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自闭症的微小身体异常:荟萃分析。

Minor physical anomalies in autism: a meta-analysis.

机构信息

Department of Child and Adolescent Psychiatry, University Medical Centre, Utrecht, The Netherlands.

出版信息

Mol Psychiatry. 2010 Mar;15(3):300-7. doi: 10.1038/mp.2008.75. Epub 2008 Jul 15.

Abstract

Autism is a complex neurodevelopmental disorder in which the interactions of genetic, epigenetic and environmental influences play a causal role. Despite the compelling evidence for a strong heritability, the etiology and molecular mechanisms underlying autism remain unclear. High phenotypic variability and genetic heterogeneity confounds the identification of susceptibility genes. The lack of robust indicators to tackle this complexity in autism has led researchers to seek for novel diagnostic tools to create homogenous subgroups. Several studies have indicated that patients with autism have higher rates of minor physical anomalies (MPAs) and that MPAs may serve as a diagnostic tool; however, the results have been inconsistent. Using the cumulative data from seven studies on MPAs in autism, this meta-analysis seeks to examine whether the aggregate data provide evidence of a large mean effect size and statistical significance for MPAs in autism. It covers the studies using multiple research methods till June 2007. The current results from seven studies suggested a significant association of MPAs in autism with a robust pooled effect size (d=0.84), and thereby provide the strongest evidence to date about the close association between MPAs and autism. Our results emphasize the importance of MPAs in the identification of heterogeneity in autism and suggest that the success of future autism genetics research will be exploited by the use of MPAs. Implications for the design of future studies on MPAs in autism are discussed and suggestions for further investigation of these important markers are proposed. Clarifying this relation might improve understanding of risk factors and molecular mechanisms in autism.

摘要

自闭症是一种复杂的神经发育障碍,其中遗传、表观遗传和环境影响的相互作用起着因果作用。尽管有强有力的证据表明自闭症具有很强的遗传性,但自闭症的病因和分子机制仍不清楚。表型的高度可变性和遗传异质性使易感基因的识别变得复杂。由于缺乏解决自闭症复杂性的强大指标,研究人员一直在寻求新的诊断工具来创建同质的亚组。几项研究表明,自闭症患者的轻微身体异常 (MPAs) 发生率较高,MPAs 可能作为一种诊断工具;然而,结果并不一致。本荟萃分析利用自闭症中 MPAs 的七个研究的累积数据,旨在检查汇总数据是否为自闭症中 MPAs 的大平均效应量和统计学意义提供证据。它涵盖了直到 2007 年 6 月使用多种研究方法的研究。目前来自七个研究的结果表明,MPAs 与自闭症之间存在显著关联,具有稳健的汇总效应量(d=0.84),从而为 MPAs 与自闭症之间的密切关联提供了迄今为止最强有力的证据。我们的结果强调了 MPAs 在自闭症异质性识别中的重要性,并表明未来自闭症遗传学研究的成功将通过使用 MPAs 来实现。讨论了对自闭症中 MPAs 进行未来研究的设计的影响,并提出了进一步研究这些重要标记物的建议。阐明这种关系可能有助于更好地理解自闭症中的风险因素和分子机制。

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