Sex Differences in the Striatal Contributions to Longitudinal Fine Motor Development in Autistic Children.

IF 9.6 1区 医学 Q1 NEUROSCIENCES
Olivia Surgent, Derek S Andrews, Joshua K Lee, Joseph Boyle, Andrew Dakopolos, Meghan Miller, Sally Ozonoff, Sally J Rogers, Marjorie Solomon, David G Amaral, Christine Wu Nordahl
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引用次数: 0

Abstract

Background: Fine motor challenges are prevalent in autistic populations. However, little is known about their neurobiological underpinnings or how their related neural mechanisms are influenced by sex. The dorsal striatum, comprised of the caudate nucleus and putamen, is associated with motor learning and control and may hold critical information. We investigated how autism diagnosis and sex assigned at birth influence associations between the dorsal striatum and fine motor development in autistic and non-autistic children.

Methods: We used multimodal assessment of striatal structures (volume and cortico-striatal white matter microstructure) and longitudinal assessment of fine motor skills, first at approximately 3 years of age (Time 1) and again 2-3 years later (Follow-up). Fine motor and magnetic resonance imaging (T1 and diffusion) data were collected at Time 1 from 356 children (234 autistic; 128 female) and at Follow-up from 195 children (113 autistic; 76 female).

Results: At Time 1, associations among fine motor skills, putamen volume, and sensorimotor-striatal fractional anisotropy (sensorimotor-affiliated dorsal striatal structures) were different in autistic boys compared to autistic girls and were not significant for non-autistic children. Further, Time 1 sensorimotor-striatal and prefrontal-striatal microstructure predicted fine motor development for autistic girls but not boys.

Conclusions: Sensorimotor-affiliated dorsal striatum structures may contribute to concurrent motor ability and predict fine motor improvement during critical windows of development in a sex-specific and diagnosis-dependent way. Moreover, the dorsal striatum may play a key role in the distinct neural mechanisms underlying motor challenges in autistic males and females.

自闭症儿童纹状体纵向精细运动发育的性别差异。
背景:精细运动障碍在自闭症人群中普遍存在。然而,人们对它们的神经生物学基础知之甚少,也不知道它们的相关神经机制是如何受性别影响的。背纹状体由尾状核和壳核组成,与运动学习和控制有关,并可能保存关键信息。我们研究了自闭症诊断和出生时的性别如何影响自闭症和非自闭症儿童背纹状体和精细运动发育之间的联系。方法:我们对纹状体结构(体积和皮质纹状体白质微观结构)进行了多模式评估,并对精细运动技能进行了纵向评估,第一次是在大约3岁时(时间1),第二次是在2-3年后(随访)。从356名儿童(234名自闭症儿童;128名女性),195名儿童(113名自闭症儿童;76女性)。结果:在时间1,精细运动技能、壳核体积和感觉运动纹状体分数各向异性(与感觉运动相关的背纹状体结构)在自闭症男孩和自闭症女孩中存在差异,而在非自闭症儿童中无显著性。此外,时间1感觉运动纹状体和前额叶纹状体微观结构预测自闭症女孩的精细运动发育,而不是男孩。结论:感觉运动相关的背纹状体结构可能有助于并发运动能力,并以性别特异性和诊断依赖的方式预测发育关键窗口期精细运动的改善。此外,背纹状体可能在自闭症男性和女性运动挑战的不同神经机制中发挥关键作用。
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来源期刊
Biological Psychiatry
Biological Psychiatry 医学-精神病学
CiteScore
18.80
自引率
2.80%
发文量
1398
审稿时长
33 days
期刊介绍: Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.
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