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自闭症谱系障碍的病因分类。

An etiologic classification of autism spectrum disorders.

作者信息

Gabis Lidia V, Pomeroy John

出版信息

Isr Med Assoc J. 2014 May;16(5):295-8.

Abstract

BACKGROUND

Autism spectrum disorders (ASD) represent a common phenotype related to multiple etiologies, such as genetic, brain injury (e.g., prematurity), environmental (e.g., viral, toxic), multiple or unknown causes.

OBJECTIVES

To devise a clinical classification of children diagnosed with ASD according to etiologic workup.

METHODS

Children diagnosed with ASD (n = 436) from two databases were divided into groups of symptomatic cryptogenic or idiopathic, and variables within each database and diagnostic category were compared.

RESULTS

By analyzing the two separate databases, 5.4% of the children were classified as symptomatic, 27% as cryptogenic and 67.75% as idiopathic. Among other findings, the entire symptomatic group demonstrated language delays, but almost none showed evidence for regression. Our results indicate similarities between the idiopathic and cryptogenic subgroups in most of the examined variables, and mutual differences from the symptomatic subgroup. The similarities between the first two subgroups support prior evidence that most perinatal factors and minor physical anomalies do not contribute to the development of core symptoms of autism.

CONCLUSIONS

Differences in gender and clinical and diagnostic features were found when etiology was used to create subtypes of ASD. This classification could have heuristic importance in the search for an autism gene(s).

摘要

背景

自闭症谱系障碍(ASD)是一种与多种病因相关的常见表型,这些病因包括遗传、脑损伤(如早产)、环境因素(如病毒、毒素)、多种病因或不明原因。

目的

根据病因检查结果对诊断为ASD的儿童进行临床分类。

方法

将来自两个数据库的436例诊断为ASD的儿童分为症状性隐源性或特发性组,并比较每个数据库和诊断类别中的变量。

结果

通过分析两个独立的数据库,5.4%的儿童被归类为症状性,27%为隐源性,67.75%为特发性。其他研究结果包括,整个症状性组均表现出语言发育迟缓,但几乎没有证据表明存在倒退现象。我们的结果表明,在大多数检查变量中,特发性和隐源性亚组之间存在相似性,且与症状性亚组存在相互差异。前两个亚组之间的相似性支持了先前的证据,即大多数围产期因素和轻微身体异常与自闭症核心症状的发展无关。

结论

当根据病因对ASD进行亚型分类时,发现了性别、临床和诊断特征方面的差异。这种分类在寻找自闭症基因方面可能具有启发意义。

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