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自闭症谱系障碍的流行病学

The epidemiology of autism spectrum disorders.

作者信息

Newschaffer Craig J, Croen Lisa A, Daniels Julie, Giarelli Ellen, Grether Judith K, Levy Susan E, Mandell David S, Miller Lisa A, Pinto-Martin Jennifer, Reaven Judy, Reynolds Ann M, Rice Catherine E, Schendel Diana, Windham Gayle C

机构信息

Department of Epidemiology and Biostatistics, Drexel University School of Public Health, Philadelphia, PA 19102, USA.

出版信息

Annu Rev Public Health. 2007;28:235-58. doi: 10.1146/annurev.publhealth.28.021406.144007.

Abstract

Autism spectrum disorders (ASDs) are complex, lifelong, neurodevelopmental conditions of largely unknown cause. They are much more common than previously believed, second in frequency only to mental retardation among the serious developmental disorders. Although a heritable component has been demonstrated in ASD etiology, putative risk genes have yet to be identified. Environmental risk factors may also play a role, perhaps via complex gene-environment interactions, but no specific exposures with significant population effects are known. A number of endogenous biomarkers associated with autism risk have been investigated, and these may help identify significant biologic pathways that, in turn, will aid in the discovery of specific genes and exposures. Future epidemiologic research should focus on expanding population-based descriptive data on ASDs, exploring candidate risk factors in large well-designed studies incorporating both genetic and environmental exposure data and addressing possible etiologic heterogeneity in studies that can stratify case groups and consider alternate endophenotypes.

摘要

自闭症谱系障碍(ASD)是复杂的、终身的神经发育疾病,其病因大多未知。它们比之前认为的更为常见,在严重发育障碍中发病率仅次于智力迟钝。虽然在ASD病因学中已证实有遗传因素,但尚未确定假定的风险基因。环境风险因素可能也起作用,或许是通过复杂的基因-环境相互作用,但尚无已知的对大量人群有显著影响的特定暴露因素。已经对一些与自闭症风险相关的内源性生物标志物进行了研究,这些生物标志物可能有助于识别重要的生物学途径,进而有助于发现特定基因和暴露因素。未来的流行病学研究应着重于扩大基于人群的ASD描述性数据,在纳入基因和环境暴露数据的大型精心设计的研究中探索候选风险因素,并在能够对病例组进行分层并考虑替代内表型的研究中解决可能的病因异质性问题。

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