自闭症谱系障碍中的线粒体功能障碍。

Maheen F Siddiqui, Clare Elwell, Mark H Johnson
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引用次数: 0

摘要

自闭症谱系障碍(ASD)被归类为以社会交流和互动减少为特征的神经发育障碍。最近,越来越多的证据表明,很大一部分自闭症患者同时患有线粒体疾病和能量产生异常等疾病。因此,这导致了自闭症可能与线粒体功能障碍有关的假设。我们回顾了在自闭症个体中报道的线粒体电子传递链(ETC)复合物活性降低和线粒体基因,特别是呼吸链复合物基因表达降低的研究。总的来说,这些发现支持了自闭症谱系障碍与线粒体功能受损有关的假设;然而,许多研究的样本量很小,所使用的技术也存在差异。因此,为了更好地建立自闭症和线粒体功能障碍之间的联系,迫切需要利用新的成像技术,如近红外光谱,这将允许对神经元活动的代谢标志物(如细胞色素c氧化酶)进行无创测量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial Dysfunction in Autism Spectrum Disorders.

Autism spectrum disorders (ASD) are classified as neurodevelopmental disorders characterised by diminished social communication and interaction. Recently, evidence has accrued that a significant proportion of individuals with autism have concomitant diseases such as mitochondrial disease and abnormalities of energy generation. This has therefore led to the hypothesis that autism may be linked to mitochondrial dysfunction. We review such studies reporting decreased activity of mitochondrial electron transport chain (ETC) complexes and reduced gene expression of mitochondrial genes, in particular genes of respiratory chain complexes, in individuals with autism. Overall, the findings support the hypothesis that there is an association of ASD with impaired mitochondrial function; however, many of the studies have small sample sizes and there is variability in the techniques utilised. There is therefore a vital need to utilise novel imaging techniques, such as near-infrared spectroscopy, that will allow non-invasive measurement of metabolic markers for neuronal activity such as cytochrome c oxidase, in order to better establish the link between autism and mitochondrial dysfunction.

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