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A PRELIMINARY VOLUMETRIC MRI STUDY OF AMYGDALA AND HIPPOCAMPAL SUBFIELDS IN AUTISM DURING INFANCY

机译:婴儿期扁桃体和海马亚区的早期体积MRI研究

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摘要

Currently, autism spectrum disorder (ASD) is mainly diagnosed by the observation of core behavioral symptoms. Consequently, the window of opportunity for effective intervention may have passed, when the disorder is detected until 3 years of age. Thus, it is of great importance to identify imaging-based biomarkers for early diagnosis of ASD. Previous findings indicate that an abnormal pattern of the amygdala and hippocampal development in autism persists through childhood and adolescence. However, due to the low tissue contrast and small structural size of amygdala and hippocampal subfields, our knowledge on their growth in autistics in early stage still remains very limited. In this paper, for the first time, we propose a volume-based analysis of the amygdala and hippocampal subfields of the infant subjects with risk of ASD at around 24 months of age. Specifically, to address the challenge of low tissue contrast, we propose a novel deep-learning approach, i.e., dilated-dense U-Net, to automatically segment the amygdala and hippocampal subfields. Experimental results on National Database for Autism Research (NDAR) show the advantages of our proposed method in terms of segmentation accuracy. Our volume-based analysis shows the overgrowths of amygdala and CA1–3 of hippocampus, which may link to the emergence of autism spectrum disorder.
机译:当前,自闭症谱系障碍(ASD)主要通过观察核心行为症状来诊断。因此,当疾病被检测到3岁时,有效干预的机会之窗可能已经过去。因此,鉴定用于早期诊断ASD的基于成像的生物标志物非常重要。先前的发现表明自闭症中杏仁核和海马发育的异常模式一直持续到儿童期和青春期。但是,由于杏仁核和海马亚区的组织对比度较低且结构尺寸较小,因此我们对它们在自闭症早期阶段的生长的认识仍然非常有限。在本文中,我们首次提出了对24个月左右有ASD风险的婴儿受试者的杏仁核和海马亚区进行基于体积的分析。具体而言,为了解决组织对比度低的挑战,我们提出了一种新颖的深度学习方法,即扩张密集的U-Net,以自动分割杏仁核和海马亚区。国家自闭症研究数据库(NDAR)的实验结果显示了我们提出的方法在分割准确性方面的优势。我们基于数量的分析显示杏仁核和海马CA1-3过度生长,这可能与自闭症谱系障碍的出现有关。

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