McKinney Walker S, Kelly Shannon E, Unruh Kathryn E, Shafer Robin L, Sweeney John A, Styner Martin, Mosconi Matthew W
Schiefelbusch Institute for Life Span Studies and Kansas Center for Autism Research and Training (K-CART), University of Kansas, Lawrence, KS, United States.
Clinical Child Psychology Program, University of Kansas, Lawrence, KS, United States.
Front Integr Neurosci. 2022 May 3;16:821109. doi: 10.3389/fnint.2022.821109. eCollection 2022.
Sensorimotor issues are common in autism spectrum disorder (ASD), though their neural bases are not well understood. The cerebellum is vital to sensorimotor control and reduced cerebellar volumes in ASD have been documented. Our study examined the extent to which cerebellar volumes are associated with multiple sensorimotor behaviors in ASD.
Fifty-eight participants with ASD and 34 typically developing (TD) controls (8-30 years) completed a structural MRI scan and precision grip testing, oculomotor testing, or both. Force variability during precision gripping as well as absolute error and trial-to-trial error variability of visually guided saccades were examined. Volumes of cerebellar lobules, vermis, and white matter were quantified. The relationships between each cerebellar region of interest (ROI) and force variability, saccade error, and saccade error variability were examined.
Relative to TD controls, individuals with ASD showed increased force variability. Individuals with ASD showed a reduced volume of cerebellar vermis VI-VII relative to TD controls. Relative to TD females, females with ASD showed a reduced volume of bilateral cerebellar Crus II/lobule VIIB. Increased volume of Crus I was associated with increased force variability. Increased volume of vermal lobules VI-VII was associated with reduced saccade error for TD controls but not individuals with ASD. Increased right lobule VIII and cerebellar white matter volumes as well as reduced right lobule VI and right lobule X volumes were associated with greater ASD symptom severity. Reduced volumes of right Crus II/lobule VIIB were associated with greater ASD symptom severity in only males, while reduced volumes of right Crus I were associated with more severe restricted and repetitive behaviors only in females.
Our finding that increased force variability in ASD is associated with greater cerebellar Crus I volumes indicates that disruption of sensory feedback processing supported by Crus I may contribute to skeletomotor differences in ASD. Results showing that volumes of vermal lobules VI-VII are associated with saccade precision in TD but not ASD implicates atypical organization of the brain systems supporting oculomotor control in ASD. Associations between volumes of cerebellar subregions and ASD symptom severity suggest cerebellar pathological processes may contribute to multiple developmental challenges in ASD.
感觉运动问题在自闭症谱系障碍(ASD)中很常见,但其神经基础尚未得到很好的理解。小脑对感觉运动控制至关重要,并且已有文献记载ASD患者的小脑体积减小。我们的研究考察了小脑体积与ASD中多种感觉运动行为的关联程度。
58名患有ASD的参与者和34名发育正常(TD)的对照者(8至30岁)完成了一次结构磁共振成像扫描以及精确抓握测试、动眼神经测试或两者皆有。检测了精确抓握过程中的力变异性以及视觉引导扫视的绝对误差和逐次试验误差变异性。对小脑小叶、蚓部和白质的体积进行了量化。研究了每个小脑感兴趣区域(ROI)与力变异性、扫视误差和扫视误差变异性之间的关系。
相对于TD对照者,ASD患者表现出更大的力变异性。相对于TD对照者,ASD患者的小脑蚓部VI - VII体积减小。相对于TD女性,患有ASD的女性双侧小脑 Crus II/小叶VIIB体积减小。Crus I体积增加与力变异性增加相关。对于TD对照者,蚓部小叶VI - VII体积增加与扫视误差减小相关,但ASD患者并非如此。右侧小叶VIII和小脑白质体积增加以及右侧小叶VI和右侧小叶X体积减小与更严重的ASD症状严重程度相关。仅在男性中,右侧Crus II/小叶VIIB体积减小与更严重的ASD症状严重程度相关,而仅在女性中,右侧Crus I体积减小与更严重的受限和重复行为相关。
我们的研究发现,ASD中力变异性增加与小脑Crus I体积增大有关,这表明Crus I支持的感觉反馈处理中断可能导致ASD中的骨骼运动差异。结果表明,蚓部小叶VI - VII体积与TD中的扫视精度相关,但与ASD无关,这意味着支持ASD中动眼神经控制的脑系统存在非典型组织。小脑亚区域体积与ASD症状严重程度之间的关联表明,小脑病理过程可能导致ASD中的多种发育挑战。