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杜氏肌营养不良症与自闭症谱系障碍的关联。

Association of Duchenne muscular dystrophy with autism spectrum disorder.

作者信息

Wu Joyce Y, Kuban Karl C K, Allred Elizabeth, Shapiro Frederic, Darras Basil T

机构信息

Division of Pediatric Neurology, David Geffen School of Medicine, Mattel Children's Hospital at UCLA, Los Angeles, CA, USA.

出版信息

J Child Neurol. 2005 Oct;20(10):790-5. doi: 10.1177/08830738050200100201.

Abstract

We hypothesize that Duchenne muscular dystrophy and autism spectrum disorder/pervasive developmental disorder co-occur with a greater than random frequency. In this study, we set out to reject the hypothesis that Duchenne muscular dystrophy and autism spectrum disorder/pervasive developmental disorder co-occur no more often than expected by chance. Two index cases and six additional boys with concomitant Duchenne muscular dystrophy and autism spectrum disorder were identified in a muscular dystrophy clinic that approximates the total number of Duchenne muscular dystrophy boys (158) in the state of Massachusetts. The rate of prevalence (6 of 158) was compared with the prevalence rate of autism spectrum disorder in boys in the general population (1.6 in 1,000). We rejected the hypothesis that Duchenne muscular dystrophy and autism spectrum disorder co-occurrence was likely to be explained by chance (P = .006). We identify a previously unrecognized association of Duchenne muscular dystrophy with autism spectrum disorder. Further work might elucidate the level of association between these two conditions, either at the genetic or at the protein level, and might clarify, at least partially, the neurobiologic mechanisms associated with autism spectrum disorder.

摘要

我们推测杜氏肌营养不良症与自闭症谱系障碍/广泛性发育障碍同时出现的频率高于随机概率。在本研究中,我们试图推翻“杜氏肌营养不良症与自闭症谱系障碍/广泛性发育障碍同时出现的频率不高于偶然预期”这一假设。在一家肌营养不良症诊所中,我们识别出了两例索引病例以及另外六名同时患有杜氏肌营养不良症和自闭症谱系障碍的男孩,该诊所的病例数接近马萨诸塞州杜氏肌营养不良症男孩的总数(158名)。将患病率(158例中有6例)与普通人群中男孩自闭症谱系障碍的患病率(千分之1.6)进行了比较。我们推翻了“杜氏肌营养不良症与自闭症谱系障碍同时出现可能是由偶然因素导致”这一假设(P = .006)。我们发现了杜氏肌营养不良症与自闭症谱系障碍之间一种此前未被认识到的关联。进一步的研究可能会阐明这两种病症在基因或蛋白质水平上的关联程度,并可能至少部分地阐明与自闭症谱系障碍相关的神经生物学机制。

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