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神经纤维瘤病 1 型患者的孤独症谱系障碍症状学。

Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1.

机构信息

The Jennifer and Daniel Gilbert Neurofibromatosis Institute, Washington, DC.

Center for Neuroscience and Behavioral Medicine at Children's National Medical Center, Washington, DC.

出版信息

Dev Med Child Neurol. 2013 Feb;55(2):131-138. doi: 10.1111/dmcn.12038. Epub 2012 Nov 16.

Abstract

AIM

Difficulties in neurocognition and social interaction are the most prominent causes of morbidity and long-term disability in children with neurofibromatosis type 1 (NF1). Symptoms of attention-deficit-hyperactivity disorder (ADHD) have also been extensively recognized in NF1. However, systematic evaluation of symptoms of autism spectrum disorder (ASD) in children with NF1 has been limited.

METHOD

We present a retrospective, cross-sectional study of the prevalence of symptoms of ASD and ADHD and their relationship in a consecutive series of 66 patients from our NF1 clinic. The Social Responsiveness Scale and the Vanderbilt ADHD Diagnostic Parent Rating Scale were used to assess symptoms of ASD and ADHD.

RESULTS

Sixty-six participants (42 males, 24 females) were included in this study. Mean age at assessment was 10 years 11 months (SD 5 y 4 mo). Forty percent of our NF1 sample had raised symptom levels reaching clinical significance on the Social Responsiveness Scale (T ≥ 60), and 14% reached levels consistent with those seen in children with ASDs (T ≥ 75). These raised levels were not explained by NF1 disease severity or externalizing/internalizing behavioral disorders. There was a statistically significant relationship between symptoms of ADHD and ASD (χ(2) =9.11, df=1, p=0.003, φ=0.56). Particularly salient were the relationships between attention and hyperactivity deficits, with impairments in social awareness and social motivation.

INTERPRETATION

We found that symptoms of ASD in our NF1 population were raised, consistent with previous reports. Further characterization of the specific ASD symptoms and their impact on daily function is fundamental to the development and implementation of effective interventions in this population, which will probably include a combination of medical and behavioral approaches.

摘要

目的

神经认知和社交互动方面的障碍是导致 1 型神经纤维瘤病(NF1)患儿发病和长期残疾的最主要原因。NF1 患儿还广泛存在注意力缺陷多动障碍(ADHD)的症状。然而,NF1 患儿自闭症谱系障碍(ASD)症状的系统评估较为有限。

方法

我们对来自 NF1 临床诊疗中心的连续 66 例患儿进行了 ASD 和 ADHD 症状的患病率及其相关性的回顾性、横断面研究。采用社交反应量表和范德比尔特多动症诊断父母评定量表评估 ASD 和 ADHD 症状。

结果

本研究共纳入 66 名参与者(42 名男性,24 名女性)。评估时的平均年龄为 10 岁 11 个月(SD 5 岁 4 个月)。我们 NF1 样本中有 40%的患儿社会反应量表的评分升高到临床显著水平(T≥60),14%达到了与 ASD 患儿相似的水平(T≥75)。这些升高的水平不能用 NF1 疾病严重程度或外在/内在行为障碍来解释。ADHD 和 ASD 症状之间存在显著的统计学关系(χ²=9.11,df=1,p=0.003,φ=0.56)。特别是在注意力和多动缺陷、社会意识和社会动机缺陷之间存在显著的相关性。

结论

我们发现,我们 NF1 人群中的 ASD 症状升高,与之前的报道一致。进一步明确特定 ASD 症状及其对日常功能的影响,对于这一人群中有效干预措施的制定和实施至关重要,这些干预措施可能包括医疗和行为相结合的方法。

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