Péter Zsanett, Oliphant Melody E, Fernandez Thomas V
Department of Biology, Sewanee: The University of the SouthSewanee, TN, USA; Department of Chemistry, Sewanee: The University of the SouthSewanee, TN, USA.
Yale Child Study Center, Yale University School of Medicine New Haven, CT, USA.
Front Neurosci. 2017 Mar 29;11:171. doi: 10.3389/fnins.2017.00171. eCollection 2017.
Motor stereotypies are common, repetitive, rhythmic movements with typical onset in early childhood. While most often described in children with autism spectrum disorder (ASD) and intellectual disability (ID), stereotypies can also present without developmental delay and persist into adulthood. Stereotypies are often disruptive and harmful, both physically and socially, and effective evidence-based treatments are lacking. This can be attributed, in part, to our incomplete knowledge of the underlying biological and environmental risk. Several studies implicate various neurotransmitters, brain circuits, anatomical loci, and pre- and post-natal environmental influences in stereotypy onset and symptom severity. However, there are few points of convergence among a relatively small number of studies, indicating that more research is needed to confirm the underlying bases of risk. Of particular note is the lack of published genetic studies of stereotypies, despite evidence for Mendelian inheritance patterns in some families. Focusing future studies on typically-developing children with primary motor stereotypies may be a useful approach to minimize potential biological, environmental, and genetic heterogeneity that could theoretically hinder consistent findings. Ultimately, a deeper understanding of the underlying biology and risk factors for motor stereotypies will lead us closer to more effective targeted therapies that will alleviate suffering in affected children.
运动刻板行为是常见的、重复性的、有节奏的动作,通常在儿童早期出现。虽然刻板行为最常出现在自闭症谱系障碍(ASD)和智力障碍(ID)儿童中,但也可能在没有发育迟缓的情况下出现,并持续到成年。刻板行为往往具有破坏性,在身体和社交方面都有害,而且缺乏有效的循证治疗方法。这在一定程度上可归因于我们对潜在生物和环境风险的认识不完整。多项研究表明,各种神经递质、脑回路、解剖位点以及产前和产后环境影响与刻板行为的发生及症状严重程度有关。然而,相对较少的研究之间几乎没有交集,这表明需要更多研究来证实潜在的风险基础。特别值得注意的是,尽管在一些家庭中有孟德尔遗传模式的证据,但关于刻板行为的已发表基因研究却很少。将未来的研究重点放在患有原发性运动刻板行为的发育正常儿童身上,可能是一种有用的方法,可最大限度地减少理论上可能阻碍得出一致结果的潜在生物、环境和基因异质性。最终,对运动刻板行为的潜在生物学和风险因素有更深入的了解,将使我们更接近找到更有效的靶向治疗方法,从而减轻受影响儿童的痛苦。