之间存在显著相关性。在 ASD 参与者中,ROI 与 Beery VMI 的表现没有明显的相关性。在群体水平上,尽管 ASD 参与者的视觉运动能力有所下降,但并未观察到与运动或感觉知觉 ROI 的系统性关系。在TD组中,研究结果与前额回在运动控制中的假定作用以及额叶在计划、组织和执行监控中的参与相一致,而这些都是VMI表现所必需的。鉴于在 ASD 患者中未观察到 VMI 与 ROI 之间的类似关联,ASD 组参与者的神经发育可能并不遵循同质模式,因此不太可能观察到这些脑区的相关性。
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Beery VMI and Brain Volumetric Relations in Autism Spectrum Disorder.

Although diminished proficiency on tasks that require visual-motor integration (VMI) has been reported in individuals with autism spectrum disorder (ASD), very few studies have examined the association between VMI performance and neuroanatomical regions of interest (ROI) involved in motor and perceptual functioning. To address these issues, the current study included an all-male sample of 41 ASD (ages 3-23 years) and 27 typically developing (TD) participants (ages 5-26 years) who completed the Beery-Buktenica Developmental Test of Visual-Motor Integration (Beery VMI) as part of a comprehensive neuropsychological battery. All participants underwent 3.0 T magnetic resonance imaging (MRI) with image quantification (FreeSurfer software v5.3). The groups were statistically matched on age, handedness, and intracranial volume (ICV). ASD participants performed significantly lower on VMI and IQ measures compared with the TD group. VMI performance was significantly correlated with FSIQ and PIQ in the TD group only. No pre-defined neuroanatomical ROIs were significantly different between groups. Significant correlations were observed in the TD group between VMI and total precentral gyrus gray matter volume (r = .51, p = .006) and total frontal lobe gray matter volume (r = .46, p = .017). There were no significant ROI correlations with Beery VMI performance in ASD participants. At the group level, despite ASD participants exhibiting reduced visuomotor abilities, no systematic relation with motor or sensory-perceptual ROIs was observed. In the TD group, results were consistent with the putative role of the precentral gyrus in motor control along with frontal involvement in planning, organization, and execution monitoring, all essential for VMI performance. Given that similar associations between VMI and ROIs were not observed in those with ASD, neurodevelopment in ASD group participants may not follow homogenous patterns making correlations in these brain regions unlikely to be observed.

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